Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8036 |
| ensemblid | ENSG00000108061.13 |
| hgncid | 15454 |
| symbol | SHOC2 |
| name | SHOC2 leucine rich repeat scaffold protein |
| refseq_nuc | NM_007373.4 |
| refseq_prot | NP_031399.2 |
| ensembl_nuc | ENST00000369452.9 |
| ensembl_prot | ENSP00000358464.5 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 110919604 |
| end | 111013665 |
| strand | + |
| ver | v1.2 |
| region | chr10:110919604-111013665 |
| region5000 | chr10:110914604-111018665 |
| regionname0 | SHOC2_chr10_110919604_111013665 |
| regionname5000 | SHOC2_chr10_110914604_111018665 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 582 | 380 | 87 | 51 | 190 | 8 | 42 | 152 | SHOC2_chr10_110914604_111018665 | SHOC2 | MSSSL others(577): Show |
chr10 | 110914604 | 111018665 |
| a0002 | 0/0 | 582 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | MSSSL others(577): Show |
chr10 | 110914604 | 111018665 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1746 | 377 | 86 | 50 | 189 | 8 | 42 | SHOC2_chr10_110914604_111018665 | SHOC2 | ATGAG others(1741): Show |
chr10 | 110914604 | 111018665 | ||
| a0001c0003 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | ATGAG others(1741): Show |
chr10 | 110914604 | 111018665 | ||
| a0001c0004 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | ATGAG others(1741): Show |
chr10 | 110914604 | 111018665 | ||
| a0001c0005 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | ATGAG others(1741): Show |
chr10 | 110914604 | 111018665 | ||
| a0002c0002 | 0/0 | 1746 | 6 | 5 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | ATGAG others(1741): Show |
chr10 | 110914604 | 111018665 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3884 | 256 | 55 | 33 | 128 | 7 | 31 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0002 | 0/0 | 3884 | 89 | 15 | 13 | 56 | 0 | 5 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0003 | 0/0 | 3883 | 12 | 10 | 1 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3878): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0004 | 0/0 | 3884 | 3 | 0 | 2 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0005 | 0/0 | 3885 | 2 | 0 | 0 | 0 | 0 | 2 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3880): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0006 | 0/0 | 3884 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0007 | 0/0 | 3884 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0008 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0009 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0010 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0011 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0013 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0014 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3880): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0015 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0016 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0017 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0018 | 0/0 | 3884 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0019 | 0/0 | 3884 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0020 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0001t0021 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0003t0001 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0004t0012 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| a0001c0005t0003 | 0/0 | 3883 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3878): Show |
chr10 | 110914604 | 111018665 |
| a0002c0002t0001 | 0/0 | 3884 | 6 | 5 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | GAAGA others(3879): Show |
chr10 | 110914604 | 111018665 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0320 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0011g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0013g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0015g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0016g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0018g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0019g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0020g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0001t0021g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0004t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0001c0005t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0002c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00423 | hp1 | a0001 | c0001 | t0015 | g0073 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0302 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0241 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01074 | hp2 | a0001 | c0005 | t0003 | g0340 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0334 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0346 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0098 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0269 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CDX | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0147 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0338 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02622 | hp2 | a0001 | c0004 | t0012 | g0143 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0124 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02723 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0347 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0344 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0345 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03017 | hp2 | a0001 | c0001 | t0018 | g0327 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0332 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0337 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0103 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0245 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0123 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04204 | hp1 | a0001 | c0001 | t0019 | g0238 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0121 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CHB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18959 | hp2 | a0001 | c0001 | t0020 | g0153 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18967 | hp1 | a0001 | c0001 | t0011 | g0048 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0163 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0339 | AFR | ASW | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ASW | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0333 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0335 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0122 | REF | REF | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0320 | REF | REF | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:111011663 | A | G | 1 | a0002 | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.1594A>G | p.Ser532Gly | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1882/3884 | 1594/1749 | 532/582 | chr10 | 111011663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:110964815 | C | T | 1 | a0001c0005 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.457C>T | p.Leu153Leu | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | 745/3884 | 457/1749 | 153/582 | chr10 | 110964815 | |||
| chr10:111004680 | T | C | 1 | a0001c0003 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.1047T>C | p.Gly349Gly | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/9 | 1335/3884 | 1047/1749 | 349/582 | chr10 | 111004680 | |||
| chr10:111009265 | C | T | 1 | a0001c0004 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1302C>T | p.Asn434Asn | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/9 | 1590/3884 | 1302/1749 | 434/582 | chr10 | 111009265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:110919648 | G | T | 1 | a0001c0001t0021 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-244G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/9 | 44711 | chr10 | 110919648 | ||||||
| chr10:110964157 | A | G | 1 | a0001c0001t0020 | 1 | NA18959.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-202A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | chr10 | 110964157 | |||||||
| chr10:110964171 | A | G | 1 | a0001c0001t0019 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-188A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | 188 | chr10 | 110964171 | ||||||
| chr10:110964196 | T | A | 1 | a0001c0001t0006 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-163T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | 163 | chr10 | 110964196 | ||||||
| chr10:111011887 | A | G | 1 | a0001c0001t0018 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*69A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 69 | chr10 | 111011887 | ||||||
| chr10:111011982 | T | A | 1 | a0001c0001t0004 | 3 | HG01069.hp2 HG01071.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*164T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 164 | chr10 | 111011982 | ||||||
| chr10:111012111 | G | A | 1 | a0001c0001t0007 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 293 | chr10 | 111012111 | ||||||
| chr10:111012319 | A | G | 1 | a0001c0001t0017 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 501 | chr10 | 111012319 | ||||||
| chr10:111012322 | T | C | 1 | a0001c0001t0008 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 504 | chr10 | 111012322 | ||||||
| chr10:111012324 | T | C | 1 | a0001c0001t0007 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 506 | chr10 | 111012324 | ||||||
| chr10:111012341 | T | C | 1 | a0001c0001t0009 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*523T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 523 | chr10 | 111012341 | ||||||
| chr10:111012591 | G | A | 1 | a0001c0001t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 773 | chr10 | 111012591 | ||||||
| chr10:111012732 | G | A | 1 | a0001c0001t0011 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*914G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 914 | chr10 | 111012732 | ||||||
| chr10:111012842 | G | T | 1 | a0001c0001t0016 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1024G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1024 | chr10 | 111012842 | ||||||
| chr10:111012924 | A | C | 1 | a0001c0001t0015 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1106A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1106 | chr10 | 111012924 | ||||||
| chr10:111013115 | G | A | 1 | a0001c0004t0012 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1297G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1297 | chr10 | 111013115 | ||||||
| chr10:111013141 | C | T | 1 | a0001c0001t0005 | 2 | HG02698.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1323C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1323 | chr10 | 111013141 | ||||||
| chr10:111013303 | G | GT | 2 | a0001c0001t0005 a0001c0001t0014 |
3 | HG02698.hp1 HG04199.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1486dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1487 | INFO_REALIGN_3_PRIME | chr10 | 111013303 | |||||
| chr10:111013304 | TG | T | 2 | a0001c0001t0003 a0001c0005t0003 |
13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1487delG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1487 | chr10 | 111013304 | ||||||
| chr10:111013305 | G | GT | 2 | a0001c0001t0001 a0001c0001t0002 |
8 | HG00738.hp2 HG01978.hp1 HG02135.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1500dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1501 | INFO_REALIGN_3_PRIME | chr10 | 111013305 | |||||
| chr10:111013305 | G | T | 3 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 |
6 | HG01081.hp1 HG02698.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1487G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1487 | chr10 | 111013305 | ||||||
| chr10:111013305 | GT | G | 2 | a0001c0001t0001 a0002c0002t0001 |
16 | HG01081.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1500delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1500 | INFO_REALIGN_3_PRIME | chr10 | 111013305 | |||||
| chr10:111013308 | T | G | 1 | a0001c0001t0013 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1490T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1490 | chr10 | 111013308 | ||||||
| chr10:111013321 | A | G | 2 | a0001c0001t0002 a0001c0001t0009 |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1503A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1503 | chr10 | 111013321 | ||||||
| chr10:111013593 | T | C | 1 | a0001c0001t0009 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1775T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1775 | chr10 | 111013593 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:110919758 | C | G | 2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | NA18990.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-235+101C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919758 | |||||||
| chr10:110919805 | C | G | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-235+148C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919805 | |||||||
| chr10:110919855 | T | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
8 | HG00544.hp1 HG00597.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+198T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919855 | |||||||
| chr10:110919872 | G | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
14 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+215G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919872 | |||||||
| chr10:110919990 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
6 | HG02165.hp1 NA18966.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+333C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919990 | |||||||
| chr10:110920101 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
88 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.-235+444G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920101 | |||||||
| chr10:110920110 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-235+453G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920110 | |||||||
| chr10:110920148 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-235+491T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920148 | |||||||
| chr10:110920192 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-235+535C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920192 | |||||||
| chr10:110920241 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-235+584T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920241 | |||||||
| chr10:110920337 | G | C | 1 | a0001c0001t0002g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-235+680G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920337 | |||||||
| chr10:110920453 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-235+796T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920453 | |||||||
| chr10:110920485 | A | G | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+828A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920485 | |||||||
| chr10:110920550 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-235+893C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920550 | |||||||
| chr10:110920680 | A | T | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+1023A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920680 | |||||||
| chr10:110920924 | A | G | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-235+1267A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920924 | |||||||
| chr10:110920960 | T | G | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+1303T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920960 | |||||||
| chr10:110921071 | C | G | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+1414C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921071 | |||||||
| chr10:110921192 | A | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+1535A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921192 | |||||||
| chr10:110921270 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-235+1613T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921270 | |||||||
| chr10:110921383 | A | G | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+1726A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921383 | |||||||
| chr10:110921574 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+1917T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921574 | |||||||
| chr10:110921628 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-235+1971T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921628 | |||||||
| chr10:110921717 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0330 a0001c0001t0001g0331 |
4 | HG02027.hp1 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+2060A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921717 | |||||||
| chr10:110921804 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-235+2147C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921804 | |||||||
| chr10:110921809 | T | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-235+2152T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921809 | |||||||
| chr10:110921852 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-235+2195A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921852 | |||||||
| chr10:110921973 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-235+2316T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921973 | |||||||
| chr10:110922002 | A | G | 2 | a0001c0001t0001g0328 a0001c0001t0018g0327 |
2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-235+2345A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922002 | |||||||
| chr10:110922129 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-235+2472T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922129 | |||||||
| chr10:110922166 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-235+2509G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922166 | |||||||
| chr10:110922246 | A | G | 4 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG02074.hp1 HG02165.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+2589A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922246 | |||||||
| chr10:110922309 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+2652C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922309 | |||||||
| chr10:110922343 | G | T | 1 | a0001c0001t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-235+2686G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922343 | |||||||
| chr10:110922452 | C | CTG | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(323): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-235+2796_-235+279 others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110922452 | ||||||
| chr10:110922468 | T | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+2811T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922468 | |||||||
| chr10:110922499 | T | G | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+2842T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922499 | |||||||
| chr10:110922669 | A | T | 1 | a0001c0003t0001g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-235+3012A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922669 | |||||||
| chr10:110922753 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+3096G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922753 | |||||||
| chr10:110922858 | T | C | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-235+3201T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922858 | |||||||
| chr10:110922959 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+3302G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922959 | |||||||
| chr10:110923325 | C | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+3668C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923325 | |||||||
| chr10:110923359 | A | G | 1 | a0001c0001t0002g0301 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-235+3702A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923359 | |||||||
| chr10:110923404 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-235+3747T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923404 | |||||||
| chr10:110923650 | A | G | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-235+3993A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923650 | |||||||
| chr10:110923685 | GAA | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-235+4030_-235+403 others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110923685 | ||||||
| chr10:110923702 | G | A | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+4045G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923702 | |||||||
| chr10:110923875 | T | C | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+4218T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923875 | |||||||
| chr10:110924110 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+4453A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924110 | |||||||
| chr10:110924150 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+4493A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924150 | |||||||
| chr10:110924236 | G | A | 3 | a0001c0001t0003g0333 a0001c0001t0003g0334 a0001c0001t0003g0335 |
3 | HG01168.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-235+4579G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924236 | |||||||
| chr10:110924262 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-235+4605C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924262 | |||||||
| chr10:110924297 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-235+4640C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924297 | |||||||
| chr10:110924329 | A | G | 13 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(10): Show |
13 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-235+4672A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924329 | |||||||
| chr10:110924570 | C | A | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+4913C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924570 | |||||||
| chr10:110924585 | T | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+4928T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924585 | |||||||
| chr10:110924775 | A | G | 17 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0306 others(14): Show |
