Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 158401 |
| ensemblid | ENSG00000165181.17 |
| hgncid | 26535 |
| symbol | SHOC1 |
| name | shortage in chiasmata 1 |
| refseq_nuc | NM_001378211.1 |
| refseq_prot | NP_001365140.1 |
| ensembl_nuc | ENST00000682961.1 |
| ensembl_prot | ENSP00000508388.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 111686171 |
| end | 111794937 |
| strand | - |
| ver | v1.2 |
| region | chr9:111686171-111794937 |
| region5000 | chr9:111681171-111799937 |
| regionname0 | SHOC1_chr9_111686171_111794937 |
| regionname5000 | SHOC1_chr9_111681171_111799937 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1508 | 101 | 9 | 19 | 56 | 6 | 11 | 35 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0002 | 0/0 | 1508 | 63 | 25 | 6 | 20 | 0 | 12 | 17 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0003 | 0/0 | 1508 | 29 | 6 | 16 | 2 | 1 | 4 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0004 | 1/0 | 1508 | 27 | 0 | 9 | 9 | 2 | 6 | 7 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0005 | 0/0 | 1508 | 21 | 11 | 1 | 5 | 0 | 4 | 3 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0006 | 0/0 | 1508 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0007 | 0/0 | 1508 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0008 | 0/0 | 1508 | 10 | 7 | 3 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0009 | 0/0 | 1508 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0010 | 0/0 | 1508 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0011 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0012 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0013 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0014 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0015 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0016 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0017 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0018 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0019 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0020 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0021 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0022 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| a0023 | 0/1 | 1508 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | MFSAL others(1503): Show |
chr9 | 111681171 | 111799937 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4524 | 99 | 9 | 19 | 55 | 6 | 10 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0001c0022 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0001c0026 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0002c0002 | 0/0 | 4524 | 36 | 0 | 4 | 20 | 0 | 12 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0002c0007 | 0/0 | 4524 | 12 | 11 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0002c0010 | 0/0 | 4524 | 6 | 6 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0002c0011 | 0/0 | 4524 | 5 | 4 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0002c0012 | 0/0 | 4524 | 4 | 4 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0003c0003 | 0/0 | 4524 | 29 | 6 | 16 | 2 | 1 | 4 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0004c0004 | 1/0 | 4524 | 27 | 0 | 9 | 9 | 2 | 6 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0005c0005 | 0/0 | 4524 | 21 | 11 | 1 | 5 | 0 | 4 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0006c0006 | 0/0 | 4524 | 16 | 15 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0007c0008 | 0/0 | 4524 | 11 | 10 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0008c0009 | 0/0 | 4524 | 10 | 7 | 3 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0009c0017 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0009c0018 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0010c0013 | 0/0 | 4524 | 2 | 0 | 0 | 0 | 2 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0011c0014 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0012c0025 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0013c0024 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0014c0021 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0015c0029 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0016c0015 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0017c0016 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0018c0027 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0019c0028 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0020c0020 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0021c0019 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0022c0023 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 | ||
| a0023c0030 | 0/1 | 4524 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ATGTT others(4519): Show |
chr9 | 111681171 | 111799937 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5200 | 99 | 9 | 19 | 55 | 6 | 10 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0001c0022t0001 | 0/0 | 5200 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0001c0026t0001 | 0/0 | 5200 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0002t0002 | 0/0 | 5200 | 36 | 0 | 4 | 20 | 0 | 12 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0007t0001 | 0/0 | 5200 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0007t0002 | 0/0 | 5200 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0007t0004 | 0/0 | 5200 | 7 | 7 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0007t0006 | 0/0 | 5200 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0007t0008 | 0/0 | 5200 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCA others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0010t0002 | 0/0 | 5200 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0010t0004 | 0/0 | 5200 | 4 | 4 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0011t0005 | 0/0 | 5200 | 5 | 4 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0002c0012t0006 | 0/0 | 5200 | 4 | 4 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0003c0003t0002 | 0/0 | 5200 | 29 | 6 | 16 | 2 | 1 | 4 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0004c0004t0002 | 1/0 | 5200 | 25 | 0 | 9 | 7 | 2 | 6 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0004c0004t0007 | 0/0 | 5200 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0005c0005t0003 | 0/0 | 5200 | 21 | 11 | 1 | 5 | 0 | 4 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0006c0006t0001 | 0/0 | 5200 | 16 | 15 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0007c0008t0001 | 0/0 | 5200 | 11 | 10 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0008c0009t0001 | 0/0 | 5200 | 10 | 7 | 3 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0009c0017t0002 | 0/0 | 5200 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0009c0018t0002 | 0/0 | 5200 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0010c0013t0002 | 0/0 | 5200 | 2 | 0 | 0 | 0 | 2 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0011c0014t0002 | 0/0 | 5200 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0012c0025t0005 | 0/0 | 5200 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0013c0024t0001 | 0/0 | 5200 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0014c0021t0002 | 0/0 | 5200 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0015c0029t0002 | 0/0 | 5200 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0016c0015t0003 | 0/0 | 5200 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0017c0016t0002 | 0/0 | 5200 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0018c0027t0001 | 0/0 | 5200 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0019c0028t0001 | 0/0 | 5200 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0020c0020t0002 | 0/0 | 5200 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0021c0019t0002 | 0/0 | 5200 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0022c0023t0001 | 0/0 | 5200 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| a0023c0030t0002 | 0/1 | 5200 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | ACCCC others(5195): Show |
chr9 | 111681171 | 111799937 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0022t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0001c0026t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0007t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0010t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0010t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0010t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0010t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0010t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0011t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0011t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0011t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0011t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0011t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0012t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0012t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0012t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0002c0012t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0003c0003t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0004c0004t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0001 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0005c0005t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0006c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0007c0008t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0007c0008t0001g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0007c0008t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0007c0008t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0007c0008t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0007c0008t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0008c0009t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0009c0017t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0009c0018t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0010c0013t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0010c0013t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0011c0014t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0011c0014t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0012c0025t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0013c0024t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0014c0021t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0015c0029t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0016c0015t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0017c0016t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0018c0027t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0019c0028t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0020c0020t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0021c0019t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0022c0023t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| a0023c0030t0002g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00099 | hp2 | a0004 | c0004 | t0002 | g0066 | EUR | GBR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00140 | hp1 | a0003 | c0003 | t0002 | g0088 | EUR | GBR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0020 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00544 | hp1 | a0005 | c0005 | t0003 | g0038 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00621 | hp1 | a0005 | c0005 | t0003 | g0037 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00639 | hp1 | a0009 | c0018 | t0002 | g0040 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0111 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00673 | hp1 | a0001 | c0022 | t0001 | g0196 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00738 | hp1 | a0004 | c0004 | t0002 | g0009 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0202 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00741 | hp1 | a0004 | c0004 | t0002 | g0065 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01069 | hp2 | a0004 | c0004 | t0002 | g0058 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0077 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01074 | hp1 | a0003 | c0003 | t0002 | g0083 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01081 | hp1 | a0003 | c0003 | t0002 | g0093 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01081 | hp2 | a0006 | c0006 | t0001 | g0002 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01099 | hp1 | a0004 | c0004 | t0002 | g0009 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01109 | hp2 | a0012 | c0025 | t0005 | g0264 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0108 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0095 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01192 | hp1 | a0008 | c0009 | t0001 | g0084 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01192 | hp2 | a0002 | c0007 | t0008 | g0019 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01243 | hp1 | a0008 | c0009 | t0001 | g0102 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01243 | hp2 | a0002 | c0011 | t0005 | g0123 | AMR | PUR | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01255 | hp1 | a0007 | c0008 | t0001 | g0005 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01255 | hp2 | a0004 | c0004 | t0002 | g0055 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01256 | hp1 | a0004 | c0004 | t0002 | g0008 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01256 | hp2 | a0003 | c0003 | t0002 | g0099 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01258 | hp2 | a0004 | c0004 | t0002 | g0008 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01261 | hp1 | a0003 | c0003 | t0002 | g0092 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01261 | hp2 | a0005 | c0005 | t0003 | g0033 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0094 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01515 | hp1 | a0004 | c0004 | t0002 | g0075 | EUR | IBS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01516 | hp1 | a0010 | c0013 | t0002 | g0043 | EUR | IBS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01884 | hp1 | a0006 | c0006 | t0001 | g0035 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01884 | hp2 | a0002 | c0010 | t0004 | g0165 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01891 | hp2 | a0008 | c0009 | t0001 | g0101 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01928 | hp2 | a0003 | c0003 | t0002 | g0173 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01934 | hp1 | a0004 | c0004 | t0002 | g0068 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01952 | hp1 | a0003 | c0003 | t0002 | g0170 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01975 | hp1 | a0008 | c0009 | t0001 | g0171 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0169 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02027 | hp1 | a0004 | c0004 | t0007 | g0062 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02027 | hp2 | a0013 | c0024 | t0001 | g0151 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02055 | hp1 | a0003 | c0003 | t0002 | g0087 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02055 | hp2 | a0006 | c0006 | t0001 | g0052 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02145 | hp1 | a0002 | c0007 | t0004 | g0257 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02145 | hp2 | a0005 | c0005 | t0003 | g0001 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02148 | hp1 | a0004 | c0004 | t0002 | g0057 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02148 | hp2 | a0003 | c0003 | t0002 | g0172 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02165 | hp2 | a0004 | c0004 | t0002 | g0061 | EAS | CDX | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02257 | hp2 | a0005 | c0005 | t0003 | g0001 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02258 | hp1 | a0007 | c0008 | t0001 | g0079 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02258 | hp2 | a0002 | c0010 | t0002 | g0013 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02273 | hp1 | a0003 | c0003 | t0002 | g0174 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02280 | hp1 | a0015 | c0029 | t0002 | g0089 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02280 | hp2 | a0016 | c0015 | t0003 | g0024 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0097 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02451 | hp1 | a0007 | c0008 | t0001 | g0004 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02451 | hp2 | a0011 | c0014 | t0002 | g0027 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02572 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02572 | hp2 | a0002 | c0007 | t0004 | g0214 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02602 | hp1 | a0001 | c0026 | t0001 | g0252 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0194 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02615 | hp1 | a0002 | c0010 | t0004 | g0114 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02615 | hp2 | a0007 | c0008 | t0001 | g0005 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02622 | hp1 | a0005 | c0005 | t0003 | g0031 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02622 | hp2 | a0003 | c0003 | t0002 | g0085 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02630 | hp1 | a0005 | c0005 | t0003 | g0028 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02630 | hp2 | a0007 | c0008 | t0001 | g0080 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02717 | hp1 | a0006 | c0006 | t0001 | g0034 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02717 | hp2 | a0008 | c0009 | t0001 | g0103 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02735 | hp1 | a0004 | c0004 | t0002 | g0070 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02738 | hp1 | a0003 | c0003 | t0002 | g0106 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0205 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02809 | hp1 | a0007 | c0008 | t0001 | g0004 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02809 | hp2 | a0003 | c0003 | t0002 | g0096 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02818 | hp1 | a0008 | c0009 | t0001 | g0107 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02818 | hp2 | a0002 | c0007 | t0004 | g0256 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02886 | hp1 | a0005 | c0005 | t0003 | g0001 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02886 | hp2 | a0006 | c0006 | t0001 | g0041 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02895 | hp1 | a0006 | c0006 | t0001 | g0050 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02895 | hp2 | a0002 | c0012 | t0006 | g0212 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02896 | hp1 | a0006 | c0006 | t0001 | g0053 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02897 | hp2 | a0002 | c0012 | t0006 | g0211 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02922 | hp1 | a0002 | c0012 | t0006 | g0209 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02922 | hp2 | a0008 | c0009 | t0001 | g0110 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02965 | hp1 | a0007 | c0008 | t0001 | g0010 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02965 | hp2 | a0005 | c0005 | t0003 | g0022 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02970 | hp1 | a0002 | c0011 | t0005 | g0160 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02970 | hp2 | a0002 | c0007 | t0004 | g0254 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03041 | hp1 | a0002 | c0011 | t0005 | g0124 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03041 | hp2 | a0006 | c0006 | t0001 | g0051 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03098 | hp2 | a0003 | c0003 | t0002 | g0091 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03130 | hp1 | a0006 | c0006 | t0001 | g0002 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03130 | hp2 | a0005 | c0005 | t0003 | g0032 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03139 | hp1 | a0002 | c0010 | t0004 | g0113 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03195 | hp1 | a0002 | c0010 | t0004 | g0112 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03195 | hp2 | a0008 | c0009 | t0001 | g0109 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03209 | hp1 | a0005 | c0005 | t0003 | g0026 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03225 | hp1 | a0011 | c0014 | t0002 | g0029 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03225 | hp2 | a0006 | c0006 | t0001 | g0002 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03239 | hp1 | a0017 | c0016 | t0002 | g0081 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0177 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03453 | hp1 | a0007 | c0008 | t0001 | g0004 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03486 | hp1 | a0002 | c0011 | t0005 | g0122 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03486 | hp2 | a0008 | c0009 | t0001 | g0100 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03491 | hp1 | a0005 | c0005 | t0003 | g0006 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0206 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03492 | hp2 | a0005 | c0005 | t0003 | g0006 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03516 | hp1 | a0007 | c0008 | t0001 | g0078 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03516 | hp2 | a0002 | c0012 | t0006 | g0208 | AFR | ESN | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03540 | hp1 | a0007 | c0008 | t0001 | g0005 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03540 | hp2 | a0002 | c0007 | t0004 | g0253 | AFR | GWD | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03579 | hp1 | a0002 | c0007 | t0002 | g0128 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03579 | hp2 | a0002 | c0007 | t0006 | g0207 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0190 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0176 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0011 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03688 | hp1 | a0005 | c0005 | t0003 | g0001 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03688 | hp2 | a0004 | c0004 | t0002 | g0069 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03710 | hp1 | a0004 | c0004 | t0002 | g0048 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03831 | hp2 | a0004 | c0004 | t0002 | g0047 | SAS | BEB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03834 | hp1 | a0003 | c0003 | t0002 | g0098 | SAS | BEB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0198 | SAS | BEB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0195 | SAS | BEB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0204 | SAS | BEB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0175 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG04115 | hp2 | a0004 | c0004 | t0002 | g0045 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0191 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG04204 | hp1 | a0004 | c0004 | t0002 | g0056 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG04204 | hp2 | a0005 | c0005 | t0003 | g0266 | SAS | STU | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18522 | hp1 | a0006 | c0006 | t0001 | g0054 | AFR | YRI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18522 | hp2 | a0007 | c0008 | t0001 | g0010 | AFR | YRI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18906 | hp1 | a0019 | c0028 | t0001 | g0215 | AFR | YRI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18906 | hp2 | a0005 | c0005 | t0003 | g0021 | AFR | YRI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18952 | hp1 | a0004 | c0004 | t0002 | g0007 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18966 | hp1 | a0004 | c0004 | t0002 | g0064 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18970 | hp2 | a0020 | c0020 | t0002 | g0044 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18998 | hp2 | a0003 | c0003 | t0002 | g0082 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19000 | hp2 | a0004 | c0004 | t0007 | g0063 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19005 | hp1 | a0021 | c0019 | t0002 | g0193 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19007 | hp2 | a0005 | c0005 | t0003 | g0036 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19030 | hp1 | a0006 | c0006 | t0001 | g0072 | AFR | LWK | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19030 | hp2 | a0002 | c0007 | t0001 | g0167 | AFR | LWK | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19043 | hp1 | a0008 | c0009 | t0001 | g0104 | AFR | LWK | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19043 | hp2 | a0002 | c0007 | t0006 | g0213 | AFR | LWK | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19062 | hp1 | a0004 | c0004 | t0002 | g0071 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19070 | hp1 | a0004 | c0004 | t0002 | g0060 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19078 | hp2 | a0005 | c0005 | t0003 | g0023 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19079 | hp1 | a0004 | c0004 | t0002 | g0059 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19084 | hp2 | a0005 | c0005 | t0003 | g0039 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19091 | hp1 | a0022 | c0023 | t0001 | g0265 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19091 | hp2 | a0004 | c0004 | t0002 | g0007 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19240 | hp1 | a0002 | c0011 | t0005 | g0121 | AFR | YRI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA19240 | hp2 | a0002 | c0007 | t0004 | g0168 | AFR | YRI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0105 | AFR | ASW | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20752 | hp1 | a0010 | c0013 | t0002 | g0076 | EUR | TSI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20805 | hp1 | a0009 | c0017 | t0002 | g0049 | EUR | TSI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | GIH | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA20905 | hp2 | a0003 | c0003 | t0002 | g0011 | SAS | GIH | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0189 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0086 | AMR | CLM | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02109 | hp1 | a0002 | c0010 | t0002 | g0013 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02109 | hp2 | a0014 | c0021 | t0002 | g0210 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02559 | hp1 | a0002 | c0007 | t0004 | g0255 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG02559 | hp2 | a0006 | c0006 | t0001 | g0073 | AFR | ACB | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03471 | hp1 | a0006 | c0006 | t0001 | g0042 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG03471 | hp2 | a0018 | c0027 | t0001 | g0147 | AFR | MSL | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG06807 | hp1 | a0006 | c0006 | t0001 | g0074 | AFR | USA | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| HG06807 | hp2 | a0005 | c0005 | t0003 | g0030 | AFR | USA | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA21309 | hp1 | a0005 | c0005 | t0003 | g0025 | AFR | LWK | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| NA21309 | hp2 | a0003 | c0003 | t0002 | g0090 | AFR | LWK | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| homoSapiens | chm13v2 | a0023 | c0030 | t0002 | g0046 | REF | REF | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0002 | g0067 | REF | REF | SHOC1_chr9_111681171_111799937 | SHOC1 | chr9 | 111681171 | 111799937 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111686832 | G | A | 1 | a0007 | 11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
missense_variant | MODERATE | c.4465C>T | p.Arg1489Cys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 4539/5200 | 4465/4527 | 1489/1508 | chr9 | 111686832 | |||
| chr9:111691563 | C | T | 1 | a0014 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.4414G>A | p.Glu1472Lys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/28 | 4488/5200 | 4414/4527 | 1472/1508 | chr9 | 111691563 | |||
| chr9:111691645 | G | T | 2 | a0005 a0016 |
22 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(19): Show |
missense_variant | MODERATE | c.4332C>A | p.Asn1444Lys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/28 | 4406/5200 | 4332/4527 | 1444/1508 | chr9 | 111691645 | |||
| chr9:111691835 | G | T | 1 | a0013 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.4142C>A | p.Thr1381Asn | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/28 | 4216/5200 | 4142/4527 | 1381/1508 | chr9 | 111691835 | |||
| chr9:111692264 | T | C | 7 | a0001 a0006 a0007 others(4): Show |
141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
missense_variant | MODERATE | c.3713A>G | p.Glu1238Gly | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/28 | 3787/5200 | 3713/4527 | 1238/1508 | chr9 | 111692264 | |||
| chr9:111693885 | T | C | 1 | a0020 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.3379A>G | p.Lys1127Glu | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/28 | 3453/5200 | 3379/4527 | 1127/1508 | chr9 | 111693885 | |||
| chr9:111700042 | A | G | 16 | a0001 a0002 a0003 others(13): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
missense_variant | MODERATE | c.3095T>C | p.Leu1032Pro | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/28 | 3169/5200 | 3095/4527 | 1032/1508 | chr9 | 111700042 | |||
| chr9:111702121 | C | T | 1 | a0022 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.3073G>A | p.Glu1025Lys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/28 | 3147/5200 | 3073/4527 | 1025/1508 | chr9 | 111702121 | |||
| chr9:111702207 | T | C | 17 | a0001 a0002 a0003 others(14): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
missense_variant | MODERATE | c.2987A>G | p.Tyr996Cys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/28 | 3061/5200 | 2987/4527 | 996/1508 | chr9 | 111702207 | |||
| chr9:111706686 | A | C | 7 | a0003 a0005 a0008 others(4): Show |
65 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
missense_variant | MODERATE | c.2619T>G | p.Asn873Lys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/28 | 2693/5200 | 2619/4527 | 873/1508 | chr9 | 111706686 | |||
| chr9:111707858 | C | T | 4 | a0005 a0011 a0012 others(1): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
missense_variant | MODERATE | c.2555G>A | p.Arg852Lys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/28 | 2629/5200 | 2555/4527 | 852/1508 | chr9 | 111707858 | |||
| chr9:111713124 | T | G | 4 | a0005 a0011 a0012 others(1): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
missense_variant | MODERATE | c.2464A>C | p.Ile822Leu | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/28 | 2538/5200 | 2464/4527 | 822/1508 | chr9 | 111713124 | |||
| chr9:111714468 | T | A | 4 | a0003 a0008 a0015 others(1): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
missense_variant | MODERATE | c.2392A>T | p.Met798Leu | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/28 | 2466/5200 | 2392/4527 | 798/1508 | chr9 | 111714468 | |||
| chr9:111714499 | T | C | 1 | a0018 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.2361A>G | p.Ile787Met | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/28 | 2435/5200 | 2361/4527 | 787/1508 | chr9 | 111714499 | |||
| chr9:111718282 | A | G | 3 | a0005 a0011 a0016 |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
missense_variant | MODERATE | c.2138T>C | p.Ile713Thr | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/28 | 2212/5200 | 2138/4527 | 713/1508 | chr9 | 111718282 | |||
| chr9:111722464 | T | G | 1 | a0019 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2076A>C | p.Gln692His | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/28 | 2150/5200 | 2076/4527 | 692/1508 | chr9 | 111722464 | |||
| chr9:111728028 | T | C | 15 | a0001 a0002 a0003 others(12): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
missense_variant | MODERATE | c.1439A>G | p.His480Arg | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/28 | 1513/5200 | 1439/4527 | 480/1508 | chr9 | 111728028 | |||
| chr9:111738406 | C | T | 1 | a0021 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1291G>A | p.Ala431Thr | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/28 | 1365/5200 | 1291/4527 | 431/1508 | chr9 | 111738406 | |||
| chr9:111746277 | G | A | 1 | a0010 | 2 | HG01516.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.1036C>T | p.Arg346Cys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/28 | 1110/5200 | 1036/4527 | 346/1508 | chr9 | 111746277 | |||
