Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22828 |
| ensemblid | ENSG00000213079.10 |
| hgncid | 20959 |
| symbol | SCAF8 |
| name | SR-related CTD associated factor 8 |
| refseq_nuc | NM_014892.5 |
| refseq_prot | NP_055707.3 |
| ensembl_nuc | ENST00000367178.8 |
| ensembl_prot | ENSP00000356146.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 154733416 |
| end | 154834221 |
| strand | + |
| ver | v1.2 |
| region | chr6:154733416-154834221 |
| region5000 | chr6:154728416-154839221 |
| regionname0 | SCAF8_chr6_154733416_154834221 |
| regionname5000 | SCAF8_chr6_154728416_154839221 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1271 | 270 | 79 | 62 | 86 | 11 | 30 | 52 | SCAF8_chr6_154728416_154839221 | SCAF8 | MEAVK others(1266): Show |
chr6 | 154728416 | 154839221 |
| a0002 | 0/0 | 1271 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | MEAVK others(1266): Show |
chr6 | 154728416 | 154839221 |
| a0003 | 0/0 | 1271 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | MEAVK others(1266): Show |
chr6 | 154728416 | 154839221 |
| a0004 | 0/0 | 1271 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | MEAVK others(1266): Show |
chr6 | 154728416 | 154839221 |
| a0005 | 0/0 | 1271 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | MEAVK others(1266): Show |
chr6 | 154728416 | 154839221 |
| a0006 | 0/0 | 1271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | MEAVK others(1266): Show |
chr6 | 154728416 | 154839221 |
| a0007 | 0/0 | 1271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | MEAVK others(1266): Show |
chr6 | 154728416 | 154839221 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3813 | 256 | 74 | 57 | 85 | 11 | 28 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0002 | 0/0 | 3813 | 6 | 0 | 5 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0006 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0008 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0011 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0012 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0013 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0014 | 0/1 | 3813 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0001c0015 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0002c0004 | 0/0 | 3813 | 3 | 2 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0003c0003 | 0/0 | 3813 | 3 | 3 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0004c0007 | 0/0 | 3813 | 2 | 1 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0005c0005 | 0/0 | 3813 | 2 | 1 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0006c0009 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 | ||
| a0007c0010 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATGGA others(3808): Show |
chr6 | 154728416 | 154839221 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5127 | 161 | 45 | 24 | 64 | 8 | 19 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0002 | 0/0 | 5127 | 69 | 20 | 24 | 18 | 2 | 5 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0003 | 0/0 | 5127 | 9 | 8 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0004 | 0/0 | 5128 | 8 | 0 | 7 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5123): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0005 | 0/0 | 5127 | 3 | 0 | 0 | 0 | 0 | 3 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0006 | 0/0 | 5113 | 2 | 0 | 0 | 2 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5108): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0007 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0008 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0009 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5110): Show |
chr6 | 154728416 | 154839221 |
| a0001c0001t0010 | 0/0 | 5128 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5123): Show |
chr6 | 154728416 | 154839221 |
| a0001c0002t0002 | 0/0 | 5127 | 6 | 0 | 5 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0006t0001 | 0/0 | 5127 | 2 | 2 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0008t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0011t0001 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0012t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0013t0002 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0014t0002 | 0/1 | 5127 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0001c0015t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0002c0004t0001 | 0/0 | 5127 | 3 | 2 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0003c0003t0002 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0004c0007t0001 | 0/0 | 5127 | 2 | 1 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0005c0005t0002 | 0/0 | 5127 | 2 | 1 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0006c0009t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| a0007c0010t0001 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | ATATT others(5122): Show |
chr6 | 154728416 | 154839221 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0009g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0001t0010g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0008t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0011t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0012t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0013t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0014t0002g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0001c0015t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0002c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0002c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0002c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0003c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0003c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0003c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0004c0007t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0004c0007t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0005c0005t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0005c0005t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0006c0009t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| a0007c0010t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0244 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | GBR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0088 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0219 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0215 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01891 | hp2 | a0001 | c0012 | t0002 | g0279 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0228 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02071 | hp2 | a0001 | c0015 | t0001 | g0109 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02145 | hp1 | a0002 | c0004 | t0001 | g0181 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02257 | hp1 | a0004 | c0007 | t0001 | g0172 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0249 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0248 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02735 | hp1 | a0002 | c0004 | t0001 | g0182 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02886 | hp1 | a0005 | c0005 | t0002 | g0256 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0144 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0221 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03195 | hp2 | a0003 | c0003 | t0002 | g0273 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0274 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03540 | hp1 | a0001 | c0008 | t0002 | g0257 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03710 | hp2 | a0001 | c0013 | t0002 | g0101 | SAS | PJL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03834 | hp1 | a0004 | c0007 | t0001 | g0134 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0191 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0209 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18522 | hp1 | a0002 | c0004 | t0001 | g0183 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18987 | hp2 | a0001 | c0001 | t0008 | g0149 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18994 | hp1 | a0006 | c0009 | t0001 | g0143 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19043 | hp1 | a0003 | c0003 | t0002 | g0272 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19088 | hp2 | a0007 | c0010 | t0001 | g0094 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ASW | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20752 | hp2 | a0005 | c0005 | t0002 | g0255 | EUR | TSI | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | USA | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| NA21309 | hp2 | a0001 | c0011 | t0001 | g0208 | AFR | LWK | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| homoSapiens | chm13v2 | a0001 | c0014 | t0002 | g0053 | REF | REF | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0031 | REF | REF | SCAF8_chr6_154728416_154839221 | SCAF8 | chr6 | 154728416 | 154839221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154808146 | A | T | 1 | a0004 | 2 | HG02257.hp1 HG03834.hp1 |
missense_variant | MODERATE | c.1058A>T | p.Gln353Leu | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/20 | 1543/5127 | 1058/3816 | 353/1271 | chr6 | 154808146 | |||
| chr6:154822368 | A | G | 1 | a0002 | 3 | HG02145.hp1 HG02735.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1885A>G | p.Thr629Ala | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/20 | 2370/5127 | 1885/3816 | 629/1271 | chr6 | 154822368 | |||
| chr6:154832173 | G | A | 1 | a0005 | 2 | HG02886.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.2594G>A | p.Ser865Asn | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 3079/5127 | 2594/3816 | 865/1271 | chr6 | 154832173 | |||
| chr6:154832706 | A | G | 1 | a0007 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.3127A>G | p.Ile1043Val | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 3612/5127 | 3127/3816 | 1043/1271 | chr6 | 154832706 | |||
| chr6:154832982 | G | A | 1 | a0006 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.3403G>A | p.Gly1135Ser | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 3888/5127 | 3403/3816 | 1135/1271 | chr6 | 154832982 | |||
| chr6:154833096 | A | G | 1 | a0003 | 3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.3517A>G | p.Met1173Val | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 4002/5127 | 3517/3816 | 1173/1271 | chr6 | 154833096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154787917 | A | G | 1 | a0001c0015 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.216A>G | p.Gln72Gln | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/20 | 701/5127 | 216/3816 | 72/1271 | chr6 | 154787917 | |||
| chr6:154808198 | A | G | 1 | a0001c0006 | 2 | HG02257.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.1110A>G | p.Gln370Gln | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/20 | 1595/5127 | 1110/3816 | 370/1271 | chr6 | 154808198 | |||
| chr6:154818577 | G | T | 1 | a0001c0013 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1620G>T | p.Gly540Gly | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/20 | 2105/5127 | 1620/3816 | 540/1271 | chr6 | 154818577 | |||
| chr6:154820179 | C | T | 1 | a0001c0002 | 6 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.1638C>T | p.Ile546Ile | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/20 | 2123/5127 | 1638/3816 | 546/1271 | chr6 | 154820179 | |||
| chr6:154820248 | A | G | 1 | a0001c0012 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1707A>G | p.Thr569Thr | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/20 | 2192/5127 | 1707/3816 | 569/1271 | chr6 | 154820248 | |||
| chr6:154820332 | T | C | 1 | a0001c0008 | 1 | HG03540.hp1 | splice_region_variant&synonymous_variant | LOW | c.1791T>C | p.Thr597Thr | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/20 | 2276/5127 | 1791/3816 | 597/1271 | chr6 | 154820332 | |||
| chr6:154824368 | A | G | 1 | a0001c0011 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2061A>G | p.Gln687Gln | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/20 | 2546/5127 | 2061/3816 | 687/1271 | chr6 | 154824368 | |||
| chr6:154831997 | G | A | 1 | a0005c0005 | 2 | HG02886.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.2418G>A | p.Val806Val | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 2903/5127 | 2418/3816 | 806/1271 | chr6 | 154831997 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154733530 | G | A | 1 | a0001c0001t0005 | 3 | HG03017.hp1 HG03942.hp1 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-371G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 371 | chr6 | 154733530 | ||||||
| chr6:154733559 | AGGGGCTA others(7): Show |
A | 1 | a0001c0001t0006 | 2 | NA18994.hp2 NA19065.hp1 |
5_prime_UTR_variant | MODIFIER | c.-337_-324delCTAGAG others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 324 | INFO_REALIGN_3_PRIME | chr6 | 154733559 | |||||
| chr6:154733681 | T | C | 1 | a0001c0001t0003 | 9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-220T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 220 | chr6 | 154733681 | ||||||
| chr6:154733742 | G | A | 1 | a0001c0001t0007 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 159 | chr6 | 154733742 | ||||||
| chr6:154733815 | G | A | 1 | a0001c0001t0008 | 1 | NA18987.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 86 | chr6 | 154733815 | ||||||
| chr6:154733854 | GCCGCCGC others(5): Show |
G | 1 | a0001c0001t0009 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38_-27delTCTTCCGC others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/20 | 27 | INFO_REALIGN_3_PRIME | chr6 | 154733854 | |||||
| chr6:154833581 | A | G | 1 | a0001c0001t0010 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 186 | chr6 | 154833581 | ||||||
| chr6:154833905 | C | T | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(7): Show |
95 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*510C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 510 | chr6 | 154833905 | ||||||
| chr6:154833961 | T | TA | 2 | a0001c0001t0004 a0001c0001t0010 |
9 | HG00099.hp1 HG01081.hp1 HG01255.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*572dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 20/20 | 573 | INFO_REALIGN_3_PRIME | chr6 | 154833961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:154734183 | C | T | 8 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+253C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734183 | |||||||
| chr6:154734185 | A | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+255A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734185 | |||||||
| chr6:154734189 | C | T | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+259C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734189 | |||||||
| chr6:154734227 | C | G | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+297C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734227 | |||||||
| chr6:154734232 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+302C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734232 | |||||||
| chr6:154734287 | C | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+357C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734287 | |||||||
| chr6:154734301 | A | T | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.30+371A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734301 | |||||||
| chr6:154734403 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+473G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734403 | |||||||
| chr6:154734419 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18960.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.30+489G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734419 | |||||||
| chr6:154734470 | G | A | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | NA18951.hp2 NA18993.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+540G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734470 | |||||||
| chr6:154734615 | C | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0002 |
2 | HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.30+685C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734615 | |||||||
| chr6:154734622 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.30+692C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734622 | |||||||
| chr6:154734993 | A | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+1063A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154734993 | |||||||
| chr6:154735024 | T | C | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+1094T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735024 | |||||||
| chr6:154735035 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.30+1105A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735035 | |||||||
| chr6:154735038 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+1108C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735038 | |||||||
| chr6:154735108 | AG | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG00438.hp1 HG02040.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.30+1179delG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735108 | |||||||
| chr6:154735120 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+1190T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735120 | |||||||
| chr6:154735123 | A | C | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+1193A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735123 | |||||||
| chr6:154735124 | C | CA | 13 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(10): Show |
13 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+1208dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154735124 | ||||||
| chr6:154735206 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+1276A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735206 | |||||||
| chr6:154735402 | T | C | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.30+1472T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735402 | |||||||
| chr6:154735422 | A | G | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+1492A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735422 | |||||||
| chr6:154735519 | C | CT | 136 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(133): Show |
136 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.30+1605dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154735519 | ||||||
| chr6:154735519 | C | CTT | 70 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0193 others(67): Show |
70 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.30+1604_30+1605dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154735519 | ||||||
| chr6:154735519 | C | CTTT | 5 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG02922.hp1 NA18998.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+1603_30+1605dup others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154735519 | ||||||
| chr6:154735554 | T | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+1624T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735554 | |||||||
| chr6:154735575 | A | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+1645A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735575 | |||||||
| chr6:154735726 | C | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+1796C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735726 | |||||||
| chr6:154735908 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01070.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.30+1978C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735908 | |||||||
| chr6:154735915 | C | T | 5 | a0001c0001t0001g0180 a0001c0001t0001g0184 a0002c0004t0001g0181 others(2): Show |
5 | HG02145.hp1 HG02735.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+1985C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735915 | |||||||
| chr6:154735919 | C | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+1989C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735919 | |||||||
| chr6:154735986 | T | C | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.30+2056T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154735986 | |||||||
| chr6:154736176 | A | AC | 22 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0091 others(19): Show |
22 | HG00621.hp2 HG00733.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.30+2249dupC | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736176 | ||||||
| chr6:154736180 | T | C | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.30+2250T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736180 | |||||||
| chr6:154736265 | C | CT | 168 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(165): Show |
168 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.30+2356dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | ||||||
| chr6:154736265 | C | CTT | 30 | a0001c0001t0001g0100 a0001c0001t0001g0168 a0001c0001t0001g0169 others(27): Show |
30 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.30+2355_30+2356dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | ||||||
| chr6:154736265 | CT | C | 8 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(5): Show |
8 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+2356delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | ||||||
| chr6:154736265 | CTTTT | C | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+2353_30+2356del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | ||||||
| chr6:154736265 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.30+2345_30+2356del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736265 | ||||||
| chr6:154736346 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+2416A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736346 | |||||||
| chr6:154736394 | C | T | 6 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(3): Show |
6 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+2464C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736394 | |||||||
| chr6:154736518 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.30+2588C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736518 | |||||||
| chr6:154736563 | C | T | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.30+2633C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736563 | |||||||
| chr6:154736634 | A | G | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+2704A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736634 | |||||||
| chr6:154736738 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+2808C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736738 | |||||||
| chr6:154736740 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+2810G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736740 | |||||||
| chr6:154736773 | T | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+2843T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736773 | |||||||
| chr6:154736788 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.30+2858T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736788 | |||||||
| chr6:154736849 | CTTAT | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0015t0001g0109 |
3 | HG00408.hp1 HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.30+2928_30+2931del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154736849 | ||||||
| chr6:154736953 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+3023A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736953 | |||||||
| chr6:154736974 | T | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+3044T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154736974 | |||||||
| chr6:154737097 | G | T | 13 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 others(10): Show |
13 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+3167G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737097 | |||||||
| chr6:154737285 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+3355A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737285 | |||||||
| chr6:154737323 | TAGCTCTA others(9): Show |
T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+3396_30+3411del others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154737323 | ||||||
| chr6:154737403 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.30+3473C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737403 | |||||||
| chr6:154737427 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0110 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+3497T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737427 | |||||||
| chr6:154737504 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+3574C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737504 | |||||||
| chr6:154737536 | T | G | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+3606T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737536 | |||||||
| chr6:154737573 | A | T | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.30+3643A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737573 | |||||||
| chr6:154737663 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.30+3733C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737663 | |||||||
| chr6:154737711 | G | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+3781G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737711 | |||||||
| chr6:154737805 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.30+3875A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737805 | |||||||
| chr6:154737813 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.30+3883G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737813 | |||||||
| chr6:154737885 | A | G | 5 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | NA18951.hp2 NA18993.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+3955A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737885 | |||||||
| chr6:154737916 | T | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02602.hp1 HG02735.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+3986T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737916 | |||||||
| chr6:154737945 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4015C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154737945 | |||||||
| chr6:154738106 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.30+4176G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738106 | |||||||
| chr6:154738165 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+4235T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738165 | |||||||
| chr6:154738210 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+4280G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738210 | |||||||
| chr6:154738291 | A | C | 1 | a0001c0001t0004g0244 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.30+4361A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738291 | |||||||
| chr6:154738304 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.30+4374G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738304 | |||||||
| chr6:154738580 | G | A | 1 | a0001c0001t0002g0008 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+4650G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738580 | |||||||
| chr6:154738606 | A | G | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+4676A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738606 | |||||||
| chr6:154738714 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.30+4784A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738714 | |||||||
| chr6:154738880 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.30+4950A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738880 | |||||||
| chr6:154738995 | G | T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG00438.hp1 HG02040.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.30+5065G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154738995 | |||||||
| chr6:154739001 | A | G | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+5071A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739001 | |||||||
| chr6:154739033 | T | C | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+5103T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739033 | |||||||
| chr6:154739098 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+5168G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739098 | |||||||
| chr6:154739294 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.30+5364A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739294 | |||||||
| chr6:154739317 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+5387T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739317 | |||||||
| chr6:154739402 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.30+5472C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739402 | |||||||
| chr6:154739454 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30+5524T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739454 | |||||||