18 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.-235+5118A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924775 | |||||||
| chr10:110924795 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-235+5138C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924795 | |||||||
| chr10:110924840 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
8 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-235+5183C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924840 | |||||||
| chr10:110924841 | G | A | 1 | a0001c0001t0010g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-235+5184G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924841 | |||||||
| chr10:110924890 | C | A | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-235+5233C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924890 | |||||||
| chr10:110924996 | G | A | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+5339G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924996 | |||||||
| chr10:110925070 | C | CA | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-235+5435dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925070 | ||||||
| chr10:110925070 | C | CAA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(25): Show |
29 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.-235+5434_-235+543 others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925070 | ||||||
| chr10:110925070 | CA | C | 20 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0319 others(17): Show |
21 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-235+5435delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925070 | ||||||
| chr10:110925087 | A | T | 1 | a0001c0001t0001g0236 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-235+5430A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925087 | |||||||
| chr10:110925089 | AAAATT | A | 20 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0035 others(17): Show |
22 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.-235+5436_-235+544 others(9): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925089 | ||||||
| chr10:110925094 | T | A | 1 | a0001c0001t0001g0236 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-235+5437T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925094 | |||||||
| chr10:110925098 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-235+5441A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925098 | |||||||
| chr10:110925115 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+5458A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925115 | |||||||
| chr10:110925390 | A | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+5733A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925390 | |||||||
| chr10:110925449 | T | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+5792T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925449 | |||||||
| chr10:110925523 | T | C | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+5866T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925523 | |||||||
| chr10:110925526 | G | T | 4 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG02074.hp1 HG02165.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+5869G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925526 | |||||||
| chr10:110925572 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-235+5915T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925572 | |||||||
| chr10:110925573 | T | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-235+5916T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925573 | |||||||
| chr10:110925656 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(188): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-235+5999C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925656 | |||||||
| chr10:110925942 | G | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0167 others(7): Show |
14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+6285G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925942 | |||||||
| chr10:110925960 | T | G | 3 | a0001c0001t0003g0333 a0001c0001t0003g0334 a0001c0001t0003g0335 |
3 | HG01168.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-235+6303T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925960 | |||||||
| chr10:110926563 | C | T | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+6906C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926563 | |||||||
| chr10:110926565 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.-235+6908C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926565 | |||||||
| chr10:110926634 | C | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+6977C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926634 | |||||||
| chr10:110926676 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-235+7019A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926676 | |||||||
| chr10:110926710 | G | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+7053G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926710 | |||||||
| chr10:110926763 | C | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | NA18951.hp1 NA18959.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-235+7106C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926763 | |||||||
| chr10:110926765 | A | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01175.hp2 HG01978.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-235+7108A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926765 | |||||||
| chr10:110926955 | A | G | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-235+7298A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926955 | |||||||
| chr10:110926976 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-235+7319G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926976 | |||||||
| chr10:110927118 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-235+7461A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927118 | |||||||
| chr10:110927313 | C | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-235+7656C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927313 | |||||||
| chr10:110927325 | A | G | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+7668A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927325 | |||||||
| chr10:110927766 | C | G | 1 | a0001c0001t0002g0228 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-235+8109C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927766 | |||||||
| chr10:110927768 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+8111A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927768 | |||||||
| chr10:110927908 | T | C | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-235+8251T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927908 | |||||||
| chr10:110927971 | A | G | 2 | a0001c0001t0004g0248 a0001c0001t0009g0227 |
2 | HG01069.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-235+8314A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927971 | |||||||
| chr10:110928087 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+8430C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928087 | |||||||
| chr10:110928155 | A | G | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+8498A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928155 | |||||||
| chr10:110928319 | C | T | 81 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(78): Show |
93 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.-235+8662C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928319 | |||||||
| chr10:110928578 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+8921A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928578 | |||||||
| chr10:110928766 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-235+9109G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928766 | |||||||
| chr10:110928825 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+9168G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928825 | |||||||
| chr10:110928851 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+9194T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928851 | |||||||
| chr10:110928911 | A | T | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+9254A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928911 | |||||||
| chr10:110929273 | T | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0156 others(4): Show |
9 | HG01261.hp1 HG02027.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+9616T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929273 | |||||||
| chr10:110929545 | A | G | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-235+9888A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929545 | |||||||
| chr10:110929614 | T | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+9957T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929614 | |||||||
| chr10:110929864 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+10207A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929864 | |||||||
| chr10:110929894 | G | A | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-235+10237G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929894 | |||||||
| chr10:110929931 | C | T | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+10274C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929931 | |||||||
| chr10:110929973 | T | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+10316T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929973 | |||||||
| chr10:110930052 | TATATG | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+10397_-235+10 others(11): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930052 | ||||||
| chr10:110930189 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-235+10532A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930189 | |||||||
| chr10:110930224 | T | G | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+10567T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930224 | |||||||
| chr10:110930409 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-235+10752T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930409 | |||||||
| chr10:110930497 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-235+10840C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930497 | |||||||
| chr10:110930593 | A | T | 1 | a0001c0001t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-235+10936A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930593 | |||||||
| chr10:110930611 | T | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+10954T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930611 | |||||||
| chr10:110930621 | A | C | 9 | a0001c0001t0001g0247 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02071.hp1 NA18942.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+10964A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930621 | |||||||
| chr10:110930735 | C | CTT | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-235+11092_-235+11 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | ||||||
| chr10:110930735 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0239 a0001c0001t0001g0249 others(3): Show |
8 | HG00140.hp1 HG00642.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+11086_-235+11 others(14): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | ||||||
| chr10:110930735 | C | CTTTTTTT others(2): Show |
104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-235+11085_-235+11 others(15): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | ||||||
| chr10:110930735 | C | CTTTTTTT others(3): Show |
139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(136): Show |
153 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-235+11084_-235+11 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | ||||||
| chr10:110930735 | C | CTTTTTTT others(4): Show |
21 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0064 others(18): Show |
21 | HG00642.hp1 HG00673.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-235+11083_-235+11 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | ||||||
| chr10:110930764 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+11107T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930764 | |||||||
| chr10:110930891 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-235+11234G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930891 | |||||||
| chr10:110931127 | C | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+11470C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931127 | |||||||
| chr10:110931202 | G | C | 1 | a0001c0001t0001g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-235+11545G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931202 | |||||||
| chr10:110931252 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-235+11595G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931252 | |||||||
| chr10:110931290 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0341 |
3 | HG01884.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-235+11633A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931290 | |||||||
| chr10:110931389 | C | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(282): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-235+11732C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931389 | |||||||
| chr10:110931411 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+11754T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931411 | |||||||
| chr10:110931744 | GTTAT | G | 12 | a0001c0001t0001g0225 a0001c0001t0003g0027 a0001c0001t0003g0226 others(9): Show |
13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-235+12092_-235+12 others(10): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110931744 | ||||||
| chr10:110931830 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-235+12173G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931830 | |||||||
| chr10:110931845 | T | G | 1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-235+12188T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931845 | |||||||
| chr10:110931852 | C | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+12195C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931852 | |||||||
| chr10:110931889 | G | A | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-235+12232G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931889 | |||||||
| chr10:110931937 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-235+12280T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931937 | |||||||
| chr10:110931995 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+12338A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931995 | |||||||
| chr10:110932051 | C | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG01081.hp2 HG01496.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-235+12394C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932051 | |||||||
| chr10:110932104 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-235+12447A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932104 | |||||||
| chr10:110932307 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+12650T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932307 | |||||||
| chr10:110932493 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+12836A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932493 | |||||||
| chr10:110932618 | C | A | 14 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
16 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-235+12961C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932618 | |||||||
| chr10:110932622 | T | G | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-235+12965T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932622 | |||||||
| chr10:110932689 | A | G | 1 | a0001c0005t0003g0340 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-235+13032A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932689 | |||||||
| chr10:110932692 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-235+13035G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932692 | |||||||
| chr10:110932702 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-235+13045G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932702 | |||||||
| chr10:110932728 | A | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(21): Show |
26 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.-235+13071A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932728 | |||||||
| chr10:110932729 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-235+13072C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932729 | |||||||
| chr10:110932820 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0106 |
5 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-235+13163A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932820 | |||||||
| chr10:110932866 | C | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-235+13209C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932866 | |||||||
| chr10:110932907 | G | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
26 | HG00408.hp2 HG00642.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.-235+13250G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932907 | |||||||
| chr10:110932985 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-235+13328C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932985 | |||||||
| chr10:110933044 | G | A | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-235+13387G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933044 | |||||||
| chr10:110933135 | G | T | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+13478G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933135 | |||||||
| chr10:110933216 | G | A | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+13559G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933216 | |||||||
| chr10:110933217 | CT | C | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+13567delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110933217 | ||||||
| chr10:110933470 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-235+13813G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933470 | |||||||
| chr10:110933570 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-235+13913T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933570 | |||||||
| chr10:110933822 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+14165A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933822 | |||||||
| chr10:110933847 | C | T | 13 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-235+14190C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933847 | |||||||
| chr10:110933868 | A | AT | 11 | a0001c0001t0001g0061 a0001c0001t0002g0021 a0001c0001t0002g0022 others(8): Show |
13 | HG00408.hp2 HG02015.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-235+14221dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110933868 | ||||||
| chr10:110934272 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.-235+14615A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934272 | |||||||
| chr10:110934367 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0095 |
2 | HG00544.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-235+14710A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934367 | |||||||
| chr10:110934448 | G | T | 1 | a0001c0001t0002g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-235+14791G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934448 | |||||||
| chr10:110934551 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0281 a0001c0001t0017g0023 |
3 | HG01884.hp2 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-235+14894A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934551 | |||||||
| chr10:110934558 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+14901G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934558 | |||||||
| chr10:110934584 | G | A | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(323): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-235+14927G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934584 | |||||||
| chr10:110934662 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-235+15005C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934662 | |||||||
| chr10:110935100 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+15443A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935100 | |||||||
| chr10:110935267 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-235+15610A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935267 | |||||||
| chr10:110935272 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+15615C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935272 | |||||||
| chr10:110935514 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-235+15857G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935514 | |||||||
| chr10:110935915 | TG | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-235+16260delG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110935915 | ||||||
| chr10:110936085 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+16428T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936085 | |||||||
| chr10:110936095 | A | AT | 37 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0094 others(34): Show |
40 | HG01074.hp2 HG01168.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.-235+16456dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936095 | ||||||
| chr10:110936095 | AT | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0071 a0001c0001t0001g0072 others(4): Show |
7 | HG02922.hp1 HG03041.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-235+16456delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936095 | ||||||
| chr10:110936135 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-235+16478C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936135 | |||||||
| chr10:110936158 | G | A | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-235+16501G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936158 | |||||||
| chr10:110936172 | C | T | 2 | a0001c0001t0002g0210 a0001c0001t0002g0211 |
2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-235+16515C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936172 | |||||||
| chr10:110936212 | T | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | NA19055.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-235+16555T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936212 | |||||||