| chr9:111748193 | G | C | 3 | a0005 a0011 a0016 |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
missense_variant | MODERATE | c.869C>G | p.Thr290Ser | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/28 | 943/5200 | 869/4527 | 290/1508 | chr9 | 111748193 | |||
| chr9:111758806 | C | T | 1 | a0009 | 2 | HG00639.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.485G>A | p.Arg162Lys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/28 | 559/5200 | 485/4527 | 162/1508 | chr9 | 111758806 | |||
| chr9:111775889 | A | T | 1 | a0017 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.344T>A | p.Val115Glu | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/28 | 418/5200 | 344/4527 | 115/1508 | chr9 | 111775889 | |||
| chr9:111775895 | A | G | 1 | a0016 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.338T>C | p.Ile113Thr | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/28 | 412/5200 | 338/4527 | 113/1508 | chr9 | 111775895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111691948 | C | T | 1 | a0018c0027 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.4029G>A | p.Ser1343Ser | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/28 | 4103/5200 | 4029/4527 | 1343/1508 | chr9 | 111691948 | |||
| chr9:111692452 | C | T | 2 | a0005c0005 a0016c0015 |
22 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(19): Show |
synonymous_variant | LOW | c.3525G>A | p.Pro1175Pro | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/28 | 3599/5200 | 3525/4527 | 1175/1508 | chr9 | 111692452 | |||
| chr9:111692455 | T | C | 2 | a0002c0011 a0012c0025 |
6 | HG01109.hp2 HG01243.hp2 HG02970.hp1 others(3): Show |
synonymous_variant | LOW | c.3522A>G | p.Ser1174Ser | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/28 | 3596/5200 | 3522/4527 | 1174/1508 | chr9 | 111692455 | |||
| chr9:111713143 | G | A | 1 | a0001c0026 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.2445C>T | p.Asp815Asp | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/28 | 2519/5200 | 2445/4527 | 815/1508 | chr9 | 111713143 | |||
| chr9:111722503 | A | G | 4 | a0003c0003 a0008c0009 a0015c0029 others(1): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
synonymous_variant | LOW | c.2037T>C | p.Pro679Pro | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/28 | 2111/5200 | 2037/4527 | 679/1508 | chr9 | 111722503 | |||
| chr9:111722557 | G | T | 3 | a0001c0022 a0002c0002 a0021c0019 |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
synonymous_variant | LOW | c.1983C>A | p.Leu661Leu | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/28 | 2057/5200 | 1983/4527 | 661/1508 | chr9 | 111722557 | |||
| chr9:111727709 | G | A | 1 | a0009c0018 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.1758C>T | p.Ser586Ser | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/28 | 1832/5200 | 1758/4527 | 586/1508 | chr9 | 111727709 | |||
| chr9:111727949 | T | G | 4 | a0003c0003 a0008c0009 a0015c0029 others(1): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
synonymous_variant | LOW | c.1518A>C | p.Ala506Ala | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/28 | 1592/5200 | 1518/4527 | 506/1508 | chr9 | 111727949 | |||
| chr9:111728045 | A | G | 1 | a0002c0012 | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.1422T>C | p.Cys474Cys | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/28 | 1496/5200 | 1422/4527 | 474/1508 | chr9 | 111728045 | |||
| chr9:111746245 | C | T | 1 | a0002c0010 | 6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
synonymous_variant | LOW | c.1068G>A | p.Pro356Pro | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/28 | 1142/5200 | 1068/4527 | 356/1508 | chr9 | 111746245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111686189 | T | A | 11 | a0001c0001t0001 a0001c0022t0001 a0001c0026t0001 others(8): Show |
143 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*581A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 581 | chr9 | 111686189 | ||||||
| chr9:111686238 | C | T | 2 | a0002c0007t0006 a0002c0012t0006 |
6 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*532G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 532 | chr9 | 111686238 | ||||||
| chr9:111686240 | G | A | 17 | a0001c0001t0001 a0001c0022t0001 a0001c0026t0001 others(14): Show |
182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*530C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 530 | chr9 | 111686240 | ||||||
| chr9:111686407 | T | G | 2 | a0005c0005t0003 a0016c0015t0003 |
22 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*363A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 363 | chr9 | 111686407 | ||||||
| chr9:111686517 | G | A | 1 | a0002c0007t0008 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*253C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 253 | chr9 | 111686517 | ||||||
| chr9:111686527 | G | C | 1 | a0004c0004t0007 | 2 | HG02027.hp1 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*243C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 243 | chr9 | 111686527 | ||||||
| chr9:111686527 | G | T | 2 | a0002c0011t0005 a0012c0025t0005 |
6 | HG01109.hp2 HG01243.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 28/28 | 243 | chr9 | 111686527 | ||||||
| chr9:111794933 | G | T | 1 | a0002c0007t0008 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/28 | 3515 | chr9 | 111794933 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111686902 | A | G | 2 | a0008c0009t0001g0109 a0008c0009t0001g0110 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4427-32T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111686902 | |||||||
| chr9:111686939 | C | CT | 50 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0117 others(47): Show |
51 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.4427-70dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111686939 | |||||||
| chr9:111686939 | C | CTT | 44 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(41): Show |
51 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.4427-71_4427-70dup others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111686939 | |||||||
| chr9:111686939 | CT | C | 96 | a0001c0026t0001g0252 a0002c0002t0002g0014 a0002c0002t0002g0166 others(93): Show |
102 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.4427-70delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111686939 | |||||||
| chr9:111686939 | CTT | C | 7 | a0002c0002t0002g0177 a0002c0011t0005g0121 a0002c0011t0005g0122 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.4427-71_4427-70del others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111686939 | |||||||
| chr9:111687033 | G | A | 1 | a0003c0003t0002g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4427-163C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687033 | |||||||
| chr9:111687478 | C | G | 2 | a0006c0006t0001g0041 a0006c0006t0001g0042 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4427-608G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687478 | |||||||
| chr9:111687690 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(117): Show |
136 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.4427-820G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687690 | |||||||
| chr9:111687752 | CTTCT | C | 30 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(27): Show |
34 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.4427-886_4427-883d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687752 | |||||||
| chr9:111687755 | CT | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(129): Show |
148 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.4427-886delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687755 | |||||||
| chr9:111687857 | G | A | 4 | a0005c0005t0003g0025 a0005c0005t0003g0026 a0005c0005t0003g0028 others(1): Show |
4 | HG02280.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4427-987C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687857 | |||||||
| chr9:111687896 | G | A | 36 | a0002c0002t0002g0014 a0002c0002t0002g0166 a0002c0002t0002g0175 others(33): Show |
37 | HG00558.hp2 HG00733.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.4427-1026C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687896 | |||||||
| chr9:111687906 | T | C | 1 | a0004c0004t0002g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4427-1036A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687906 | |||||||
| chr9:111687923 | C | T | 22 | a0002c0010t0004g0112 a0002c0010t0004g0113 a0002c0010t0004g0114 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.4427-1053G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111687923 | |||||||
| chr9:111688082 | T | TACC | 6 | a0005c0005t0003g0006 a0005c0005t0003g0023 a0005c0005t0003g0036 others(3): Show |
7 | HG00544.hp1 HG00621.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.4427-1215_4427-121 others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688082 | |||||||
| chr9:111688184 | T | C | 6 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.4427-1314A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688184 | |||||||
| chr9:111688249 | C | A | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4427-1379G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688249 | |||||||
| chr9:111688333 | C | T | 1 | a0001c0022t0001g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4427-1463G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688333 | |||||||
| chr9:111688352 | A | C | 2 | a0005c0005t0003g0021 a0005c0005t0003g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4427-1482T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688352 | |||||||
| chr9:111688591 | G | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.4427-1721C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688591 | |||||||
| chr9:111688699 | G | T | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4427-1829C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688699 | |||||||
| chr9:111688751 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0162 |
2 | HG02040.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.4427-1881T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688751 | |||||||
| chr9:111688828 | T | TG | 169 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(166): Show |
189 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.4427-1959_4427-195 others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111688828 | |||||||
| chr9:111689175 | C | G | 1 | a0021c0019t0002g0193 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4427-2305G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689175 | |||||||
| chr9:111689329 | C | CAAT | 13 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0139 others(10): Show |
13 | HG00099.hp1 HG02135.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.4426+2219_4426+222 others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689329 | |||||||
| chr9:111689345 | A | AATT | 38 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0135 others(35): Show |
42 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.4426+2205_4426+220 others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689345 | |||||||
| chr9:111689348 | A | AATT | 111 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(108): Show |
127 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.4426+2200_4426+220 others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689348 | |||||||
| chr9:111689348 | A | T | 41 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0135 others(38): Show |
45 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.4426+2203T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689348 | |||||||
| chr9:111689351 | T | A | 4 | a0002c0002t0002g0181 a0002c0002t0002g0183 a0004c0004t0002g0007 others(1): Show |
5 | NA18952.hp1 NA18970.hp2 NA19083.hp1 others(2): Show |
intron_variant | MODIFIER | c.4426+2200A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689351 | |||||||
| chr9:111689600 | AATAAATT others(5): Show |
A | 166 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(163): Show |
186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.4426+1939_4426+195 others(16): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689600 | |||||||
| chr9:111689601 | A | C | 4 | a0002c0010t0004g0112 a0002c0010t0004g0113 a0002c0010t0004g0114 others(1): Show |
4 | HG01884.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4426+1950T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689601 | |||||||
| chr9:111689602 | TAAATTTT others(5): Show |
T | 4 | a0002c0010t0004g0112 a0002c0010t0004g0113 a0002c0010t0004g0114 others(1): Show |
4 | HG01884.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4426+1937_4426+194 others(16): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689602 | |||||||
| chr9:111689613 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(163): Show |
186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.4426+1938A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689613 | |||||||
| chr9:111689614 | A | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(163): Show |
186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.4426+1937T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689614 | |||||||
| chr9:111689615 | A | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(167): Show |
190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.4426+1936T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689615 | |||||||
| chr9:111689616 | T | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(167): Show |
190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.4426+1935A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689616 | |||||||
| chr9:111689724 | A | G | 16 | a0002c0002t0002g0014 a0002c0002t0002g0176 a0002c0002t0002g0178 others(13): Show |
17 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.4426+1827T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689724 | |||||||
| chr9:111689735 | C | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(160): Show |
183 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.4426+1816G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111689735 | |||||||
| chr9:111690094 | C | CATAA | 164 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(161): Show |
184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.4426+1453_4426+145 others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111690094 | |||||||
| chr9:111690403 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(261): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.4426+1148A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111690403 | |||||||
| chr9:111690656 | A | G | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4426+895T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111690656 | |||||||
| chr9:111690726 | G | A | 31 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0117 others(28): Show |
32 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.4426+825C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111690726 | |||||||
| chr9:111690856 | T | C | 1 | a0010c0013t0002g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4426+695A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111690856 | |||||||
| chr9:111690896 | C | T | 1 | a0002c0002t0002g0198 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4426+655G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111690896 | |||||||
| chr9:111691255 | C | G | 1 | a0002c0002t0002g0180 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4426+296G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111691255 | |||||||
| chr9:111691332 | T | G | 1 | a0002c0002t0002g0189 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4426+219A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 27/27 | chr9 | 111691332 | |||||||
| chr9:111692606 | G | A | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3466-95C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111692606 | |||||||
| chr9:111692727 | T | C | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3466-216A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111692727 | |||||||
| chr9:111692801 | T | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(159): Show |
182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3466-290A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111692801 | |||||||
| chr9:111693090 | G | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(41): Show |
51 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.3466-579C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693090 | |||||||
| chr9:111693213 | C | T | 2 | a0011c0014t0002g0027 a0011c0014t0002g0029 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3465+586G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693213 | |||||||
| chr9:111693239 | G | A | 4 | a0002c0012t0006g0208 a0002c0012t0006g0209 a0002c0012t0006g0211 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3465+560C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693239 | |||||||
| chr9:111693421 | C | CA | 36 | a0002c0002t0002g0203 a0002c0007t0002g0128 a0002c0007t0004g0253 others(33): Show |
37 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.3465+377dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693421 | |||||||
| chr9:111693421 | CA | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(110): Show |
121 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.3465+377delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693421 | |||||||
| chr9:111693421 | CAA | C | 21 | a0001c0001t0001g0159 a0001c0001t0001g0246 a0002c0002t0002g0014 others(18): Show |
22 | HG00621.hp1 HG01192.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.3465+376_3465+377d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693421 | |||||||
| chr9:111693421 | CAAA | C | 36 | a0002c0002t0002g0191 a0002c0007t0001g0167 a0002c0010t0004g0113 others(33): Show |
48 | HG00544.hp1 HG01081.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.3465+375_3465+377d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693421 | |||||||
| chr9:111693421 | CAAAA | C | 10 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0135 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3465+374_3465+377d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 26/27 | chr9 | 111693421 | |||||||
| chr9:111694042 | T | TTAAG | 163 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(160): Show |
183 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.3316-95_3316-94ins others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 25/27 | chr9 | 111694042 | |||||||
| chr9:111694116 | C | T | 35 | a0002c0002t0002g0014 a0002c0002t0002g0166 a0002c0002t0002g0175 others(32): Show |
36 | HG00558.hp2 HG00733.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.3315+115G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 25/27 | chr9 | 111694116 | |||||||
| chr9:111694120 | T | C | 2 | a0002c0012t0006g0208 a0002c0012t0006g0209 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3315+111A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 25/27 | chr9 | 111694120 | |||||||
| chr9:111694651 | A | G | 3 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0019c0028t0001g0215 |
3 | HG02572.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3184-289T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111694651 | |||||||
| chr9:111694768 | A | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3184-406T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111694768 | |||||||
| chr9:111694819 | A | T | 22 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0135 others(19): Show |
30 | HG01081.hp2 HG01255.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3184-457T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111694819 | |||||||
| chr9:111694926 | C | T | 1 | a0001c0026t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3184-564G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111694926 | |||||||
| chr9:111695038 | C | T | 1 | a0003c0003t0002g0086 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3184-676G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695038 | |||||||
| chr9:111695070 | T | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3184-708A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695070 | |||||||
| chr9:111695086 | GA | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(159): Show |
182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3184-725delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695086 | |||||||
| chr9:111695348 | T | C | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3184-986A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695348 | |||||||
| chr9:111695421 | A | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3184-1059T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695421 | |||||||
| chr9:111695438 | G | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(159): Show |
182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3184-1076C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695438 | |||||||
| chr9:111695550 | C | T | 36 | a0002c0002t0002g0014 a0002c0002t0002g0166 a0002c0002t0002g0175 others(33): Show |
37 | HG00558.hp2 HG00733.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.3184-1188G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695550 | |||||||
| chr9:111695637 | A | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(159): Show |
182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3184-1275T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695637 | |||||||
| chr9:111695702 | G | A | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3184-1340C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695702 | |||||||
| chr9:111695853 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3184-1491T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695853 | |||||||
| chr9:111695917 | C | T | 1 | a0006c0006t0001g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3184-1555G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111695917 | |||||||
| chr9:111696165 | C | A | 4 | a0002c0010t0004g0112 a0002c0010t0004g0113 a0002c0010t0004g0114 others(1): Show |
4 | HG01884.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3184-1803G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696165 | |||||||
| chr9:111696272 | A | G | 206 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(203): Show |
227 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.3184-1910T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696272 | |||||||
| chr9:111696320 | C | T | 82 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0139 others(79): Show |
91 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.3184-1958G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696320 | |||||||
| chr9:111696346 | T | A | 21 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0139 others(18): Show |
21 | HG00099.hp1 HG00597.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.3184-1984A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696346 | |||||||
| chr9:111696372 | A | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3184-2010T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696372 | |||||||
| chr9:111696426 | A | C | 4 | a0007c0008t0001g0004 a0007c0008t0001g0078 a0007c0008t0001g0079 others(1): Show |
6 | HG02258.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3184-2064T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696426 | |||||||
| chr9:111696453 | T | A | 37 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(34): Show |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.3184-2091A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696453 | |||||||
| chr9:111696621 | C | T | 3 | a0002c0002t0002g0014 a0002c0002t0002g0178 a0002c0002t0002g0197 |
4 | NA19000.hp1 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.3184-2259G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696621 | |||||||
| chr9:111696631 | A | G | 6 | a0002c0007t0006g0213 a0002c0010t0002g0013 a0002c0012t0006g0208 others(3): Show |
7 | HG02109.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3184-2269T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696631 | |||||||
| chr9:111696660 | AT | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(90): Show |
102 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.3184-2299delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111696660 | |||||||
| chr9:111697029 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0235 |
2 | HG00741.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3184-2667T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697029 | |||||||
| chr9:111697049 | G | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3184-2687C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697049 | |||||||
| chr9:111697146 | A | G | 6 | a0002c0007t0006g0207 a0002c0007t0006g0213 a0002c0012t0006g0208 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3184-2784T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697146 | |||||||
| chr9:111697190 | C | CT | 57 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(54): Show |
62 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3183+2763dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697190 | |||||||
| chr9:111697203 | T | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3183+2751A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697203 | |||||||
| chr9:111697233 | T | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.3183+2721A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697233 | |||||||
| chr9:111697254 | T | C | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3183+2700A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697254 | |||||||
| chr9:111697279 | A | T | 1 | a0002c0007t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3183+2675T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697279 | |||||||
| chr9:111697326 | T | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3183+2628A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697326 | |||||||
| chr9:111697345 | C | T | 2 | a0006c0006t0001g0041 a0006c0006t0001g0042 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3183+2609G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697345 | |||||||
| chr9:111697356 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3183+2598C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697356 | |||||||
| chr9:111697435 | T | C | 11 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3183+2519A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697435 | |||||||
| chr9:111697489 | G | C | 11 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3183+2465C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697489 | |||||||
| chr9:111697506 | G | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(177): Show |
194 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.3183+2448C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697506 | |||||||
| chr9:111697511 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.3183+2443C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697511 | |||||||
| chr9:111697565 | C | A | 1 | a0007c0008t0001g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3183+2389G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697565 | |||||||
| chr9:111697702 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0001c0001t0001g0150 |
4 | HG01099.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3183+2252A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697702 | |||||||
| chr9:111697809 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3183+2145G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697809 | |||||||
| chr9:111697876 | C | T | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3183+2078G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697876 | |||||||
| chr9:111697929 | A | C | 44 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(41): Show |
45 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.3183+2025T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697929 | |||||||
| chr9:111697994 | G | A | 6 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3183+1960C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111697994 | |||||||
| chr9:111698009 | A | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.3183+1945T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698009 | |||||||
| chr9:111698029 | G | A | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.3183+1925C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698029 | |||||||
| chr9:111698093 | C | T | 1 | a0003c0003t0002g0108 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3183+1861G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698093 | |||||||
| chr9:111698229 | G | A | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3183+1725C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698229 | |||||||
| chr9:111698239 | T | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3183+1715A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698239 | |||||||
| chr9:111698303 | T | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3183+1651A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698303 | |||||||
| chr9:111698306 | G | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.3183+1648C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698306 | |||||||
| chr9:111698599 | T | TGTAGTAT others(4): Show |
40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.3183+1354_3183+135 others(15): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698599 | |||||||
| chr9:111698655 | AGC | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3183+1297_3183+129 others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698655 | |||||||
| chr9:111698657 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(86): Show |
97 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.3183+1297G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698657 | |||||||
| chr9:111698712 | G | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3183+1242C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698712 | |||||||
| chr9:111698720 | G | A | 1 | a0002c0002t0002g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3183+1234C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698720 | |||||||
| chr9:111698797 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3183+1157G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698797 | |||||||
| chr9:111698807 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3183+1147C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698807 | |||||||
| chr9:111698961 | G | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(156): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.3183+993C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111698961 | |||||||
| chr9:111699173 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.3183+781C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699173 | |||||||
| chr9:111699192 | C | T | 1 | a0002c0002t0002g0205 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3183+762G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699192 | |||||||
| chr9:111699423 | A | C | 1 | a0009c0018t0002g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3183+531T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699423 | |||||||
| chr9:111699546 | T | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3183+408A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699546 | |||||||
| chr9:111699575 | G | C | 1 | a0002c0002t0002g0175 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3183+379C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699575 | |||||||
| chr9:111699600 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3183+354T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699600 | |||||||
| chr9:111699623 | A | T | 1 | a0005c0005t0003g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3183+331T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699623 | |||||||
| chr9:111699641 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0153 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3183+313A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699641 | |||||||