| chr6:154739515 | T | C | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0116 others(2): Show |
5 | HG00642.hp1 HG01358.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+5585T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739515 | |||||||
| chr6:154739627 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.30+5697G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739627 | |||||||
| chr6:154739654 | C | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0187 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+5724C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739654 | |||||||
| chr6:154739858 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+5928A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154739858 | |||||||
| chr6:154740107 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+6177T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740107 | |||||||
| chr6:154740301 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.30+6371T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740301 | |||||||
| chr6:154740524 | A | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+6594A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740524 | |||||||
| chr6:154740602 | ATTTTCTT others(5): Show |
A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+6689_30+6700del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154740602 | ||||||
| chr6:154740625 | C | CT | 97 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0085 others(94): Show |
97 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.30+6709dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154740625 | ||||||
| chr6:154740625 | C | CTT | 89 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.30+6708_30+6709dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154740625 | ||||||
| chr6:154740772 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+6842C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740772 | |||||||
| chr6:154740810 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+6880G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154740810 | |||||||
| chr6:154741081 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.30+7151G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741081 | |||||||
| chr6:154741093 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+7163C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741093 | |||||||
| chr6:154741151 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.30+7221T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741151 | |||||||
| chr6:154741294 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.30+7364G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741294 | |||||||
| chr6:154741596 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.30+7666G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741596 | |||||||
| chr6:154741649 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.30+7719C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741649 | |||||||
| chr6:154741653 | C | T | 1 | a0001c0001t0002g0010 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.30+7723C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741653 | |||||||
| chr6:154741669 | A | T | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+7739A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741669 | |||||||
| chr6:154741670 | G | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+7740G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741670 | |||||||
| chr6:154741697 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.30+7767G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741697 | |||||||
| chr6:154741702 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG02015.hp1 HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.30+7772C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741702 | |||||||
| chr6:154741730 | G | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.30+7800G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154741730 | |||||||
| chr6:154742076 | G | A | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.30+8146G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742076 | |||||||
| chr6:154742156 | T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+8226T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742156 | |||||||
| chr6:154742233 | A | G | 6 | a0001c0001t0001g0098 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+8303A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742233 | |||||||
| chr6:154742506 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.30+8576A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742506 | |||||||
| chr6:154742649 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.30+8719T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742649 | |||||||
| chr6:154742742 | CTTTA | C | 205 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.30+8819_30+8822del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154742742 | ||||||
| chr6:154742833 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.30+8903A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742833 | |||||||
| chr6:154742914 | C | T | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+8984C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742914 | |||||||
| chr6:154742925 | T | C | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.30+8995T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154742925 | |||||||
| chr6:154742953 | A | AT | 157 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.30+9032dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154742953 | ||||||
| chr6:154743541 | G | A | 223 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.30+9611G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154743541 | |||||||
| chr6:154743662 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+9732C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154743662 | |||||||
| chr6:154743945 | A | C | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+10015A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154743945 | |||||||
| chr6:154743979 | AATTTACC others(4): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+10055_30+10065d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154743979 | ||||||
| chr6:154744145 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.30+10215T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744145 | |||||||
| chr6:154744215 | C | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+10285C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744215 | |||||||
| chr6:154744485 | C | T | 2 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
2 | HG01496.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.30+10555C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744485 | |||||||
| chr6:154744768 | C | A | 221 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.30+10838C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744768 | |||||||
| chr6:154744768 | C | G | 2 | a0003c0003t0002g0273 a0003c0003t0002g0274 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.30+10838C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744768 | |||||||
| chr6:154744928 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+10998G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744928 | |||||||
| chr6:154744972 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.30+11042G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154744972 | |||||||
| chr6:154745111 | C | A | 1 | a0001c0001t0002g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.30+11181C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745111 | |||||||
| chr6:154745138 | G | A | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+11208G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745138 | |||||||
| chr6:154745206 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.30+11276T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745206 | |||||||
| chr6:154745381 | T | A | 56 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(53): Show |
56 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.30+11451T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745381 | |||||||
| chr6:154745407 | TC | T | 11 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(8): Show |
11 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+11478delC | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745407 | |||||||
| chr6:154745545 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+11615T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745545 | |||||||
| chr6:154745570 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+11640G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745570 | |||||||
| chr6:154745811 | T | G | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+11881T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745811 | |||||||
| chr6:154745894 | T | C | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.30+11964T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745894 | |||||||
| chr6:154745976 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0184 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.30+12046C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154745976 | |||||||
| chr6:154746126 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+12196T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746126 | |||||||
| chr6:154746176 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.30+12246G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746176 | |||||||
| chr6:154746192 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0174 |
2 | HG00621.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.30+12262A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746192 | |||||||
| chr6:154746392 | A | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+12462A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746392 | |||||||
| chr6:154746431 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30+12501T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746431 | |||||||
| chr6:154746491 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+12561A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746491 | |||||||
| chr6:154746536 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.30+12606C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746536 | |||||||
| chr6:154746654 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0247 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+12724G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746654 | |||||||
| chr6:154746657 | A | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0247 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+12727A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746657 | |||||||
| chr6:154746659 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0247 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+12729C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746659 | |||||||
| chr6:154746699 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+12769T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154746699 | |||||||
| chr6:154747258 | A | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+13328A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747258 | |||||||
| chr6:154747410 | G | C | 10 | a0001c0001t0002g0012 a0001c0001t0002g0017 a0001c0001t0002g0018 others(7): Show |
10 | HG00597.hp1 HG00673.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+13480G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747410 | |||||||
| chr6:154747419 | G | A | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.30+13489G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747419 | |||||||
| chr6:154747432 | T | G | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+13502T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747432 | |||||||
| chr6:154747624 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.30+13694C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747624 | |||||||
| chr6:154747646 | C | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+13716C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747646 | |||||||
| chr6:154747666 | T | C | 9 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(6): Show |
9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+13736T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747666 | |||||||
| chr6:154747702 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.30+13772T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747702 | |||||||
| chr6:154747764 | T | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13834T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747764 | |||||||
| chr6:154747896 | C | CTATG | 4 | a0001c0001t0002g0072 a0001c0001t0002g0075 a0001c0001t0002g0276 others(1): Show |
4 | HG00621.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13967_30+13968i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | C | CTATGTG | 9 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0078 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+13967_30+13968i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | C | CTG | 43 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0093 others(40): Show |
43 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.30+14006_30+14007d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | C | CTGTG | 17 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0098 others(14): Show |
17 | HG00642.hp1 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.30+14004_30+14007d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | C | CTGTGTG | 15 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0099 others(12): Show |
15 | HG00558.hp1 HG01070.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+14002_30+14007d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | C | CTGTGTGT others(1): Show |
6 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00597.hp2 HG01256.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+14000_30+14007d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.30+13998_30+14007d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0196 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.30+13996_30+14007d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTG | C | 44 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0102 others(41): Show |
44 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.30+14006_30+14007d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTGTG | C | 18 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0001g0124 others(15): Show |
18 | HG00544.hp2 HG00673.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+14004_30+14007d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTGTGTG | C | 57 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0097 others(54): Show |
57 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+14002_30+14007d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTGTGTGT others(1): Show |
C | 9 | a0001c0001t0001g0180 a0001c0001t0001g0184 a0001c0001t0005g0144 others(6): Show |
9 | HG02145.hp1 HG03017.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+14000_30+14007d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTGTGTGT others(3): Show |
C | 1 | a0002c0004t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.30+13998_30+14007d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0167 |
2 | HG02717.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.30+13996_30+14007d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTGTGTGT others(7): Show |
C | 5 | a0001c0001t0003g0084 a0001c0001t0003g0267 a0001c0001t0003g0268 others(2): Show |
5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+13994_30+14007d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747896 | CTGTGTGT others(9): Show |
C | 5 | a0001c0001t0002g0026 a0001c0001t0003g0080 a0001c0001t0003g0081 others(2): Show |
5 | HG02129.hp1 HG02258.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+13992_30+14007d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154747896 | ||||||
| chr6:154747900 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.30+13970G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154747900 | |||||||
| chr6:154748008 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.30+14078T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748008 | |||||||
| chr6:154748108 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.30+14178G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748108 | |||||||
| chr6:154748462 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+14532A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748462 | |||||||
| chr6:154748525 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0110 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+14595G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748525 | |||||||
| chr6:154748727 | T | G | 1 | a0001c0001t0002g0018 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.30+14797T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748727 | |||||||
| chr6:154748814 | A | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0247 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.30+14884A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154748814 | |||||||
| chr6:154749025 | T | G | 4 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0051 others(1): Show |
4 | HG00642.hp2 HG01123.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+15095T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749025 | |||||||
| chr6:154749092 | G | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+15162G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749092 | |||||||
| chr6:154749123 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.30+15193G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749123 | |||||||
| chr6:154749175 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.30+15245C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749175 | |||||||
| chr6:154749188 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.30+15258G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749188 | |||||||
| chr6:154749231 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0001g0247 a0001c0011t0001g0208 |
3 | HG03098.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.30+15301G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749231 | |||||||
| chr6:154749247 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.30+15317C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749247 | |||||||
| chr6:154749494 | T | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00558.hp1 HG03942.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+15564T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749494 | |||||||
| chr6:154749614 | G | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02723.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+15684G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749614 | |||||||
| chr6:154749654 | A | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+15724A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749654 | |||||||
| chr6:154749673 | G | A | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+15743G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749673 | |||||||
| chr6:154749693 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
3 | HG02451.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.30+15763G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749693 | |||||||
| chr6:154749712 | G | C | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+15782G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154749712 | |||||||
| chr6:154750018 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.30+16088G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750018 | |||||||
| chr6:154750251 | T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+16321T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750251 | |||||||
| chr6:154750298 | A | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.30+16368A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750298 | |||||||
| chr6:154750380 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+16450G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750380 | |||||||
| chr6:154750434 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+16504T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750434 | |||||||
| chr6:154750453 | T | G | 17 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0167 others(14): Show |
17 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.30+16523T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750453 | |||||||
| chr6:154750631 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.30+16701A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750631 | |||||||
| chr6:154750886 | T | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.30+16956T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750886 | |||||||
| chr6:154750954 | T | C | 1 | a0001c0001t0010g0088 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.30+17024T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154750954 | |||||||
| chr6:154751033 | T | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0264 |
2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.30+17103T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751033 | |||||||
| chr6:154751186 | G | A | 86 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.30+17256G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751186 | |||||||
| chr6:154751269 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+17339C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751269 | |||||||
| chr6:154751301 | T | C | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17371T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751301 | |||||||
| chr6:154751309 | A | C | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17379A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751309 | |||||||
| chr6:154751854 | T | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0110 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.30+17924T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154751854 | |||||||
| chr6:154752029 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.30+18099C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752029 | |||||||
| chr6:154752072 | T | G | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.30+18142T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752072 | |||||||
| chr6:154752098 | T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30+18168T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752098 | |||||||
| chr6:154752154 | C | G | 5 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0046 others(2): Show |
5 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+18224C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752154 | |||||||
| chr6:154752422 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+18492C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752422 | |||||||
| chr6:154752423 | T | C | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.30+18493T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752423 | |||||||
| chr6:154752523 | C | T | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+18593C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752523 | |||||||
| chr6:154752729 | T | C | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+18799T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752729 | |||||||
| chr6:154752978 | G | C | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.30+19048G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154752978 | |||||||
| chr6:154753012 | G | GT | 7 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(4): Show |
7 | HG02055.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.30+19093dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154753012 | ||||||
| chr6:154753016 | T | TG | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.30+19086_30+19087i others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753016 | |||||||
| chr6:154753050 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.30+19120C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753050 | |||||||
| chr6:154753158 | G | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+19228G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753158 | |||||||
| chr6:154753371 | T | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.30+19441T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753371 | |||||||
| chr6:154753382 | G | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.30+19452G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753382 | |||||||
| chr6:154753502 | A | G | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+19572A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753502 | |||||||
| chr6:154753532 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.30+19602G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753532 | |||||||
| chr6:154753671 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.30+19741T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753671 | |||||||
| chr6:154753954 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.30+20024C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753954 | |||||||
| chr6:154753984 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0008t0002g0257 |
3 | HG01070.hp1 HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.31-20005C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154753984 | |||||||
| chr6:154754042 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.31-19947G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754042 | |||||||
| chr6:154754087 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.31-19902A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754087 | |||||||
| chr6:154754321 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-19668C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754321 | |||||||
| chr6:154754377 | G | A | 1 | a0001c0001t0009g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-19612G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754377 | |||||||
| chr6:154754472 | A | G | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-19517A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754472 | |||||||
| chr6:154754524 | G | A | 11 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-19465G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754524 | |||||||
| chr6:154754716 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.31-19273T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754716 | |||||||
| chr6:154754794 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-19195T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754794 | |||||||
| chr6:154754797 | T | C | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-19192T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754797 | |||||||
| chr6:154754835 | T | A | 2 | a0003c0003t0002g0273 a0003c0003t0002g0274 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.31-19154T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754835 | |||||||
| chr6:154754859 | C | G | 1 | a0001c0001t0002g0008 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.31-19130C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754859 | |||||||
| chr6:154754886 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.31-19103A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754886 | |||||||
| chr6:154754958 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31-19031T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754958 | |||||||
| chr6:154754959 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31-19030C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154754959 | |||||||
| chr6:154755013 | G | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.31-18976G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755013 | |||||||
| chr6:154755081 | A | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-18908A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755081 | |||||||
| chr6:154755349 | G | A | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.31-18640G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755349 | |||||||
| chr6:154755367 | T | C | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-18622T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755367 | |||||||
| chr6:154755414 | C | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-18575C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755414 | |||||||
| chr6:154755489 | G | A | 185 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.31-18500G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755489 | |||||||
| chr6:154755502 | C | T | 1 | a0002c0004t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.31-18487C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755502 | |||||||