| chr10:110936286 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0015g0073 |
3 | HG00423.hp1 NA18998.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-235+16629T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936286 | |||||||
| chr10:110936381 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+16724G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936381 | |||||||
| chr10:110936414 | T | C | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+16757T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936414 | |||||||
| chr10:110936423 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+16766A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936423 | |||||||
| chr10:110936430 | C | A | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+16773C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936430 | |||||||
| chr10:110936458 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+16801A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936458 | |||||||
| chr10:110936494 | T | A | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-235+16837T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936494 | |||||||
| chr10:110936527 | A | T | 1 | a0001c0001t0002g0209 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-235+16870A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936527 | |||||||
| chr10:110936589 | C | CTTT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-235+16945_-235+16 others(9): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTT | 6 | a0001c0001t0001g0075 a0002c0002t0001g0028 a0002c0002t0001g0117 others(3): Show |
7 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-235+16944_-235+16 others(10): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0074 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-235+16939_-235+16 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0041 a0001c0001t0002g0167 a0001c0001t0002g0177 others(3): Show |
6 | HG01943.hp1 HG02976.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+16939_-235+16 others(15): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTTTTT others(3): Show |
86 | a0001c0001t0001g0053 a0001c0001t0001g0068 a0001c0001t0001g0071 others(83): Show |
96 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.-235+16938_-235+16 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTTTTT others(4): Show |
150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(147): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-235+16937_-235+16 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTTTTT others(5): Show |
22 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0060 others(19): Show |
23 | HG00558.hp2 HG00738.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-235+16936_-235+16 others(18): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-235+16935_-235+16 others(19): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+16947_-235+16 others(22): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936589 | CT | C | 36 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(33): Show |
38 | HG00438.hp2 HG00621.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-235+16947delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | ||||||
| chr10:110936604 | T | TTTTTTTT others(3): Show |
1 | a0001c0001t0001g0030 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-235+16947_-235+16 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936604 | |||||||
| chr10:110936604 | T | TTTTTTTT others(4): Show |
5 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
6 | HG00544.hp1 HG00597.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.-235+16947_-235+16 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936604 | |||||||
| chr10:110936611 | C | T | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+16954C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936611 | |||||||
| chr10:110936876 | C | G | 1 | a0001c0001t0002g0233 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-235+17219C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936876 | |||||||
| chr10:110936885 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-235+17228G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936885 | |||||||
| chr10:110936954 | G | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-235+17297G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936954 | |||||||
| chr10:110936966 | G | A | 1 | a0001c0003t0001g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-235+17309G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936966 | |||||||
| chr10:110936983 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+17326A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936983 | |||||||
| chr10:110937030 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-235+17373T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937030 | |||||||
| chr10:110937036 | A | C | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+17379A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937036 | |||||||
| chr10:110937123 | G | A | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+17466G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937123 | |||||||
| chr10:110937259 | CT | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
6 | NA18949.hp2 NA18973.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+17615delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110937259 | ||||||
| chr10:110937279 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+17622A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937279 | |||||||
| chr10:110937483 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(285): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-235+17826C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937483 | |||||||
| chr10:110937556 | C | T | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-235+17899C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937556 | |||||||
| chr10:110937751 | G | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(324): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-235+18094G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937751 | |||||||
| chr10:110937998 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-235+18341C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937998 | |||||||
| chr10:110938298 | T | A | 1 | a0001c0001t0010g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-235+18641T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938298 | |||||||
| chr10:110938396 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-235+18739T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938396 | |||||||
| chr10:110938604 | A | C | 1 | a0001c0001t0007g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-235+18947A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938604 | |||||||
| chr10:110938824 | A | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-235+19167A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938824 | |||||||
| chr10:110938881 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+19224C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938881 | |||||||
| chr10:110939097 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-235+19440C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939097 | |||||||
| chr10:110939104 | T | C | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-235+19447T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939104 | |||||||
| chr10:110939216 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-235+19559A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939216 | |||||||
| chr10:110939570 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0262 |
2 | HG00639.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-235+19913G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939570 | |||||||
| chr10:110939597 | G | A | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02027.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-235+19940G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939597 | |||||||
| chr10:110939609 | C | T | 2 | a0001c0001t0003g0344 a0001c0001t0014g0163 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-235+19952C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939609 | |||||||
| chr10:110939636 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(284): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-235+19979A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939636 | |||||||
| chr10:110939638 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-235+19981C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939638 | |||||||
| chr10:110939661 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-235+20004A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939661 | |||||||
| chr10:110939827 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-235+20170A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939827 | |||||||
| chr10:110940152 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-235+20495A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940152 | |||||||
| chr10:110940221 | T | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(324): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-235+20564T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940221 | |||||||
| chr10:110940262 | T | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+20605T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940262 | |||||||
| chr10:110940289 | C | A | 1 | a0001c0001t0001g0323 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-235+20632C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940289 | |||||||
| chr10:110940349 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-235+20692C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940349 | |||||||
| chr10:110940403 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+20746G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940403 | |||||||
| chr10:110940538 | C | G | 1 | a0001c0001t0002g0207 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-235+20881C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940538 | |||||||
| chr10:110940539 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-235+20882A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940539 | |||||||
| chr10:110940910 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | NA18980.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-235+21282_-235+21 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-235+21281_-235+21 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-235+21276_-235+21 others(22): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | G | GTTTTTTT others(15): Show |
1 | a0001c0001t0001g0343 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-235+21270_-235+21 others(28): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0162 others(3): Show |
6 | HG02258.hp1 HG02683.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+21281_-235+21 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(5): Show |
G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(15): Show |
20 | HG01081.hp1 HG01175.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-235+21280_-235+21 others(18): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(6): Show |
G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0225 a0001c0001t0003g0226 others(1): Show |
4 | HG03139.hp1 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+21279_-235+21 others(19): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0003g0335 a0001c0001t0021g0121 |
2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-235+21278_-235+21 others(20): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(8): Show |
G | 9 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(6): Show |
10 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-235+21277_-235+21 others(21): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+21276_-235+21 others(22): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(10): Show |
G | 8 | a0001c0001t0002g0022 a0001c0001t0002g0165 a0001c0001t0002g0203 others(5): Show |
9 | HG00597.hp2 HG02300.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+21275_-235+21 others(23): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(11): Show |
G | 77 | a0001c0001t0001g0039 a0001c0001t0001g0069 a0001c0001t0001g0091 others(74): Show |
86 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+21274_-235+21 others(24): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(12): Show |
G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(195): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-235+21273_-235+21 others(25): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0001g0285 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-235+21272_-235+21 others(26): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940910 | GTTTTTTT others(15): Show |
G | 1 | a0001c0001t0001g0309 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-235+21270_-235+21 others(28): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | ||||||
| chr10:110940919 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+21262T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940919 | |||||||
| chr10:110940922 | T | G | 6 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0162 others(3): Show |
6 | HG02258.hp1 HG02683.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+21265T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940922 | |||||||
| chr10:110940923 | T | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(15): Show |
20 | HG01081.hp1 HG01175.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-235+21266T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940923 | |||||||
| chr10:110940924 | T | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0225 a0001c0001t0003g0226 others(1): Show |
4 | HG03139.hp1 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+21267T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940924 | |||||||
| chr10:110940925 | T | G | 2 | a0001c0001t0003g0335 a0001c0001t0021g0121 |
2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-235+21268T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940925 | |||||||
| chr10:110940926 | T | G | 9 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(6): Show |
10 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-235+21269T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940926 | |||||||
| chr10:110940927 | T | G | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+21270T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940927 | |||||||
| chr10:110940928 | T | G | 8 | a0001c0001t0002g0022 a0001c0001t0002g0165 a0001c0001t0002g0203 others(5): Show |
9 | HG00597.hp2 HG02300.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+21271T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940928 | |||||||
| chr10:110940929 | T | G | 77 | a0001c0001t0001g0039 a0001c0001t0001g0069 a0001c0001t0001g0091 others(74): Show |
86 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+21272T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940929 | |||||||
| chr10:110940930 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(195): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-235+21273T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940930 | |||||||
| chr10:110940931 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-235+21274T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940931 | |||||||
| chr10:110940934 | T | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+21277T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940934 | |||||||
| chr10:110940937 | T | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+21280T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940937 | |||||||
| chr10:110940947 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-235+21290T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940947 | |||||||
| chr10:110941072 | C | A | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+21415C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941072 | |||||||
| chr10:110941122 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-235+21465A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941122 | |||||||
| chr10:110941129 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-235+21472C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941129 | |||||||
| chr10:110941190 | T | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+21533T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941190 | |||||||
| chr10:110941262 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-235+21605A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941262 | |||||||
| chr10:110941417 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-235+21760C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941417 | |||||||
| chr10:110941472 | C | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0139 |
3 | HG02809.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-235+21815C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941472 | |||||||
| chr10:110941488 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+21831T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941488 | |||||||
| chr10:110941552 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0001g0067 others(7): Show |
11 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-235+21895G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941552 | |||||||
| chr10:110941556 | TC | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+21901delC | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110941556 | ||||||
| chr10:110941596 | T | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+21939T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941596 | |||||||
| chr10:110941608 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-235+21951C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941608 | |||||||
| chr10:110941751 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+22094G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941751 | |||||||
| chr10:110941824 | T | G | 13 | a0001c0001t0001g0225 a0001c0001t0003g0027 a0001c0001t0003g0226 others(10): Show |
14 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+22167T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941824 | |||||||
| chr10:110941951 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-234-22174A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941951 | |||||||
| chr10:110942086 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-22039G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942086 | |||||||
| chr10:110942124 | T | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-22001T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942124 | |||||||
| chr10:110942131 | T | TCTGGAAA others(3): Show |
288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(285): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-234-21990_-234-21 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110942131 | ||||||
| chr10:110942615 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-21510T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942615 | |||||||
| chr10:110942670 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-234-21455G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942670 | |||||||
| chr10:110942680 | A | G | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-21445A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942680 | |||||||
| chr10:110942689 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-234-21436T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942689 | |||||||
| chr10:110942818 | T | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-234-21307T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942818 | |||||||
| chr10:110943066 | C | T | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-234-21059C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943066 | |||||||
| chr10:110943179 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-234-20946G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943179 | |||||||
| chr10:110943197 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-234-20928A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943197 | |||||||
| chr10:110943230 | C | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-20895C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943230 | |||||||
| chr10:110943240 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-234-20885G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943240 | |||||||
| chr10:110943257 | CT | C | 12 | a0001c0001t0001g0225 a0001c0001t0003g0027 a0001c0001t0003g0226 others(9): Show |
13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-234-20855delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110943257 | ||||||
| chr10:110943687 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-234-20438G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943687 | |||||||
| chr10:110943785 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-234-20340C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943785 | |||||||
| chr10:110943807 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-234-20318G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943807 | |||||||
| chr10:110943903 | C | A | 1 | a0001c0001t0002g0019 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-234-20222C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943903 | |||||||
| chr10:110943981 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-234-20144C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943981 | |||||||
| chr10:110944120 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-20005T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944120 | |||||||
| chr10:110944173 | C | T | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-234-19952C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944173 | |||||||
| chr10:110944293 | T | A | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-234-19832T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944293 | |||||||
| chr10:110944384 | C | CA | 316 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(313): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-234-19725dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110944384 | ||||||
| chr10:110944384 | C | CAA | 6 | a0001c0001t0001g0094 a0001c0001t0001g0125 a0001c0001t0001g0130 others(3): Show |