| chr9:111699788 | C | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3183+166G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 24/27 | chr9 | 111699788 | |||||||
| chr9:111700186 | G | T | 85 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0117 others(82): Show |
91 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.3090-139C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700186 | |||||||
| chr9:111700257 | C | T | 5 | a0002c0012t0006g0208 a0002c0012t0006g0209 a0002c0012t0006g0211 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3090-210G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700257 | |||||||
| chr9:111700318 | T | A | 1 | a0018c0027t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3090-271A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700318 | |||||||
| chr9:111700342 | C | CA | 46 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(43): Show |
53 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3090-296dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700342 | |||||||
| chr9:111700374 | CT | C | 38 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(35): Show |
39 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.3090-328delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700374 | |||||||
| chr9:111700413 | G | C | 1 | a0006c0006t0001g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3090-366C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700413 | |||||||
| chr9:111700425 | G | A | 1 | a0002c0010t0004g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3090-378C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700425 | |||||||
| chr9:111700569 | CAA | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.3090-524_3090-523d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700569 | |||||||
| chr9:111700596 | T | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3090-549A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700596 | |||||||
| chr9:111700654 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3090-607T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700654 | |||||||
| chr9:111700675 | C | T | 60 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(57): Show |
65 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.3090-628G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700675 | |||||||
| chr9:111700700 | C | T | 3 | a0004c0004t0002g0060 a0004c0004t0002g0064 a0004c0004t0002g0071 |
3 | NA18966.hp1 NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.3090-653G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700700 | |||||||
| chr9:111700711 | T | G | 1 | a0004c0004t0002g0069 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3090-664A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700711 | |||||||
| chr9:111700723 | T | C | 3 | a0003c0003t0002g0092 a0003c0003t0002g0094 a0003c0003t0002g0111 |
3 | HG00642.hp2 HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.3090-676A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700723 | |||||||
| chr9:111700767 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.3090-720T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700767 | |||||||
| chr9:111700980 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3090-933G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111700980 | |||||||
| chr9:111701080 | T | C | 2 | a0002c0012t0006g0208 a0002c0012t0006g0209 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3089+1025A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111701080 | |||||||
| chr9:111701220 | C | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3089+885G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111701220 | |||||||
| chr9:111701766 | G | A | 21 | a0001c0001t0001g0249 a0005c0005t0003g0001 a0005c0005t0003g0006 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.3089+339C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111701766 | |||||||
| chr9:111701910 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3089+195G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111701910 | |||||||
| chr9:111701938 | C | T | 1 | a0008c0009t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3089+167G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111701938 | |||||||
| chr9:111702055 | T | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3089+50A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111702055 | |||||||
| chr9:111702075 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3089+30T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111702075 | |||||||
| chr9:111702095 | G | A | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3089+10C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 23/27 | chr9 | 111702095 | |||||||
| chr9:111702254 | A | C | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2968-28T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702254 | |||||||
| chr9:111702453 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(81): Show |
92 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2968-227G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702453 | |||||||
| chr9:111702490 | A | G | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2968-264T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702490 | |||||||
| chr9:111702528 | T | A | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2968-302A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702528 | |||||||
| chr9:111702601 | T | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2968-375A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702601 | |||||||
| chr9:111702688 | A | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2968-462T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702688 | |||||||
| chr9:111702722 | G | A | 6 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2968-496C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702722 | |||||||
| chr9:111702772 | A | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(144): Show |
157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2968-546T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702772 | |||||||
| chr9:111702924 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2968-698T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111702924 | |||||||
| chr9:111703023 | T | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2968-797A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703023 | |||||||
| chr9:111703064 | C | T | 3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2967+817G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703064 | |||||||
| chr9:111703079 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(139): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.2967+802G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703079 | |||||||
| chr9:111703224 | A | G | 37 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(34): Show |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2967+657T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703224 | |||||||
| chr9:111703298 | T | G | 1 | a0003c0003t0002g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2967+583A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703298 | |||||||
| chr9:111703312 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0263 |
2 | NA18955.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2967+569C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703312 | |||||||
| chr9:111703327 | C | A | 3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2967+554G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703327 | |||||||
| chr9:111703399 | G | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2967+482C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703399 | |||||||
| chr9:111703437 | T | C | 1 | a0001c0026t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2967+444A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703437 | |||||||
| chr9:111703580 | G | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2967+301C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703580 | |||||||
| chr9:111703603 | A | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2967+278T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703603 | |||||||
| chr9:111703761 | T | C | 6 | a0002c0007t0006g0207 a0002c0007t0006g0213 a0002c0012t0006g0208 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2967+120A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 22/27 | chr9 | 111703761 | |||||||
| chr9:111704238 | C | A | 4 | a0002c0002t0002g0189 a0002c0002t0002g0204 a0002c0002t0002g0205 others(1): Show |
4 | HG01123.hp1 HG02738.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2856-246G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111704238 | |||||||
| chr9:111704461 | T | C | 11 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2856-469A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111704461 | |||||||
| chr9:111704623 | C | T | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2855+624G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111704623 | |||||||
| chr9:111704746 | GT | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(156): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.2855+500delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111704746 | |||||||
| chr9:111704832 | A | C | 60 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(57): Show |
65 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2855+415T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111704832 | |||||||
| chr9:111704883 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2855+364T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111704883 | |||||||
| chr9:111704905 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2855+342G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111704905 | |||||||
| chr9:111705069 | A | G | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2855+178T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705069 | |||||||
| chr9:111705162 | A | AATATATA others(1): Show |
20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2855+77_2855+84dup others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705162 | |||||||
| chr9:111705162 | AAT | A | 33 | a0001c0001t0001g0229 a0002c0007t0008g0019 a0003c0003t0002g0011 others(30): Show |
34 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2855+83_2855+84del others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705162 | |||||||
| chr9:111705166 | T | TACACAC | 10 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0221 others(7): Show |
14 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2855+80_2855+81ins others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705166 | |||||||
| chr9:111705166 | T | TACACACA others(1): Show |
11 | a0001c0001t0001g0016 a0001c0001t0001g0157 a0001c0001t0001g0163 others(8): Show |
12 | HG00558.hp1 HG00642.hp1 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.2855+80_2855+81ins others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705166 | |||||||
| chr9:111705166 | T | TACACACA others(3): Show |
37 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0115 others(34): Show |
39 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2855+80_2855+81ins others(10): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705166 | |||||||
| chr9:111705166 | T | TACACACA others(5): Show |
27 | a0001c0001t0001g0012 a0001c0001t0001g0117 a0001c0001t0001g0118 others(24): Show |
28 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.2855+80_2855+81ins others(12): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705166 | |||||||
| chr9:111705166 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0146 others(1): Show |
4 | HG00544.hp2 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.2855+80_2855+81ins others(14): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705166 | |||||||
| chr9:111705166 | T | TACACACA others(9): Show |
5 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0153 others(2): Show |
5 | HG02040.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2855+80_2855+81ins others(16): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705166 | |||||||
| chr9:111705168 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(94): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2855+79A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705168 | |||||||
| chr9:111705168 | T | TACACAC | 17 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0176 others(14): Show |
18 | HG00673.hp1 HG01123.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2855+78_2855+79ins others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705168 | |||||||
| chr9:111705168 | T | TACACACA others(1): Show |
14 | a0002c0002t0002g0166 a0002c0002t0002g0175 a0002c0002t0002g0179 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2855+78_2855+79ins others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705168 | |||||||
| chr9:111705168 | T | TACACACA others(3): Show |
2 | a0002c0002t0002g0185 a0002c0002t0002g0190 |
2 | HG03654.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2855+78_2855+79ins others(10): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705168 | |||||||
| chr9:111705168 | T | TACACACA others(7): Show |
5 | a0002c0002t0002g0177 a0002c0002t0002g0181 a0002c0002t0002g0182 others(2): Show |
5 | HG00558.hp2 HG02135.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2855+78_2855+79ins others(14): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705168 | |||||||
| chr9:111705168 | TATAC | T | 7 | a0008c0009t0001g0084 a0008c0009t0001g0100 a0008c0009t0001g0101 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2855+75_2855+78del others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705168 | |||||||
| chr9:111705170 | T | C | 144 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(141): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2855+77A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705170 | |||||||
| chr9:111705170 | T | TAC | 12 | a0006c0006t0001g0002 a0006c0006t0001g0034 a0006c0006t0001g0035 others(9): Show |
15 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2855+75_2855+76dup others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705170 | |||||||
| chr9:111705170 | T | TATATATA others(3): Show |
1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2855+76_2855+77ins others(10): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705170 | |||||||
| chr9:111705170 | TAC | T | 6 | a0002c0007t0006g0207 a0002c0007t0006g0213 a0002c0012t0006g0208 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2855+75_2855+76del others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705170 | |||||||
| chr9:111705172 | C | T | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2855+75G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705172 | |||||||
| chr9:111705195 | A | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2855+52T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705195 | |||||||
| chr9:111705196 | C | CACACAT | 10 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2855+50_2855+51ins others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705196 | |||||||
| chr9:111705196 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2855+51G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705196 | |||||||
| chr9:111705198 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(95): Show |
106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2855+49A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705198 | |||||||
| chr9:111705200 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0244 a0001c0001t0001g0260 |
3 | HG02135.hp2 NA18999.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2855+47A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705200 | |||||||
| chr9:111705202 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2855+45A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705202 | |||||||
| chr9:111705204 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2855+43A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705204 | |||||||
| chr9:111705206 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2855+41A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705206 | |||||||
| chr9:111705208 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2855+39T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705208 | |||||||
| chr9:111705209 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2855+38A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705209 | |||||||
| chr9:111705210 | G | T | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2855+37C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705210 | |||||||
| chr9:111705211 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2855+36A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705211 | |||||||
| chr9:111705219 | T | C | 1 | a0006c0006t0001g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2855+28A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 21/27 | chr9 | 111705219 | |||||||
| chr9:111705391 | T | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2738-27A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705391 | |||||||
| chr9:111705412 | C | A | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2738-48G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705412 | |||||||
| chr9:111705415 | CTCTT | C | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.2738-55_2738-52del others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705415 | |||||||
| chr9:111705423 | C | CT | 98 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(95): Show |
106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2738-60dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705423 | |||||||
| chr9:111705423 | CT | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2738-60delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705423 | |||||||
| chr9:111705545 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2738-181G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705545 | |||||||
| chr9:111705873 | C | T | 1 | a0008c0009t0001g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2738-509G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705873 | |||||||
| chr9:111705941 | G | T | 60 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(57): Show |
65 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2738-577C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705941 | |||||||
| chr9:111705991 | A | G | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2737+577T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111705991 | |||||||
| chr9:111706014 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2737+554G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111706014 | |||||||
| chr9:111706110 | C | T | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2737+458G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111706110 | |||||||
| chr9:111706142 | G | A | 60 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(57): Show |
65 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2737+426C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111706142 | |||||||
| chr9:111706321 | T | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2737+247A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111706321 | |||||||
| chr9:111706350 | A | C | 37 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(34): Show |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2737+218T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 20/27 | chr9 | 111706350 | |||||||
| chr9:111706798 | T | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2559-52A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111706798 | |||||||
| chr9:111706876 | G | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2559-130C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111706876 | |||||||
| chr9:111706903 | A | G | 14 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0139 others(11): Show |
14 | HG00099.hp1 HG00597.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.2559-157T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111706903 | |||||||
| chr9:111706905 | A | G | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2559-159T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111706905 | |||||||
| chr9:111706981 | T | C | 2 | a0002c0002t0002g0176 a0002c0002t0002g0200 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2559-235A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111706981 | |||||||
| chr9:111707018 | C | T | 4 | a0002c0012t0006g0208 a0002c0012t0006g0209 a0002c0012t0006g0211 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2559-272G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707018 | |||||||
| chr9:111707023 | T | A | 37 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(34): Show |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2559-277A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707023 | |||||||
| chr9:111707204 | T | C | 5 | a0006c0006t0001g0002 a0006c0006t0001g0050 a0006c0006t0001g0052 others(2): Show |
8 | HG01081.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2559-458A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707204 | |||||||
| chr9:111707254 | A | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2559-508T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707254 | |||||||
| chr9:111707267 | C | A | 39 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(36): Show |
40 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.2559-521G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707267 | |||||||
| chr9:111707394 | GA | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2558+460delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707394 | |||||||
| chr9:111707819 | C | G | 1 | a0002c0007t0002g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2558+36G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707819 | |||||||
| chr9:111707826 | T | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2558+29A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707826 | |||||||
| chr9:111707847 | A | G | 21 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0139 others(18): Show |
21 | HG00099.hp1 HG00597.hp1 HG02040.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.2558+8T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 19/27 | chr9 | 111707847 | |||||||
| chr9:111707966 | A | C | 1 | a0002c0010t0002g0013 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2489-42T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111707966 | |||||||
| chr9:111708096 | C | T | 1 | a0003c0003t0002g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2489-172G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708096 | |||||||
| chr9:111708104 | A | G | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2489-180T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708104 | |||||||
| chr9:111708165 | A | G | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2489-241T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708165 | |||||||
| chr9:111708198 | A | AAT | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2489-275_2489-274i others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708198 | |||||||
| chr9:111708201 | T | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2489-277A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708201 | |||||||
| chr9:111708208 | T | TA | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2489-285_2489-284i others(3): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708208 | |||||||
| chr9:111708209 | T | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2489-285A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708209 | |||||||
| chr9:111708212 | A | T | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2489-288T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708212 | |||||||
| chr9:111708215 | T | TA | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2489-292_2489-291i others(3): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708215 | |||||||
| chr9:111708234 | G | A | 1 | a0002c0002t0002g0166 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2489-310C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708234 | |||||||
| chr9:111708260 | T | C | 1 | a0002c0007t0004g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2489-336A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708260 | |||||||
| chr9:111708289 | G | A | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2489-365C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708289 | |||||||
| chr9:111708314 | T | C | 3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2489-390A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708314 | |||||||
| chr9:111708350 | C | T | 1 | a0002c0007t0004g0214 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2489-426G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708350 | |||||||
| chr9:111708352 | G | A | 1 | a0003c0003t0002g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2489-428C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708352 | |||||||
| chr9:111708541 | A | G | 37 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(34): Show |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2489-617T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708541 | |||||||
| chr9:111708664 | T | G | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2489-740A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708664 | |||||||
| chr9:111708677 | G | A | 1 | a0003c0003t0002g0174 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2489-753C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708677 | |||||||
| chr9:111708945 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2489-1021G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708945 | |||||||
| chr9:111708966 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2489-1042G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708966 | |||||||
| chr9:111708982 | T | C | 1 | a0002c0002t0002g0239 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2489-1058A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708982 | |||||||
| chr9:111708986 | G | A | 7 | a0008c0009t0001g0084 a0008c0009t0001g0100 a0008c0009t0001g0101 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2489-1062C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111708986 | |||||||
| chr9:111709129 | T | C | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2489-1205A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111709129 | |||||||
| chr9:111709405 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2489-1481G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111709405 | |||||||
| chr9:111709501 | T | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(237): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.2489-1577A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111709501 | |||||||
| chr9:111709532 | T | C | 1 | a0004c0004t0002g0007 | 2 | NA18952.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2489-1608A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111709532 | |||||||
| chr9:111709537 | G | A | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2489-1613C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111709537 | |||||||
| chr9:111709849 | C | T | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2489-1925G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111709849 | |||||||
| chr9:111709936 | G | C | 1 | a0002c0007t0002g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2489-2012C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111709936 | |||||||
| chr9:111710148 | C | G | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2489-2224G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710148 | |||||||
| chr9:111710154 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2489-2230G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710154 | |||||||
| chr9:111710299 | A | G | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2489-2375T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710299 | |||||||
| chr9:111710454 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2489-2530G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710454 | |||||||
| chr9:111710467 | C | G | 61 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(58): Show |
66 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2489-2543G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710467 | |||||||
| chr9:111710675 | G | T | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2488+2425C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710675 | |||||||
| chr9:111710692 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2488+2408T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710692 | |||||||
| chr9:111710839 | G | A | 2 | a0009c0017t0002g0049 a0009c0018t0002g0040 |
2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2488+2261C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710839 | |||||||
| chr9:111710929 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2488+2171C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710929 | |||||||
| chr9:111710942 | C | T | 21 | a0002c0010t0002g0013 a0005c0005t0003g0001 a0005c0005t0003g0006 others(18): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.2488+2158G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111710942 | |||||||
| chr9:111711066 | C | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | NA19005.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2488+2034G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711066 | |||||||
| chr9:111711194 | G | C | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488+1906C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711194 | |||||||
| chr9:111711312 | C | T | 2 | a0004c0004t0002g0008 a0004c0004t0002g0075 |
3 | HG01256.hp1 HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2488+1788G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711312 | |||||||
| chr9:111711356 | G | A | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2488+1744C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711356 | |||||||
| chr9:111711491 | G | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2488+1609C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711491 | |||||||
| chr9:111711571 | G | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+1529C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711571 | |||||||
| chr9:111711576 | G | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+1524C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711576 | |||||||
| chr9:111711613 | A | G | 3 | a0001c0001t0001g0228 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | NA18955.hp1 NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2488+1487T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711613 | |||||||
| chr9:111711718 | C | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2488+1382G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711718 | |||||||
| chr9:111711767 | A | G | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2488+1333T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711767 | |||||||
| chr9:111711813 | T | G | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488+1287A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711813 | |||||||
| chr9:111711833 | A | G | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488+1267T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711833 | |||||||
| chr9:111711834 | T | A | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2488+1266A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711834 | |||||||
| chr9:111711877 | A | G | 9 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(6): Show |
9 | HG02572.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488+1223T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711877 | |||||||
| chr9:111711922 | T | A | 5 | a0002c0007t0006g0213 a0002c0012t0006g0208 a0002c0012t0006g0209 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488+1178A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111711922 | |||||||
| chr9:111712088 | A | G | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+1012T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712088 | |||||||