| chr6:154755503 | G | A | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-18486G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755503 | |||||||
| chr6:154755503 | G | C | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-18486G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755503 | |||||||
| chr6:154755529 | A | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-18460A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755529 | |||||||
| chr6:154755596 | A | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-18393A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755596 | |||||||
| chr6:154755719 | C | T | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-18270C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755719 | |||||||
| chr6:154755892 | C | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-18097C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755892 | |||||||
| chr6:154755894 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.31-18095C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755894 | |||||||
| chr6:154755941 | G | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-18048G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154755941 | |||||||
| chr6:154756017 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31-17972A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756017 | |||||||
| chr6:154756075 | A | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0263 |
2 | HG01515.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.31-17914A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756075 | |||||||
| chr6:154756238 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-17751C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756238 | |||||||
| chr6:154756727 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.31-17262A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756727 | |||||||
| chr6:154756737 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-17252G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756737 | |||||||
| chr6:154756749 | G | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-17240G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756749 | |||||||
| chr6:154756831 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.31-17158C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756831 | |||||||
| chr6:154756835 | C | T | 9 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0111 others(6): Show |
9 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-17154C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756835 | |||||||
| chr6:154756848 | A | G | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-17141A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756848 | |||||||
| chr6:154756857 | G | A | 1 | a0001c0002t0002g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.31-17132G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756857 | |||||||
| chr6:154756933 | T | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | NA18951.hp2 NA18993.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-17056T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756933 | |||||||
| chr6:154756939 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-17050G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154756939 | |||||||
| chr6:154757088 | C | T | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-16901C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757088 | |||||||
| chr6:154757315 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31-16674C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757315 | |||||||
| chr6:154757360 | G | C | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-16629G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757360 | |||||||
| chr6:154757507 | C | T | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-16482C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757507 | |||||||
| chr6:154757863 | C | T | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-16126C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757863 | |||||||
| chr6:154757909 | C | CT | 5 | a0001c0001t0001g0140 a0001c0001t0001g0245 a0001c0001t0002g0030 others(2): Show |
5 | HG00544.hp1 HG00741.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-16061dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154757909 | ||||||
| chr6:154757914 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-16075T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757914 | |||||||
| chr6:154757950 | A | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-16039A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154757950 | |||||||
| chr6:154758033 | C | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-15956C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758033 | |||||||
| chr6:154758174 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-15815A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758174 | |||||||
| chr6:154758236 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-15753A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758236 | |||||||
| chr6:154758267 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31-15722A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758267 | |||||||
| chr6:154758329 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.31-15660C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758329 | |||||||
| chr6:154758335 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.31-15654C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758335 | |||||||
| chr6:154758451 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.31-15538A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758451 | |||||||
| chr6:154758462 | T | C | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-15527T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758462 | |||||||
| chr6:154758508 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.31-15481G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758508 | |||||||
| chr6:154758531 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31-15458C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758531 | |||||||
| chr6:154758551 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-15438A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758551 | |||||||
| chr6:154758611 | C | CT | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-15372dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154758611 | ||||||
| chr6:154758978 | A | C | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-15011A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154758978 | |||||||
| chr6:154759104 | T | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0278 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.31-14885T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759104 | |||||||
| chr6:154759125 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.31-14864C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759125 | |||||||
| chr6:154759483 | G | A | 4 | a0004c0007t0001g0134 a0004c0007t0001g0172 a0005c0005t0002g0255 others(1): Show |
4 | HG02257.hp1 HG02886.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-14506G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759483 | |||||||
| chr6:154759505 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.31-14484A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759505 | |||||||
| chr6:154759664 | A | AT | 153 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(150): Show |
153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.31-14307dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154759664 | ||||||
| chr6:154759664 | AT | A | 32 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(29): Show |
32 | HG00621.hp2 HG01109.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-14307delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154759664 | ||||||
| chr6:154759767 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.31-14222G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759767 | |||||||
| chr6:154759831 | A | G | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-14158A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759831 | |||||||
| chr6:154759849 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-14140A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759849 | |||||||
| chr6:154759987 | G | A | 9 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(6): Show |
9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-14002G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154759987 | |||||||
| chr6:154760029 | C | T | 205 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.31-13960C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760029 | |||||||
| chr6:154760087 | T | TA | 9 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(6): Show |
9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-13899dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154760087 | ||||||
| chr6:154760512 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.31-13477G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760512 | |||||||
| chr6:154760563 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.31-13426A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760563 | |||||||
| chr6:154760713 | GT | G | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-13268delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154760713 | ||||||
| chr6:154760839 | A | G | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-13150A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760839 | |||||||
| chr6:154760974 | T | A | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-13015T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760974 | |||||||
| chr6:154760985 | A | G | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0250 others(1): Show |
4 | NA18983.hp1 NA18998.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-13004A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154760985 | |||||||
| chr6:154761067 | G | T | 8 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0136 others(5): Show |
8 | HG00140.hp1 HG00733.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-12922G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761067 | |||||||
| chr6:154761164 | C | A | 1 | a0001c0001t0002g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31-12825C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761164 | |||||||
| chr6:154761311 | C | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-12678C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761311 | |||||||
| chr6:154761523 | T | C | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-12466T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761523 | |||||||
| chr6:154761540 | C | T | 1 | a0001c0001t0002g0017 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.31-12449C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761540 | |||||||
| chr6:154761668 | A | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-12321A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761668 | |||||||
| chr6:154761845 | C | G | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.31-12144C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154761845 | |||||||
| chr6:154762090 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-11899A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762090 | |||||||
| chr6:154762123 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-11866C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762123 | |||||||
| chr6:154762183 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.31-11806A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762183 | |||||||
| chr6:154762213 | T | G | 1 | a0001c0001t0003g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.31-11776T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762213 | |||||||
| chr6:154762585 | A | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-11404A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762585 | |||||||
| chr6:154762687 | A | G | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-11302A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762687 | |||||||
| chr6:154762755 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0264 |
2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.31-11234T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762755 | |||||||
| chr6:154762898 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31-11091T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762898 | |||||||
| chr6:154762921 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.31-11068T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154762921 | |||||||
| chr6:154763135 | C | G | 214 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.31-10854C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763135 | |||||||
| chr6:154763251 | T | C | 169 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.31-10738T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763251 | |||||||
| chr6:154763274 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.31-10715T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763274 | |||||||
| chr6:154763289 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-10700T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763289 | |||||||
| chr6:154763310 | T | C | 2 | a0003c0003t0002g0273 a0003c0003t0002g0274 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.31-10679T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763310 | |||||||
| chr6:154763311 | C | T | 279 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.31-10678C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763311 | |||||||
| chr6:154763411 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.31-10578T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763411 | |||||||
| chr6:154763759 | A | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-10230A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763759 | |||||||
| chr6:154763793 | C | G | 168 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.31-10196C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763793 | |||||||
| chr6:154763960 | G | A | 223 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.31-10029G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154763960 | |||||||
| chr6:154764067 | T | C | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-9922T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764067 | |||||||
| chr6:154764100 | A | G | 5 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9889A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764100 | |||||||
| chr6:154764142 | T | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9847T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764142 | |||||||
| chr6:154764277 | C | CT | 200 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.31-9698dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154764277 | ||||||
| chr6:154764340 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.31-9649A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764340 | |||||||
| chr6:154764385 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.31-9604A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764385 | |||||||
| chr6:154764519 | A | C | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31-9470A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764519 | |||||||
| chr6:154764761 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.31-9228A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764761 | |||||||
| chr6:154764797 | T | G | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31-9192T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154764797 | |||||||
| chr6:154765019 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-8970G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765019 | |||||||
| chr6:154765099 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31-8890A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765099 | |||||||
| chr6:154765104 | C | G | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31-8885C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765104 | |||||||
| chr6:154765186 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.31-8803C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765186 | |||||||
| chr6:154765459 | T | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-8530T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765459 | |||||||
| chr6:154765504 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-8485C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765504 | |||||||
| chr6:154765540 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0236 |
2 | HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.31-8449G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765540 | |||||||
| chr6:154765632 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.31-8357C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765632 | |||||||
| chr6:154765700 | A | ATTAT | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-8285_31-8282dup others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154765700 | ||||||
| chr6:154765943 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.31-8046A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154765943 | |||||||
| chr6:154766041 | A | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-7948A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766041 | |||||||
| chr6:154766052 | A | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0206 |
3 | HG00609.hp1 HG02155.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.31-7937A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766052 | |||||||
| chr6:154766061 | TTAAAG | T | 47 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0156 others(44): Show |
47 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.31-7924_31-7920del others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766061 | ||||||
| chr6:154766068 | A | G | 1 | a0001c0001t0004g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31-7921A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766068 | |||||||
| chr6:154766083 | GTTA | G | 89 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.31-7902_31-7900del others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766083 | ||||||
| chr6:154766100 | C | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-7889C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766100 | |||||||
| chr6:154766123 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-7866A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766123 | |||||||
| chr6:154766428 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-7561C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766428 | |||||||
| chr6:154766659 | AC | A | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-7320delC | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766659 | ||||||
| chr6:154766668 | C | CT | 4 | a0001c0001t0001g0163 a0001c0001t0001g0239 a0001c0001t0001g0265 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7321_31-7320ins others(1): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766668 | |||||||
| chr6:154766668 | C | CTT | 5 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0148 others(2): Show |
5 | HG02602.hp1 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-7321_31-7320ins others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766668 | |||||||
| chr6:154766668 | C | T | 2 | a0001c0001t0001g0162 a0001c0013t0002g0101 |
2 | HG03209.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.31-7321C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766668 | |||||||
| chr6:154766669 | C | CCT | 32 | a0001c0001t0001g0097 a0001c0001t0001g0178 a0001c0001t0001g0179 others(29): Show |
32 | HG00621.hp2 HG01123.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-7320_31-7319ins others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766669 | |||||||
| chr6:154766669 | C | CT | 51 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0091 others(48): Show |
51 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.31-7305dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766669 | ||||||
| chr6:154766669 | C | CTT | 18 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0001t0001g0151 others(15): Show |
18 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-7306_31-7305dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766669 | ||||||
| chr6:154766669 | C | CTTT | 60 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(57): Show |
60 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.31-7307_31-7305dup others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154766669 | ||||||
| chr6:154766669 | C | T | 15 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0148 others(12): Show |
15 | HG01109.hp1 HG02486.hp2 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-7320C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766669 | |||||||
| chr6:154766670 | T | C | 1 | a0001c0001t0006g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.31-7319T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766670 | |||||||
| chr6:154766708 | A | T | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-7281A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766708 | |||||||
| chr6:154766749 | A | C | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-7240A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766749 | |||||||
| chr6:154766828 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-7161G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766828 | |||||||
| chr6:154766855 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-7134C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766855 | |||||||
| chr6:154766932 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-7057G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154766932 | |||||||
| chr6:154767376 | A | AT | 5 | a0001c0001t0001g0105 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG00438.hp2 HG03834.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-6600dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767376 | ||||||
| chr6:154767481 | G | A | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-6508G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767481 | |||||||
| chr6:154767507 | C | T | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-6482C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767507 | |||||||
| chr6:154767529 | C | CT | 5 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0267 others(2): Show |
5 | HG01109.hp1 HG02258.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-6433dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | ||||||
| chr6:154767529 | CT | C | 49 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(46): Show |
49 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.31-6433delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | ||||||
| chr6:154767529 | CTT | C | 11 | a0001c0001t0002g0011 a0001c0001t0002g0033 a0001c0001t0002g0072 others(8): Show |
11 | HG00621.hp2 HG01106.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-6434_31-6433del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | ||||||
| chr6:154767529 | CTTT | C | 32 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0167 others(29): Show |
32 | HG01123.hp1 HG01167.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-6435_31-6433del others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | ||||||
| chr6:154767529 | CTTTTTTT others(3): Show |
C | 166 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.31-6442_31-6433del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154767529 | ||||||
| chr6:154767657 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-6332A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767657 | |||||||
| chr6:154767911 | A | T | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.31-6078A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767911 | |||||||
| chr6:154767971 | C | G | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31-6018C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154767971 | |||||||
| chr6:154768015 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31-5974T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768015 | |||||||
| chr6:154768336 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-5653T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768336 | |||||||
| chr6:154768483 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | NA18993.hp2 NA19088.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.31-5506A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768483 | |||||||
| chr6:154768492 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-5497G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768492 | |||||||
| chr6:154768578 | C | G | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.31-5411C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154768578 | |||||||
| chr6:154769036 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.31-4953G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769036 | |||||||
| chr6:154769044 | C | G | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-4945C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769044 | |||||||
| chr6:154769060 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31-4929C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769060 | |||||||
| chr6:154769062 | CA | C | 56 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(53): Show |
56 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.31-4903delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | ||||||
| chr6:154769062 | CAA | C | 14 | a0001c0001t0001g0105 a0001c0001t0001g0166 a0001c0001t0001g0178 others(11): Show |
14 | HG00642.hp2 HG01169.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-4904_31-4903del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | ||||||
| chr6:154769062 | CAAA | C | 106 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0085 others(103): Show |
106 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.31-4905_31-4903del others(3): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | ||||||
| chr6:154769062 | CAAAA | C | 84 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(81): Show |
84 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.31-4906_31-4903del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154769062 | ||||||
| chr6:154769063 | A | C | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.31-4926A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769063 | |||||||
| chr6:154769201 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-4788G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769201 | |||||||
| chr6:154769628 | G | A | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4361G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154769628 | |||||||
| chr6:154770074 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-3915G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770074 | |||||||
| chr6:154770101 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-3888G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770101 | |||||||
| chr6:154770210 | G | T | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-3779G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770210 | |||||||
| chr6:154770276 | A | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3713A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770276 | |||||||
| chr6:154770334 | T | C | 194 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.31-3655T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770334 | |||||||
| chr6:154770339 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0238 |
2 | NA18949.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.31-3650C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770339 | |||||||
| chr6:154770386 | ACACTCTC others(7): Show |
A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0118 |
3 | HG01074.hp2 HG02647.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.31-3601_31-3588del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770386 | ||||||
| chr6:154770388 | A | ACACACTC others(23): Show |
1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.31-3600_31-3599ins others(30): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | A | ACACACTC others(51): Show |
1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.31-3600_31-3599ins others(58): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | A | ACT | 8 | a0001c0001t0002g0012 a0001c0001t0002g0017 a0001c0001t0002g0018 others(5): Show |
8 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-3566_31-3565dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | A | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(5): Show |
8 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-3601A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770388 | |||||||
| chr6:154770388 | ACTCT | A | 8 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0015 others(5): Show |