6 | HG02055.hp2 HG04199.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-234-19726_-234-19 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110944384 | ||||||
| chr10:110944420 | A | G | 5 | a0001c0001t0002g0019 a0001c0001t0002g0118 a0001c0001t0002g0201 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-234-19705A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944420 | |||||||
| chr10:110944576 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-19549G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944576 | |||||||
| chr10:110944622 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(282): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.-234-19503T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944622 | |||||||
| chr10:110944982 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
105 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-234-19143G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944982 | |||||||
| chr10:110945147 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
46 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-234-18978T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945147 | |||||||
| chr10:110945203 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-18922C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945203 | |||||||
| chr10:110945204 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0341 |
3 | HG01884.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-234-18921G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945204 | |||||||
| chr10:110945238 | T | C | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-18887T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945238 | |||||||
| chr10:110945263 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-234-18862T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945263 | |||||||
| chr10:110945353 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-18772A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945353 | |||||||
| chr10:110945430 | A | C | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-18695A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945430 | |||||||
| chr10:110945605 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-234-18520T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945605 | |||||||
| chr10:110945606 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-234-18519C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945606 | |||||||
| chr10:110945624 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-234-18501T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945624 | |||||||
| chr10:110945913 | T | TG | 3 | a0001c0001t0001g0054 a0001c0001t0001g0072 a0001c0001t0001g0090 |
3 | NA18939.hp2 NA18956.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-234-18211dupG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110945913 | ||||||
| chr10:110945940 | C | T | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-18185C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945940 | |||||||
| chr10:110946056 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-234-18069T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946056 | |||||||
| chr10:110946128 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-17997A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946128 | |||||||
| chr10:110946265 | T | A | 1 | a0001c0001t0002g0235 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-234-17860T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946265 | |||||||
| chr10:110946291 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-234-17834T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946291 | |||||||
| chr10:110946306 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-234-17819A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946306 | |||||||
| chr10:110946470 | A | C | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-234-17655A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946470 | |||||||
| chr10:110946730 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-234-17395T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946730 | |||||||
| chr10:110946741 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-234-17384G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946741 | |||||||
| chr10:110946789 | G | A | 19 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0322 others(16): Show |
20 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-234-17336G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946789 | |||||||
| chr10:110946816 | T | A | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-17309T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946816 | |||||||
| chr10:110946821 | T | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-17304T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946821 | |||||||
| chr10:110946855 | G | A | 12 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(9): Show |
13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-234-17270G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946855 | |||||||
| chr10:110947024 | C | T | 1 | a0001c0004t0012g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-234-17101C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947024 | |||||||
| chr10:110947345 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(282): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-234-16780G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947345 | |||||||
| chr10:110947388 | G | A | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-234-16737G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947388 | |||||||
| chr10:110947655 | A | T | 1 | a0001c0001t0002g0178 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-234-16470A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947655 | |||||||
| chr10:110947712 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-234-16413G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947712 | |||||||
| chr10:110947726 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-234-16399C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947726 | |||||||
| chr10:110947766 | C | CA | 60 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
67 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-234-16343dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110947766 | ||||||
| chr10:110947766 | C | CAA | 7 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0109 others(4): Show |
7 | HG00099.hp1 HG03139.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-234-16344_-234-16 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110947766 | ||||||
| chr10:110947766 | CA | C | 14 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-234-16343delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110947766 | ||||||
| chr10:110947814 | T | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-16311T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947814 | |||||||
| chr10:110947827 | G | A | 1 | a0001c0001t0002g0183 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-234-16298G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947827 | |||||||
| chr10:110947834 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-234-16291C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947834 | |||||||
| chr10:110947949 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(284): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-234-16176C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947949 | |||||||
| chr10:110947956 | T | A | 1 | a0001c0001t0010g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-234-16169T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947956 | |||||||
| chr10:110947964 | T | A | 3 | a0001c0001t0001g0225 a0001c0001t0003g0226 a0001c0001t0021g0121 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-234-16161T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947964 | |||||||
| chr10:110948322 | A | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-15803A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948322 | |||||||
| chr10:110948527 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-15598C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948527 | |||||||
| chr10:110948653 | G | A | 1 | a0001c0001t0013g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-234-15472G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948653 | |||||||
| chr10:110948840 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-234-15285A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948840 | |||||||
| chr10:110948842 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0129 a0001c0001t0001g0131 |
4 | HG02145.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-234-15283C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948842 | |||||||
| chr10:110949016 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-234-15109T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949016 | |||||||
| chr10:110949128 | G | C | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-14997G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949128 | |||||||
| chr10:110949157 | G | A | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-14968G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949157 | |||||||
| chr10:110949189 | G | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-14936G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949189 | |||||||
| chr10:110949232 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-234-14893A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949232 | |||||||
| chr10:110949326 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-14799C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949326 | |||||||
| chr10:110949664 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-14461G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949664 | |||||||
| chr10:110949669 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-234-14456C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949669 | |||||||
| chr10:110949744 | G | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-234-14381G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949744 | |||||||
| chr10:110949905 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-234-14220A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949905 | |||||||
| chr10:110949958 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-14167A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949958 | |||||||
| chr10:110950027 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-14098A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950027 | |||||||
| chr10:110950110 | G | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-14015G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950110 | |||||||
| chr10:110950127 | A | G | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-234-13998A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950127 | |||||||
| chr10:110950286 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-234-13839A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950286 | |||||||
| chr10:110950367 | A | G | 1 | a0001c0001t0006g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-234-13758A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950367 | |||||||
| chr10:110950448 | C | G | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-234-13677C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950448 | |||||||
| chr10:110950624 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-234-13501A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950624 | |||||||
| chr10:110950684 | C | T | 18 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0322 others(15): Show |
19 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-234-13441C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950684 | |||||||
| chr10:110951040 | A | G | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-13085A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951040 | |||||||
| chr10:110951080 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-13045G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951080 | |||||||
| chr10:110951164 | T | C | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-12961T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951164 | |||||||
| chr10:110951283 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0322 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-234-12842C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951283 | |||||||
| chr10:110951287 | A | G | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-234-12838A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951287 | |||||||
| chr10:110951306 | C | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-234-12819C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951306 | |||||||
| chr10:110951376 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-234-12749C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951376 | |||||||
| chr10:110951389 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-234-12736G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951389 | |||||||
| chr10:110951448 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-234-12677C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951448 | |||||||
| chr10:110951488 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-12637A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951488 | |||||||
| chr10:110951502 | T | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0281 a0001c0001t0017g0023 |
3 | HG01884.hp2 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-234-12623T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951502 | |||||||
| chr10:110951769 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0330 a0001c0001t0001g0331 |
4 | HG02027.hp1 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-234-12356G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951769 | |||||||
| chr10:110951772 | C | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-12353C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951772 | |||||||
| chr10:110951967 | C | T | 10 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0167 others(7): Show |
14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-234-12158C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951967 | |||||||
| chr10:110952071 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-234-12054G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952071 | |||||||
| chr10:110952113 | AT | A | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-234-12006delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110952113 | ||||||
| chr10:110952114 | T | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-12011T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952114 | |||||||
| chr10:110952159 | A | G | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-234-11966A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952159 | |||||||
| chr10:110952167 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-11958A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952167 | |||||||
| chr10:110952218 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-234-11907A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952218 | |||||||
| chr10:110952290 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-11835G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952290 | |||||||
| chr10:110952368 | T | C | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-11757T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952368 | |||||||
| chr10:110952410 | A | G | 1 | a0001c0001t0002g0018 | 2 | NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-234-11715A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952410 | |||||||
| chr10:110952613 | G | T | 17 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0306 others(14): Show |
18 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.-234-11512G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952613 | |||||||
| chr10:110952711 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.-234-11414C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952711 | |||||||
| chr10:110952719 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.-234-11406C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952719 | |||||||
| chr10:110952783 | A | G | 1 | a0001c0001t0002g0221 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-234-11342A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952783 | |||||||
| chr10:110952791 | T | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0281 a0001c0001t0017g0023 |
3 | HG01884.hp2 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-234-11334T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952791 | |||||||
| chr10:110952794 | T | C | 1 | a0001c0001t0002g0183 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-234-11331T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952794 | |||||||
| chr10:110952845 | A | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-11280A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952845 | |||||||
| chr10:110953065 | C | A | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-11060C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953065 | |||||||
| chr10:110953124 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-234-11001T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953124 | |||||||
| chr10:110953142 | A | G | 1 | a0001c0001t0003g0334 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-234-10983A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953142 | |||||||
| chr10:110953193 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-234-10932C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953193 | |||||||
| chr10:110953231 | GT | G | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-234-10891delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110953231 | ||||||
| chr10:110953243 | T | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
14 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-234-10882T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953243 | |||||||
| chr10:110953385 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-10740C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953385 | |||||||
| chr10:110953470 | T | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-10655T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953470 | |||||||
| chr10:110953537 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-234-10588A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953537 | |||||||
| chr10:110953559 | A | T | 10 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0166 others(7): Show |
12 | HG02015.hp1 HG02074.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-234-10566A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953559 | |||||||
| chr10:110953703 | G | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-10422G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953703 | |||||||
| chr10:110953713 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-234-10412T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953713 | |||||||
| chr10:110953730 | G | GTA | 3 | a0001c0001t0001g0115 a0001c0001t0002g0184 a0001c0001t0002g0199 |
3 | HG03831.hp2 NA18964.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-234-10379_-234-10 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110953730 | ||||||
| chr10:110953730 | GTA | G | 4 | a0001c0001t0003g0344 a0001c0001t0005g0123 a0001c0001t0005g0124 others(1): Show |
4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-234-10379_-234-10 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110953730 | ||||||
| chr10:110953732 | A | G | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-234-10393A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953732 | |||||||
| chr10:110953853 | T | G | 1 | a0001c0001t0006g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-234-10272T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953853 | |||||||
| chr10:110954057 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-234-10068G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954057 | |||||||
| chr10:110954156 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-234-9969A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954156 | |||||||
| chr10:110954400 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-234-9725G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954400 | |||||||
| chr10:110954420 | A | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-9705A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954420 | |||||||
| chr10:110954529 | T | TAATC | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(287): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-234-9594_-234-959 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110954529 | ||||||
| chr10:110954593 | G | T | 5 | a0001c0001t0002g0019 a0001c0001t0002g0118 a0001c0001t0002g0201 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-234-9532G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954593 | |||||||
| chr10:110954611 | G | A | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-234-9514G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954611 | |||||||
| chr10:110954720 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-234-9405A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954720 | |||||||
| chr10:110954739 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-9386G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954739 | |||||||
| chr10:110954813 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(324): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-234-9312A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954813 | |||||||
| chr10:110954934 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-234-9191A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954934 | |||||||
| chr10:110954939 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-234-9186G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954939 | |||||||
| chr10:110954957 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-9168G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954957 | |||||||