| chr9:111712113 | C | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+987G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712113 | |||||||
| chr9:111712156 | A | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2488+944T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712156 | |||||||
| chr9:111712247 | T | C | 1 | a0003c0003t0002g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2488+853A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712247 | |||||||
| chr9:111712387 | A | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+713T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712387 | |||||||
| chr9:111712420 | G | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+680C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712420 | |||||||
| chr9:111712439 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2488+661T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712439 | |||||||
| chr9:111712448 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+652G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712448 | |||||||
| chr9:111712449 | G | C | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488+651C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712449 | |||||||
| chr9:111712450 | G | GTA | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+648_2488+649d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712450 | |||||||
| chr9:111712527 | C | G | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+573G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712527 | |||||||
| chr9:111712543 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2488+557T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712543 | |||||||
| chr9:111712549 | C | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.2488+551G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712549 | |||||||
| chr9:111712597 | G | T | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2488+503C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712597 | |||||||
| chr9:111712691 | A | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(94): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2488+409T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712691 | |||||||
| chr9:111712795 | GT | G | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488+304delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712795 | |||||||
| chr9:111712916 | G | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2488+184C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712916 | |||||||
| chr9:111712982 | T | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.2488+118A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 18/27 | chr9 | 111712982 | |||||||
| chr9:111713281 | A | G | 2 | a0006c0006t0001g0041 a0006c0006t0001g0042 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2416-109T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713281 | |||||||
| chr9:111713384 | A | G | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2416-212T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713384 | |||||||
| chr9:111713527 | C | T | 21 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(18): Show |
22 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.2416-355G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713527 | |||||||
| chr9:111713543 | G | C | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2416-371C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713543 | |||||||
| chr9:111713571 | G | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2416-399C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713571 | |||||||
| chr9:111713617 | A | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2416-445T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713617 | |||||||
| chr9:111713646 | C | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | NA18955.hp1 NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2416-474G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713646 | |||||||
| chr9:111713662 | G | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2416-490C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713662 | |||||||
| chr9:111713668 | G | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2416-496C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713668 | |||||||
| chr9:111713918 | T | G | 2 | a0005c0005t0003g0021 a0005c0005t0003g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2415+527A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713918 | |||||||
| chr9:111713986 | T | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2415+459A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111713986 | |||||||
| chr9:111714189 | A | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2415+256T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 17/27 | chr9 | 111714189 | |||||||
| chr9:111714679 | C | T | 1 | a0002c0007t0004g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2237-56G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111714679 | |||||||
| chr9:111714762 | A | ATACT | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2237-140_2237-139i others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111714762 | |||||||
| chr9:111714763 | C | G | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2237-140G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111714763 | |||||||
| chr9:111714866 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2237-243G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111714866 | |||||||
| chr9:111714990 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2237-367C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111714990 | |||||||
| chr9:111715076 | C | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2237-453G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111715076 | |||||||
| chr9:111715190 | C | T | 4 | a0003c0003t0002g0083 a0003c0003t0002g0095 a0003c0003t0002g0097 others(1): Show |
4 | HG01074.hp1 HG01169.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.2237-567G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111715190 | |||||||
| chr9:111715281 | T | A | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2237-658A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111715281 | |||||||
| chr9:111715824 | T | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2237-1201A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111715824 | |||||||
| chr9:111715941 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2237-1318C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111715941 | |||||||
| chr9:111716050 | T | C | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2237-1427A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716050 | |||||||
| chr9:111716217 | A | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237-1594T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716217 | |||||||
| chr9:111716233 | C | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2237-1610G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716233 | |||||||
| chr9:111716345 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(141): Show |
154 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2237-1722C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716345 | |||||||
| chr9:111716381 | C | CT | 14 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(11): Show |
14 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2237-1759dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716381 | |||||||
| chr9:111716381 | CT | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
114 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.2237-1759delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716381 | |||||||
| chr9:111716381 | CTT | C | 52 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0231 others(49): Show |
55 | HG00140.hp1 HG00642.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.2237-1760_2237-175 others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716381 | |||||||
| chr9:111716381 | CTTT | C | 23 | a0002c0002t0002g0200 a0002c0010t0004g0112 a0002c0010t0004g0113 others(20): Show |
24 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2237-1761_2237-175 others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716381 | |||||||
| chr9:111716381 | CTTTTTT | C | 18 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(15): Show |
22 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.2237-1764_2237-175 others(10): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716381 | |||||||
| chr9:111716532 | A | G | 5 | a0002c0007t0006g0213 a0002c0012t0006g0208 a0002c0012t0006g0209 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236+1652T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716532 | |||||||
| chr9:111716564 | A | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2236+1620T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716564 | |||||||
| chr9:111716851 | T | C | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236+1333A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111716851 | |||||||
| chr9:111717205 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2236+979C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717205 | |||||||
| chr9:111717278 | A | T | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2236+906T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717278 | |||||||
| chr9:111717461 | C | T | 1 | a0003c0003t0002g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2236+723G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717461 | |||||||
| chr9:111717510 | A | T | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2236+674T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717510 | |||||||
| chr9:111717570 | G | A | 1 | a0021c0019t0002g0193 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2236+614C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717570 | |||||||
| chr9:111717594 | C | CA | 24 | a0002c0002t0002g0197 a0002c0002t0002g0205 a0002c0010t0004g0165 others(21): Show |
28 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.2236+589dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717594 | |||||||
| chr9:111717594 | CA | C | 11 | a0001c0001t0001g0119 a0002c0007t0004g0168 a0002c0007t0004g0214 others(8): Show |
11 | HG01167.hp1 HG02572.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.2236+589delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717594 | |||||||
| chr9:111717677 | T | C | 1 | a0022c0023t0001g0265 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2236+507A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717677 | |||||||
| chr9:111717758 | C | G | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236+426G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717758 | |||||||
| chr9:111717767 | A | G | 1 | a0005c0005t0003g0266 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2236+417T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717767 | |||||||
| chr9:111717874 | C | G | 7 | a0008c0009t0001g0084 a0008c0009t0001g0100 a0008c0009t0001g0101 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2236+310G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717874 | |||||||
| chr9:111717907 | A | G | 4 | a0002c0012t0006g0208 a0002c0012t0006g0209 a0002c0012t0006g0211 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2236+277T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111717907 | |||||||
| chr9:111718059 | G | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2236+125C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111718059 | |||||||
| chr9:111718067 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2236+117A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 16/27 | chr9 | 111718067 | |||||||
| chr9:111718322 | C | A | 159 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(156): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.2132-34G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111718322 | |||||||
| chr9:111718380 | T | G | 1 | a0004c0004t0002g0007 | 2 | NA18952.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2132-92A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111718380 | |||||||
| chr9:111718628 | T | C | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2132-340A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111718628 | |||||||
| chr9:111718681 | T | C | 2 | a0003c0003t0002g0091 a0003c0003t0002g0096 |
2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2132-393A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111718681 | |||||||
| chr9:111718790 | CAA | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2132-504_2132-503d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111718790 | |||||||
| chr9:111718879 | G | A | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2132-591C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111718879 | |||||||
| chr9:111719019 | T | C | 1 | a0003c0003t0002g0172 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2132-731A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111719019 | |||||||
| chr9:111719351 | G | A | 41 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(38): Show |
42 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.2132-1063C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111719351 | |||||||
| chr9:111719375 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2132-1087G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111719375 | |||||||
| chr9:111719899 | G | A | 1 | a0002c0007t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2132-1611C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111719899 | |||||||
| chr9:111720082 | C | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2132-1794G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720082 | |||||||
| chr9:111720300 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG00408.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2132-2012A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720300 | |||||||
| chr9:111720358 | A | G | 1 | a0005c0005t0003g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2131+2051T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720358 | |||||||
| chr9:111720503 | T | G | 9 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(6): Show |
9 | HG02572.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2131+1906A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720503 | |||||||
| chr9:111720700 | C | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(141): Show |
154 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2131+1709G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720700 | |||||||
| chr9:111720742 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.2131+1667A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720742 | |||||||
| chr9:111720877 | T | C | 2 | a0006c0006t0001g0041 a0006c0006t0001g0042 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2131+1532A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720877 | |||||||
| chr9:111720940 | T | G | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2131+1469A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720940 | |||||||
| chr9:111720998 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2131+1411A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111720998 | |||||||
| chr9:111721011 | T | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2131+1398A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721011 | |||||||
| chr9:111721021 | A | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2131+1388T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721021 | |||||||
| chr9:111721036 | C | T | 6 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0112 others(3): Show |
7 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2131+1373G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721036 | |||||||
| chr9:111721155 | T | C | 1 | a0008c0009t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2131+1254A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721155 | |||||||
| chr9:111721340 | T | G | 3 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0019c0028t0001g0215 |
3 | HG02572.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2131+1069A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721340 | |||||||
| chr9:111721362 | C | T | 4 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(1): Show |
5 | HG02109.hp1 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2131+1047G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721362 | |||||||
| chr9:111721443 | G | A | 2 | a0005c0005t0003g0021 a0005c0005t0003g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2131+966C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721443 | |||||||
| chr9:111721560 | G | A | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2131+849C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721560 | |||||||
| chr9:111721586 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2131+823G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721586 | |||||||
| chr9:111721755 | T | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2131+654A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721755 | |||||||
| chr9:111721770 | C | A | 1 | a0003c0003t0002g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2131+639G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721770 | |||||||
| chr9:111721809 | C | T | 1 | a0006c0006t0001g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2131+600G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721809 | |||||||
| chr9:111721868 | C | A | 19 | a0002c0002t0002g0166 a0002c0002t0002g0175 a0002c0002t0002g0177 others(16): Show |
19 | HG00558.hp2 HG02135.hp1 HG03239.hp2 others(16): Show |
intron_variant | MODIFIER | c.2131+541G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721868 | |||||||
| chr9:111721936 | T | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2131+473A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111721936 | |||||||
| chr9:111722123 | T | C | 37 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(34): Show |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2131+286A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111722123 | |||||||
| chr9:111722141 | G | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2131+268C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111722141 | |||||||
| chr9:111722312 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(261): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.2131+97C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111722312 | |||||||
| chr9:111722402 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
splice_region_variant&intron_variant | LOW | c.2131+7A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 15/27 | chr9 | 111722402 | |||||||
| chr9:111722675 | C | T | 2 | a0008c0009t0001g0109 a0008c0009t0001g0110 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1955-90G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111722675 | |||||||
| chr9:111722729 | CTTATT | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(98): Show |
109 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1955-149_1955-145d others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111722729 | |||||||
| chr9:111722837 | C | T | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1955-252G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111722837 | |||||||
| chr9:111722889 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1955-304A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111722889 | |||||||
| chr9:111722947 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1955-362C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111722947 | |||||||
| chr9:111722981 | C | A | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1955-396G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111722981 | |||||||
| chr9:111723031 | C | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1955-446G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723031 | |||||||
| chr9:111723071 | C | T | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1955-486G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723071 | |||||||
| chr9:111723138 | A | T | 1 | a0003c0003t0002g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1955-553T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723138 | |||||||
| chr9:111723468 | A | C | 1 | a0001c0001t0001g0260 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1954+324T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723468 | |||||||
| chr9:111723470 | A | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(156): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1954+322T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723470 | |||||||
| chr9:111723588 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1954+204G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723588 | |||||||
| chr9:111723630 | G | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1954+162C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723630 | |||||||
| chr9:111723668 | G | C | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1954+124C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723668 | |||||||
| chr9:111723711 | A | T | 2 | a0004c0004t0002g0045 a0004c0004t0002g0066 |
2 | HG00099.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1954+81T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 14/27 | chr9 | 111723711 | |||||||
| chr9:111723939 | T | A | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1835-28A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111723939 | |||||||
| chr9:111724058 | T | C | 1 | a0004c0004t0002g0069 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1835-147A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111724058 | |||||||
| chr9:111724122 | G | A | 1 | a0006c0006t0001g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1835-211C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111724122 | |||||||
| chr9:111724417 | G | A | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1835-506C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111724417 | |||||||
| chr9:111724447 | C | T | 1 | a0002c0002t0002g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1835-536G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111724447 | |||||||
| chr9:111724626 | C | T | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1835-715G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111724626 | |||||||
| chr9:111724761 | C | T | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1835-850G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111724761 | |||||||
| chr9:111725005 | A | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1835-1094T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111725005 | |||||||
| chr9:111725065 | A | G | 9 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(6): Show |
9 | HG02572.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1835-1154T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111725065 | |||||||
| chr9:111725097 | A | G | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1835-1186T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111725097 | |||||||
| chr9:111725491 | G | C | 1 | a0002c0007t0004g0214 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1835-1580C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111725491 | |||||||
| chr9:111725651 | T | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1835-1740A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111725651 | |||||||
| chr9:111725711 | T | C | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1835-1800A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111725711 | |||||||
| chr9:111725849 | A | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1834+1784T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111725849 | |||||||
| chr9:111726184 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1834+1449T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726184 | |||||||
| chr9:111726500 | C | T | 38 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(35): Show |
39 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1834+1133G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726500 | |||||||
| chr9:111726565 | A | G | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1834+1068T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726565 | |||||||
| chr9:111726576 | T | C | 1 | a0002c0002t0002g0268 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1834+1057A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726576 | |||||||
| chr9:111726625 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1834+1008T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726625 | |||||||
| chr9:111726725 | T | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1834+908A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726725 | |||||||
| chr9:111726791 | A | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1834+842T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726791 | |||||||
| chr9:111726954 | G | A | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1834+679C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726954 | |||||||
| chr9:111726963 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1834+670T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111726963 | |||||||
| chr9:111727019 | A | C | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1834+614T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111727019 | |||||||
| chr9:111727125 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1834+508G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111727125 | |||||||
| chr9:111727129 | AT | A | 6 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1834+503delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111727129 | |||||||
| chr9:111727468 | T | G | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1834+165A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111727468 | |||||||
| chr9:111727607 | C | T | 159 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(156): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1834+26G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 13/27 | chr9 | 111727607 | |||||||
| chr9:111728085 | C | T | 6 | a0005c0005t0003g0025 a0005c0005t0003g0026 a0005c0005t0003g0028 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1418-36G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111728085 | |||||||
| chr9:111728258 | G | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(42): Show |
52 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1418-209C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111728258 | |||||||
| chr9:111728802 | A | T | 2 | a0005c0005t0003g0021 a0005c0005t0003g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1418-753T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111728802 | |||||||
| chr9:111729103 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1418-1054C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729103 | |||||||
| chr9:111729109 | T | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1418-1060A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729109 | |||||||
| chr9:111729117 | T | TC | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1418-1069dupG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729117 | |||||||
| chr9:111729118 | C | G | 1 | a0003c0003t0002g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1418-1069G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729118 | |||||||
| chr9:111729195 | A | AACCTCCA others(25): Show |
40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1418-1178_1418-114 others(36): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729195 | |||||||
| chr9:111729358 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1418-1309A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729358 | |||||||
| chr9:111729384 | G | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1418-1335C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729384 | |||||||
| chr9:111729391 | G | T | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1418-1342C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729391 | |||||||
| chr9:111729401 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1418-1352G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729401 | |||||||
| chr9:111729408 | G | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0244 a0001c0001t0001g0245 |
3 | HG02071.hp2 NA19005.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1418-1359C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729408 | |||||||
| chr9:111729625 | G | A | 2 | a0006c0006t0001g0041 a0006c0006t0001g0042 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1418-1576C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729625 | |||||||
| chr9:111729651 | T | C | 6 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1418-1602A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729651 | |||||||
| chr9:111729761 | G | A | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1418-1712C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729761 | |||||||
| chr9:111729769 | G | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1418-1720C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729769 | |||||||
| chr9:111729823 | C | T | 2 | a0002c0012t0006g0208 a0002c0012t0006g0209 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1418-1774G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729823 | |||||||
| chr9:111729888 | C | CA | 87 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(84): Show |
93 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1418-1840dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729888 | |||||||
| chr9:111729888 | C | CAA | 131 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(128): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1418-1841_1418-184 others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729888 | |||||||
| chr9:111729905 | T | C | 37 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(34): Show |
38 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1418-1856A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111729905 | |||||||
| chr9:111730051 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1418-2002T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730051 | |||||||
| chr9:111730152 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1418-2103A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730152 | |||||||
| chr9:111730212 | T | G | 38 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(35): Show |
39 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1418-2163A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730212 | |||||||
| chr9:111730322 | A | C | 9 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(6): Show |
9 | HG02572.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1418-2273T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730322 | |||||||
| chr9:111730393 | G | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1418-2344C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730393 | |||||||
| chr9:111730455 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1418-2406C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730455 | |||||||
| chr9:111730532 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1418-2483A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730532 | |||||||
| chr9:111730867 | G | A | 1 | a0003c0003t0002g0172 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1418-2818C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730867 | |||||||
| chr9:111730886 | A | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1418-2837T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730886 | |||||||
| chr9:111730977 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1418-2928A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111730977 | |||||||
| chr9:111731074 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(42): Show |
52 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1418-3025A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731074 | |||||||