8 | HG00642.hp2 HG01123.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-3568_31-3565del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | ACTCTCT | A | 7 | a0001c0001t0002g0195 a0001c0001t0003g0080 a0001c0001t0003g0081 others(4): Show |
7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-3570_31-3565del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | ACTCTCTC others(3): Show |
A | 14 | a0001c0001t0002g0073 a0001c0001t0002g0075 a0001c0001t0002g0076 others(11): Show |
14 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-3574_31-3565del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | ACTCTCTC others(5): Show |
A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG00558.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-3576_31-3565del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | ACTCTCTC others(7): Show |
A | 173 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.31-3578_31-3565del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | ACTCTCTC others(11): Show |
A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0239 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.31-3582_31-3565del others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770388 | ACTCTCTC others(13): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.31-3584_31-3565del others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154770388 | ||||||
| chr6:154770390 | T | A | 4 | a0001c0008t0002g0257 a0003c0003t0002g0272 a0003c0003t0002g0273 others(1): Show |
4 | HG03195.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3599T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770390 | |||||||
| chr6:154770392 | T | A | 2 | a0003c0003t0002g0272 a0003c0003t0002g0274 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-3597T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770392 | |||||||
| chr6:154770396 | T | A | 2 | a0001c0001t0002g0195 a0001c0013t0002g0101 |
2 | HG02717.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.31-3593T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770396 | |||||||
| chr6:154770398 | T | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-3591T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770398 | |||||||
| chr6:154770400 | T | A | 8 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-3589T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770400 | |||||||
| chr6:154770402 | T | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0265 a0001c0001t0001g0271 others(1): Show |
4 | HG00558.hp2 HG02723.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3587T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770402 | |||||||
| chr6:154770404 | T | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG00609.hp2 HG02040.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.31-3585T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770404 | |||||||
| chr6:154770425 | A | C | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.31-3564A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770425 | |||||||
| chr6:154770457 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.31-3532G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770457 | |||||||
| chr6:154770537 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-3452C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770537 | |||||||
| chr6:154770540 | C | T | 1 | a0001c0002t0002g0050 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.31-3449C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770540 | |||||||
| chr6:154770816 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-3173C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770816 | |||||||
| chr6:154770954 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-3035A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154770954 | |||||||
| chr6:154771047 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.31-2942G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771047 | |||||||
| chr6:154771065 | T | C | 156 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.31-2924T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771065 | |||||||
| chr6:154771126 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-2863G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771126 | |||||||
| chr6:154771268 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31-2721C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771268 | |||||||
| chr6:154771323 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.31-2666A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771323 | |||||||
| chr6:154771467 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-2522A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771467 | |||||||
| chr6:154771651 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-2338C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154771651 | |||||||
| chr6:154772021 | C | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-1968C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772021 | |||||||
| chr6:154772158 | GTTAA | G | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-1826_31-1823del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 154772158 | ||||||
| chr6:154772231 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.31-1758C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772231 | |||||||
| chr6:154772324 | G | T | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.31-1665G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772324 | |||||||
| chr6:154772432 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.31-1557G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772432 | |||||||
| chr6:154772470 | G | A | 2 | a0003c0003t0002g0273 a0003c0003t0002g0274 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.31-1519G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772470 | |||||||
| chr6:154772489 | A | G | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31-1500A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772489 | |||||||
| chr6:154772637 | C | T | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.31-1352C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772637 | |||||||
| chr6:154772702 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.31-1287A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772702 | |||||||
| chr6:154772713 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.31-1276A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772713 | |||||||
| chr6:154772919 | T | C | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.31-1070T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154772919 | |||||||
| chr6:154773148 | C | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-841C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773148 | |||||||
| chr6:154773231 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.31-758C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773231 | |||||||
| chr6:154773416 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-573G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773416 | |||||||
| chr6:154773630 | A | G | 205 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.31-359A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773630 | |||||||
| chr6:154773717 | C | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-272C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773717 | |||||||
| chr6:154773854 | G | A | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.31-135G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773854 | |||||||
| chr6:154773868 | G | T | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-121G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 1/19 | chr6 | 154773868 | |||||||
| chr6:154774118 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+46A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774118 | |||||||
| chr6:154774233 | C | G | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+161C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774233 | |||||||
| chr6:154774272 | C | G | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+200C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774272 | |||||||
| chr6:154774357 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.114+285G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774357 | |||||||
| chr6:154774430 | C | A | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.114+358C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774430 | |||||||
| chr6:154774997 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0139 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.114+925A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154774997 | |||||||
| chr6:154775137 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.114+1065A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775137 | |||||||
| chr6:154775253 | C | T | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.114+1181C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775253 | |||||||
| chr6:154775273 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.114+1201T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775273 | |||||||
| chr6:154775328 | T | C | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.114+1256T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775328 | |||||||
| chr6:154775534 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+1462G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775534 | |||||||
| chr6:154775640 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.114+1568C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775640 | |||||||
| chr6:154775652 | C | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1580C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775652 | |||||||
| chr6:154775653 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.114+1581C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775653 | |||||||
| chr6:154775959 | G | A | 209 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.114+1887G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775959 | |||||||
| chr6:154775959 | G | C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0184 a0002c0004t0001g0181 others(2): Show |
5 | HG02145.hp1 HG02735.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1887G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154775959 | |||||||
| chr6:154776287 | GTGTATAT others(7): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.115-1712_115-1699d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154776287 | ||||||
| chr6:154776289 | GTATATAT others(7): Show |
G | 185 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.115-1693_115-1680d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154776289 | ||||||
| chr6:154776297 | GTA | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(2): Show |
5 | HG02451.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-1692_115-1691d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154776297 | ||||||
| chr6:154776396 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.115-1605A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154776396 | |||||||
| chr6:154776536 | A | G | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.115-1465A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154776536 | |||||||
| chr6:154777019 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.115-982A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777019 | |||||||
| chr6:154777168 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.115-833G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777168 | |||||||
| chr6:154777172 | G | C | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.115-829G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777172 | |||||||
| chr6:154777183 | A | AG | 7 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(4): Show |
7 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-814dupG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | 154777183 | ||||||
| chr6:154777188 | A | G | 9 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(6): Show |
9 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-813A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777188 | |||||||
| chr6:154777253 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.115-748T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777253 | |||||||
| chr6:154777429 | C | T | 1 | a0001c0006t0001g0249 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.115-572C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777429 | |||||||
| chr6:154777468 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.115-533T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777468 | |||||||
| chr6:154777589 | A | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-412A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777589 | |||||||
| chr6:154777756 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.115-245A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777756 | |||||||
| chr6:154777834 | C | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.115-167C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777834 | |||||||
| chr6:154777849 | A | G | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.115-152A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 2/19 | chr6 | 154777849 | |||||||
| chr6:154778237 | C | T | 205 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.159+192C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778237 | |||||||
| chr6:154778280 | C | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+235C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778280 | |||||||
| chr6:154778348 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0278 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159+303C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778348 | |||||||
| chr6:154778378 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+333A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778378 | |||||||
| chr6:154778380 | T | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.159+335T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778380 | |||||||
| chr6:154778546 | C | G | 86 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.159+501C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778546 | |||||||
| chr6:154778768 | A | AGT | 9 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0076 others(6): Show |
9 | HG00621.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+723_159+724ins others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778768 | |||||||
| chr6:154778768 | A | AGTGT | 4 | a0001c0001t0002g0075 a0001c0001t0002g0077 a0001c0001t0002g0276 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+723_159+724ins others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778768 | |||||||
| chr6:154778768 | A | AGTGTGT | 5 | a0001c0001t0002g0074 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | HG01123.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+723_159+724ins others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778768 | |||||||
| chr6:154778769 | A | ATG | 77 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0090 others(74): Show |
77 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.159+764_159+765dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | A | ATGTG | 24 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0128 others(21): Show |
24 | HG00642.hp2 HG01074.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.159+762_159+765dup others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | A | ATGTGTG | 6 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0138 others(3): Show |
6 | HG00140.hp1 HG00741.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+760_159+765dup others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0246 a0001c0001t0001g0259 a0001c0001t0001g0260 others(4): Show |
7 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+758_159+765dup others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | A | G | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+724A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778769 | |||||||
| chr6:154778769 | ATG | A | 8 | a0001c0001t0001g0112 a0001c0001t0001g0165 a0001c0001t0001g0170 others(5): Show |
8 | HG01070.hp2 HG01981.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+764_159+765del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | ATGTG | A | 20 | a0001c0001t0001g0064 a0001c0001t0001g0100 a0001c0001t0001g0113 others(17): Show |
20 | HG02148.hp1 HG02258.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.159+762_159+765del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | ATGTGTG | A | 6 | a0001c0001t0001g0166 a0001c0001t0003g0267 a0001c0001t0003g0268 others(3): Show |
6 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+760_159+765del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0167 a0001c0001t0002g0021 |
2 | HG02132.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.159+756_159+765del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778769 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.159+752_159+765del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154778769 | ||||||
| chr6:154778836 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.159+791T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778836 | |||||||
| chr6:154778937 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.159+892G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778937 | |||||||
| chr6:154778943 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+898C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154778943 | |||||||
| chr6:154779024 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+979T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779024 | |||||||
| chr6:154779071 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159+1026C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779071 | |||||||
| chr6:154779088 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.159+1043A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779088 | |||||||
| chr6:154779276 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159+1231T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779276 | |||||||
| chr6:154779359 | T | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+1314T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779359 | |||||||
| chr6:154779414 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.159+1369G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779414 | |||||||
| chr6:154779673 | G | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+1628G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779673 | |||||||
| chr6:154779758 | G | GGT | 5 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0040 others(2): Show |
5 | HG02273.hp2 HG02280.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1736_159+1737d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779758 | ||||||
| chr6:154779759 | G | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1714G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779759 | |||||||
| chr6:154779777 | GTGTGTAT others(5): Show |
G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.159+1734_159+1745d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779777 | ||||||
| chr6:154779779 | GTGTATAT others(3): Show |
G | 12 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0167 others(9): Show |
12 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1736_159+1745d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779779 | ||||||
| chr6:154779779 | GTGTATAT others(5): Show |
G | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.159+1736_159+1747d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779779 | ||||||
| chr6:154779781 | G | GTGTA | 5 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0046 others(2): Show |
5 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+1737_159+1738i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779781 | G | GTGTATAT others(1): Show |
3 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 |
3 | HG01109.hp1 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.159+1737_159+1738i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779781 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0003g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159+1737_159+1738i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779781 | GTA | G | 58 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0118 others(55): Show |
58 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.159+1755_159+1756d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779781 | GTATA | G | 19 | a0001c0001t0001g0064 a0001c0001t0001g0090 a0001c0001t0001g0100 others(16): Show |
19 | HG00140.hp1 HG00733.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+1753_159+1756d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779781 | GTATATA | G | 81 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(78): Show |
81 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.159+1751_159+1756d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779781 | GTATATAT others(1): Show |
G | 21 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(18): Show |
21 | HG00621.hp2 HG01167.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.159+1749_159+1756d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779781 | GTATATAT others(3): Show |
G | 4 | a0003c0003t0002g0273 a0003c0003t0002g0274 a0005c0005t0002g0255 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1747_159+1756d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154779781 | ||||||
| chr6:154779783 | A | G | 62 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(59): Show |
62 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.159+1738A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779783 | |||||||
| chr6:154779785 | A | G | 67 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0097 others(64): Show |
67 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.159+1740A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779785 | |||||||
| chr6:154779787 | A | G | 12 | a0001c0001t0001g0064 a0001c0001t0001g0090 a0001c0001t0001g0100 others(9): Show |
12 | HG00140.hp1 HG00733.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1742A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779787 | |||||||
| chr6:154779789 | A | G | 93 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.159+1744A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779789 | |||||||
| chr6:154779791 | A | G | 17 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(14): Show |
17 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.159+1746A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779791 | |||||||
| chr6:154779793 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+1748A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779793 | |||||||
| chr6:154779813 | T | A | 15 | a0001c0001t0002g0039 a0001c0001t0002g0075 a0001c0001t0002g0076 others(12): Show |
15 | HG01358.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+1768T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154779813 | |||||||
| chr6:154780019 | G | A | 4 | a0001c0001t0001g0220 a0001c0001t0001g0240 a0001c0001t0001g0242 others(1): Show |
4 | HG02015.hp2 HG02155.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1974G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780019 | |||||||
| chr6:154780354 | C | CT | 40 | a0001c0001t0001g0111 a0001c0001t0001g0174 a0001c0001t0002g0028 others(37): Show |
40 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.159+2327dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154780354 | ||||||
| chr6:154780354 | CT | C | 19 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0113 others(16): Show |
19 | HG00140.hp2 HG01070.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+2327delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154780354 | ||||||
| chr6:154780405 | CAT | C | 59 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(56): Show |
59 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.159+2362_159+2363d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154780405 | ||||||
| chr6:154780453 | C | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2408C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780453 | |||||||
| chr6:154780534 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.159+2489C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780534 | |||||||
| chr6:154780583 | T | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+2538T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780583 | |||||||
| chr6:154780772 | T | C | 4 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0051 others(1): Show |
4 | HG00642.hp2 HG01123.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2727T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780772 | |||||||
| chr6:154780809 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+2764C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780809 | |||||||
| chr6:154780819 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.159+2774G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780819 | |||||||
| chr6:154780957 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+2912C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154780957 | |||||||
| chr6:154781103 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.159+3058A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781103 | |||||||
| chr6:154781117 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.159+3072T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781117 | |||||||
| chr6:154781156 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0232 |
2 | HG02132.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.159+3111A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781156 | |||||||
| chr6:154781498 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.159+3453C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781498 | |||||||
| chr6:154781551 | A | G | 19 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0145 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+3506A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781551 | |||||||
| chr6:154781668 | T | C | 170 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.159+3623T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781668 | |||||||
| chr6:154781673 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.159+3628A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781673 | |||||||
| chr6:154781687 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.159+3642C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781687 | |||||||
| chr6:154781977 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.159+3932A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154781977 | |||||||
| chr6:154782116 | A | G | 78 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0097 others(75): Show |
78 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.159+4071A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782116 | |||||||
| chr6:154782222 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.159+4177C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782222 | |||||||
| chr6:154782286 | G | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
5 | HG02723.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+4241G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782286 | |||||||
| chr6:154782404 | G | T | 9 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0111 others(6): Show |
9 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+4359G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782404 | |||||||
| chr6:154782417 | T | TCAAAACA others(3): Show |
2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+4382_159+4391d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154782417 | ||||||
| chr6:154782417 | T | TCAAAACA others(8): Show |
1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+4377_159+4391d others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154782417 | ||||||
| chr6:154782549 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.159+4504T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782549 | |||||||
| chr6:154782572 | A | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+4527A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782572 | |||||||
| chr6:154782747 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.159+4702C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782747 | |||||||
| chr6:154782761 | G | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.159+4716G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154782761 | |||||||
| chr6:154783117 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.160-4744A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783117 | |||||||