| chr10:110955175 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-234-8950G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955175 | |||||||
| chr10:110955242 | C | T | 2 | a0001c0001t0002g0168 a0001c0001t0002g0172 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-234-8883C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955242 | |||||||
| chr10:110955262 | G | C | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-8863G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955262 | |||||||
| chr10:110955284 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-8841A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955284 | |||||||
| chr10:110955290 | A | G | 1 | a0001c0001t0002g0165 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-234-8835A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955290 | |||||||
| chr10:110955293 | A | G | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-234-8832A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955293 | |||||||
| chr10:110955367 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-8758C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955367 | |||||||
| chr10:110955380 | C | A | 1 | a0001c0001t0003g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-234-8745C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955380 | |||||||
| chr10:110955601 | G | A | 17 | a0001c0001t0001g0225 a0001c0001t0003g0027 a0001c0001t0003g0226 others(14): Show |
18 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-234-8524G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955601 | |||||||
| chr10:110955732 | C | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-8393C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955732 | |||||||
| chr10:110955777 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-234-8348G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955777 | |||||||
| chr10:110955863 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0068 others(9): Show |
13 | HG00558.hp2 NA18939.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.-234-8262C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955863 | |||||||
| chr10:110955866 | T | G | 1 | a0002c0002t0001g0345 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-234-8259T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955866 | |||||||
| chr10:110955949 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-234-8176T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955949 | |||||||
| chr10:110956192 | CT | C | 77 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(74): Show |
87 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-234-7922delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110956192 | ||||||
| chr10:110956209 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-234-7916G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956209 | |||||||
| chr10:110956307 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-7818G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956307 | |||||||
| chr10:110956390 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-234-7735T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956390 | |||||||
| chr10:110956484 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-7641A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956484 | |||||||
| chr10:110956518 | T | A | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-7607T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956518 | |||||||
| chr10:110956639 | T | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-234-7486T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956639 | |||||||
| chr10:110956755 | T | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-7370T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956755 | |||||||
| chr10:110956897 | T | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(282): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-234-7228T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956897 | |||||||
| chr10:110956898 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-234-7227G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956898 | |||||||
| chr10:110956913 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-7212A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956913 | |||||||
| chr10:110957042 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-234-7083T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957042 | |||||||
| chr10:110957101 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0139 |
3 | HG02809.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-234-7024A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957101 | |||||||
| chr10:110957113 | A | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-7012A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957113 | |||||||
| chr10:110957201 | G | A | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-6924G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957201 | |||||||
| chr10:110957239 | G | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-234-6886G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957239 | |||||||
| chr10:110957416 | C | T | 15 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0306 others(12): Show |
16 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-234-6709C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957416 | |||||||
| chr10:110957462 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-6663G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957462 | |||||||
| chr10:110957532 | A | AC | 109 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0063 others(106): Show |
121 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.-234-6583dupC | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110957532 | ||||||
| chr10:110957536 | C | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0279 |
2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-234-6589C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957536 | |||||||
| chr10:110957537 | C | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
15 | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.-234-6588C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957537 | |||||||
| chr10:110957771 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-234-6354C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957771 | |||||||
| chr10:110958088 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
46 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-234-6037A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958088 | |||||||
| chr10:110958141 | C | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-234-5984C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958141 | |||||||
| chr10:110958220 | C | CT | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-234-5892dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110958220 | ||||||
| chr10:110958365 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-234-5760C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958365 | |||||||
| chr10:110958381 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-5744T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958381 | |||||||
| chr10:110958458 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(287): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-234-5667T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958458 | |||||||
| chr10:110959057 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.-234-5068T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959057 | |||||||
| chr10:110959099 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-234-5026T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959099 | |||||||
| chr10:110959157 | T | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-234-4968T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959157 | |||||||
| chr10:110959541 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-234-4584C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959541 | |||||||
| chr10:110959554 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(285): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-234-4571A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959554 | |||||||
| chr10:110959568 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-234-4557C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959568 | |||||||
| chr10:110959585 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-234-4540G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959585 | |||||||
| chr10:110959672 | A | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-4453A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959672 | |||||||
| chr10:110959813 | T | G | 1 | a0001c0001t0001g0292 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-234-4312T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959813 | |||||||
| chr10:110959973 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-234-4152A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959973 | |||||||
| chr10:110960152 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-234-3973A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960152 | |||||||
| chr10:110960219 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-3906T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960219 | |||||||
| chr10:110960350 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-234-3775G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960350 | |||||||
| chr10:110960352 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-234-3773C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960352 | |||||||
| chr10:110960394 | G | A | 16 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(13): Show |
16 | HG01175.hp2 HG01978.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-234-3731G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960394 | |||||||
| chr10:110960609 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-234-3516A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960609 | |||||||
| chr10:110960726 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-3399A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960726 | |||||||
| chr10:110960969 | G | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-3156G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960969 | |||||||
| chr10:110961242 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(285): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-234-2883A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961242 | |||||||
| chr10:110961258 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-2867C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961258 | |||||||
| chr10:110961296 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-2829A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961296 | |||||||
| chr10:110961398 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-234-2727T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961398 | |||||||
| chr10:110961493 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-234-2632T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961493 | |||||||
| chr10:110961650 | G | T | 14 | a0001c0001t0001g0225 a0001c0001t0003g0027 a0001c0001t0003g0226 others(11): Show |
15 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-234-2475G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961650 | |||||||
| chr10:110961954 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-2171G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961954 | |||||||
| chr10:110962048 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0322 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-234-2077T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962048 | |||||||
| chr10:110962114 | A | G | 13 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(10): Show |
13 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-234-2011A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962114 | |||||||
| chr10:110962254 | G | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-1871G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962254 | |||||||
| chr10:110962682 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-234-1443C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962682 | |||||||
| chr10:110962828 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-234-1297C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962828 | |||||||
| chr10:110962830 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-1295A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962830 | |||||||
| chr10:110963095 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-234-1030G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963095 | |||||||
| chr10:110963147 | T | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-978T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963147 | |||||||
| chr10:110963195 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-930C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963195 | |||||||
| chr10:110963266 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-859C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963266 | |||||||
| chr10:110963473 | C | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-652C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963473 | |||||||
| chr10:110963529 | C | G | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-234-596C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963529 | |||||||
| chr10:110963531 | C | A | 1 | a0001c0001t0002g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-234-594C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963531 | |||||||
| chr10:110963564 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-561T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963564 | |||||||
| chr10:110963752 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-234-373A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963752 | |||||||
| chr10:110963858 | G | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-267G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963858 | |||||||
| chr10:110965141 | C | A | 1 | a0001c0001t0001g0266 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.703+80C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965141 | |||||||
| chr10:110965160 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.703+99C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965160 | |||||||
| chr10:110965380 | G | GT | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.703+322dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110965380 | ||||||
| chr10:110965501 | C | T | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+440C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965501 | |||||||
| chr10:110965521 | G | C | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703+460G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965521 | |||||||
| chr10:110965530 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.703+469A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965530 | |||||||
| chr10:110965536 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.703+475G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965536 | |||||||
| chr10:110965562 | A | T | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.703+501A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965562 | |||||||
| chr10:110965563 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.703+502T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965563 | |||||||
| chr10:110965773 | C | T | 1 | a0001c0001t0001g0011 | 2 | NA18998.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.703+712C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965773 | |||||||
| chr10:110965778 | G | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+717G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965778 | |||||||
| chr10:110966101 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
46 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.703+1040G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966101 | |||||||
| chr10:110966317 | A | T | 1 | a0001c0001t0001g0331 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.703+1256A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966317 | |||||||
| chr10:110966384 | TA | T | 3 | a0001c0001t0001g0197 a0001c0001t0002g0196 a0001c0001t0002g0198 |
3 | HG02602.hp2 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.703+1324delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966384 | |||||||
| chr10:110966513 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0349 |
2 | NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.703+1452T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966513 | |||||||
| chr10:110966583 | T | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+1522T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966583 | |||||||
| chr10:110966623 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.703+1562A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966623 | |||||||
| chr10:110966694 | A | G | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+1633A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966694 | |||||||
| chr10:110966734 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.703+1673T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966734 | |||||||
| chr10:110966941 | A | T | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703+1880A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966941 | |||||||
| chr10:110967169 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.703+2108A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967169 | |||||||
| chr10:110967213 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.703+2152C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967213 | |||||||
| chr10:110967466 | T | C | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+2405T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967466 | |||||||
| chr10:110967576 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.703+2515T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967576 | |||||||
| chr10:110967643 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.703+2582C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967643 | |||||||
| chr10:110967663 | A | G | 1 | a0001c0001t0002g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+2602A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967663 | |||||||
| chr10:110968068 | T | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.703+3007T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968068 | |||||||
| chr10:110968196 | T | G | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.703+3135T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968196 | |||||||
| chr10:110968352 | A | G | 2 | a0001c0001t0002g0168 a0001c0001t0002g0172 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.703+3291A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968352 | |||||||
| chr10:110968549 | A | C | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.703+3488A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968549 | |||||||
| chr10:110968550 | TTTATA | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0096 others(1): Show |
5 | HG00408.hp2 HG02040.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3498_703+3502d others(7): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110968550 | ||||||
| chr10:110968585 | A | G | 1 | a0001c0001t0019g0238 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.703+3524A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968585 | |||||||
| chr10:110968646 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.703+3585A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968646 | |||||||
| chr10:110968650 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+3589G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968650 | |||||||
| chr10:110968740 | G | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0065 others(10): Show |
14 | HG00558.hp2 NA18939.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.703+3679G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968740 | |||||||
| chr10:110968828 | T | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.703+3767T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968828 | |||||||
| chr10:110968840 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.703+3779G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968840 | |||||||
| chr10:110968920 | A | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+3859A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968920 | |||||||
| chr10:110969306 | A | G | 2 | a0001c0001t0003g0344 a0001c0001t0014g0163 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703+4245A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969306 | |||||||
| chr10:110969357 | C | T | 13 | a0001c0001t0001g0225 a0001c0001t0003g0027 a0001c0001t0003g0226 others(10): Show |
14 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+4296C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969357 | |||||||
| chr10:110969540 | C | T | 2 | a0001c0001t0003g0344 a0001c0001t0014g0163 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703+4479C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969540 | |||||||
| chr10:110969541 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.703+4480G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969541 | |||||||
| chr10:110969549 | T | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0102 a0001c0001t0001g0105 |
3 | NA18971.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.703+4488T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969549 | |||||||
| chr10:110969617 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.703+4556G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969617 | |||||||
| chr10:110969890 | TATGAGAA others(6): Show |
T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+4845_703+4857d others(15): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110969890 | ||||||
| chr10:110970001 | C | T | 1 | a0001c0001t0020g0153 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.703+4940C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970001 | |||||||
| chr10:110970149 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.703+5088A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970149 | |||||||