| chr9:111731140 | TTGTG | T | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1418-3095_1418-309 others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731140 | |||||||
| chr9:111731145 | G | C | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1418-3096C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731145 | |||||||
| chr9:111731146 | C | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1418-3097G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731146 | |||||||
| chr9:111731195 | G | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1418-3146C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731195 | |||||||
| chr9:111731219 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1418-3170C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731219 | |||||||
| chr9:111731347 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1418-3298A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731347 | |||||||
| chr9:111731402 | C | T | 1 | a0003c0003t0002g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1418-3353G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731402 | |||||||
| chr9:111731455 | G | A | 1 | a0003c0003t0002g0020 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1418-3406C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731455 | |||||||
| chr9:111731486 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1418-3437C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731486 | |||||||
| chr9:111731497 | G | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1418-3448C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731497 | |||||||
| chr9:111731514 | G | A | 38 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(35): Show |
39 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1418-3465C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731514 | |||||||
| chr9:111731542 | T | A | 38 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(35): Show |
39 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1418-3493A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731542 | |||||||
| chr9:111731803 | AAACAT | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1418-3759_1418-375 others(9): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731803 | |||||||
| chr9:111731808 | T | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(197): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1418-3759A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731808 | |||||||
| chr9:111731972 | C | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1418-3923G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731972 | |||||||
| chr9:111731987 | A | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1418-3938T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731987 | |||||||
| chr9:111731999 | TA | T | 6 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1418-3951delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111731999 | |||||||
| chr9:111732000 | A | T | 30 | a0001c0001t0001g0236 a0002c0010t0002g0013 a0002c0010t0004g0112 others(27): Show |
35 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.1418-3951T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732000 | |||||||
| chr9:111732266 | C | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1418-4217G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732266 | |||||||
| chr9:111732276 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1418-4227A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732276 | |||||||
| chr9:111732367 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0153 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1418-4318A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732367 | |||||||
| chr9:111732527 | T | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(156): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1418-4478A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732527 | |||||||
| chr9:111732708 | AATAC | A | 7 | a0008c0009t0001g0084 a0008c0009t0001g0100 a0008c0009t0001g0101 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1418-4663_1418-466 others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732708 | |||||||
| chr9:111732750 | A | G | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1418-4701T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732750 | |||||||
| chr9:111732870 | G | T | 4 | a0002c0012t0006g0208 a0002c0012t0006g0209 a0002c0012t0006g0211 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1418-4821C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111732870 | |||||||
| chr9:111733039 | CT | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1418-4991delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733039 | |||||||
| chr9:111733041 | T | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1418-4992A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733041 | |||||||
| chr9:111733220 | T | C | 1 | a0004c0004t0002g0048 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1417+5060A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733220 | |||||||
| chr9:111733335 | A | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1417+4945T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733335 | |||||||
| chr9:111733341 | C | T | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1417+4939G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733341 | |||||||
| chr9:111733552 | T | C | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1417+4728A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733552 | |||||||
| chr9:111733614 | T | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1417+4666A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733614 | |||||||
| chr9:111733642 | C | A | 3 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0019c0028t0001g0215 |
3 | HG02572.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1417+4638G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733642 | |||||||
| chr9:111733764 | A | G | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1417+4516T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733764 | |||||||
| chr9:111733796 | A | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(98): Show |
109 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1417+4484T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733796 | |||||||
| chr9:111733857 | CA | C | 42 | a0001c0001t0001g0126 a0002c0002t0002g0179 a0002c0007t0008g0019 others(39): Show |
43 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1417+4422delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111733857 | |||||||
| chr9:111734070 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1417+4210C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734070 | |||||||
| chr9:111734235 | CATA | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(156): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1417+4042_1417+404 others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734235 | |||||||
| chr9:111734509 | C | T | 1 | a0006c0006t0001g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1417+3771G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734509 | |||||||
| chr9:111734680 | G | C | 40 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1417+3600C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734680 | |||||||
| chr9:111734687 | A | G | 1 | a0002c0002t0002g0190 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1417+3593T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734687 | |||||||
| chr9:111734814 | T | TA | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1417+3465dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734814 | |||||||
| chr9:111734819 | T | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1417+3461A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734819 | |||||||
| chr9:111734960 | A | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1417+3320T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734960 | |||||||
| chr9:111734978 | C | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1417+3302G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111734978 | |||||||
| chr9:111735248 | A | G | 3 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0019c0028t0001g0215 |
3 | HG02572.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1417+3032T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735248 | |||||||
| chr9:111735330 | C | T | 47 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0117 others(44): Show |
48 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1417+2950G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735330 | |||||||
| chr9:111735351 | C | A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(162): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1417+2929G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735351 | |||||||
| chr9:111735586 | T | C | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1417+2694A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735586 | |||||||
| chr9:111735589 | A | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1417+2691T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735589 | |||||||
| chr9:111735829 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0240 |
2 | HG02523.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1417+2451G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735829 | |||||||
| chr9:111735872 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1417+2408G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735872 | |||||||
| chr9:111735873 | G | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1417+2407C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735873 | |||||||
| chr9:111735897 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1417+2383A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111735897 | |||||||
| chr9:111736056 | A | G | 1 | a0002c0011t0005g0121 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1417+2224T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111736056 | |||||||
| chr9:111736452 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1417+1828A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111736452 | |||||||
| chr9:111736527 | A | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1417+1753T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111736527 | |||||||
| chr9:111736534 | C | T | 2 | a0002c0002t0002g0181 a0002c0002t0002g0183 |
2 | NA19083.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1417+1746G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111736534 | |||||||
| chr9:111736604 | T | C | 1 | a0002c0007t0004g0214 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1417+1676A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111736604 | |||||||
| chr9:111736608 | A | G | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+1672T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111736608 | |||||||
| chr9:111736987 | A | G | 2 | a0004c0004t0002g0064 a0004c0004t0002g0071 |
2 | NA18966.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1417+1293T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111736987 | |||||||
| chr9:111737051 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1417+1229A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737051 | |||||||
| chr9:111737111 | G | T | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417+1169C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737111 | |||||||
| chr9:111737145 | T | A | 2 | a0002c0002t0002g0014 a0002c0002t0002g0197 |
3 | NA19010.hp1 NA19080.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1417+1135A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737145 | |||||||
| chr9:111737166 | A | T | 1 | a0003c0003t0002g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1417+1114T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737166 | |||||||
| chr9:111737181 | A | T | 9 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(6): Show |
9 | HG02572.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1417+1099T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737181 | |||||||
| chr9:111737226 | C | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0262 |
3 | NA18992.hp2 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1417+1054G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737226 | |||||||
| chr9:111737361 | T | C | 1 | a0004c0004t0002g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1417+919A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737361 | |||||||
| chr9:111737594 | A | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1417+686T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737594 | |||||||
| chr9:111737660 | AAAAC | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(98): Show |
109 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1417+616_1417+619d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737660 | |||||||
| chr9:111737688 | AC | A | 27 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(24): Show |
36 | HG00544.hp1 HG00621.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.1417+591delG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737688 | |||||||
| chr9:111737688 | ACCC | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(193): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1417+589_1417+591d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737688 | |||||||
| chr9:111737698 | C | A | 1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1417+582G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737698 | |||||||
| chr9:111737805 | CCTT | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(162): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1417+472_1417+474d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 12/27 | chr9 | 111737805 | |||||||
| chr9:111738546 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1175-24A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111738546 | |||||||
| chr9:111738594 | A | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1175-72T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111738594 | |||||||
| chr9:111738956 | T | TAGTC | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1175-435_1175-434i others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111738956 | |||||||
| chr9:111738958 | G | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1175-436C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111738958 | |||||||
| chr9:111739042 | C | T | 1 | a0002c0010t0004g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1175-520G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111739042 | |||||||
| chr9:111739225 | G | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(162): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1175-703C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111739225 | |||||||
| chr9:111739426 | G | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1175-904C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111739426 | |||||||
| chr9:111739842 | A | G | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1175-1320T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111739842 | |||||||
| chr9:111739899 | CCAGA | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(162): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1175-1381_1175-137 others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111739899 | |||||||
| chr9:111740084 | T | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1174+1392A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111740084 | |||||||
| chr9:111740351 | G | C | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1174+1125C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111740351 | |||||||
| chr9:111740409 | C | G | 44 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(41): Show |
51 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1174+1067G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111740409 | |||||||
| chr9:111740462 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1174+1014C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111740462 | |||||||
| chr9:111741014 | C | G | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1174+462G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111741014 | |||||||
| chr9:111741086 | C | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1174+390G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111741086 | |||||||
| chr9:111741210 | T | C | 54 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(51): Show |
59 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1174+266A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111741210 | |||||||
| chr9:111741213 | T | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(134): Show |
146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1174+263A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111741213 | |||||||
| chr9:111741405 | C | A | 1 | a0002c0010t0004g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1174+71G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 11/27 | chr9 | 111741405 | |||||||
| chr9:111741597 | C | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1080-27G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111741597 | |||||||
| chr9:111741664 | C | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1080-94G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111741664 | |||||||
| chr9:111741820 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1080-250G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111741820 | |||||||
| chr9:111741875 | G | A | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080-305C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111741875 | |||||||
| chr9:111742001 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1080-431T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111742001 | |||||||
| chr9:111742105 | C | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(216): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.1080-535G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111742105 | |||||||
| chr9:111742193 | C | A | 1 | a0002c0007t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1080-623G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111742193 | |||||||
| chr9:111742480 | G | GGGGT | 77 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(74): Show |
82 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1080-914_1080-911d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111742480 | |||||||
| chr9:111742488 | C | G | 69 | a0001c0022t0001g0196 a0001c0026t0001g0252 a0002c0002t0002g0014 others(66): Show |
71 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.1080-918G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111742488 | |||||||
| chr9:111742942 | G | A | 1 | a0002c0010t0004g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1080-1372C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111742942 | |||||||
| chr9:111743212 | CCTT | C | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1080-1645_1080-164 others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111743212 | |||||||
| chr9:111743639 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1080-2069G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111743639 | |||||||
| chr9:111743685 | C | T | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1080-2115G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111743685 | |||||||
| chr9:111743817 | A | T | 6 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080-2247T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111743817 | |||||||
| chr9:111743872 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1080-2302C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111743872 | |||||||
| chr9:111744194 | GAT | G | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1079+2038_1079+203 others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111744194 | |||||||
| chr9:111744341 | T | C | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1079+1893A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111744341 | |||||||
| chr9:111744555 | A | C | 3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1079+1679T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111744555 | |||||||
| chr9:111744609 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0001c0001t0001g0150 |
4 | HG01099.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079+1625G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111744609 | |||||||
| chr9:111744840 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(212): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1079+1394G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111744840 | |||||||
| chr9:111745034 | C | T | 4 | a0003c0003t0002g0077 a0003c0003t0002g0086 a0003c0003t0002g0087 others(1): Show |
4 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079+1200G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745034 | |||||||
| chr9:111745083 | A | G | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1079+1151T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745083 | |||||||
| chr9:111745099 | G | A | 21 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(18): Show |
22 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1079+1135C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745099 | |||||||
| chr9:111745154 | G | C | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1079+1080C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745154 | |||||||
| chr9:111745309 | G | A | 51 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0117 others(48): Show |
52 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1079+925C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745309 | |||||||
| chr9:111745333 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1079+901T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745333 | |||||||
| chr9:111745365 | G | C | 2 | a0002c0002t0002g0195 a0002c0002t0002g0198 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1079+869C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745365 | |||||||
| chr9:111745389 | C | T | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079+845G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745389 | |||||||
| chr9:111745537 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1079+697T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745537 | |||||||
| chr9:111745573 | G | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0153 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1079+661C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745573 | |||||||
| chr9:111745751 | G | C | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079+483C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111745751 | |||||||
| chr9:111746175 | T | C | 1 | a0019c0028t0001g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1079+59A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111746175 | |||||||
| chr9:111746206 | A | G | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1079+28T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111746206 | |||||||
| chr9:111746216 | G | A | 3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1079+18C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 10/27 | chr9 | 111746216 | |||||||
| chr9:111746457 | T | C | 7 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.971-115A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111746457 | |||||||
| chr9:111746693 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.971-351A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111746693 | |||||||
| chr9:111747051 | G | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(178): Show |
195 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.971-709C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747051 | |||||||
| chr9:111747124 | A | C | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.971-782T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747124 | |||||||
| chr9:111747469 | T | C | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+623A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747469 | |||||||
| chr9:111747542 | C | T | 6 | a0002c0007t0006g0213 a0002c0012t0006g0208 a0002c0012t0006g0209 others(3): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.970+550G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747542 | |||||||
| chr9:111747659 | C | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.970+433G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747659 | |||||||
| chr9:111747702 | T | C | 1 | a0009c0017t0002g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.970+390A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747702 | |||||||
| chr9:111747883 | C | A | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.970+209G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747883 | |||||||
| chr9:111747992 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.970+100C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 9/27 | chr9 | 111747992 | |||||||
| chr9:111748202 | G | A | 5 | a0002c0010t0002g0013 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.863-3C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748202 | |||||||
| chr9:111748257 | C | A | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.863-58G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748257 | |||||||
| chr9:111748521 | C | T | 2 | a0002c0012t0006g0208 a0002c0012t0006g0209 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.863-322G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748521 | |||||||
| chr9:111748580 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.863-381C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748580 | |||||||
| chr9:111748625 | T | A | 1 | a0003c0003t0002g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.863-426A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748625 | |||||||
| chr9:111748721 | C | CT | 13 | a0002c0007t0001g0167 a0002c0007t0004g0253 a0002c0007t0004g0254 others(10): Show |
18 | HG01109.hp2 HG01255.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.863-523dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748721 | |||||||
| chr9:111748759 | TC | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.863-561delG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748759 | |||||||
| chr9:111748760 | C | CCTT | 192 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(189): Show |
211 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.863-564_863-562dup others(3): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748760 | |||||||
| chr9:111748766 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.863-567G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748766 | |||||||
| chr9:111748781 | C | A | 2 | a0005c0005t0003g0023 a0005c0005t0003g0039 |
2 | NA19078.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.863-582G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748781 | |||||||
| chr9:111748789 | T | C | 1 | a0003c0003t0002g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.863-590A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748789 | |||||||
| chr9:111748789 | T | TC | 38 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0126 others(35): Show |
38 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-591dupG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748789 | |||||||
| chr9:111748790 | C | T | 1 | a0003c0003t0002g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.863-591G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748790 | |||||||
| chr9:111748794 | CCCTT | C | 35 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0002c0010t0002g0013 others(32): Show |
37 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.863-599_863-596del others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748794 | |||||||
| chr9:111748806 | TCCTTCCT others(9): Show |
T | 3 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0019c0028t0001g0215 |
3 | HG02572.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.863-623_863-608del others(16): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748806 | |||||||
| chr9:111748971 | CCCCT | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.863-776_863-773del others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111748971 | |||||||
| chr9:111749092 | CTTCTT | C | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-898_863-894del others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749092 | |||||||
| chr9:111749129 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(152): Show |
165 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.863-930G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749129 | |||||||
| chr9:111749158 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.863-959G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749158 | |||||||
| chr9:111749170 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.863-971A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749170 | |||||||
| chr9:111749392 | T | G | 1 | a0005c0005t0003g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.863-1193A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749392 | |||||||
| chr9:111749558 | G | T | 1 | a0003c0003t0002g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.863-1359C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749558 | |||||||
| chr9:111749562 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.863-1363C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749562 | |||||||
| chr9:111749770 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.863-1571A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749770 | |||||||
| chr9:111749771 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0018c0027t0001g0147 |
3 | HG03139.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.863-1572C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749771 | |||||||
| chr9:111749771 | G | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.863-1572C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749771 | |||||||
| chr9:111749990 | T | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(164): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.863-1791A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749990 | |||||||
| chr9:111749991 | G | A | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.863-1792C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111749991 | |||||||
| chr9:111750099 | G | A | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.863-1900C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750099 | |||||||
| chr9:111750142 | A | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(224): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.863-1943T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750142 | |||||||
| chr9:111750181 | C | T | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.863-1982G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750181 | |||||||
| chr9:111750291 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.863-2092T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750291 | |||||||
| chr9:111750305 | A | G | 1 | a0004c0004t0002g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.863-2106T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750305 | |||||||
| chr9:111750325 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(104): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.863-2126G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750325 | |||||||
| chr9:111750326 | G | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.863-2127C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750326 | |||||||
| chr9:111750427 | C | A | 5 | a0006c0006t0001g0002 a0006c0006t0001g0050 a0006c0006t0001g0052 others(2): Show |
8 | HG01081.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.863-2228G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750427 | |||||||
| chr9:111750523 | C | T | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.863-2324G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750523 | |||||||
| chr9:111750635 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.863-2436T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111750635 | |||||||
| chr9:111751036 | G | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0119 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.863-2837C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111751036 | |||||||