| chr6:154783140 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.160-4721T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783140 | |||||||
| chr6:154783231 | T | C | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-4630T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783231 | |||||||
| chr6:154783249 | T | A | 16 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0167 others(13): Show |
16 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.160-4612T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783249 | |||||||
| chr6:154783298 | C | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160-4563C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783298 | |||||||
| chr6:154783310 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.160-4551T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783310 | |||||||
| chr6:154783357 | A | G | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-4504A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783357 | |||||||
| chr6:154783694 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-4167A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783694 | |||||||
| chr6:154783700 | A | G | 17 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0166 others(14): Show |
17 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.160-4161A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783700 | |||||||
| chr6:154783897 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-3964C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783897 | |||||||
| chr6:154783908 | A | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-3953A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783908 | |||||||
| chr6:154783974 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160-3887G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154783974 | |||||||
| chr6:154784050 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-3811G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784050 | |||||||
| chr6:154784105 | T | C | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.160-3756T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784105 | |||||||
| chr6:154784120 | G | GAGAGAGA others(3): Show |
1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160-3740_160-3739i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GAT | 10 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0100 others(7): Show |
10 | HG00140.hp2 HG01109.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-3704_160-3703d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATAT | 4 | a0001c0001t0001g0154 a0001c0001t0001g0185 a0001c0001t0002g0058 others(1): Show |
4 | HG01516.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-3706_160-3703d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATAT | 7 | a0001c0001t0001g0170 a0001c0001t0001g0186 a0001c0001t0002g0032 others(4): Show |
7 | HG00735.hp2 HG01070.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-3708_160-3703d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(1): Show |
5 | a0001c0001t0001g0106 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-3710_160-3703d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(3): Show |
2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.160-3712_160-3703d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(5): Show |
1 | a0001c0001t0002g0037 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160-3714_160-3703d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(7): Show |
1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160-3716_160-3703d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(9): Show |
5 | a0001c0001t0001g0092 a0001c0001t0001g0150 a0001c0001t0001g0167 others(2): Show |
5 | HG02080.hp1 HG02717.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3718_160-3703d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(11): Show |
2 | a0001c0001t0001g0127 a0001c0001t0007g0107 |
2 | HG02886.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.160-3720_160-3703d others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(13): Show |
1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.160-3722_160-3703d others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(15): Show |
1 | a0001c0001t0001g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160-3724_160-3703d others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(17): Show |
1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-3726_160-3703d others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | G | GATATATA others(23): Show |
1 | a0001c0001t0001g0189 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.160-3732_160-3703d others(32): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GAT | G | 16 | a0001c0001t0001g0099 a0001c0001t0001g0152 a0001c0001t0002g0002 others(13): Show |
16 | HG00733.hp2 HG01070.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.160-3704_160-3703d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATAT | G | 20 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0010 others(17): Show |
20 | HG00597.hp1 HG00642.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-3706_160-3703d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATAT | G | 5 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0271 others(2): Show |
5 | HG02080.hp2 HG03486.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-3708_160-3703d others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(1): Show |
G | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3710_160-3703d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(3): Show |
G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0157 a0001c0001t0001g0159 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3712_160-3703d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(5): Show |
G | 8 | a0001c0001t0001g0136 a0001c0001t0002g0075 a0001c0001t0002g0076 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-3714_160-3703d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(7): Show |
G | 6 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3716_160-3703d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(9): Show |
G | 2 | a0001c0001t0002g0072 a0001c0001t0002g0074 |
2 | HG00621.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.160-3718_160-3703d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(15): Show |
G | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.160-3724_160-3703d others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(17): Show |
G | 79 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0097 others(76): Show |
79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.160-3726_160-3703d others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784120 | GATATATA others(23): Show |
G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-3732_160-3703d others(32): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784120 | ||||||
| chr6:154784122 | T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160-3739T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784122 | |||||||
| chr6:154784124 | T | G | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(1): Show |
4 | HG01167.hp1 HG01433.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-3737T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784124 | |||||||
| chr6:154784126 | T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160-3735T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784126 | |||||||
| chr6:154784128 | T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160-3733T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784128 | |||||||
| chr6:154784138 | T | TATATAG | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0095 others(3): Show |
6 | HG00642.hp1 HG01358.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-3718_160-3717i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784138 | ||||||
| chr6:154784147 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160-3710_160-3699d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784147 | ||||||
| chr6:154784149 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.160-3708_160-3699d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784149 | ||||||
| chr6:154784155 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.160-3703_160-3702i others(21): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0137 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160-3703_160-3702i others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0102 |
2 | HG00733.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.160-3703_160-3702i others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0131 others(1): Show |
4 | HG01952.hp2 HG02602.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(7): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0229 others(3): Show |
6 | HG00735.hp1 HG02071.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0173 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.160-3703_160-3702i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(3): Show |
6 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0128 others(3): Show |
6 | HG00408.hp1 HG02004.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(1): Show |
8 | a0001c0001t0001g0089 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG00558.hp1 HG01891.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.160-3703_160-3702i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATT | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0096 others(3): Show |
6 | HG02257.hp1 HG03490.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATATTT others(3): Show |
5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0141 others(2): Show |
5 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-3703_160-3702i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATT | 5 | a0001c0001t0001g0070 a0001c0001t0001g0135 a0001c0001t0001g0158 others(2): Show |
5 | HG02723.hp1 NA18942.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-3692_160-3689d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATATTTAT others(1): Show |
3 | a0001c0001t0001g0125 a0001c0001t0001g0162 a0001c0001t0001g0206 |
3 | HG01261.hp1 HG02155.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.160-3696_160-3689d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATTTATT | 3 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0148 |
3 | HG01515.hp1 HG01517.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.160-3705_160-3704i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | ATTTATTT others(3): Show |
1 | a0001c0001t0001g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.160-3705_160-3704i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154784155 | ||||||
| chr6:154784155 | A | T | 28 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0095 others(25): Show |
28 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.160-3706A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784155 | |||||||
| chr6:154784159 | T | A | 2 | a0001c0001t0001g0167 a0005c0005t0002g0255 |
2 | HG02717.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160-3702T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784159 | |||||||
| chr6:154784393 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.160-3468T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784393 | |||||||
| chr6:154784453 | C | A | 1 | a0001c0001t0002g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.160-3408C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784453 | |||||||
| chr6:154784784 | C | A | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-3077C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784784 | |||||||
| chr6:154784851 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-3010T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784851 | |||||||
| chr6:154784863 | C | T | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.160-2998C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784863 | |||||||
| chr6:154784918 | A | G | 156 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.160-2943A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784918 | |||||||
| chr6:154784960 | C | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160-2901C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154784960 | |||||||
| chr6:154785015 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.160-2846G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785015 | |||||||
| chr6:154785017 | C | A | 185 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.160-2844C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785017 | |||||||
| chr6:154785101 | A | G | 8 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0111 others(5): Show |
8 | HG00621.hp1 HG00741.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-2760A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785101 | |||||||
| chr6:154785143 | T | C | 1 | a0001c0001t0006g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.160-2718T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785143 | |||||||
| chr6:154785154 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.160-2707T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785154 | |||||||
| chr6:154785249 | T | C | 1 | a0001c0006t0001g0249 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-2612T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785249 | |||||||
| chr6:154785414 | A | C | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.160-2447A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785414 | |||||||
| chr6:154785445 | C | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-2416C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785445 | |||||||
| chr6:154785588 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03579.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.160-2273C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785588 | |||||||
| chr6:154785684 | A | ATTAT | 223 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.160-2174_160-2173i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154785684 | ||||||
| chr6:154785824 | G | T | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-2037G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785824 | |||||||
| chr6:154785838 | C | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-2023C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785838 | |||||||
| chr6:154785906 | A | G | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.160-1955A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785906 | |||||||
| chr6:154785948 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-1913G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154785948 | |||||||
| chr6:154786029 | C | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-1832C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786029 | |||||||
| chr6:154786423 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.160-1438C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786423 | |||||||
| chr6:154786602 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0036 |
2 | HG01070.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.160-1259G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786602 | |||||||
| chr6:154786624 | G | A | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160-1237G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786624 | |||||||
| chr6:154786772 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.160-1089G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154786772 | |||||||
| chr6:154786886 | A | AAAGAACT others(30): Show |
1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.160-972_160-936dup others(37): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | 154786886 | ||||||
| chr6:154787005 | A | T | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.160-856A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787005 | |||||||
| chr6:154787044 | A | G | 1 | a0001c0001t0002g0010 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.160-817A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787044 | |||||||
| chr6:154787071 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.160-790G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787071 | |||||||
| chr6:154787091 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-770G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787091 | |||||||
| chr6:154787253 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.160-608G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787253 | |||||||
| chr6:154787547 | T | G | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-314T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787547 | |||||||
| chr6:154787640 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.160-221A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 3/19 | chr6 | 154787640 | |||||||
| chr6:154788175 | G | A | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.321+153G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788175 | |||||||
| chr6:154788226 | CTGTGTTA others(30): Show |
C | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.321+207_321+243del others(37): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154788226 | ||||||
| chr6:154788272 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+250A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788272 | |||||||
| chr6:154788290 | C | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.321+268C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788290 | |||||||
| chr6:154788545 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0239 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.321+523T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788545 | |||||||
| chr6:154788698 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.321+676C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788698 | |||||||
| chr6:154788700 | A | G | 5 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0046 others(2): Show |
5 | HG01928.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+678A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788700 | |||||||
| chr6:154788729 | C | G | 1 | a0001c0001t0002g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.321+707C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788729 | |||||||
| chr6:154788792 | T | G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG01106.hp1 HG01261.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+770T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788792 | |||||||
| chr6:154788913 | G | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.321+891G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788913 | |||||||
| chr6:154788970 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0159 |
2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.321+948G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154788970 | |||||||
| chr6:154789216 | C | G | 85 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.321+1194C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789216 | |||||||
| chr6:154789224 | T | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.321+1202T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789224 | |||||||
| chr6:154789300 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.321+1278A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789300 | |||||||
| chr6:154789343 | C | T | 2 | a0003c0003t0002g0273 a0003c0003t0002g0274 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.321+1321C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789343 | |||||||
| chr6:154789544 | A | AT | 16 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG00621.hp2 HG01106.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.321+1541dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154789544 | ||||||
| chr6:154789770 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.321+1748C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789770 | |||||||
| chr6:154789787 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+1765C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789787 | |||||||
| chr6:154789837 | G | T | 1 | a0002c0004t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.321+1815G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789837 | |||||||
| chr6:154789872 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+1850A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789872 | |||||||
| chr6:154789931 | A | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.321+1909A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154789931 | |||||||
| chr6:154790225 | G | T | 214 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.321+2203G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790225 | |||||||
| chr6:154790291 | G | T | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.321+2269G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790291 | |||||||
| chr6:154790432 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.322-2391C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790432 | |||||||
| chr6:154790489 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0002g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.322-2305_322-2295d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.322-2306_322-2295d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0002g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.322-2307_322-2295d others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0002g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.322-2309_322-2295d others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0002g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.322-2311_322-2295d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0002g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.322-2313_322-2295d others(21): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | AT | A | 15 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-2295delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATT | A | 12 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0002g0038 others(9): Show |
12 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.322-2296_322-2295d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0252 a0001c0001t0004g0192 others(3): Show |
6 | HG00735.hp1 HG01255.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-2303_322-2295d others(11): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(3): Show |
A | 23 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0110 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.322-2304_322-2295d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(4): Show |
A | 68 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(65): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
intron_variant | MODIFIER | c.322-2305_322-2295d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(5): Show |
A | 57 | a0001c0001t0001g0064 a0001c0001t0001g0071 a0001c0001t0001g0087 others(54): Show |
57 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.322-2306_322-2295d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(6): Show |
A | 11 | a0001c0001t0001g0089 a0001c0001t0001g0111 a0001c0001t0001g0114 others(8): Show |
11 | HG01515.hp1 HG01516.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.322-2307_322-2295d others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(7): Show |
A | 6 | a0001c0001t0001g0187 a0001c0001t0002g0074 a0001c0001t0002g0276 others(3): Show |
6 | HG01123.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2308_322-2295d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(8): Show |
A | 22 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(19): Show |
22 | HG00621.hp2 HG01496.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.322-2309_322-2295d others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(9): Show |
A | 6 | a0001c0001t0001g0167 a0001c0001t0001g0259 a0001c0001t0001g0260 others(3): Show |
6 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2310_322-2295d others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(10): Show |
A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2311_322-2295d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0002g0063 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.322-2313_322-2295d others(21): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0002g0060 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.322-2314_322-2295d others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790489 | ATTTTTTT others(14): Show |
A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.322-2315_322-2295d others(23): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154790489 | ||||||
| chr6:154790505 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.322-2318T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790505 | |||||||
| chr6:154790589 | C | T | 223 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.322-2234C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790589 | |||||||
| chr6:154790619 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.322-2204T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790619 | |||||||
| chr6:154790687 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.322-2136T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790687 | |||||||
| chr6:154790790 | G | A | 210 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.322-2033G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790790 | |||||||
| chr6:154790911 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.322-1912A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790911 | |||||||
| chr6:154790934 | A | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.322-1889A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154790934 | |||||||
| chr6:154791160 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0242 |
2 | HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.322-1663A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791160 | |||||||
| chr6:154791166 | T | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-1657T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791166 | |||||||
| chr6:154791238 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.322-1585C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791238 | |||||||
| chr6:154791421 | T | A | 1 | a0001c0001t0002g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322-1402T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791421 | |||||||
| chr6:154791570 | C | G | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.322-1253C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791570 | |||||||
| chr6:154791640 | G | GT | 73 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0118 others(70): Show |
73 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.322-1176dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154791640 | ||||||
| chr6:154791647 | T | TA | 89 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.322-1170dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | 154791647 | ||||||
| chr6:154791706 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.322-1117C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791706 | |||||||
| chr6:154791730 | G | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-1093G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791730 | |||||||
| chr6:154791789 | A | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.322-1034A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791789 | |||||||
| chr6:154791974 | T | C | 179 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.322-849T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791974 | |||||||
| chr6:154791992 | A | G | 163 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.322-831A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154791992 | |||||||
| chr6:154792098 | C | T | 89 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.322-725C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792098 | |||||||
| chr6:154792239 | A | C | 1 | a0001c0001t0002g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322-584A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792239 | |||||||
| chr6:154792466 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.322-357C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792466 | |||||||
| chr6:154792574 | T | C | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.322-249T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792574 | |||||||
| chr6:154792738 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.322-85C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 4/19 | chr6 | 154792738 | |||||||
| chr6:154792994 | A | G | 2 | a0001c0006t0001g0221 a0001c0006t0001g0249 |
2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.475+18A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154792994 | |||||||
| chr6:154793063 | G | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+87G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793063 | |||||||