| chr10:110970238 | C | A | 1 | a0001c0001t0002g0207 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703+5177C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970238 | |||||||
| chr10:110970288 | A | G | 1 | a0001c0001t0002g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.703+5227A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970288 | |||||||
| chr10:110970505 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+5444G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970505 | |||||||
| chr10:110970639 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.703+5578A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970639 | |||||||
| chr10:110970667 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.703+5606G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970667 | |||||||
| chr10:110970706 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+5645T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970706 | |||||||
| chr10:110970729 | GT | G | 300 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.703+5683delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110970729 | ||||||
| chr10:110970729 | GTT | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0086 a0001c0001t0001g0114 others(5): Show |
8 | HG02145.hp1 HG02965.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+5682_703+5683d others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110970729 | ||||||
| chr10:110970729 | GTTT | G | 15 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0306 others(12): Show |
16 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+5681_703+5683d others(5): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110970729 | ||||||
| chr10:110970734 | T | G | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.703+5673T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970734 | |||||||
| chr10:110970744 | T | G | 1 | a0001c0001t0001g0303 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.703+5683T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970744 | |||||||
| chr10:110970844 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.703+5783G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970844 | |||||||
| chr10:110970920 | T | A | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.703+5859T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970920 | |||||||
| chr10:110971175 | T | C | 1 | a0001c0001t0003g0336 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.703+6114T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971175 | |||||||
| chr10:110971322 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0016g0332 |
2 | HG03098.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.703+6261A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971322 | |||||||
| chr10:110971413 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0297 |
5 | HG00140.hp1 HG00642.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+6352G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971413 | |||||||
| chr10:110971428 | C | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+6367C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971428 | |||||||
| chr10:110971564 | A | ATTTTTTC others(3): Show |
1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.703+6509_703+6510i others(12): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110971564 | ||||||
| chr10:110971568 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.703+6507T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971568 | |||||||
| chr10:110971741 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.703+6680A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971741 | |||||||
| chr10:110971901 | T | C | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(339): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.703+6840T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971901 | |||||||
| chr10:110971944 | A | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0158 others(1): Show |
4 | HG03490.hp1 HG03492.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+6883A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971944 | |||||||
| chr10:110972089 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.703+7028C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972089 | |||||||
| chr10:110972217 | C | G | 25 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0053 others(22): Show |
27 | HG00099.hp1 HG01175.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.703+7156C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972217 | |||||||
| chr10:110972629 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+7568G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972629 | |||||||
| chr10:110972679 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(298): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.703+7618T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972679 | |||||||
| chr10:110972688 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.703+7627T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972688 | |||||||
| chr10:110972727 | C | T | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+7666C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972727 | |||||||
| chr10:110972764 | T | C | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+7703T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972764 | |||||||
| chr10:110973008 | C | T | 1 | a0001c0001t0006g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+7947C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973008 | |||||||
| chr10:110973010 | A | C | 1 | a0001c0001t0006g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+7949A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973010 | |||||||
| chr10:110973056 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+7995G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973056 | |||||||
| chr10:110973274 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.703+8213G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973274 | |||||||
| chr10:110973327 | G | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.703+8266G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973327 | |||||||
| chr10:110973335 | C | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.703+8274C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973335 | |||||||
| chr10:110973384 | A | G | 1 | a0001c0001t0007g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.703+8323A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973384 | |||||||
| chr10:110973402 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0096 others(1): Show |
5 | HG00408.hp2 HG02040.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+8341C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973402 | |||||||
| chr10:110973467 | A | C | 1 | a0001c0001t0002g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.703+8406A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973467 | |||||||
| chr10:110973477 | T | A | 1 | a0001c0001t0002g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.703+8416T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973477 | |||||||
| chr10:110973638 | G | A | 1 | a0001c0001t0015g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.703+8577G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973638 | |||||||
| chr10:110973673 | G | GT | 15 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0001g0070 others(12): Show |
16 | HG02071.hp1 HG02135.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+8620dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110973673 | ||||||
| chr10:110973793 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.703+8732G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973793 | |||||||
| chr10:110973865 | C | CAT | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+8816_703+8817d others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110973865 | ||||||
| chr10:110974009 | G | A | 4 | a0001c0001t0003g0344 a0001c0001t0005g0123 a0001c0001t0005g0124 others(1): Show |
4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+8948G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974009 | |||||||
| chr10:110974389 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+9328G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974389 | |||||||
| chr10:110974473 | G | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+9412G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974473 | |||||||
| chr10:110974649 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.703+9588G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974649 | |||||||
| chr10:110974699 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0330 a0001c0001t0001g0331 |
4 | HG02027.hp1 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+9638T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974699 | |||||||
| chr10:110974991 | C | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+9930C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974991 | |||||||
| chr10:110975158 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+10097C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975158 | |||||||
| chr10:110975158 | CT | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
10 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+10112delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110975158 | ||||||
| chr10:110975176 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703+10115G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975176 | |||||||
| chr10:110975280 | C | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+10219C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975280 | |||||||
| chr10:110975338 | G | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.703+10277G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975338 | |||||||
| chr10:110975414 | T | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0139 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.704-10214T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975414 | |||||||
| chr10:110975443 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.704-10185A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975443 | |||||||
| chr10:110975593 | CTTTG | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.704-10031_704-1002 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110975593 | ||||||
| chr10:110975697 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.704-9931A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975697 | |||||||
| chr10:110975879 | C | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-9749C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975879 | |||||||
| chr10:110975903 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.704-9725T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975903 | |||||||
| chr10:110975908 | T | G | 1 | a0001c0001t0011g0048 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.704-9720T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975908 | |||||||
| chr10:110975915 | C | CT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
89 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.704-9703dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110975915 | ||||||
| chr10:110976175 | G | T | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704-9453G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976175 | |||||||
| chr10:110976232 | A | G | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.704-9396A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976232 | |||||||
| chr10:110976316 | C | CT | 6 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0231 others(3): Show |
6 | HG01081.hp1 HG02572.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-9299dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110976316 | ||||||
| chr10:110976344 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.704-9284C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976344 | |||||||
| chr10:110976396 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0278 |
2 | HG01928.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.704-9232C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976396 | |||||||
| chr10:110976923 | GCT | G | 3 | a0001c0001t0001g0312 a0001c0001t0005g0123 a0001c0001t0005g0124 |
3 | HG02698.hp1 HG04199.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-8702_704-8701d others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110976923 | ||||||
| chr10:110977126 | G | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-8502G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977126 | |||||||
| chr10:110977165 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.704-8463T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977165 | |||||||
| chr10:110977171 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.704-8457T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977171 | |||||||
| chr10:110977256 | G | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-8372G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977256 | |||||||
| chr10:110977397 | C | T | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-8231C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977397 | |||||||
| chr10:110977406 | C | T | 1 | a0001c0001t0003g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704-8222C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977406 | |||||||
| chr10:110977408 | G | A | 1 | a0002c0002t0001g0347 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.704-8220G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977408 | |||||||
| chr10:110977642 | T | C | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-7986T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977642 | |||||||
| chr10:110977696 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0050 |
3 | NA18968.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.704-7932G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977696 | |||||||
| chr10:110977858 | C | T | 2 | a0001c0001t0003g0344 a0001c0001t0014g0163 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-7770C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977858 | |||||||
| chr10:110977910 | C | T | 4 | a0001c0001t0003g0344 a0001c0001t0005g0123 a0001c0001t0005g0124 others(1): Show |
4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-7718C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977910 | |||||||
| chr10:110977939 | A | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(298): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.704-7689A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977939 | |||||||
| chr10:110977972 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.704-7656G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977972 | |||||||
| chr10:110978015 | C | G | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-7613C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978015 | |||||||
| chr10:110978166 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.704-7462T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978166 | |||||||
| chr10:110978207 | C | T | 3 | a0001c0001t0002g0170 a0001c0001t0003g0027 a0001c0001t0003g0341 |
4 | HG01884.hp1 HG01891.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-7421C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978207 | |||||||
| chr10:110978212 | G | A | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-7416G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978212 | |||||||
| chr10:110978231 | T | G | 1 | a0001c0001t0002g0168 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.704-7397T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978231 | |||||||
| chr10:110978264 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.704-7364A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978264 | |||||||
| chr10:110978413 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.704-7215C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978413 | |||||||
| chr10:110978583 | C | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-7045C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978583 | |||||||
| chr10:110978593 | A | T | 6 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0097 others(3): Show |
6 | NA18951.hp2 NA18960.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-7035A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978593 | |||||||
| chr10:110978600 | G | C | 6 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0097 others(3): Show |
6 | NA18951.hp2 NA18960.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-7028G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978600 | |||||||
| chr10:110978817 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.704-6811T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978817 | |||||||
| chr10:110979053 | T | G | 2 | a0001c0001t0001g0328 a0001c0001t0018g0327 |
2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.704-6575T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979053 | |||||||
| chr10:110979210 | A | G | 1 | a0001c0001t0002g0218 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.704-6418A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979210 | |||||||
| chr10:110979309 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-6319A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979309 | |||||||
| chr10:110979377 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.704-6251T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979377 | |||||||
| chr10:110979451 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-6177G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979451 | |||||||
| chr10:110979469 | G | A | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.704-6159G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979469 | |||||||
| chr10:110979488 | A | T | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-6140A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979488 | |||||||
| chr10:110979602 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.704-6026A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979602 | |||||||
| chr10:110979610 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(300): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.704-6018T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979610 | |||||||
| chr10:110979738 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-5890G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979738 | |||||||
| chr10:110979834 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.704-5794C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979834 | |||||||
| chr10:110979840 | A | G | 1 | a0001c0001t0002g0018 | 2 | NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.704-5788A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979840 | |||||||
| chr10:110979884 | T | TTTG | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(339): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.704-5735_704-5733d others(5): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110979884 | ||||||
| chr10:110980040 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-5588A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980040 | |||||||
| chr10:110980152 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.704-5476C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980152 | |||||||
| chr10:110980158 | C | CT | 8 | a0001c0001t0001g0231 a0001c0001t0001g0319 a0001c0001t0002g0206 others(5): Show |
9 | HG00597.hp2 HG01081.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.704-5452dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110980158 | ||||||
| chr10:110980158 | CT | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
22 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-5452delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110980158 | ||||||
| chr10:110980238 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-5390G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980238 | |||||||
| chr10:110980281 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0096 others(1): Show |
5 | HG00408.hp2 HG02040.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-5347C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980281 | |||||||
| chr10:110980517 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.704-5111C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980517 | |||||||
| chr10:110980626 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704-5002A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980626 | |||||||
| chr10:110980700 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-4928A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980700 | |||||||
| chr10:110980757 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-4871C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980757 | |||||||
| chr10:110980801 | T | TC | 5 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0313 others(2): Show |
5 | HG00438.hp2 HG00621.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-4826dupC | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110980801 | ||||||
| chr10:110980998 | G | A | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-4630G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980998 | |||||||
| chr10:110981233 | C | T | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.704-4395C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981233 | |||||||
| chr10:110981234 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02683.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.704-4394G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981234 | |||||||
| chr10:110981408 | A | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
16 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.704-4220A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981408 | |||||||
| chr10:110981693 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-3935C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981693 | |||||||
| chr10:110981793 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.704-3835C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981793 | |||||||
| chr10:110981866 | A | T | 9 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0097 others(6): Show |
9 | HG02015.hp2 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-3762A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981866 | |||||||