| chr9:111751073 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.863-2874G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111751073 | |||||||
| chr9:111751316 | G | A | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.863-3117C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111751316 | |||||||
| chr9:111751319 | T | C | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-3120A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111751319 | |||||||
| chr9:111751557 | T | G | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.863-3358A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111751557 | |||||||
| chr9:111751575 | T | C | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.863-3376A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111751575 | |||||||
| chr9:111751579 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.863-3380C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111751579 | |||||||
| chr9:111752053 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(184): Show |
201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.863-3854C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752053 | |||||||
| chr9:111752065 | A | C | 4 | a0003c0003t0002g0077 a0003c0003t0002g0086 a0003c0003t0002g0087 others(1): Show |
4 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-3866T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752065 | |||||||
| chr9:111752067 | T | C | 2 | a0003c0003t0002g0011 a0003c0003t0002g0098 |
3 | HG03669.hp2 HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.863-3868A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752067 | |||||||
| chr9:111752351 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.862+3974C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752351 | |||||||
| chr9:111752406 | A | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.862+3919T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752406 | |||||||
| chr9:111752482 | G | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.862+3843C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752482 | |||||||
| chr9:111752731 | T | C | 1 | a0015c0029t0002g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.862+3594A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752731 | |||||||
| chr9:111752854 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.862+3471C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752854 | |||||||
| chr9:111752924 | G | A | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.862+3401C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111752924 | |||||||
| chr9:111753012 | A | C | 2 | a0008c0009t0001g0109 a0008c0009t0001g0110 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.862+3313T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753012 | |||||||
| chr9:111753013 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.862+3312C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753013 | |||||||
| chr9:111753053 | A | C | 5 | a0002c0002t0002g0177 a0002c0002t0002g0181 a0002c0002t0002g0182 others(2): Show |
5 | HG00558.hp2 HG02135.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.862+3272T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753053 | |||||||
| chr9:111753081 | G | T | 1 | a0002c0007t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.862+3244C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753081 | |||||||
| chr9:111753238 | T | A | 39 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(36): Show |
40 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.862+3087A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753238 | |||||||
| chr9:111753239 | A | T | 5 | a0002c0007t0006g0213 a0002c0012t0006g0208 a0002c0012t0006g0209 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.862+3086T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753239 | |||||||
| chr9:111753247 | C | T | 32 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(29): Show |
33 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.862+3078G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753247 | |||||||
| chr9:111753584 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(104): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.862+2741G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753584 | |||||||
| chr9:111753890 | G | T | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.862+2435C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753890 | |||||||
| chr9:111753912 | T | C | 6 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0112 others(3): Show |
7 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.862+2413A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111753912 | |||||||
| chr9:111754100 | T | A | 1 | a0001c0001t0001g0262 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.862+2225A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754100 | |||||||
| chr9:111754261 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.862+2064A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754261 | |||||||
| chr9:111754361 | G | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.862+1964C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754361 | |||||||
| chr9:111754411 | G | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(140): Show |
152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.862+1914C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754411 | |||||||
| chr9:111754571 | T | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.862+1754A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754571 | |||||||
| chr9:111754613 | A | G | 2 | a0002c0011t0005g0124 a0002c0011t0005g0160 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.862+1712T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754613 | |||||||
| chr9:111754699 | C | CTTT | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.862+1625_862+1626i others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754699 | |||||||
| chr9:111754795 | G | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.862+1530C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111754795 | |||||||
| chr9:111755004 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.862+1321T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111755004 | |||||||
| chr9:111755030 | C | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(164): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.862+1295G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111755030 | |||||||
| chr9:111755200 | G | GC | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.862+1124_862+1125i others(3): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111755200 | |||||||
| chr9:111755584 | T | C | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.862+741A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111755584 | |||||||
| chr9:111755875 | C | T | 4 | a0002c0011t0005g0122 a0002c0011t0005g0123 a0002c0011t0005g0124 others(1): Show |
4 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+450G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111755875 | |||||||
| chr9:111756017 | G | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(184): Show |
201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.862+308C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111756017 | |||||||
| chr9:111756027 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.862+298A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111756027 | |||||||
| chr9:111756053 | C | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.862+272G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111756053 | |||||||
| chr9:111756122 | C | T | 2 | a0002c0007t0001g0167 a0012c0025t0005g0264 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.862+203G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111756122 | |||||||
| chr9:111756123 | G | GACAACA | 21 | a0001c0001t0001g0218 a0005c0005t0003g0001 a0005c0005t0003g0006 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.862+196_862+201dup others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 8/27 | chr9 | 111756123 | |||||||
| chr9:111756534 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.709-56G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111756534 | |||||||
| chr9:111756535 | G | A | 4 | a0003c0003t0002g0077 a0003c0003t0002g0086 a0003c0003t0002g0087 others(1): Show |
4 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-57C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111756535 | |||||||
| chr9:111756675 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.709-197G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111756675 | |||||||
| chr9:111757035 | G | GA | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.709-558dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757035 | |||||||
| chr9:111757115 | G | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.709-637C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757115 | |||||||
| chr9:111757319 | G | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(104): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.708+765C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757319 | |||||||
| chr9:111757530 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(237): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.708+554C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757530 | |||||||
| chr9:111757559 | G | A | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.708+525C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757559 | |||||||
| chr9:111757723 | T | G | 2 | a0004c0004t0002g0008 a0004c0004t0002g0075 |
3 | HG01256.hp1 HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.708+361A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757723 | |||||||
| chr9:111757864 | A | C | 4 | a0004c0004t0002g0047 a0004c0004t0002g0055 a0004c0004t0002g0056 others(1): Show |
4 | HG01255.hp2 HG02148.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+220T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757864 | |||||||
| chr9:111757883 | T | A | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.708+201A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757883 | |||||||
| chr9:111757974 | T | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.708+110A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 7/27 | chr9 | 111757974 | |||||||
| chr9:111758198 | T | G | 1 | a0002c0002t0002g0188 | 1 | NA18944.hp1 | splice_region_variant&intron_variant | LOW | c.597-3A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758198 | |||||||
| chr9:111758250 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597-55C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758250 | |||||||
| chr9:111758298 | G | A | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.597-103C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758298 | |||||||
| chr9:111758318 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.597-123C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758318 | |||||||
| chr9:111758333 | C | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.597-138G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758333 | |||||||
| chr9:111758425 | G | A | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.597-230C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758425 | |||||||
| chr9:111758468 | C | T | 2 | a0004c0004t0002g0058 a0004c0004t0002g0065 |
2 | HG00741.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.596+227G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758468 | |||||||
| chr9:111758488 | C | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.596+207G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758488 | |||||||
| chr9:111758507 | T | C | 1 | a0014c0021t0002g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.596+188A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758507 | |||||||
| chr9:111758520 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(184): Show |
201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.596+175G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758520 | |||||||
| chr9:111758521 | G | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0262 |
3 | NA18992.hp2 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.596+174C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758521 | |||||||
| chr9:111758537 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.596+158G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758537 | |||||||
| chr9:111758538 | G | A | 1 | a0005c0005t0003g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.596+157C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758538 | |||||||
| chr9:111758602 | A | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0262 |
3 | NA18992.hp2 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.596+93T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 6/27 | chr9 | 111758602 | |||||||
| chr9:111759350 | A | G | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-502T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111759350 | |||||||
| chr9:111759695 | C | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0135 |
3 | HG01891.hp1 HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.443-847G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111759695 | |||||||
| chr9:111759707 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.443-859T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111759707 | |||||||
| chr9:111759873 | T | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0135 |
3 | HG01891.hp1 HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.443-1025A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111759873 | |||||||
| chr9:111759928 | A | G | 1 | a0019c0028t0001g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.443-1080T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111759928 | |||||||
| chr9:111760121 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.443-1273T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760121 | |||||||
| chr9:111760380 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.443-1532G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760380 | |||||||
| chr9:111760387 | T | C | 32 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(29): Show |
33 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.443-1539A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760387 | |||||||
| chr9:111760461 | C | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.443-1613G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760461 | |||||||
| chr9:111760507 | G | C | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.443-1659C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760507 | |||||||
| chr9:111760541 | G | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.443-1693C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760541 | |||||||
| chr9:111760620 | GT | G | 23 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(20): Show |
24 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.443-1773delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760620 | |||||||
| chr9:111760714 | T | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-1866A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760714 | |||||||
| chr9:111760741 | T | C | 1 | a0003c0003t0002g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.443-1893A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760741 | |||||||
| chr9:111760822 | CTA | C | 32 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(29): Show |
33 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.443-1976_443-1975d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111760822 | |||||||
| chr9:111761137 | C | T | 3 | a0002c0002t0002g0014 a0002c0002t0002g0178 a0002c0002t0002g0197 |
4 | NA19000.hp1 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-2289G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761137 | |||||||
| chr9:111761212 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.443-2364C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761212 | |||||||
| chr9:111761299 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.443-2451G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761299 | |||||||
| chr9:111761420 | T | C | 11 | a0003c0003t0002g0085 a0003c0003t0002g0105 a0003c0003t0002g0106 others(8): Show |
11 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.443-2572A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761420 | |||||||
| chr9:111761424 | C | G | 3 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0019c0028t0001g0215 |
3 | HG02572.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.443-2576G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761424 | |||||||
| chr9:111761487 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.443-2639C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761487 | |||||||
| chr9:111761509 | AAAAC | A | 15 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0004g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.443-2665_443-2662d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761509 | |||||||
| chr9:111761580 | A | G | 15 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0004g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.443-2732T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761580 | |||||||
| chr9:111761632 | A | C | 2 | a0008c0009t0001g0109 a0008c0009t0001g0110 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.443-2784T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761632 | |||||||
| chr9:111761768 | T | C | 54 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(51): Show |
59 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.443-2920A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111761768 | |||||||
| chr9:111762041 | A | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-3193T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762041 | |||||||
| chr9:111762077 | G | A | 5 | a0002c0007t0006g0213 a0002c0012t0006g0208 a0002c0012t0006g0209 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-3229C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762077 | |||||||
| chr9:111762102 | A | T | 2 | a0008c0009t0001g0109 a0008c0009t0001g0110 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.443-3254T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762102 | |||||||
| chr9:111762118 | A | T | 6 | a0005c0005t0003g0025 a0005c0005t0003g0026 a0005c0005t0003g0028 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-3270T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762118 | |||||||
| chr9:111762308 | G | T | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.443-3460C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762308 | |||||||
| chr9:111762526 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0001c0001t0001g0150 |
4 | HG01099.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-3678G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762526 | |||||||
| chr9:111762757 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(147): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.443-3909T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762757 | |||||||
| chr9:111762776 | T | A | 4 | a0002c0002t0002g0189 a0002c0002t0002g0204 a0002c0002t0002g0205 others(1): Show |
4 | HG01123.hp1 HG02738.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-3928A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762776 | |||||||
| chr9:111762830 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.443-3982G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762830 | |||||||
| chr9:111762845 | C | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.443-3997G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762845 | |||||||
| chr9:111762853 | G | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.443-4005C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111762853 | |||||||
| chr9:111763151 | A | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.443-4303T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763151 | |||||||
| chr9:111763166 | A | G | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.443-4318T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763166 | |||||||
| chr9:111763239 | G | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-4391C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763239 | |||||||
| chr9:111763284 | T | C | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.443-4436A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763284 | |||||||
| chr9:111763490 | T | G | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.443-4642A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763490 | |||||||
| chr9:111763566 | A | T | 3 | a0002c0002t0002g0014 a0002c0002t0002g0178 a0002c0002t0002g0197 |
4 | NA19000.hp1 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-4718T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763566 | |||||||
| chr9:111763616 | A | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0263 |
2 | NA18955.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.443-4768T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763616 | |||||||
| chr9:111763644 | T | C | 4 | a0002c0012t0006g0208 a0002c0012t0006g0209 a0002c0012t0006g0211 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-4796A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763644 | |||||||
| chr9:111763806 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.443-4958G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111763806 | |||||||
| chr9:111764100 | G | A | 1 | a0005c0005t0003g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.443-5252C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764100 | |||||||
| chr9:111764116 | TC | T | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-5269delG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764116 | |||||||
| chr9:111764178 | T | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-5330A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764178 | |||||||
| chr9:111764342 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.443-5494C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764342 | |||||||
| chr9:111764483 | C | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(164): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.443-5635G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764483 | |||||||
| chr9:111764501 | T | C | 2 | a0008c0009t0001g0109 a0008c0009t0001g0110 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.443-5653A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764501 | |||||||
| chr9:111764504 | A | C | 1 | a0001c0026t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.443-5656T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764504 | |||||||
| chr9:111764586 | A | G | 2 | a0006c0006t0001g0041 a0006c0006t0001g0042 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.443-5738T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111764586 | |||||||
| chr9:111765032 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.443-6184G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765032 | |||||||
| chr9:111765105 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.443-6257G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765105 | |||||||
| chr9:111765136 | G | A | 1 | a0002c0007t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.443-6288C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765136 | |||||||
| chr9:111765140 | CA | C | 40 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0137 others(37): Show |
41 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.443-6293delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765140 | |||||||
| chr9:111765161 | T | C | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.443-6313A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765161 | |||||||
| chr9:111765333 | G | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.443-6485C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765333 | |||||||
| chr9:111765599 | AC | A | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-6752delG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765599 | |||||||
| chr9:111765600 | CAAAACAA others(4): Show |
C | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.443-6763_443-6753d others(13): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765600 | |||||||
| chr9:111765606 | A | G | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-6758T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765606 | |||||||
| chr9:111765645 | C | T | 6 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0112 others(3): Show |
7 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-6797G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765645 | |||||||
| chr9:111765775 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(217): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.443-6927T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765775 | |||||||
| chr9:111765777 | G | A | 13 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG00099.hp1 HG00597.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.443-6929C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765777 | |||||||
| chr9:111765828 | C | G | 3 | a0002c0002t0002g0014 a0002c0002t0002g0178 a0002c0002t0002g0197 |
4 | NA19000.hp1 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-6980G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765828 | |||||||
| chr9:111765912 | G | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-7064C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765912 | |||||||
| chr9:111765950 | G | T | 1 | a0003c0003t0002g0020 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.443-7102C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111765950 | |||||||
| chr9:111766041 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443-7193G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766041 | |||||||
| chr9:111766080 | G | A | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.443-7232C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766080 | |||||||
| chr9:111766306 | C | T | 3 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0165 |
4 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-7458G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766306 | |||||||
| chr9:111766407 | G | C | 1 | a0001c0022t0001g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.443-7559C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766407 | |||||||
| chr9:111766615 | G | T | 1 | a0002c0002t0002g0239 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.443-7767C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766615 | |||||||
| chr9:111766694 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(218): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.443-7846A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766694 | |||||||
| chr9:111766769 | G | A | 1 | a0002c0002t0002g0190 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.443-7921C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766769 | |||||||
| chr9:111766797 | A | G | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-7949T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766797 | |||||||
| chr9:111766812 | A | G | 1 | a0004c0004t0002g0064 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.443-7964T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111766812 | |||||||
| chr9:111767014 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.443-8166A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767014 | |||||||
| chr9:111767038 | AT | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(198): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.443-8191delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767038 | |||||||
| chr9:111767038 | ATT | A | 20 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(17): Show |
24 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.443-8192_443-8191d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767038 | |||||||
| chr9:111767149 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.443-8301G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767149 | |||||||
| chr9:111767250 | C | CA | 187 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(184): Show |
201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.443-8403dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767250 | |||||||
| chr9:111767543 | A | G | 1 | a0008c0009t0001g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442+8248T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767543 | |||||||
| chr9:111767733 | G | C | 1 | a0003c0003t0002g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442+8058C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767733 | |||||||
| chr9:111767914 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0235 |
2 | HG00741.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.442+7877A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767914 | |||||||
| chr9:111767954 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.442+7837C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111767954 | |||||||
| chr9:111768224 | T | C | 1 | a0001c0026t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.442+7567A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111768224 | |||||||
| chr9:111768228 | A | AT | 52 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(49): Show |
57 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.442+7562dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111768228 | |||||||
| chr9:111768516 | G | A | 3 | a0002c0002t0002g0014 a0002c0002t0002g0178 a0002c0002t0002g0197 |
4 | NA19000.hp1 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+7275C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111768516 | |||||||
| chr9:111768713 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG00408.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.442+7078A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111768713 | |||||||
| chr9:111768836 | T | C | 4 | a0002c0012t0006g0208 a0002c0012t0006g0209 a0002c0012t0006g0211 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+6955A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111768836 | |||||||
| chr9:111768881 | G | GA | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.442+6909dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111768881 | |||||||
| chr9:111768942 | G | C | 1 | a0003c0003t0002g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442+6849C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111768942 | |||||||
| chr9:111769016 | C | T | 7 | a0008c0009t0001g0084 a0008c0009t0001g0100 a0008c0009t0001g0101 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+6775G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769016 | |||||||
| chr9:111769268 | T | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.442+6523A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769268 | |||||||
| chr9:111769479 | T | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+6312A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769479 | |||||||
| chr9:111769502 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.442+6289C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769502 | |||||||
| chr9:111769506 | C | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+6285G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769506 | |||||||
| chr9:111769714 | C | A | 1 | a0002c0002t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.442+6077G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769714 | |||||||
| chr9:111769957 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+5834G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769957 | |||||||
| chr9:111769973 | CTGTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0219 a0001c0001t0001g0222 |
3 | HG01515.hp2 HG02897.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.442+5807_442+5817d others(13): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769973 | |||||||
| chr9:111769976 | TTTTTTTT others(3): Show |
T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(92): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.442+5805_442+5814d others(12): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769976 | |||||||