| chr6:154793080 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0211 |
2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.475+104G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793080 | |||||||
| chr6:154793252 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.475+276G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793252 | |||||||
| chr6:154793343 | T | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.475+367T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793343 | |||||||
| chr6:154793380 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.475+404T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793380 | |||||||
| chr6:154793412 | T | A | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.475+436T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793412 | |||||||
| chr6:154793454 | A | T | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.475+478A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793454 | |||||||
| chr6:154793455 | A | T | 168 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.475+479A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793455 | |||||||
| chr6:154793466 | A | C | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+490A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793466 | |||||||
| chr6:154793471 | T | C | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+495T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793471 | |||||||
| chr6:154793510 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.475+534G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793510 | |||||||
| chr6:154793565 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.475+589A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793565 | |||||||
| chr6:154793575 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.475+599G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793575 | |||||||
| chr6:154793622 | C | G | 1 | a0001c0001t0008g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.475+646C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793622 | |||||||
| chr6:154793674 | G | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0236 |
2 | HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.475+698G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793674 | |||||||
| chr6:154793734 | G | T | 16 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0167 others(13): Show |
16 | HG01167.hp1 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.475+758G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793734 | |||||||
| chr6:154793771 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.475+795C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793771 | |||||||
| chr6:154793815 | C | CA | 146 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(143): Show |
146 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.475+863dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793815 | ||||||
| chr6:154793815 | C | CAA | 33 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0104 others(30): Show |
33 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.475+862_475+863dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793815 | ||||||
| chr6:154793815 | CA | C | 9 | a0001c0001t0002g0021 a0001c0001t0002g0026 a0001c0001t0002g0029 others(6): Show |
9 | HG00621.hp2 HG02129.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+863delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793815 | ||||||
| chr6:154793839 | A | AT | 10 | a0001c0001t0001g0086 a0001c0001t0001g0176 a0001c0001t0001g0177 others(7): Show |
10 | HG01884.hp1 HG02300.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+870dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793839 | ||||||
| chr6:154793839 | A | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+863A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793839 | |||||||
| chr6:154793840 | T | A | 2 | a0001c0001t0001g0233 a0001c0001t0002g0006 |
2 | HG02135.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.475+864T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154793840 | |||||||
| chr6:154793905 | G | GTGTGTGT others(5): Show |
214 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.475+932_475+943dup others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154793905 | ||||||
| chr6:154794017 | C | G | 214 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.476-992C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794017 | |||||||
| chr6:154794220 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.476-789G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794220 | |||||||
| chr6:154794628 | A | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.476-381A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794628 | |||||||
| chr6:154794759 | T | TG | 36 | a0001c0001t0001g0097 a0001c0001t0001g0167 a0001c0001t0001g0200 others(33): Show |
36 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.476-237dupG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794759 | ||||||
| chr6:154794759 | TG | T | 16 | a0001c0001t0001g0091 a0001c0001t0001g0177 a0001c0001t0001g0187 others(13): Show |
16 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.476-237delG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794759 | ||||||
| chr6:154794769 | G | C | 81 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.476-240G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794769 | |||||||
| chr6:154794769 | G | GC | 4 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0122 others(1): Show |
4 | HG01192.hp1 HG01361.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-240_476-239ins others(1): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794769 | |||||||
| chr6:154794771 | G | T | 1 | a0001c0001t0002g0028 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.476-238G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794771 | |||||||
| chr6:154794772 | GT | G | 29 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0105 others(26): Show |
29 | HG00099.hp1 HG00544.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.476-236delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | |||||||
| chr6:154794772 | GTGTGGGG others(3): Show |
G | 3 | a0001c0001t0001g0145 a0001c0001t0002g0075 a0001c0001t0005g0191 |
3 | HG00558.hp2 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.476-236_476-227del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | |||||||
| chr6:154794772 | GTGTGGGG others(5): Show |
G | 1 | a0001c0001t0002g0282 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.476-236_476-225del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | |||||||
| chr6:154794772 | GTGTGGGG others(7): Show |
G | 3 | a0001c0001t0001g0212 a0001c0001t0002g0074 a0001c0001t0002g0076 |
3 | HG01123.hp1 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.476-236_476-223del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | |||||||
| chr6:154794772 | GTGTGGGG others(9): Show |
G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0004g0226 |
3 | HG02148.hp2 HG03490.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.476-236_476-221del others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | |||||||
| chr6:154794772 | GTGTGGGG others(11): Show |
G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0237 a0001c0001t0001g0247 |
3 | HG02109.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.476-236_476-219del others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794772 | |||||||
| chr6:154794773 | T | G | 21 | a0001c0001t0001g0155 a0001c0001t0001g0180 a0001c0001t0001g0224 others(18): Show |
21 | HG00597.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.476-236T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794773 | |||||||
| chr6:154794775 | T | G | 3 | a0001c0001t0002g0007 a0001c0001t0006g0019 a0001c0008t0002g0257 |
3 | HG03130.hp2 HG03540.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.476-234T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794775 | |||||||
| chr6:154794777 | G | T | 53 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0105 others(50): Show |
53 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.476-232G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794777 | |||||||
| chr6:154794777 | GGGGGTGT others(26): Show |
G | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.476-230_476-198del others(33): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794777 | ||||||
| chr6:154794778 | G | T | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.476-231G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794778 | |||||||
| chr6:154794778 | GGGGTGT | G | 11 | a0001c0001t0001g0119 a0001c0001t0001g0187 a0001c0001t0001g0202 others(8): Show |
11 | HG00673.hp1 HG01081.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.476-229_476-224del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(1): Show |
G | 11 | a0001c0001t0001g0118 a0001c0001t0001g0176 a0001c0001t0001g0189 others(8): Show |
11 | HG00408.hp2 HG01074.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.476-229_476-222del others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(3): Show |
G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0177 a0001c0001t0001g0184 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-229_476-220del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(5): Show |
G | 1 | a0002c0004t0001g0183 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.476-229_476-218del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(7): Show |
G | 2 | a0001c0001t0002g0079 a0006c0009t0001g0143 |
2 | HG02647.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.476-229_476-216del others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(9): Show |
G | 3 | a0001c0001t0001g0164 a0001c0001t0002g0077 a0001c0001t0002g0078 |
3 | HG02965.hp2 NA18971.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.476-229_476-214del others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(11): Show |
G | 6 | a0001c0001t0001g0193 a0001c0001t0001g0210 a0001c0011t0001g0208 others(3): Show |
6 | HG02630.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-229_476-212del others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0211 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.476-229_476-210del others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(17): Show |
G | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.476-229_476-206del others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794778 | GGGGTGTG others(27): Show |
G | 87 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.476-229_476-196del others(34): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794778 | ||||||
| chr6:154794779 | G | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.476-230G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794779 | |||||||
| chr6:154794780 | G | GGT | 11 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0014 others(8): Show |
11 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.476-180_476-179dup others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0002g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.476-190_476-179dup others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | G | T | 10 | a0001c0001t0001g0097 a0001c0001t0001g0194 a0001c0001t0001g0200 others(7): Show |
10 | HG00438.hp2 HG00609.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.476-229G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794780 | |||||||
| chr6:154794780 | GGT | G | 12 | a0001c0001t0001g0085 a0001c0001t0001g0218 a0001c0001t0001g0220 others(9): Show |
12 | HG00099.hp1 HG00741.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.476-180_476-179del others(2): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGT | G | 11 | a0001c0001t0001g0180 a0001c0001t0001g0197 a0001c0001t0001g0240 others(8): Show |
11 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.476-182_476-179del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGTGT | G | 23 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0155 others(20): Show |
23 | HG00642.hp2 HG01109.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.476-184_476-179del others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGTGTG others(3): Show |
G | 1 | a0001c0002t0002g0047 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.476-188_476-179del others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGTGTG others(5): Show |
G | 7 | a0001c0001t0002g0062 a0001c0001t0002g0276 a0001c0001t0002g0277 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-190_476-179del others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0213 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.476-198_476-179del others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGTGTG others(17): Show |
G | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.476-202_476-179del others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGTGTG others(29): Show |
G | 1 | a0001c0001t0001g0242 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.476-214_476-179del others(36): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794780 | GGTGTGTG others(31): Show |
G | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-216_476-179del others(38): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 154794780 | ||||||
| chr6:154794782 | T | G | 6 | a0001c0001t0002g0003 a0001c0001t0002g0026 a0001c0001t0002g0029 others(3): Show |
6 | HG02129.hp1 HG03540.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.476-227T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794782 | |||||||
| chr6:154794784 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.476-225T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794784 | |||||||
| chr6:154794785 | GTGTGTGT others(10): Show |
G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.476-223_476-207del others(17): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794785 | |||||||
| chr6:154794786 | T | G | 1 | a0001c0001t0002g0023 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.476-223T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794786 | |||||||
| chr6:154794787 | GT | G | 3 | a0001c0001t0001g0145 a0001c0001t0002g0075 a0001c0001t0005g0191 |
3 | HG00558.hp2 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.476-221delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794787 | |||||||
| chr6:154794788 | T | G | 1 | a0001c0001t0002g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.476-221T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794788 | |||||||
| chr6:154794790 | T | G | 3 | a0001c0001t0001g0145 a0001c0001t0002g0075 a0001c0001t0005g0191 |
3 | HG00558.hp2 HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.476-219T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794790 | |||||||
| chr6:154794792 | T | G | 4 | a0001c0001t0001g0212 a0001c0001t0002g0072 a0001c0001t0002g0275 others(1): Show |
4 | HG00621.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-217T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794792 | |||||||
| chr6:154794793 | GT | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0004g0226 |
3 | HG02148.hp2 HG03490.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.476-215delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794793 | |||||||
| chr6:154794794 | T | G | 3 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0076 |
3 | HG01123.hp1 HG02080.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.476-215T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794794 | |||||||
| chr6:154794795 | GT | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0237 others(1): Show |
4 | HG02109.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-213delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794795 | |||||||
| chr6:154794796 | T | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0004g0226 |
3 | HG02148.hp2 HG03490.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.476-213T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794796 | |||||||
| chr6:154794798 | T | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0237 others(1): Show |
4 | HG02109.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-211T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794798 | |||||||
| chr6:154794800 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.476-209T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794800 | |||||||
| chr6:154794804 | T | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.476-205T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794804 | |||||||
| chr6:154794899 | A | G | 2 | a0001c0001t0004g0192 a0001c0001t0004g0223 |
2 | HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.476-110A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794899 | |||||||
| chr6:154794905 | G | A | 2 | a0001c0001t0001g0167 a0005c0005t0002g0256 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.476-104G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 5/19 | chr6 | 154794905 | |||||||
| chr6:154795151 | TTC | T | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.606+14_606+15delCT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154795151 | ||||||
| chr6:154795495 | C | T | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+356C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795495 | |||||||
| chr6:154795581 | A | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+442A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795581 | |||||||
| chr6:154795765 | C | G | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+626C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795765 | |||||||
| chr6:154795885 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.606+746C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154795885 | |||||||
| chr6:154796019 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.606+880T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796019 | |||||||
| chr6:154796177 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.606+1038G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796177 | |||||||
| chr6:154796280 | T | G | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.606+1141T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796280 | |||||||
| chr6:154796353 | T | TTC | 11 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(8): Show |
11 | HG00140.hp2 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.606+1252_606+1253d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | T | TTCCC | 7 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01433.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+1216_606+1217i others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | T | TTCCCTCT others(5): Show |
2 | a0001c0001t0001g0154 a0001c0001t0007g0107 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.606+1216_606+1217i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | T | TTCCCTCT others(9): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0186 |
2 | HG01070.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.606+1216_606+1217i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | T | TTCCCTCT others(15): Show |
1 | a0001c0001t0001g0173 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.606+1216_606+1217i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | T | TTCCTCTC others(4): Show |
1 | a0001c0001t0001g0171 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.606+1216_606+1217i others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | T | TTCCTCTC others(6): Show |
1 | a0001c0001t0001g0128 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.606+1216_606+1217i others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | TTC | T | 3 | a0001c0001t0001g0125 a0001c0001t0002g0007 a0001c0008t0002g0257 |
3 | HG01261.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.606+1252_606+1253d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | TTCTC | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(2): Show |
5 | HG02273.hp2 HG02486.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+1250_606+1253d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | TTCTCTCT others(5): Show |
T | 1 | a0001c0001t0002g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.606+1242_606+1253d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796353 | TTCTCTCT others(11): Show |
T | 1 | a0001c0001t0002g0022 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.606+1236_606+1253d others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796353 | ||||||
| chr6:154796354 | T | TCC | 9 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(6): Show |
9 | HG01515.hp2 HG01975.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1216_606+1217i others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796354 | ||||||
| chr6:154796356 | T | C | 158 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.606+1217T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796356 | |||||||
| chr6:154796358 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.606+1219T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796358 | |||||||
| chr6:154796385 | C | CTCTGTCT others(1): Show |
3 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03704.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.606+1249_606+1250i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796385 | ||||||
| chr6:154796385 | C | CTGTCTG | 26 | a0001c0001t0001g0118 a0001c0001t0001g0179 a0001c0001t0001g0193 others(23): Show |
26 | HG00609.hp2 HG01074.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.606+1247_606+1248i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796385 | ||||||
| chr6:154796385 | C | G | 15 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0125 others(12): Show |
15 | HG01167.hp1 HG01261.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+1246C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796385 | |||||||
| chr6:154796389 | C | CTCTCTCT others(23): Show |
1 | a0001c0001t0008g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(32): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(27): Show |
1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(36): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.606+1253_606+1254i others(30): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0095 |
2 | NA19062.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.606+1253_606+1254i others(28): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(17): Show |
4 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0204 others(1): Show |
4 | HG02257.hp1 NA18942.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(15): Show |
9 | a0001c0001t0001g0071 a0001c0001t0001g0135 a0001c0001t0001g0169 others(6): Show |
9 | HG01109.hp1 HG01496.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(24): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(13): Show |
14 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0086 others(11): Show |
14 | HG00642.hp1 HG01358.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(26): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(11): Show |
13 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0119 others(10): Show |
13 | HG00735.hp1 HG01106.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(9): Show |
16 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0090 others(13): Show |
16 | HG00140.hp1 HG00544.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(3): Show |
2 | a0001c0001t0002g0275 a0001c0012t0002g0279 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.606+1253_606+1254i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(7): Show |
15 | a0001c0001t0001g0064 a0001c0001t0001g0085 a0001c0001t0001g0096 others(12): Show |
15 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(11): Show |
1 | a0001c0001t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.606+1253_606+1254i others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(5): Show |
15 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0110 others(12): Show |
15 | HG00609.hp1 HG01515.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0142 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(18): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTGT others(3): Show |
6 | a0001c0001t0001g0100 a0001c0001t0001g0150 a0001c0001t0001g0163 others(3): Show |
6 | HG00621.hp2 HG01123.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+1253_606+1254i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTCTGT others(7): Show |
1 | a0001c0001t0001g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.606+1253_606+1254i others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTGTCT others(1): Show |
4 | a0001c0001t0001g0131 a0002c0004t0001g0181 a0002c0004t0001g0182 others(1): Show |
4 | HG02145.hp1 HG02735.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+1257_606+1258i others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTCTGTCT others(5): Show |
12 | a0001c0001t0001g0105 a0001c0001t0001g0145 a0001c0001t0001g0196 others(9): Show |
12 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.606+1257_606+1258i others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTG | 4 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(1): Show |
4 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1251_606+1252i others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTGTCTG | 9 | a0001c0001t0001g0114 a0001c0001t0001g0128 a0001c0001t0001g0171 others(6): Show |
9 | HG00597.hp2 HG01952.hp2 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1251_606+1252i others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | CTGTCTGT others(3): Show |
32 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0001t0001g0155 others(29): Show |
32 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.606+1251_606+1252i others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796389 | ||||||
| chr6:154796389 | C | G | 52 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0118 others(49): Show |
52 | HG00609.hp2 HG01070.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.606+1250C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796389 | |||||||
| chr6:154796829 | A | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.606+1690A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796829 | |||||||
| chr6:154796853 | T | G | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.606+1714T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796853 | |||||||
| chr6:154796873 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.606+1734G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796873 | |||||||
| chr6:154796881 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.606+1742A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796881 | |||||||
| chr6:154796890 | T | G | 1 | a0001c0001t0002g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.606+1751T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796890 | |||||||
| chr6:154796953 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.606+1814C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154796953 | |||||||
| chr6:154796980 | C | CA | 12 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(9): Show |
12 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+1854dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154796980 | ||||||
| chr6:154797105 | ATTTTATA others(4790): Show |
A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG01261.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.606+1972_607-64del | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154797105 | ||||||
| chr6:154797373 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0168 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.606+2234T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797373 | |||||||
| chr6:154797398 | A | AT | 7 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(4): Show |
7 | HG02258.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+2269dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154797398 | ||||||
| chr6:154797406 | T | C | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.606+2267T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797406 | |||||||
| chr6:154797437 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.606+2298C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797437 | |||||||
| chr6:154797678 | A | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.606+2539A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797678 | |||||||
| chr6:154797737 | C | G | 1 | a0001c0001t0002g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.606+2598C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154797737 | |||||||
| chr6:154798018 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.606+2879A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798018 | |||||||
| chr6:154798024 | T | G | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.606+2885T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798024 | |||||||