| chr10:110981870 | A | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0225 a0001c0001t0003g0226 |
3 | HG03139.hp1 HG03225.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.704-3758A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981870 | |||||||
| chr10:110981873 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0322 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.704-3755T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981873 | |||||||
| chr10:110981874 | T | A | 204 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.704-3754T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981874 | |||||||
| chr10:110981876 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0322 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.704-3752T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981876 | |||||||
| chr10:110981876 | T | TTATTTAT others(7): Show |
34 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0164 others(31): Show |
36 | HG00597.hp2 HG00609.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.704-3750_704-3749i others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | ||||||
| chr10:110981876 | T | TTATTTAT others(11): Show |
36 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(33): Show |
44 | HG00558.hp1 HG00673.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.704-3750_704-3749i others(20): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | ||||||
| chr10:110981876 | T | TTATTTAT others(15): Show |
2 | a0001c0001t0002g0172 a0001c0001t0002g0174 |
2 | HG02109.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.704-3750_704-3749i others(24): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | ||||||
| chr10:110981876 | T | TTATTTTT others(11): Show |
18 | a0001c0001t0001g0005 a0001c0001t0001g0249 a0001c0001t0001g0250 others(15): Show |
20 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.704-3750_704-3749i others(20): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | ||||||
| chr10:110981876 | T | TTTTTTAT others(7): Show |
104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.704-3751_704-3750i others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | ||||||
| chr10:110981961 | T | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-3667T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981961 | |||||||
| chr10:110982004 | C | T | 23 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(20): Show |
25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.704-3624C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982004 | |||||||
| chr10:110982012 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.704-3616C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982012 | |||||||
| chr10:110982030 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-3598A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982030 | |||||||
| chr10:110982038 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.704-3590A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982038 | |||||||
| chr10:110982102 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.704-3526G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982102 | |||||||
| chr10:110982140 | A | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(33): Show |
40 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.704-3488A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982140 | |||||||
| chr10:110982145 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0158 others(1): Show |
4 | HG03490.hp1 HG03492.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-3483G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982145 | |||||||
| chr10:110982319 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.704-3309T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982319 | |||||||
| chr10:110982350 | T | G | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.704-3278T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982350 | |||||||
| chr10:110982376 | C | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0277 a0001c0001t0002g0217 |
3 | HG01928.hp2 HG01975.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.704-3252C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982376 | |||||||
| chr10:110982409 | T | C | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.704-3219T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982409 | |||||||
| chr10:110982545 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-3083A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982545 | |||||||
| chr10:110982658 | T | G | 2 | a0001c0001t0003g0344 a0001c0001t0014g0163 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-2970T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982658 | |||||||
| chr10:110982769 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.704-2859T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982769 | |||||||
| chr10:110982784 | A | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01175.hp2 HG01978.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.704-2844A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982784 | |||||||
| chr10:110982792 | A | G | 16 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(13): Show |
16 | HG01175.hp2 HG01978.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.704-2836A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982792 | |||||||
| chr10:110983119 | A | G | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.704-2509A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983119 | |||||||
| chr10:110983272 | A | G | 2 | a0001c0001t0003g0344 a0001c0001t0014g0163 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-2356A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983272 | |||||||
| chr10:110983379 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.704-2249T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983379 | |||||||
| chr10:110983497 | G | GT | 6 | a0001c0001t0001g0253 a0001c0001t0001g0256 a0001c0001t0001g0265 others(3): Show |
6 | HG00408.hp1 HG02735.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-2124dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110983497 | ||||||
| chr10:110983879 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-1749A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983879 | |||||||
| chr10:110984023 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.704-1605C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984023 | |||||||
| chr10:110984117 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-1511A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984117 | |||||||
| chr10:110984131 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-1497A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984131 | |||||||
| chr10:110984219 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(301): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.704-1409T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984219 | |||||||
| chr10:110984359 | G | T | 3 | a0001c0001t0002g0191 a0001c0001t0002g0203 a0001c0001t0002g0223 |
3 | NA18969.hp1 NA19006.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.704-1269G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984359 | |||||||
| chr10:110984521 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
8 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-1107A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984521 | |||||||
| chr10:110984567 | C | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0290 others(7): Show |
11 | HG02071.hp1 NA18942.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.704-1061C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984567 | |||||||
| chr10:110984654 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-974A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984654 | |||||||
| chr10:110984749 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-879A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984749 | |||||||
| chr10:110984787 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(297): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.704-841A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984787 | |||||||
| chr10:110984808 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-820G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984808 | |||||||
| chr10:110985107 | T | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0167 others(7): Show |
14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.704-521T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985107 | |||||||
| chr10:110985158 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0039 |
2 | NA18970.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.704-470T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985158 | |||||||
| chr10:110985200 | C | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.704-428C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985200 | |||||||
| chr10:110985458 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.704-170G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985458 | |||||||
| chr10:110985498 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.704-130G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985498 | |||||||
| chr10:110985549 | T | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0067 |
3 | HG02109.hp2 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.704-79T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985549 | |||||||
| chr10:110985777 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+12G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110985777 | |||||||
| chr10:110985931 | C | T | 22 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0022 others(19): Show |
26 | HG01257.hp1 HG01952.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.841+166C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110985931 | |||||||
| chr10:110986001 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.841+236A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986001 | |||||||
| chr10:110986008 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.841+243T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986008 | |||||||
| chr10:110986259 | G | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.841+494G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986259 | |||||||
| chr10:110986470 | T | C | 1 | a0001c0001t0002g0204 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.841+705T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986470 | |||||||
| chr10:110986576 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.841+811C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986576 | |||||||
| chr10:110986618 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.841+853C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986618 | |||||||
| chr10:110986619 | G | A | 6 | a0001c0001t0001g0132 a0001c0001t0001g0240 a0001c0001t0001g0263 others(3): Show |
6 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+854G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986619 | |||||||
| chr10:110986630 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.841+865C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986630 | |||||||
| chr10:110986800 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0056 a0001c0001t0001g0058 others(3): Show |
7 | NA18953.hp1 NA18961.hp2 NA19058.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+1035G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986800 | |||||||
| chr10:110986977 | A | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(219): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.841+1212A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986977 | |||||||
| chr10:110987042 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0322 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.841+1277A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987042 | |||||||
| chr10:110987052 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+1287C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987052 | |||||||
| chr10:110987121 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG03654.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.841+1356A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987121 | |||||||
| chr10:110987163 | TGCTTGTA others(12): Show |
T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.841+1405_841+1423d others(21): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110987163 | ||||||
| chr10:110987199 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+1434G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987199 | |||||||
| chr10:110987417 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.841+1652C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987417 | |||||||
| chr10:110987460 | C | G | 1 | a0001c0001t0001g0014 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.841+1695C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987460 | |||||||
| chr10:110987484 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.841+1719A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987484 | |||||||
| chr10:110987497 | T | G | 1 | a0001c0001t0001g0330 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.841+1732T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987497 | |||||||
| chr10:110987706 | A | G | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.841+1941A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987706 | |||||||
| chr10:110987752 | T | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+1987T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987752 | |||||||
| chr10:110987760 | A | T | 1 | a0001c0001t0001g0116 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.841+1995A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987760 | |||||||
| chr10:110987770 | C | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+2005C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987770 | |||||||
| chr10:110987784 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.841+2019T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987784 | |||||||
| chr10:110987793 | G | A | 4 | a0001c0001t0003g0336 a0001c0001t0003g0337 a0001c0001t0003g0338 others(1): Show |
4 | HG02451.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+2028G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987793 | |||||||
| chr10:110987864 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.841+2099C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987864 | |||||||
| chr10:110987986 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+2221G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987986 | |||||||
| chr10:110987994 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.841+2229C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987994 | |||||||
| chr10:110988070 | G | A | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.841+2305G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988070 | |||||||
| chr10:110988448 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.841+2683A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988448 | |||||||
| chr10:110988465 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0350 |
2 | NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.841+2700A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988465 | |||||||
| chr10:110988495 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.841+2730A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988495 | |||||||
| chr10:110988658 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+2893T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988658 | |||||||
| chr10:110989044 | A | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.841+3279A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989044 | |||||||
| chr10:110989171 | G | A | 7 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0303 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+3406G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989171 | |||||||
| chr10:110989351 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(299): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.841+3586T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989351 | |||||||
| chr10:110989362 | C | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+3597C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989362 | |||||||
| chr10:110989391 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.841+3626T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989391 | |||||||
| chr10:110990153 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(184): Show |
209 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.841+4388T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990153 | |||||||
| chr10:110990157 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.841+4392G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990157 | |||||||
| chr10:110990189 | T | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(317): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.841+4424T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990189 | |||||||
| chr10:110990319 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.841+4554T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990319 | |||||||
| chr10:110990364 | G | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
10 | HG00544.hp1 HG00597.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.841+4599G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990364 | |||||||
| chr10:110990385 | A | C | 9 | a0001c0001t0002g0020 a0001c0001t0002g0179 a0001c0001t0002g0186 others(6): Show |
10 | HG00558.hp1 HG02027.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.841+4620A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990385 | |||||||
| chr10:110990485 | G | C | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+4720G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990485 | |||||||
| chr10:110990493 | G | A | 1 | a0001c0003t0001g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.841+4728G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990493 | |||||||
| chr10:110990531 | T | TG | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.841+4768dupG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110990531 | ||||||
| chr10:110990555 | G | A | 1 | a0001c0001t0002g0019 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.841+4790G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990555 | |||||||
| chr10:110990732 | A | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.841+4967A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990732 | |||||||
| chr10:110990853 | C | G | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(339): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.841+5088C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990853 | |||||||
| chr10:110990871 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(184): Show |
209 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.841+5106C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990871 | |||||||
| chr10:110991046 | G | C | 1 | a0001c0001t0002g0164 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.841+5281G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991046 | |||||||
| chr10:110991210 | C | G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG01109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.841+5445C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991210 | |||||||
| chr10:110991405 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.841+5640A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991405 | |||||||
| chr10:110991531 | G | T | 2 | a0001c0001t0002g0168 a0001c0001t0002g0172 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.841+5766G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991531 | |||||||
| chr10:110991673 | G | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+5908G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991673 | |||||||
| chr10:110992260 | A | C | 1 | a0001c0001t0001g0314 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.841+6495A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992260 | |||||||
| chr10:110992276 | A | G | 1 | a0001c0001t0013g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.841+6511A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992276 | |||||||
| chr10:110992376 | A | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.841+6611A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992376 | |||||||
| chr10:110992619 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(315): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.841+6854A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992619 | |||||||
| chr10:110992628 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.841+6863G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992628 | |||||||
| chr10:110993066 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.841+7301C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993066 | |||||||
| chr10:110993367 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.842-7048G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993367 | |||||||
| chr10:110993465 | G | T | 3 | a0001c0001t0001g0304 a0001c0001t0001g0311 a0001c0001t0001g0312 |
3 | HG02965.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.842-6950G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993465 | |||||||
| chr10:110993529 | A | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-6886A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993529 | |||||||
| chr10:110993777 | T | C | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.842-6638T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993777 | |||||||
| chr10:110993887 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.842-6528G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993887 | |||||||
| chr10:110993963 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(316): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.842-6452C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993963 | |||||||
| chr10:110994265 | A | T | 7 | a0001c0001t0001g0253 a0001c0001t0001g0256 a0001c0001t0001g0265 others(4): Show |
7 | HG00408.hp1 HG02735.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.842-6150A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994265 | |||||||