| chr9:111769979 | T | G | 86 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.442+5812A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769979 | |||||||
| chr9:111769981 | TTTTTG | T | 22 | a0002c0007t0004g0168 a0002c0007t0006g0213 a0005c0005t0003g0001 others(19): Show |
25 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.442+5805_442+5809d others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769981 | |||||||
| chr9:111769982 | TTTTG | T | 43 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(40): Show |
44 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.442+5805_442+5808d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769982 | |||||||
| chr9:111769983 | TTTG | T | 7 | a0002c0002t0002g0175 a0002c0002t0002g0189 a0002c0002t0002g0190 others(4): Show |
7 | HG01123.hp1 HG01192.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+5805_442+5807d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769983 | |||||||
| chr9:111769984 | TTG | T | 25 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0112 others(22): Show |
26 | HG00140.hp1 HG01081.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.442+5805_442+5806d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769984 | |||||||
| chr9:111769985 | TG | T | 18 | a0002c0010t0004g0114 a0002c0011t0005g0122 a0003c0003t0002g0077 others(15): Show |
18 | HG00642.hp2 HG01071.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.442+5805delC | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769985 | |||||||
| chr9:111769986 | G | T | 4 | a0003c0003t0002g0011 a0003c0003t0002g0083 a0003c0003t0002g0085 others(1): Show |
5 | HG01074.hp1 HG02622.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+5805C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769986 | |||||||
| chr9:111769988 | T | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0223 a0001c0001t0001g0243 others(1): Show |
4 | HG00642.hp1 HG00673.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+5803A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769988 | |||||||
| chr9:111769989 | T | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(92): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.442+5802A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769989 | |||||||
| chr9:111769990 | T | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0219 a0001c0001t0001g0222 |
3 | HG01515.hp2 HG02897.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.442+5801A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769990 | |||||||
| chr9:111769991 | T | G | 4 | a0003c0003t0002g0105 a0003c0003t0002g0106 a0008c0009t0001g0104 others(1): Show |
4 | HG02280.hp1 HG02738.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+5800A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769991 | |||||||
| chr9:111769992 | T | G | 2 | a0006c0006t0001g0072 a0008c0009t0001g0084 |
2 | HG01192.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.442+5799A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769992 | |||||||
| chr9:111769995 | T | G | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.442+5796A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769995 | |||||||
| chr9:111769998 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.442+5793A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111769998 | |||||||
| chr9:111770159 | G | A | 1 | a0004c0004t0002g0048 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.442+5632C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111770159 | |||||||
| chr9:111770526 | A | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+5265T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111770526 | |||||||
| chr9:111770779 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.442+5012G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111770779 | |||||||
| chr9:111770783 | G | A | 1 | a0002c0002t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.442+5008C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111770783 | |||||||
| chr9:111770803 | A | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+4988T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111770803 | |||||||
| chr9:111770935 | C | T | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.442+4856G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111770935 | |||||||
| chr9:111771132 | C | T | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.442+4659G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111771132 | |||||||
| chr9:111771340 | A | AT | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.442+4450dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111771340 | |||||||
| chr9:111772120 | G | A | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+3671C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772120 | |||||||
| chr9:111772159 | C | T | 10 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0176 others(7): Show |
11 | HG00673.hp1 HG02071.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.442+3632G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772159 | |||||||
| chr9:111772177 | T | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.442+3614A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772177 | |||||||
| chr9:111772460 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.442+3331T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772460 | |||||||
| chr9:111772550 | G | A | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.442+3241C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772550 | |||||||
| chr9:111772792 | C | T | 4 | a0002c0007t0001g0167 a0002c0010t0004g0112 a0002c0010t0004g0113 others(1): Show |
4 | HG02615.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+2999G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772792 | |||||||
| chr9:111772834 | C | G | 6 | a0005c0005t0003g0025 a0005c0005t0003g0026 a0005c0005t0003g0028 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+2957G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772834 | |||||||
| chr9:111772979 | GATT | G | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+2809_442+2811d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111772979 | |||||||
| chr9:111773003 | G | A | 3 | a0005c0005t0003g0028 a0011c0014t0002g0027 a0011c0014t0002g0029 |
3 | HG02451.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.442+2788C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773003 | |||||||
| chr9:111773004 | C | T | 3 | a0005c0005t0003g0028 a0011c0014t0002g0027 a0011c0014t0002g0029 |
3 | HG02451.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.442+2787G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773004 | |||||||
| chr9:111773026 | C | CATGGAT | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+2759_442+2764d others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773026 | |||||||
| chr9:111773096 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.442+2695A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773096 | |||||||
| chr9:111773217 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+2574G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773217 | |||||||
| chr9:111773289 | C | G | 2 | a0002c0002t0002g0195 a0002c0002t0002g0198 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.442+2502G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773289 | |||||||
| chr9:111773381 | C | T | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+2410G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773381 | |||||||
| chr9:111773456 | G | A | 1 | a0006c0006t0001g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.442+2335C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773456 | |||||||
| chr9:111773469 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.442+2322G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773469 | |||||||
| chr9:111773499 | A | G | 1 | a0015c0029t0002g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.442+2292T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773499 | |||||||
| chr9:111773535 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442+2256G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773535 | |||||||
| chr9:111773869 | TC | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.442+1921delG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773869 | |||||||
| chr9:111773966 | A | G | 1 | a0002c0007t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442+1825T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111773966 | |||||||
| chr9:111774081 | T | C | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.442+1710A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774081 | |||||||
| chr9:111774096 | G | A | 2 | a0006c0006t0001g0034 a0006c0006t0001g0035 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.442+1695C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774096 | |||||||
| chr9:111774247 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.442+1544C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774247 | |||||||
| chr9:111774271 | A | T | 1 | a0003c0003t0002g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442+1520T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774271 | |||||||
| chr9:111774375 | T | C | 1 | a0003c0003t0002g0108 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.442+1416A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774375 | |||||||
| chr9:111774447 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0259 |
3 | HG02165.hp1 HG02735.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.442+1344G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774447 | |||||||
| chr9:111774500 | A | G | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+1291T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774500 | |||||||
| chr9:111774595 | A | T | 2 | a0002c0007t0001g0167 a0012c0025t0005g0264 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.442+1196T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774595 | |||||||
| chr9:111774627 | A | G | 1 | a0010c0013t0002g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.442+1164T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774627 | |||||||
| chr9:111774698 | C | A | 9 | a0002c0002t0002g0191 a0002c0007t0006g0213 a0002c0012t0006g0208 others(6): Show |
9 | HG02109.hp2 HG02738.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+1093G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774698 | |||||||
| chr9:111774700 | A | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(172): Show |
194 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.442+1091T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774700 | |||||||
| chr9:111774702 | A | C | 97 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(94): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.442+1089T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774702 | |||||||
| chr9:111774902 | G | A | 10 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0176 others(7): Show |
11 | HG00673.hp1 HG02071.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.442+889C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111774902 | |||||||
| chr9:111775002 | A | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(183): Show |
200 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.442+789T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775002 | |||||||
| chr9:111775003 | A | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.442+788T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775003 | |||||||
| chr9:111775003 | AT | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+787delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775003 | |||||||
| chr9:111775019 | T | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.442+772A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775019 | |||||||
| chr9:111775212 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.442+579G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775212 | |||||||
| chr9:111775226 | C | T | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442+565G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775226 | |||||||
| chr9:111775537 | T | C | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.442+254A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775537 | |||||||
| chr9:111775698 | A | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.442+93T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 5/27 | chr9 | 111775698 | |||||||
| chr9:111775999 | T | G | 1 | a0003c0003t0002g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.258-24A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111775999 | |||||||
| chr9:111776180 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(104): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.258-205C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776180 | |||||||
| chr9:111776212 | T | TA | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.258-238dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776212 | |||||||
| chr9:111776287 | G | T | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.258-312C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776287 | |||||||
| chr9:111776424 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.258-449T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776424 | |||||||
| chr9:111776432 | T | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.258-457A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776432 | |||||||
| chr9:111776530 | C | T | 1 | a0002c0012t0006g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.258-555G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776530 | |||||||
| chr9:111776547 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.258-572C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776547 | |||||||
| chr9:111776672 | C | T | 1 | a0002c0002t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.258-697G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776672 | |||||||
| chr9:111776876 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.258-901C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776876 | |||||||
| chr9:111776952 | C | A | 1 | a0004c0004t0002g0057 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.258-977G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111776952 | |||||||
| chr9:111777019 | G | A | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.258-1044C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777019 | |||||||
| chr9:111777029 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.258-1054C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777029 | |||||||
| chr9:111777111 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.258-1136C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777111 | |||||||
| chr9:111777114 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.258-1139C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777114 | |||||||
| chr9:111777169 | G | A | 1 | a0006c0006t0001g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258-1194C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777169 | |||||||
| chr9:111777269 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0263 |
2 | NA18955.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.258-1294C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777269 | |||||||
| chr9:111777271 | A | G | 5 | a0002c0007t0001g0167 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
5 | HG01109.hp2 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-1296T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777271 | |||||||
| chr9:111777277 | C | G | 7 | a0008c0009t0001g0084 a0008c0009t0001g0100 a0008c0009t0001g0101 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-1302G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777277 | |||||||
| chr9:111777317 | C | T | 4 | a0008c0009t0001g0084 a0008c0009t0001g0100 a0008c0009t0001g0101 others(1): Show |
4 | HG01192.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1342G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777317 | |||||||
| chr9:111777440 | C | CA | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.258-1466dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777440 | |||||||
| chr9:111777538 | G | A | 1 | a0003c0003t0002g0020 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.258-1563C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777538 | |||||||
| chr9:111777581 | C | T | 4 | a0002c0002t0002g0189 a0002c0002t0002g0204 a0002c0002t0002g0205 others(1): Show |
4 | HG01123.hp1 HG02738.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1606G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777581 | |||||||
| chr9:111777770 | C | T | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-1795G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777770 | |||||||
| chr9:111777799 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.258-1824A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111777799 | |||||||
| chr9:111778214 | C | CACTG | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.258-2243_258-2240d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778214 | |||||||
| chr9:111778358 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0161 |
2 | HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.258-2383A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778358 | |||||||
| chr9:111778624 | A | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.257+2306T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778624 | |||||||
| chr9:111778770 | C | CAA | 19 | a0002c0002t0002g0166 a0002c0002t0002g0175 a0002c0002t0002g0177 others(16): Show |
19 | HG00558.hp2 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.257+2158_257+2159d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778770 | |||||||
| chr9:111778770 | C | CAAA | 12 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0176 others(9): Show |
13 | HG00673.hp1 HG01123.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+2157_257+2159d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778770 | |||||||
| chr9:111778770 | CA | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(154): Show |
171 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.257+2159delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778770 | |||||||
| chr9:111778770 | CAA | C | 13 | a0001c0001t0001g0139 a0001c0001t0001g0261 a0002c0007t0004g0168 others(10): Show |
13 | HG00099.hp1 HG00733.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+2158_257+2159d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778770 | |||||||
| chr9:111778804 | G | C | 1 | a0005c0005t0003g0039 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.257+2126C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778804 | |||||||
| chr9:111778885 | G | A | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.257+2045C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111778885 | |||||||
| chr9:111779113 | AAAGAG | A | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.257+1812_257+1816d others(7): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779113 | |||||||
| chr9:111779114 | AAGAG | A | 10 | a0001c0001t0001g0143 a0001c0001t0001g0219 a0002c0007t0004g0214 others(7): Show |
10 | HG01243.hp2 HG01515.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+1812_257+1815d others(6): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779114 | |||||||
| chr9:111779115 | AGAG | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(151): Show |
163 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.257+1812_257+1814d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779115 | |||||||
| chr9:111779118 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0135 a0002c0002t0002g0239 others(1): Show |
4 | HG02257.hp1 HG03139.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+1812C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779118 | |||||||
| chr9:111779134 | G | A | 1 | a0009c0017t0002g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.257+1796C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779134 | |||||||
| chr9:111779236 | T | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(94): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.257+1694A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779236 | |||||||
| chr9:111779266 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.257+1664G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779266 | |||||||
| chr9:111779299 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.257+1631C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779299 | |||||||
| chr9:111779326 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.257+1604G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779326 | |||||||
| chr9:111779436 | T | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(152): Show |
165 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.257+1494A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779436 | |||||||
| chr9:111779465 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.257+1465A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779465 | |||||||
| chr9:111779642 | TA | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.257+1287delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779642 | |||||||
| chr9:111779659 | T | A | 1 | a0002c0002t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.257+1271A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779659 | |||||||
| chr9:111779698 | T | C | 1 | a0002c0002t0002g0166 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.257+1232A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779698 | |||||||
| chr9:111779972 | T | C | 6 | a0002c0007t0006g0213 a0002c0012t0006g0208 a0002c0012t0006g0209 others(3): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+958A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779972 | |||||||
| chr9:111779989 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(237): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.257+941C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111779989 | |||||||
| chr9:111780059 | G | A | 1 | a0003c0003t0002g0108 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.257+871C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780059 | |||||||
| chr9:111780069 | A | G | 1 | a0002c0007t0008g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.257+861T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780069 | |||||||
| chr9:111780088 | A | G | 4 | a0004c0004t0002g0047 a0004c0004t0002g0055 a0004c0004t0002g0056 others(1): Show |
4 | HG01255.hp2 HG02148.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+842T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780088 | |||||||
| chr9:111780142 | C | T | 2 | a0008c0009t0001g0109 a0008c0009t0001g0110 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.257+788G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780142 | |||||||
| chr9:111780171 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.257+759G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780171 | |||||||
| chr9:111780179 | C | A | 1 | a0001c0001t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.257+751G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780179 | |||||||
| chr9:111780202 | G | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.257+728C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780202 | |||||||
| chr9:111780224 | C | T | 2 | a0002c0007t0001g0167 a0012c0025t0005g0264 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.257+706G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780224 | |||||||
| chr9:111780348 | A | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(104): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.257+582T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780348 | |||||||
| chr9:111780461 | T | G | 5 | a0002c0007t0001g0167 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
5 | HG01109.hp2 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+469A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780461 | |||||||
| chr9:111780472 | A | T | 1 | a0002c0007t0006g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.257+458T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780472 | |||||||
| chr9:111780481 | T | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.257+449A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780481 | |||||||
| chr9:111780637 | A | G | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.257+293T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780637 | |||||||
| chr9:111780795 | G | A | 6 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0112 others(3): Show |
7 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+135C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 4/27 | chr9 | 111780795 | |||||||
| chr9:111781120 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.170-103T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781120 | |||||||
| chr9:111781186 | A | T | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-169T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781186 | |||||||
| chr9:111781198 | C | T | 1 | a0001c0026t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.170-181G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781198 | |||||||
| chr9:111781199 | C | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.170-182G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781199 | |||||||
| chr9:111781200 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.170-183C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781200 | |||||||
| chr9:111781360 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.170-343T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781360 | |||||||
| chr9:111781414 | A | T | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.170-397T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781414 | |||||||
| chr9:111781628 | CAGG | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.170-614_170-612del others(3): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781628 | |||||||
| chr9:111781692 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.170-675G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781692 | |||||||
| chr9:111781724 | G | GTAAA | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-711_170-708dup others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781724 | |||||||
| chr9:111781724 | G | GTAAATAA others(1): Show |
100 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(97): Show |
108 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.170-715_170-708dup others(8): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781724 | |||||||
| chr9:111781724 | G | GTAAATAA others(5): Show |
32 | a0001c0001t0001g0135 a0001c0001t0001g0242 a0002c0010t0004g0112 others(29): Show |
36 | HG00544.hp1 HG00621.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.170-719_170-708dup others(12): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781724 | |||||||
| chr9:111781724 | G | GTAAATAA others(9): Show |
29 | a0002c0002t0002g0166 a0002c0002t0002g0175 a0002c0002t0002g0177 others(26): Show |
30 | HG00558.hp2 HG01109.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.170-723_170-708dup others(16): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781724 | |||||||
| chr9:111781724 | G | GTAAATAA others(13): Show |
19 | a0002c0002t0002g0014 a0002c0002t0002g0176 a0002c0002t0002g0178 others(16): Show |
20 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.170-727_170-708dup others(20): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781724 | |||||||
| chr9:111781724 | G | GTAAATAA others(17): Show |
3 | a0001c0022t0001g0196 a0002c0007t0001g0167 a0002c0007t0006g0213 |
3 | HG00673.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.170-731_170-708dup others(24): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781724 | |||||||
| chr9:111781746 | A | AAATTAAT others(13): Show |
2 | a0003c0003t0002g0085 a0003c0003t0002g0090 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.170-730_170-729ins others(20): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781746 | |||||||
| chr9:111781750 | A | AAATAAAT others(25): Show |
1 | a0008c0009t0001g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.170-734_170-733ins others(32): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATAAAT others(17): Show |
1 | a0008c0009t0001g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.170-734_170-733ins others(24): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATAAAT others(21): Show |
5 | a0008c0009t0001g0100 a0008c0009t0001g0101 a0008c0009t0001g0102 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-734_170-733ins others(28): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATAAAT others(17): Show |
4 | a0003c0003t0002g0098 a0003c0003t0002g0099 a0003c0003t0002g0111 others(1): Show |
4 | HG00642.hp2 HG01256.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-734_170-733ins others(24): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATAAAT others(21): Show |
2 | a0003c0003t0002g0108 a0008c0009t0001g0084 |
2 | HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.170-734_170-733ins others(28): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATAAAT others(13): Show |
3 | a0003c0003t0002g0095 a0003c0003t0002g0096 a0003c0003t0002g0097 |
3 | HG01169.hp1 HG02300.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.170-734_170-733ins others(20): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATAAAT others(17): Show |
12 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(9): Show |
13 | HG00140.hp1 HG00408.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.170-734_170-733ins others(24): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATTAAT others(9): Show |
1 | a0003c0003t0002g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.170-734_170-733ins others(16): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATTAAT others(13): Show |
1 | a0003c0003t0002g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.170-734_170-733ins others(20): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | AAATTAAT others(17): Show |
2 | a0003c0003t0002g0091 a0003c0003t0002g0105 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.170-734_170-733ins others(24): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781750 | A | T | 2 | a0003c0003t0002g0085 a0003c0003t0002g0090 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.170-733T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781750 | |||||||
| chr9:111781831 | C | CAGAATAT others(4574): Show |
1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.170-815_170-814ins others(4581): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781831 | |||||||
| chr9:111781937 | A | G | 4 | a0003c0003t0002g0085 a0003c0003t0002g0105 a0003c0003t0002g0106 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-920T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781937 | |||||||
| chr9:111781985 | G | A | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.170-968C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111781985 | |||||||
| chr9:111782027 | C | T | 1 | a0003c0003t0002g0011 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.170-1010G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782027 | |||||||
| chr9:111782028 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.170-1011T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782028 | |||||||
| chr9:111782069 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.170-1052T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782069 | |||||||
| chr9:111782143 | C | T | 1 | a0003c0003t0002g0020 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.170-1126G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782143 | |||||||
| chr9:111782384 | A | G | 2 | a0002c0012t0006g0208 a0002c0012t0006g0209 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.170-1367T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782384 | |||||||
| chr9:111782578 | G | GA | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.170-1562dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782578 | |||||||
| chr9:111782596 | C | T | 1 | a0004c0004t0002g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.170-1579G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782596 | |||||||