| chr6:154798166 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.606+3027T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798166 | |||||||
| chr6:154798392 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0168 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.606+3253T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798392 | |||||||
| chr6:154798594 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.607-3377C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798594 | |||||||
| chr6:154798903 | G | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-3068G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154798903 | |||||||
| chr6:154799126 | C | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.607-2845C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799126 | |||||||
| chr6:154799317 | T | C | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | NA18951.hp2 NA18993.hp1 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-2654T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799317 | |||||||
| chr6:154799379 | A | G | 3 | a0001c0001t0001g0167 a0001c0001t0002g0276 a0001c0001t0002g0278 |
3 | HG02717.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.607-2592A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799379 | |||||||
| chr6:154799666 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.607-2305C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799666 | |||||||
| chr6:154799685 | T | A | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.607-2286T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154799685 | |||||||
| chr6:154799775 | CTATT | C | 5 | a0001c0001t0001g0118 a0001c0001t0001g0235 a0001c0001t0001g0254 others(2): Show |
5 | HG01074.hp2 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-2173_607-2170d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154799775 | ||||||
| chr6:154799775 | CTATTTAT others(1): Show |
C | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.607-2177_607-2170d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr6 | 154799775 | ||||||
| chr6:154800125 | G | C | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.607-1846G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800125 | |||||||
| chr6:154800184 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.607-1787C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800184 | |||||||
| chr6:154800293 | C | G | 2 | a0001c0001t0002g0195 a0001c0001t0007g0107 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.607-1678C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800293 | |||||||
| chr6:154800355 | A | G | 3 | a0001c0001t0005g0144 a0001c0001t0005g0191 a0001c0001t0005g0209 |
3 | HG03017.hp1 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.607-1616A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800355 | |||||||
| chr6:154800569 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.607-1402A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800569 | |||||||
| chr6:154800640 | G | C | 2 | a0003c0003t0002g0273 a0003c0003t0002g0274 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.607-1331G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800640 | |||||||
| chr6:154800650 | GT | G | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.607-1320delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154800650 | |||||||
| chr6:154801040 | G | C | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.607-931G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801040 | |||||||
| chr6:154801063 | A | G | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.607-908A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801063 | |||||||
| chr6:154801178 | A | G | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.607-793A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801178 | |||||||
| chr6:154801257 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.607-714A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801257 | |||||||
| chr6:154801504 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.607-467A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801504 | |||||||
| chr6:154801854 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.607-117G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 6/19 | chr6 | 154801854 | |||||||
| chr6:154802254 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.783+107C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802254 | |||||||
| chr6:154802458 | T | C | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.783+311T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802458 | |||||||
| chr6:154802488 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.783+341G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802488 | |||||||
| chr6:154802567 | A | G | 1 | a0006c0009t0001g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.783+420A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802567 | |||||||
| chr6:154802617 | CA | C | 8 | a0001c0001t0001g0091 a0001c0001t0001g0243 a0001c0001t0001g0259 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+482delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 154802617 | ||||||
| chr6:154802629 | AT | A | 110 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.783+490delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 154802629 | ||||||
| chr6:154802630 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.783+483T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802630 | |||||||
| chr6:154802637 | T | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.783+490T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802637 | |||||||
| chr6:154802940 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.784-604C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154802940 | |||||||
| chr6:154803032 | G | T | 1 | a0001c0001t0006g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.784-512G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803032 | |||||||
| chr6:154803218 | A | G | 1 | a0001c0001t0002g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.784-326A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803218 | |||||||
| chr6:154803328 | A | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0157 a0001c0001t0001g0159 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-216A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803328 | |||||||
| chr6:154803449 | T | G | 214 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.784-95T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803449 | |||||||
| chr6:154803481 | A | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-63A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 7/19 | chr6 | 154803481 | |||||||
| chr6:154803647 | A | G | 1 | a0001c0001t0008g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.863+24A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154803647 | |||||||
| chr6:154803751 | G | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+128G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154803751 | |||||||
| chr6:154803775 | C | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.863+152C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154803775 | |||||||
| chr6:154804036 | A | AT | 6 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(3): Show |
6 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.863+424dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr6 | 154804036 | ||||||
| chr6:154804219 | T | C | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.863+596T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804219 | |||||||
| chr6:154804291 | A | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+668A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804291 | |||||||
| chr6:154804383 | C | G | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.863+760C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804383 | |||||||
| chr6:154804543 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.864-826C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804543 | |||||||
| chr6:154804856 | T | C | 3 | a0002c0004t0001g0181 a0002c0004t0001g0182 a0002c0004t0001g0183 |
3 | HG02145.hp1 HG02735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.864-513T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804856 | |||||||
| chr6:154804917 | A | G | 1 | a0005c0005t0002g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.864-452A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154804917 | |||||||
| chr6:154805009 | G | A | 89 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.864-360G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154805009 | |||||||
| chr6:154805107 | C | T | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.864-262C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154805107 | |||||||
| chr6:154805202 | A | AT | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.864-167_864-166ins others(1): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 8/19 | chr6 | 154805202 | |||||||
| chr6:154805561 | CT | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0218 a0001c0001t0002g0275 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+88delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr6 | 154805561 | ||||||
| chr6:154805576 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.981+90A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154805576 | |||||||
| chr6:154805720 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.981+234A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154805720 | |||||||
| chr6:154805764 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.981+278T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154805764 | |||||||
| chr6:154806035 | G | T | 3 | a0001c0008t0002g0257 a0005c0005t0002g0255 a0005c0005t0002g0256 |
3 | HG02886.hp1 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.981+549G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806035 | |||||||
| chr6:154806109 | C | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.981+623C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806109 | |||||||
| chr6:154806323 | G | T | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.981+837G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806323 | |||||||
| chr6:154806477 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.981+991G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806477 | |||||||
| chr6:154806506 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.981+1020G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806506 | |||||||
| chr6:154806802 | T | TA | 4 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0037 others(1): Show |
4 | HG01261.hp2 HG02300.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.982-1267dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr6 | 154806802 | ||||||
| chr6:154806830 | G | A | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.982-1240G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806830 | |||||||
| chr6:154806917 | A | C | 1 | a0001c0001t0004g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.982-1153A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154806917 | |||||||
| chr6:154807109 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.982-961T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807109 | |||||||
| chr6:154807198 | G | C | 211 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.982-872G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807198 | |||||||
| chr6:154807292 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
3 | HG02451.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.982-778C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807292 | |||||||
| chr6:154807353 | A | G | 1 | a0001c0001t0008g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.982-717A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807353 | |||||||
| chr6:154807405 | A | G | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.982-665A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807405 | |||||||
| chr6:154807450 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.982-620G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807450 | |||||||
| chr6:154807810 | A | G | 169 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.982-260A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807810 | |||||||
| chr6:154807904 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.982-166A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807904 | |||||||
| chr6:154807969 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.982-101A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154807969 | |||||||
| chr6:154808057 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.982-13A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 9/19 | chr6 | 154808057 | |||||||
| chr6:154808459 | A | AT | 6 | a0001c0001t0002g0051 a0001c0001t0003g0080 a0001c0001t0003g0081 others(3): Show |
6 | HG02258.hp2 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-212dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808459 | ||||||
| chr6:154808459 | AT | A | 181 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1114-212delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808459 | ||||||
| chr6:154808459 | ATT | A | 11 | a0001c0001t0001g0102 a0001c0001t0001g0148 a0001c0001t0001g0214 others(8): Show |
11 | HG02129.hp2 HG02723.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-213_1114-212d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808459 | ||||||
| chr6:154808511 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1114-175C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | chr6 | 154808511 | |||||||
| chr6:154808599 | G | A | 1 | a0001c0001t0008g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1114-87G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | chr6 | 154808599 | |||||||
| chr6:154808650 | CCTTT | C | 209 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1114-33_1114-30del others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 154808650 | ||||||
| chr6:154809020 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0229 |
2 | NA18945.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1226+222A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809020 | |||||||
| chr6:154809134 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1226+336A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809134 | |||||||
| chr6:154809245 | T | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1226+447T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809245 | |||||||
| chr6:154809250 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1226+452T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809250 | |||||||
| chr6:154809344 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1226+546C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809344 | |||||||
| chr6:154809550 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1227-465A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809550 | |||||||
| chr6:154809633 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1227-382A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809633 | |||||||
| chr6:154809703 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1227-312A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809703 | |||||||
| chr6:154809844 | G | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227-171G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809844 | |||||||
| chr6:154809955 | G | A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(8): Show |
11 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227-60G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 11/19 | chr6 | 154809955 | |||||||
| chr6:154810243 | A | C | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1420+35A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810243 | |||||||
| chr6:154810344 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1420+136T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810344 | |||||||
| chr6:154810353 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1420+145C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810353 | |||||||
| chr6:154810358 | TAGAG | T | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1420+152_1420+155d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154810358 | ||||||
| chr6:154810365 | GAGA | G | 80 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(77): Show |
80 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1420+166_1420+168d others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154810365 | ||||||
| chr6:154810492 | T | TA | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420+285dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154810492 | ||||||
| chr6:154810498 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420+290G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810498 | |||||||
| chr6:154810513 | T | C | 2 | a0003c0003t0002g0273 a0003c0003t0002g0274 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1420+305T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154810513 | |||||||
| chr6:154811048 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0239 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1420+840T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811048 | |||||||
| chr6:154811103 | C | G | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1420+895C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811103 | |||||||
| chr6:154811179 | T | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1420+971T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811179 | |||||||
| chr6:154811339 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1420+1131G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811339 | |||||||
| chr6:154811385 | T | C | 2 | a0001c0001t0003g0268 a0001c0001t0003g0269 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1420+1177T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811385 | |||||||
| chr6:154811481 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1420+1273T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811481 | |||||||
| chr6:154811524 | G | A | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1420+1316G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811524 | |||||||
| chr6:154811883 | G | A | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1420+1675G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811883 | |||||||
| chr6:154811973 | A | T | 3 | a0002c0004t0001g0181 a0002c0004t0001g0182 a0002c0004t0001g0183 |
3 | HG02145.hp1 HG02735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1420+1765A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811973 | |||||||
| chr6:154811983 | G | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1420+1775G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154811983 | |||||||
| chr6:154812068 | C | T | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1420+1860C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812068 | |||||||
| chr6:154812096 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1420+1888C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812096 | |||||||
| chr6:154812176 | C | CT | 5 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0051 others(2): Show |
5 | HG01255.hp1 HG01261.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420+1991dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812176 | ||||||
| chr6:154812176 | CT | C | 176 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1420+1991delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812176 | ||||||
| chr6:154812176 | CTT | C | 10 | a0001c0001t0001g0110 a0001c0001t0001g0124 a0001c0001t0001g0158 others(7): Show |
10 | HG01517.hp1 HG02109.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1420+1990_1420+199 others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812176 | ||||||
| chr6:154812199 | T | A | 203 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1420+1991T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812199 | |||||||
| chr6:154812199 | T | TA | 4 | a0001c0001t0002g0276 a0001c0008t0002g0257 a0003c0003t0002g0273 others(1): Show |
4 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420+1994dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812199 | ||||||
| chr6:154812263 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1420+2055A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812263 | |||||||
| chr6:154812289 | C | A | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1420+2081C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812289 | |||||||
| chr6:154812292 | C | CT | 51 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0123 others(48): Show |
51 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1420+2105dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812292 | ||||||
| chr6:154812292 | C | CTT | 6 | a0001c0001t0001g0133 a0001c0001t0002g0029 a0001c0001t0002g0034 others(3): Show |
6 | HG00642.hp2 HG01978.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420+2104_1420+210 others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812292 | ||||||
| chr6:154812292 | CT | C | 24 | a0001c0001t0001g0190 a0001c0001t0002g0073 a0001c0001t0002g0075 others(21): Show |
24 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1420+2105delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154812292 | ||||||
| chr6:154812337 | G | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1420+2129G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812337 | |||||||
| chr6:154812413 | G | C | 1 | a0005c0005t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1420+2205G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812413 | |||||||
| chr6:154812546 | C | G | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1420+2338C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812546 | |||||||
| chr6:154812608 | C | G | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1420+2400C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812608 | |||||||
| chr6:154812735 | A | G | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1420+2527A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812735 | |||||||
| chr6:154812797 | T | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0110 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1420+2589T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154812797 | |||||||
| chr6:154813022 | G | C | 1 | a0001c0001t0002g0039 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1421-2694G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813022 | |||||||
| chr6:154813039 | CA | C | 218 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1421-2661delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154813039 | ||||||
| chr6:154813080 | T | A | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1421-2636T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813080 | |||||||
| chr6:154813272 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1421-2444C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813272 | |||||||
| chr6:154813273 | C | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1421-2443C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813273 | |||||||
| chr6:154813297 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1421-2419G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813297 | |||||||
| chr6:154813492 | T | C | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1421-2224T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813492 | |||||||
| chr6:154813523 | C | T | 1 | a0001c0015t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1421-2193C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813523 | |||||||
| chr6:154813638 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1421-2078A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813638 | |||||||
| chr6:154813800 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0110 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1421-1916G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813800 | |||||||
| chr6:154813861 | C | T | 214 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1421-1855C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813861 | |||||||
| chr6:154813934 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1421-1782G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813934 | |||||||
| chr6:154813950 | G | T | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1421-1766G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154813950 | |||||||
| chr6:154814206 | T | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1421-1510T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154814206 | |||||||
| chr6:154814391 | A | G | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1421-1325A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154814391 | |||||||
| chr6:154815174 | G | A | 11 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0207 others(8): Show |
11 | HG02109.hp1 HG02630.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-542G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815174 | |||||||
| chr6:154815279 | AGAGT | A | 10 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0176 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1421-433_1421-430d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr6 | 154815279 | ||||||
| chr6:154815293 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1421-423T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815293 | |||||||
| chr6:154815304 | T | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1421-412T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815304 | |||||||
| chr6:154815329 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1421-387A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815329 | |||||||
| chr6:154815352 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1421-364G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815352 | |||||||
| chr6:154815367 | G | T | 169 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1421-349G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815367 | |||||||
| chr6:154815399 | T | C | 1 | a0001c0001t0002g0023 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1421-317T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815399 | |||||||
| chr6:154815444 | A | G | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1421-272A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 12/19 | chr6 | 154815444 | |||||||
| chr6:154815953 | G | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0184 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1521+137G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154815953 | |||||||
| chr6:154816002 | A | T | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1521+186A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816002 | |||||||
| chr6:154816010 | G | A | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1521+194G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816010 | |||||||
| chr6:154816139 | T | C | 219 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1521+323T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816139 | |||||||
| chr6:154816236 | T | G | 1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1521+420T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816236 | |||||||
| chr6:154816512 | G | GCTGT | 214 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1521+699_1521+702d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154816512 | ||||||
| chr6:154816521 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1521+705C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816521 | |||||||
| chr6:154816552 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1521+736A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816552 | |||||||
| chr6:154816825 | A | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1521+1009A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154816825 | |||||||
| chr6:154816870 | TTAAG | T | 2 | a0001c0001t0002g0277 a0001c0001t0002g0282 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1521+1058_1521+106 others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154816870 | ||||||
| chr6:154817039 | AT | A | 186 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1521+1227delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154817039 | ||||||
| chr6:154817114 | C | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1521+1298C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817114 | |||||||
| chr6:154817115 | C | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1521+1299C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817115 | |||||||
| chr6:154817116 | C | CTAGTGAT others(1): Show |
3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1521+1300_1521+130 others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817116 | |||||||