| chr9:111782653 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.170-1636A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782653 | |||||||
| chr9:111782710 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.170-1693C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782710 | |||||||
| chr9:111782714 | T | TA | 18 | a0002c0007t0004g0214 a0005c0005t0003g0001 a0005c0005t0003g0006 others(15): Show |
22 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.170-1698dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782714 | |||||||
| chr9:111782815 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.170-1798G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782815 | |||||||
| chr9:111782821 | C | T | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.170-1804G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111782821 | |||||||
| chr9:111783125 | A | T | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-2108T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783125 | |||||||
| chr9:111783177 | A | G | 1 | a0003c0003t0002g0108 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.170-2160T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783177 | |||||||
| chr9:111783287 | C | A | 6 | a0001c0001t0001g0115 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
6 | HG00408.hp1 HG02071.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-2270G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783287 | |||||||
| chr9:111783328 | A | G | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.170-2311T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783328 | |||||||
| chr9:111783353 | G | A | 2 | a0002c0007t0001g0167 a0012c0025t0005g0264 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.170-2336C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783353 | |||||||
| chr9:111783438 | T | C | 6 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0112 others(3): Show |
7 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-2421A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783438 | |||||||
| chr9:111783530 | C | T | 1 | a0002c0011t0005g0121 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.169+2382G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783530 | |||||||
| chr9:111783567 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.169+2345G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783567 | |||||||
| chr9:111783579 | T | C | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.169+2333A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783579 | |||||||
| chr9:111783598 | T | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.169+2314A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783598 | |||||||
| chr9:111783621 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG00639.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.169+2291C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783621 | |||||||
| chr9:111783744 | G | A | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.169+2168C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783744 | |||||||
| chr9:111783855 | G | A | 5 | a0002c0007t0004g0253 a0002c0007t0004g0254 a0002c0007t0004g0255 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+2057C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783855 | |||||||
| chr9:111783954 | T | G | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+1958A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783954 | |||||||
| chr9:111783998 | GT | G | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.169+1913delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111783998 | |||||||
| chr9:111784009 | G | C | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.169+1903C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111784009 | |||||||
| chr9:111784052 | T | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.169+1860A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111784052 | |||||||
| chr9:111784461 | A | G | 7 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG00597.hp2 HG02135.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+1451T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111784461 | |||||||
| chr9:111784673 | T | C | 36 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(33): Show |
37 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.169+1239A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111784673 | |||||||
| chr9:111784793 | G | C | 5 | a0002c0011t0005g0121 a0002c0011t0005g0122 a0002c0011t0005g0123 others(2): Show |
5 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+1119C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111784793 | |||||||
| chr9:111785029 | G | A | 3 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0165 |
4 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+883C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785029 | |||||||
| chr9:111785206 | T | C | 3 | a0002c0002t0002g0014 a0002c0002t0002g0178 a0002c0002t0002g0197 |
4 | NA19000.hp1 NA19010.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+706A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785206 | |||||||
| chr9:111785264 | C | T | 4 | a0003c0003t0002g0077 a0003c0003t0002g0086 a0003c0003t0002g0087 others(1): Show |
4 | HG00140.hp1 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+648G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785264 | |||||||
| chr9:111785275 | A | G | 10 | a0002c0007t0004g0168 a0002c0007t0004g0214 a0002c0007t0006g0207 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.169+637T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785275 | |||||||
| chr9:111785352 | CT | C | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.169+559delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785352 | |||||||
| chr9:111785414 | T | TA | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.169+497dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785414 | |||||||
| chr9:111785430 | C | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.169+482G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785430 | |||||||
| chr9:111785439 | G | C | 1 | a0002c0002t0002g0198 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.169+473C>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785439 | |||||||
| chr9:111785499 | T | C | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169+413A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785499 | |||||||
| chr9:111785541 | C | G | 2 | a0010c0013t0002g0043 a0010c0013t0002g0076 |
2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.169+371G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785541 | |||||||
| chr9:111785596 | T | C | 2 | a0006c0006t0001g0073 a0006c0006t0001g0074 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.169+316A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785596 | |||||||
| chr9:111785663 | T | G | 5 | a0002c0007t0001g0167 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
5 | HG01109.hp2 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+249A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785663 | |||||||
| chr9:111785884 | C | T | 1 | a0017c0016t0002g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.169+28G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 3/27 | chr9 | 111785884 | |||||||
| chr9:111786072 | T | C | 1 | a0019c0028t0001g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.46-37A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786072 | |||||||
| chr9:111786074 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.46-39A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786074 | |||||||
| chr9:111786171 | G | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(164): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.46-136C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786171 | |||||||
| chr9:111786283 | A | C | 1 | a0002c0010t0004g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.46-248T>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786283 | |||||||
| chr9:111786410 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.46-375C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786410 | |||||||
| chr9:111786483 | T | C | 1 | a0002c0010t0004g0113 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46-448A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786483 | |||||||
| chr9:111786486 | T | C | 1 | a0002c0007t0002g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46-451A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786486 | |||||||
| chr9:111786503 | A | AT | 71 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(68): Show |
82 | HG00408.hp1 HG00558.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.46-469dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786503 | |||||||
| chr9:111786503 | A | ATT | 11 | a0001c0001t0001g0129 a0001c0001t0001g0216 a0001c0001t0001g0218 others(8): Show |
12 | HG00621.hp2 HG00741.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.46-470_46-469dupAA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786503 | |||||||
| chr9:111786503 | A | ATTT | 11 | a0002c0007t0008g0019 a0002c0010t0004g0112 a0002c0010t0004g0113 others(8): Show |
11 | HG01109.hp2 HG01192.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-471_46-469dupAA others(1): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786503 | |||||||
| chr9:111786503 | AT | A | 28 | a0001c0001t0001g0127 a0001c0026t0001g0252 a0002c0002t0002g0199 others(25): Show |
32 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.46-469delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786503 | |||||||
| chr9:111786503 | ATT | A | 8 | a0003c0003t0002g0085 a0005c0005t0003g0022 a0007c0008t0001g0004 others(5): Show |
13 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-470_46-469delAA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786503 | |||||||
| chr9:111786503 | ATTT | A | 32 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(29): Show |
33 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.46-471_46-469delAA others(1): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786503 | |||||||
| chr9:111786585 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(149): Show |
162 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.46-550G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786585 | |||||||
| chr9:111786773 | T | A | 1 | a0002c0002t0002g0206 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.46-738A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786773 | |||||||
| chr9:111786931 | C | T | 3 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0165 |
4 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-896G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111786931 | |||||||
| chr9:111787052 | G | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.46-1017C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787052 | |||||||
| chr9:111787077 | C | G | 1 | a0002c0007t0002g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46-1042G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787077 | |||||||
| chr9:111787091 | A | G | 5 | a0002c0007t0001g0167 a0002c0010t0004g0112 a0002c0010t0004g0113 others(2): Show |
5 | HG01109.hp2 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-1056T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787091 | |||||||
| chr9:111787270 | A | G | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.46-1235T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787270 | |||||||
| chr9:111787324 | C | T | 2 | a0002c0002t0002g0176 a0002c0002t0002g0200 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.46-1289G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787324 | |||||||
| chr9:111787366 | C | T | 2 | a0003c0003t0002g0083 a0003c0003t0002g0174 |
2 | HG01074.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.46-1331G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787366 | |||||||
| chr9:111787432 | G | T | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.46-1397C>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787432 | |||||||
| chr9:111787647 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-1612G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787647 | |||||||
| chr9:111787945 | C | T | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.46-1910G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787945 | |||||||
| chr9:111787947 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.46-1912C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111787947 | |||||||
| chr9:111788013 | T | A | 2 | a0003c0003t0002g0105 a0003c0003t0002g0106 |
2 | HG02738.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.46-1978A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788013 | |||||||
| chr9:111788064 | C | CT | 23 | a0001c0001t0001g0119 a0001c0001t0001g0158 a0002c0002t0002g0166 others(20): Show |
24 | HG01109.hp2 HG01167.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.46-2030dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788064 | |||||||
| chr9:111788064 | C | CTT | 139 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(136): Show |
148 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.46-2031_46-2030dup others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788064 | |||||||
| chr9:111788064 | CT | C | 8 | a0004c0004t0002g0075 a0006c0006t0001g0074 a0007c0008t0001g0004 others(5): Show |
13 | HG01255.hp1 HG01515.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-2030delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788064 | |||||||
| chr9:111788192 | A | G | 1 | a0004c0004t0002g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46-2157T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788192 | |||||||
| chr9:111788195 | G | A | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-2160C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788195 | |||||||
| chr9:111788235 | T | TA | 215 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(212): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.46-2201dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788235 | |||||||
| chr9:111788377 | T | C | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-2342A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788377 | |||||||
| chr9:111788398 | C | T | 3 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0165 |
4 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-2363G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788398 | |||||||
| chr9:111788403 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.46-2368G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788403 | |||||||
| chr9:111788452 | T | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.46-2417A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788452 | |||||||
| chr9:111788718 | TG | T | 3 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0165 |
4 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2655delC | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788718 | |||||||
| chr9:111788737 | C | T | 2 | a0004c0004t0002g0007 a0020c0020t0002g0044 |
3 | NA18952.hp1 NA18970.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.45+2637G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788737 | |||||||
| chr9:111788750 | C | T | 1 | a0005c0005t0003g0023 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.45+2624G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788750 | |||||||
| chr9:111788895 | GTC | G | 32 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(29): Show |
33 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.45+2477_45+2478del others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788895 | |||||||
| chr9:111788946 | CA | C | 6 | a0002c0007t0006g0213 a0002c0012t0006g0208 a0002c0012t0006g0209 others(3): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+2427delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111788946 | |||||||
| chr9:111789035 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+2339G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789035 | |||||||
| chr9:111789039 | C | G | 1 | a0002c0007t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45+2335G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789039 | |||||||
| chr9:111789104 | T | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.45+2270A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789104 | |||||||
| chr9:111789144 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.45+2230G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789144 | |||||||
| chr9:111789149 | C | CTT | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.45+2223_45+2224dup others(2): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789149 | |||||||
| chr9:111789349 | T | G | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+2025A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789349 | |||||||
| chr9:111789418 | T | A | 3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.45+1956A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789418 | |||||||
| chr9:111789448 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+1926T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789448 | |||||||
| chr9:111789470 | T | A | 1 | a0005c0005t0003g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.45+1904A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789470 | |||||||
| chr9:111789476 | ATTTTAAG others(3): Show |
A | 3 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0165 |
4 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+1888_45+1897del others(10): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789476 | |||||||
| chr9:111789505 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.45+1869T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789505 | |||||||
| chr9:111789695 | A | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.45+1679T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789695 | |||||||
| chr9:111789698 | G | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+1676C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789698 | |||||||
| chr9:111789745 | T | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.45+1629A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789745 | |||||||
| chr9:111789916 | TTTC | T | 3 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0165 |
4 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+1455_45+1457del others(3): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789916 | |||||||
| chr9:111789936 | G | A | 51 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0117 others(48): Show |
52 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+1438C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789936 | |||||||
| chr9:111789937 | T | C | 1 | a0002c0010t0004g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+1437A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111789937 | |||||||
| chr9:111790170 | C | T | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.45+1204G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790170 | |||||||
| chr9:111790195 | T | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.45+1179A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790195 | |||||||
| chr9:111790227 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(99): Show |
110 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.45+1147T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790227 | |||||||
| chr9:111790245 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(198): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.45+1129A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790245 | |||||||
| chr9:111790301 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.45+1073G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790301 | |||||||
| chr9:111790346 | C | T | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+1028G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790346 | |||||||
| chr9:111790640 | AT | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.45+733delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790640 | |||||||
| chr9:111790710 | T | G | 6 | a0002c0007t0008g0019 a0002c0010t0002g0013 a0002c0010t0004g0112 others(3): Show |
7 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+664A>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111790710 | |||||||
| chr9:111791249 | A | G | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+125T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 2/27 | chr9 | 111791249 | |||||||
| chr9:111791568 | A | G | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36-114T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791568 | |||||||
| chr9:111791569 | T | C | 3 | a0002c0002t0002g0204 a0002c0002t0002g0205 a0002c0002t0002g0206 |
3 | HG02738.hp2 HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-36-115A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791569 | |||||||
| chr9:111791648 | C | T | 1 | a0010c0013t0002g0043 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-36-194G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791648 | |||||||
| chr9:111791752 | G | GTAACCAT others(22): Show |
1 | a0006c0006t0001g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-36-327_-36-299dup others(29): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791752 | |||||||
| chr9:111791752 | G | GTAACCAT others(51): Show |
2 | a0006c0006t0001g0073 a0006c0006t0001g0074 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-36-356_-36-299dup others(58): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791752 | |||||||
| chr9:111791752 | GTAACCAT others(22): Show |
G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(143): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-36-327_-36-299del others(29): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791752 | |||||||
| chr9:111791752 | GTAACCAT others(51): Show |
G | 68 | a0002c0002t0002g0175 a0002c0007t0001g0167 a0002c0007t0004g0168 others(65): Show |
73 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-36-356_-36-299del others(58): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791752 | |||||||
| chr9:111791752 | GTAACCAT others(80): Show |
G | 5 | a0002c0007t0006g0207 a0002c0010t0004g0165 a0003c0003t0002g0020 others(2): Show |
6 | HG00408.hp2 HG01884.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-385_-36-299del others(87): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791752 | |||||||
| chr9:111791752 | GTAACCAT others(109): Show |
G | 2 | a0002c0007t0008g0019 a0017c0016t0002g0081 |
2 | HG01192.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-36-414_-36-299del | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111791752 | |||||||
| chr9:111792057 | AAGCCTAA others(4): Show |
A | 1 | a0001c0001t0001g0162 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-36-614_-36-604del others(11): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792057 | |||||||
| chr9:111792311 | G | A | 1 | a0008c0009t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-36-857C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792311 | |||||||
| chr9:111792330 | C | T | 1 | a0001c0026t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-36-876G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792330 | |||||||
| chr9:111792349 | G | A | 2 | a0002c0007t0001g0167 a0012c0025t0005g0264 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-36-895C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792349 | |||||||
| chr9:111792351 | G | A | 32 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(29): Show |
33 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-36-897C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792351 | |||||||
| chr9:111792380 | GA | G | 5 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
5 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-927delT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792380 | |||||||
| chr9:111792674 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-36-1220A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792674 | |||||||
| chr9:111792844 | A | G | 1 | a0002c0007t0006g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-36-1390T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792844 | |||||||
| chr9:111792887 | C | CT | 8 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(5): Show |
13 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-1434dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792887 | |||||||
| chr9:111792887 | C | CTT | 32 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(29): Show |
33 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-36-1435_-36-1434d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792887 | |||||||
| chr9:111792887 | CT | C | 6 | a0003c0003t0002g0174 a0005c0005t0003g0023 a0005c0005t0003g0036 others(3): Show |
6 | HG00544.hp1 HG00621.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-1434delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792887 | |||||||
| chr9:111792957 | AC | A | 3 | a0002c0010t0004g0112 a0002c0010t0004g0113 a0002c0010t0004g0114 |
3 | HG02615.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-36-1504delG | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111792957 | |||||||
| chr9:111793040 | G | A | 1 | a0012c0025t0005g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-36-1586C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793040 | |||||||
| chr9:111793177 | C | T | 1 | a0002c0007t0001g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37+1723G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793177 | |||||||
| chr9:111793528 | A | G | 1 | a0007c0008t0001g0010 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-37+1372T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793528 | |||||||
| chr9:111793622 | A | ATGGTTAG others(19): Show |
31 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(28): Show |
32 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-37+1252_-37+1277d others(28): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793622 | |||||||
| chr9:111793622 | A | ATGGTTAG others(18): Show |
1 | a0003c0003t0002g0108 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-37+1277_-37+1278i others(27): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793622 | |||||||
| chr9:111793664 | T | A | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.-37+1236A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793664 | |||||||
| chr9:111793679 | A | AT | 46 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0166 others(43): Show |
48 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-37+1220dupA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793679 | |||||||
| chr9:111793679 | A | ATT | 63 | a0001c0001t0001g0012 a0001c0001t0001g0116 a0001c0001t0001g0117 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-37+1219_-37+1220d others(4): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793679 | |||||||
| chr9:111793679 | A | ATTT | 43 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(40): Show |
50 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-37+1218_-37+1220d others(5): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793679 | |||||||
| chr9:111793679 | AT | A | 35 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(32): Show |
36 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-37+1220delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793679 | |||||||
| chr9:111793693 | T | A | 1 | a0003c0003t0002g0111 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-37+1207A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793693 | |||||||
| chr9:111793777 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-37+1123G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793777 | |||||||
| chr9:111793798 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-37+1102C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793798 | |||||||
| chr9:111793921 | G | A | 6 | a0003c0003t0002g0169 a0003c0003t0002g0170 a0003c0003t0002g0172 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+979C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793921 | |||||||
| chr9:111793971 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-37+929G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793971 | |||||||
| chr9:111793997 | G | A | 22 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(19): Show |
26 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.-37+903C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111793997 | |||||||
| chr9:111794196 | G | A | 34 | a0003c0003t0002g0011 a0003c0003t0002g0020 a0003c0003t0002g0077 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-37+704C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794196 | |||||||
| chr9:111794273 | C | CA | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.-37+626_-37+627ins others(1): Show |
SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794273 | |||||||
| chr9:111794278 | T | TA | 44 | a0001c0022t0001g0196 a0002c0002t0002g0014 a0002c0002t0002g0175 others(41): Show |
45 | HG00558.hp2 HG00673.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-37+621dupT | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794278 | |||||||
| chr9:111794287 | A | G | 1 | a0005c0005t0003g0023 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-37+613T>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794287 | |||||||
| chr9:111794289 | A | T | 1 | a0009c0018t0002g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-37+611T>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794289 | |||||||
| chr9:111794291 | AT | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(112): Show |
127 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-37+608delA | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794291 | |||||||
| chr9:111794292 | T | A | 108 | a0001c0001t0001g0012 a0001c0001t0001g0115 a0001c0001t0001g0116 others(105): Show |
111 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-37+608A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794292 | |||||||
| chr9:111794295 | T | A | 2 | a0002c0002t0002g0267 a0002c0002t0002g0268 |
2 | NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-37+605A>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794295 | |||||||
| chr9:111794305 | C | T | 3 | a0002c0010t0004g0112 a0002c0010t0004g0113 a0002c0010t0004g0114 |
3 | HG02615.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-37+595G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794305 | |||||||
| chr9:111794306 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-37+594C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794306 | |||||||
| chr9:111794535 | G | A | 6 | a0007c0008t0001g0004 a0007c0008t0001g0005 a0007c0008t0001g0010 others(3): Show |
11 | HG01255.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37+365C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794535 | |||||||
| chr9:111794540 | T | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-37+360A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794540 | |||||||
| chr9:111794551 | G | A | 34 | a0001c0001t0001g0270 a0003c0003t0002g0011 a0003c0003t0002g0020 others(31): Show |
35 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-37+349C>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794551 | |||||||
| chr9:111794581 | C | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(186): Show |
203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-37+319G>T | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794581 | |||||||
| chr9:111794666 | T | C | 19 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0023 others(16): Show |
23 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.-37+234A>G | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794666 | |||||||
| chr9:111794836 | C | T | 21 | a0005c0005t0003g0001 a0005c0005t0003g0006 a0005c0005t0003g0021 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37+64G>A | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794836 | |||||||
| chr9:111794893 | C | G | 1 | a0003c0003t0002g0020 | 1 | HG00408.hp2 | splice_region_variant&intron_variant | LOW | c.-37+7G>C | SHOC1 | ENSG00000165181.17 | transcript | ENST00000682961.1 | protein_coding | 1/27 | chr9 | 111794893 |