| chr6:154817184 | T | C | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1522-1295T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817184 | |||||||
| chr6:154817251 | C | G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG01106.hp1 HG01261.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1522-1228C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817251 | |||||||
| chr6:154817676 | G | A | 187 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1522-803G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817676 | |||||||
| chr6:154817715 | A | G | 6 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0033 others(3): Show |
6 | HG01070.hp2 HG01106.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1522-764A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817715 | |||||||
| chr6:154817808 | T | C | 59 | a0001c0001t0001g0070 a0001c0001t0001g0086 a0001c0001t0001g0087 others(56): Show |
59 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1522-671T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154817808 | |||||||
| chr6:154818110 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1522-369G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154818110 | |||||||
| chr6:154818120 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1522-359A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154818120 | |||||||
| chr6:154818257 | CTAAT | C | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1522-220_1522-217d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 154818257 | ||||||
| chr6:154818397 | A | G | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1522-82A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 13/19 | chr6 | 154818397 | |||||||
| chr6:154818742 | T | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1635+150T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818742 | |||||||
| chr6:154818783 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1635+191G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818783 | |||||||
| chr6:154818806 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1635+214A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818806 | |||||||
| chr6:154818836 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1635+244A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154818836 | |||||||
| chr6:154819083 | G | GT | 187 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1635+498dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr6 | 154819083 | ||||||
| chr6:154819092 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1635+500A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819092 | |||||||
| chr6:154819157 | T | C | 224 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1635+565T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819157 | |||||||
| chr6:154819226 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1635+634T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819226 | |||||||
| chr6:154819468 | A | G | 4 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0002g0278 others(1): Show |
4 | HG03471.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1636-709A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819468 | |||||||
| chr6:154819798 | G | C | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1636-379G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819798 | |||||||
| chr6:154819834 | C | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1636-343C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819834 | |||||||
| chr6:154819853 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1636-324G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819853 | |||||||
| chr6:154819871 | C | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1636-306C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154819871 | |||||||
| chr6:154820139 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1636-38G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 14/19 | chr6 | 154820139 | |||||||
| chr6:154820517 | A | T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792+184A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820517 | |||||||
| chr6:154820828 | C | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1792+495C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820828 | |||||||
| chr6:154820889 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1792+556T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820889 | |||||||
| chr6:154820920 | G | T | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG00735.hp1 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792+587G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154820920 | |||||||
| chr6:154821010 | A | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 |
3 | HG02451.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1792+677A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821010 | |||||||
| chr6:154821012 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1792+679G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821012 | |||||||
| chr6:154821187 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1792+854C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821187 | |||||||
| chr6:154821231 | G | A | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1792+898G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821231 | |||||||
| chr6:154821239 | CCTGTTGG others(25): Show |
C | 6 | a0001c0001t0001g0098 a0001c0001t0001g0157 a0001c0001t0001g0159 others(3): Show |
6 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+939_1792+970d others(34): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr6 | 154821239 | ||||||
| chr6:154821331 | T | C | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1793-945T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821331 | |||||||
| chr6:154821457 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1793-819G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821457 | |||||||
| chr6:154821460 | A | G | 78 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0097 others(75): Show |
78 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1793-816A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821460 | |||||||
| chr6:154821478 | C | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793-798C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821478 | |||||||
| chr6:154821658 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1793-618A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821658 | |||||||
| chr6:154821774 | G | A | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1793-502G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821774 | |||||||
| chr6:154821818 | G | A | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1793-458G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821818 | |||||||
| chr6:154821968 | C | T | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1793-308C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821968 | |||||||
| chr6:154821994 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1793-282C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154821994 | |||||||
| chr6:154822148 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1793-128G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154822148 | |||||||
| chr6:154822151 | T | G | 27 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0200 others(24): Show |
27 | HG00099.hp1 HG00609.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1793-125T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154822151 | |||||||
| chr6:154822168 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1793-108G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 15/19 | chr6 | 154822168 | |||||||
| chr6:154822545 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1926+136A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154822545 | |||||||
| chr6:154822673 | C | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1926+264C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154822673 | |||||||
| chr6:154822935 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1926+526T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154822935 | |||||||
| chr6:154823106 | G | A | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1926+697G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823106 | |||||||
| chr6:154823136 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1926+727C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823136 | |||||||
| chr6:154823384 | T | A | 1 | a0001c0011t0001g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1927-850T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823384 | |||||||
| chr6:154823639 | GAGA | G | 4 | a0001c0001t0002g0275 a0001c0001t0002g0280 a0001c0001t0002g0281 others(1): Show |
4 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1927-591_1927-589d others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 154823639 | ||||||
| chr6:154823751 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0238 |
2 | NA18949.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1927-483A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823751 | |||||||
| chr6:154823827 | A | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0264 |
2 | HG00544.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1927-407A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823827 | |||||||
| chr6:154823883 | C | T | 69 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(66): Show |
69 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1927-351C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823883 | |||||||
| chr6:154823907 | T | A | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1927-327T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823907 | |||||||
| chr6:154823941 | T | C | 17 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(14): Show |
17 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1927-293T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154823941 | |||||||
| chr6:154824043 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1927-191A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154824043 | |||||||
| chr6:154824145 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1927-89T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 16/19 | chr6 | 154824145 | |||||||
| chr6:154824417 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2071+39A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824417 | |||||||
| chr6:154824429 | G | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2071+51G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824429 | |||||||
| chr6:154824456 | A | G | 1 | a0001c0001t0002g0039 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2071+78A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824456 | |||||||
| chr6:154824482 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2071+104C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824482 | |||||||
| chr6:154824642 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2071+264T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824642 | |||||||
| chr6:154824804 | G | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0247 a0001c0011t0001g0208 |
3 | HG03098.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2071+426G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824804 | |||||||
| chr6:154824814 | A | G | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2071+436A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824814 | |||||||
| chr6:154824836 | G | C | 4 | a0001c0001t0001g0090 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00140.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2071+458G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824836 | |||||||
| chr6:154824957 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2071+579A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154824957 | |||||||
| chr6:154824961 | G | GA | 22 | a0001c0001t0001g0252 a0001c0001t0001g0271 a0001c0001t0002g0072 others(19): Show |
22 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.2071+595dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154824961 | ||||||
| chr6:154825099 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2071+721T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825099 | |||||||
| chr6:154825129 | T | A | 1 | a0001c0001t0002g0039 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2071+751T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825129 | |||||||
| chr6:154825137 | G | C | 1 | a0003c0003t0002g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2071+759G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825137 | |||||||
| chr6:154825178 | A | G | 6 | a0001c0001t0002g0195 a0001c0001t0003g0080 a0001c0001t0003g0081 others(3): Show |
6 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2071+800A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825178 | |||||||
| chr6:154825241 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2071+863T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825241 | |||||||
| chr6:154825401 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2071+1023A>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825401 | |||||||
| chr6:154825655 | C | CA | 35 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0104 others(32): Show |
35 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.2071+1298dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | ||||||
| chr6:154825655 | C | CAA | 138 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.2071+1297_2071+129 others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | ||||||
| chr6:154825655 | C | CAAA | 26 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0099 others(23): Show |
26 | HG00544.hp1 HG00735.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2071+1296_2071+129 others(7): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | ||||||
| chr6:154825655 | C | CAAAA | 14 | a0001c0001t0002g0072 a0001c0001t0002g0075 a0001c0001t0002g0076 others(11): Show |
14 | HG00621.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2071+1295_2071+129 others(8): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 154825655 | ||||||
| chr6:154825693 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2071+1315C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825693 | |||||||
| chr6:154825852 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2072-1320G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154825852 | |||||||
| chr6:154826021 | A | G | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0116 others(2): Show |
5 | HG00642.hp1 HG01358.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2072-1151A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826021 | |||||||
| chr6:154826272 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2072-900A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826272 | |||||||
| chr6:154826706 | G | A | 4 | a0001c0013t0002g0101 a0003c0003t0002g0272 a0003c0003t0002g0273 others(1): Show |
4 | HG03195.hp2 HG03453.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2072-466G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826706 | |||||||
| chr6:154826708 | T | G | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2072-464T>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826708 | |||||||
| chr6:154826745 | G | A | 61 | a0001c0001t0001g0125 a0001c0001t0002g0001 a0001c0001t0002g0002 others(58): Show |
61 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2072-427G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826745 | |||||||
| chr6:154826849 | T | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2072-323T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826849 | |||||||
| chr6:154826864 | A | T | 1 | a0003c0003t0002g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2072-308A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826864 | |||||||
| chr6:154826993 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2072-179T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154826993 | |||||||
| chr6:154827048 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0236 |
2 | HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2072-124T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154827048 | |||||||
| chr6:154827129 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2072-43A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 17/19 | chr6 | 154827129 | |||||||
| chr6:154827250 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2140+10C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827250 | |||||||
| chr6:154827482 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2140+242G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827482 | |||||||
| chr6:154827719 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2140+479T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827719 | |||||||
| chr6:154827834 | C | CG | 95 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0071 others(92): Show |
95 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.2140+605dupG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154827834 | ||||||
| chr6:154827834 | C | CGG | 34 | a0001c0001t0001g0086 a0001c0001t0001g0103 a0001c0001t0001g0161 others(31): Show |
34 | HG00597.hp1 HG00642.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2140+604_2140+605d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154827834 | ||||||
| chr6:154827834 | CG | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0120 a0001c0001t0001g0159 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.2140+605delG | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154827834 | ||||||
| chr6:154827839 | G | A | 1 | a0001c0013t0002g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2140+599G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827839 | |||||||
| chr6:154827839 | G | C | 1 | a0006c0009t0001g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2140+599G>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827839 | |||||||
| chr6:154827839 | G | T | 2 | a0001c0001t0001g0218 a0001c0001t0002g0013 |
2 | HG00733.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2140+599G>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827839 | |||||||
| chr6:154827844 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2140+604G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154827844 | |||||||
| chr6:154828069 | T | C | 1 | a0001c0008t0002g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2140+829T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828069 | |||||||
| chr6:154828131 | A | G | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2140+891A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828131 | |||||||
| chr6:154828345 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2140+1105C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828345 | |||||||
| chr6:154828369 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2140+1129A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828369 | |||||||
| chr6:154828496 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2140+1256A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828496 | |||||||
| chr6:154828562 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2140+1322G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828562 | |||||||
| chr6:154828809 | A | G | 60 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(57): Show |
60 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.2140+1569A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828809 | |||||||
| chr6:154828922 | A | G | 1 | a0001c0001t0003g0269 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2140+1682A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828922 | |||||||
| chr6:154828971 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2140+1731T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154828971 | |||||||
| chr6:154828993 | C | CT | 16 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(13): Show |
16 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2140+1762dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154828993 | ||||||
| chr6:154829195 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2141-1727T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829195 | |||||||
| chr6:154829214 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(62): Show |
65 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2141-1708G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829214 | |||||||
| chr6:154829232 | A | AT | 59 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(56): Show |
59 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.2141-1674dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154829232 | ||||||
| chr6:154829232 | AT | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0110 a0001c0001t0001g0178 others(3): Show |
6 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2141-1674delT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154829232 | ||||||
| chr6:154829497 | C | A | 1 | a0001c0001t0001g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2141-1425C>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829497 | |||||||
| chr6:154829573 | T | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-1349T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829573 | |||||||
| chr6:154829610 | A | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(62): Show |
65 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2141-1312A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829610 | |||||||
| chr6:154829629 | G | A | 19 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(16): Show |
19 | HG00621.hp2 HG01123.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.2141-1293G>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829629 | |||||||
| chr6:154829781 | C | CCTGTAAT others(8): Show |
1 | a0001c0001t0002g0074 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2141-1138_2141-112 others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr6 | 154829781 | ||||||
| chr6:154829781 | C | T | 2 | a0005c0005t0002g0255 a0005c0005t0002g0256 |
2 | HG02886.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2141-1141C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154829781 | |||||||
| chr6:154830125 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2141-797C>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154830125 | |||||||
| chr6:154830640 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2141-282T>A | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 18/19 | chr6 | 154830640 | |||||||
| chr6:154831177 | C | G | 66 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(63): Show |
66 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.2359+37C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831177 | |||||||
| chr6:154831230 | A | G | 1 | a0001c0001t0002g0011 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2359+90A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831230 | |||||||
| chr6:154831255 | C | CT | 11 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 others(8): Show |
11 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2359+124dupT | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831255 | ||||||
| chr6:154831442 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2359+302A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831442 | |||||||
| chr6:154831567 | A | G | 3 | a0003c0003t0002g0272 a0003c0003t0002g0273 a0003c0003t0002g0274 |
3 | HG03195.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2360-372A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831567 | |||||||
| chr6:154831637 | T | TTCTAAGC others(1): Show |
4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-300_2360-293d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831637 | ||||||
| chr6:154831646 | T | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG00609.hp2 HG02040.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-293T>C | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831646 | |||||||
| chr6:154831692 | A | G | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2360-247A>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831692 | |||||||
| chr6:154831703 | T | TA | 16 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0111 others(13): Show |
16 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2360-197dupA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | T | TAA | 12 | a0001c0001t0001g0064 a0001c0001t0001g0135 a0001c0001t0001g0154 others(9): Show |
12 | HG00099.hp1 HG00673.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-198_2360-197d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | T | TAAA | 12 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0150 others(9): Show |
12 | HG01358.hp1 HG02922.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.2360-199_2360-197d others(5): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0210 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2360-213_2360-197d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | T | TAAAAAAA others(22): Show |
1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2360-225_2360-197d others(31): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TA | T | 14 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0099 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2360-197delA | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAA | T | 12 | a0001c0001t0001g0071 a0001c0001t0001g0097 a0001c0001t0001g0106 others(9): Show |
12 | HG00558.hp1 HG01070.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-198_2360-197d others(4): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAA | T | 10 | a0001c0001t0001g0115 a0001c0001t0001g0166 a0001c0001t0001g0176 others(7): Show |
10 | HG01516.hp2 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2360-200_2360-197d others(6): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAA | T | 8 | a0001c0001t0001g0091 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG01516.hp1 HG01517.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360-201_2360-197d others(7): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(1): Show |
T | 8 | a0001c0001t0001g0205 a0001c0001t0001g0212 a0001c0001t0001g0213 others(5): Show |
8 | HG01361.hp2 HG01433.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2360-204_2360-197d others(10): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(2): Show |
T | 8 | a0001c0001t0002g0024 a0001c0001t0002g0038 a0001c0001t0002g0076 others(5): Show |
8 | HG00597.hp1 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360-205_2360-197d others(11): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(3): Show |
T | 60 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0002g0001 others(57): Show |
60 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.2360-206_2360-197d others(12): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(4): Show |
T | 21 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0001t0001g0108 others(18): Show |
21 | HG00408.hp1 HG00621.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2360-207_2360-197d others(13): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(5): Show |
T | 44 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0087 others(41): Show |
44 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.2360-208_2360-197d others(14): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(6): Show |
T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0175 |
2 | HG00597.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2360-209_2360-197d others(15): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(7): Show |
T | 1 | a0002c0004t0001g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2360-210_2360-197d others(16): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0002g0028 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2360-213_2360-197d others(19): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(11): Show |
T | 1 | a0001c0001t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2360-214_2360-197d others(20): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(13): Show |
T | 5 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(2): Show |
5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-216_2360-197d others(22): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831703 | TAAAAAAA others(22): Show |
T | 5 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2360-225_2360-197d others(31): Show |
SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr6 | 154831703 | ||||||
| chr6:154831705 | A | T | 1 | a0001c0001t0007g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2360-234A>T | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831705 | |||||||
| chr6:154831843 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2360-96C>G | SCAF8 | ENSG00000213079.10 | transcript | ENST00000367178.8 | protein_coding | 19/19 | chr6 | 154831843 |