| chr10:110994721 | T | C | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(339): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.842-5694T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994721 | |||||||
| chr10:110994925 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.842-5490T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994925 | |||||||
| chr10:110994989 | A | G | 1 | a0001c0001t0001g0314 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.842-5426A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994989 | |||||||
| chr10:110995015 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.842-5400A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995015 | |||||||
| chr10:110995031 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.842-5384A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995031 | |||||||
| chr10:110995052 | GAAAA | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0341 |
3 | HG01884.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.842-5362_842-5359d others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995052 | |||||||
| chr10:110995137 | T | A | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-5278T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995137 | |||||||
| chr10:110995140 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.842-5275T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995140 | |||||||
| chr10:110995141 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.842-5274G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995141 | |||||||
| chr10:110995416 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.842-4999A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995416 | |||||||
| chr10:110995501 | A | T | 18 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0322 others(15): Show |
19 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.842-4914A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995501 | |||||||
| chr10:110995538 | A | C | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-4877A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995538 | |||||||
| chr10:110995845 | C | T | 22 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0148 others(19): Show |
24 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.842-4570C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995845 | |||||||
| chr10:110995971 | C | T | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.842-4444C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995971 | |||||||
| chr10:110996123 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.842-4292G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996123 | |||||||
| chr10:110996333 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.842-4082G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996333 | |||||||
| chr10:110996368 | A | G | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.842-4047A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996368 | |||||||
| chr10:110996410 | C | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0275 |
2 | HG02257.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.842-4005C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996410 | |||||||
| chr10:110996452 | A | G | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(339): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.842-3963A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996452 | |||||||
| chr10:110996828 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.842-3587C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996828 | |||||||
| chr10:110996889 | A | T | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.842-3526A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996889 | |||||||
| chr10:110997427 | A | G | 5 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.842-2988A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997427 | |||||||
| chr10:110997528 | CT | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(150): Show |
173 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.842-2882delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110997528 | ||||||
| chr10:110997532 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
230 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.842-2883T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997532 | |||||||
| chr10:110997533 | T | C | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(339): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.842-2882T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997533 | |||||||
| chr10:110997539 | C | G | 3 | a0001c0001t0005g0123 a0001c0001t0005g0124 a0001c0001t0011g0048 |
3 | HG02698.hp1 HG04199.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.842-2876C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997539 | |||||||
| chr10:110997604 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.842-2811G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997604 | |||||||
| chr10:110997624 | T | A | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-2791T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997624 | |||||||
| chr10:110997658 | C | A | 10 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0166 others(7): Show |
12 | HG02015.hp1 HG02074.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.842-2757C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997658 | |||||||
| chr10:110997951 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.842-2464A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997951 | |||||||
| chr10:110997998 | CT | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(177): Show |
202 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.842-2402delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110997998 | ||||||
| chr10:110998196 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.842-2219A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998196 | |||||||
| chr10:110998218 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(180): Show |
205 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.842-2197C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998218 | |||||||
| chr10:110998251 | G | C | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-2164G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998251 | |||||||
| chr10:110998365 | T | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
85 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.842-2050T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998365 | |||||||
| chr10:110998380 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.842-2035T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998380 | |||||||
| chr10:110998386 | T | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-2029T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998386 | |||||||
| chr10:110998398 | G | C | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.842-2017G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998398 | |||||||
| chr10:110998416 | C | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.842-1999C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998416 | |||||||
| chr10:110998439 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.842-1976G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998439 | |||||||
| chr10:110998485 | T | G | 2 | a0001c0001t0002g0018 a0001c0001t0002g0301 |
3 | NA18952.hp2 NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.842-1930T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998485 | |||||||
| chr10:110998683 | AAGTGGTG others(2): Show |
A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.842-1731_842-1723d others(11): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998683 | |||||||
| chr10:110998724 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.842-1691T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998724 | |||||||
| chr10:110998951 | T | G | 2 | a0001c0001t0001g0197 a0001c0001t0002g0196 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.842-1464T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998951 | |||||||
| chr10:110999038 | G | A | 4 | a0001c0001t0003g0344 a0001c0001t0005g0123 a0001c0001t0005g0124 others(1): Show |
4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.842-1377G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999038 | |||||||
| chr10:110999116 | G | T | 2 | a0001c0001t0003g0344 a0001c0001t0014g0163 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.842-1299G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999116 | |||||||
| chr10:110999236 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.842-1179C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999236 | |||||||
| chr10:110999323 | T | C | 3 | a0001c0001t0003g0337 a0001c0001t0003g0338 a0001c0001t0003g0339 |
3 | HG02451.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.842-1092T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999323 | |||||||
| chr10:110999330 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-1085C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999330 | |||||||
| chr10:110999346 | A | G | 1 | a0001c0001t0007g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.842-1069A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999346 | |||||||
| chr10:110999524 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.842-891G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999524 | |||||||
| chr10:110999672 | G | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.842-743G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999672 | |||||||
| chr10:110999736 | C | CA | 11 | a0001c0001t0001g0071 a0001c0001t0001g0225 a0001c0001t0001g0259 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-656dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999736 | C | CAA | 166 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-657_842-656dup others(2): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999736 | C | CAAA | 24 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0040 others(21): Show |
27 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.842-658_842-656dup others(3): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999736 | C | CAAAA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
6 | HG02145.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.842-659_842-656dup others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999736 | CAAAAAA | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
39 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.842-661_842-656del others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999736 | CAAAAAAA | C | 6 | a0001c0001t0001g0072 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG02683.hp2 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-662_842-656del others(7): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999736 | CAAAAAAA others(4): Show |
C | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.842-666_842-656del others(11): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999736 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.842-669_842-656del others(14): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | ||||||
| chr10:110999760 | G | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(10): Show |
15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.842-655G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999760 | |||||||
| chr10:110999850 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
45 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.842-565A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999850 | |||||||
| chr10:110999973 | T | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.842-442T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999973 | |||||||
| chr10:111000566 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.972+21A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000566 | |||||||
| chr10:111000708 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.972+163A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000708 | |||||||
| chr10:111000748 | T | C | 1 | a0001c0001t0001g0010 | 2 | NA19054.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.972+203T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000748 | |||||||
| chr10:111000786 | A | G | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(339): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.972+241A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000786 | |||||||
| chr10:111000813 | T | C | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.972+268T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000813 | |||||||
| chr10:111000822 | G | A | 5 | a0002c0002t0001g0028 a0002c0002t0001g0117 a0002c0002t0001g0345 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.972+277G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000822 | |||||||
| chr10:111000936 | A | G | 1 | a0001c0001t0006g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.972+391A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000936 | |||||||
| chr10:111000994 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0003g0344 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.972+449C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000994 | |||||||
| chr10:111001060 | C | CT | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(280): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.972+528dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001060 | ||||||
| chr10:111001157 | C | CT | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.972+629dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001157 | ||||||
| chr10:111001197 | G | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.972+652G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001197 | |||||||
| chr10:111001220 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0350 |
2 | NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.972+675C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001220 | |||||||
| chr10:111001231 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.972+686C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001231 | |||||||
| chr10:111001243 | C | G | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.972+698C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001243 | |||||||
| chr10:111001312 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.972+767G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001312 | |||||||
| chr10:111001315 | C | T | 1 | a0001c0004t0012g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.972+770C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001315 | |||||||
| chr10:111001318 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(302): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.972+773T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001318 | |||||||
| chr10:111001434 | C | T | 1 | a0001c0001t0002g0221 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.972+889C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001434 | |||||||
| chr10:111001448 | G | A | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.972+903G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001448 | |||||||
| chr10:111001760 | G | A | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.972+1215G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001760 | |||||||
| chr10:111001805 | AGGCG | A | 18 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0322 others(15): Show |
19 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.972+1266_972+1269d others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001805 | ||||||
| chr10:111001813 | G | A | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
89 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.972+1268G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001813 | |||||||
| chr10:111001951 | A | G | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.972+1406A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001951 | |||||||
| chr10:111001987 | AGTGAGCC others(3): Show |
A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0322 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.972+1447_972+1456d others(12): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001987 | ||||||
| chr10:111002003 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.972+1458G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002003 | |||||||
| chr10:111002047 | A | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.972+1502A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002047 | |||||||
| chr10:111002125 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.972+1580T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002125 | |||||||
| chr10:111002185 | G | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.972+1640G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002185 | |||||||
| chr10:111002556 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.972+2011T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002556 | |||||||
| chr10:111002622 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.973-1984A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002622 | |||||||
| chr10:111002719 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.973-1887C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002719 | |||||||
| chr10:111002746 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.973-1860G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002746 | |||||||
| chr10:111002779 | CA | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(284): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.973-1814delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111002779 | ||||||
| chr10:111002783 | A | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0156 others(4): Show |
9 | HG01261.hp1 HG02027.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.973-1823A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002783 | |||||||
| chr10:111003107 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(283): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.973-1499T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003107 | |||||||
| chr10:111003174 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.973-1432C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003174 | |||||||
| chr10:111003398 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(285): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.973-1208G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003398 | |||||||
| chr10:111003520 | G | A | 1 | a0001c0001t0004g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.973-1086G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003520 | |||||||
| chr10:111003627 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.973-979G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003627 | |||||||
| chr10:111003677 | C | A | 1 | a0001c0001t0002g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.973-929C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003677 | |||||||
| chr10:111003679 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.973-927T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003679 | |||||||
| chr10:111003680 | G | T | 1 | a0001c0001t0002g0192 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.973-926G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003680 | |||||||
| chr10:111003781 | G | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.973-825G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003781 | |||||||
| chr10:111003816 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(283): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.973-790C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003816 | |||||||
| chr10:111003913 | T | C | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
89 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.973-693T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003913 | |||||||
| chr10:111003917 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0046 |
4 | HG00140.hp2 HG00639.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.973-689G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003917 | |||||||
| chr10:111004016 | G | T | 1 | a0001c0001t0021g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.973-590G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004016 | |||||||
| chr10:111004124 | G | T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(33): Show |
40 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.973-482G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004124 | |||||||
| chr10:111004191 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.973-415A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004191 | |||||||
| chr10:111004212 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.973-394G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004212 | |||||||
| chr10:111004274 | C | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-332C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004274 | |||||||
| chr10:111004424 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.973-182C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004424 | |||||||
| chr10:111004466 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.973-140T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004466 | |||||||
| chr10:111004836 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(301): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1161+42T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111004836 | |||||||
| chr10:111004975 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0229 |
3 | HG03490.hp1 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1161+181C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111004975 | |||||||
| chr10:111004992 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1161+198T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111004992 | |||||||
| chr10:111005417 | G | A | 78 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(75): Show |
88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1161+623G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005417 | |||||||
| chr10:111005454 | C | G | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1161+660C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005454 | |||||||
| chr10:111005458 | G | A | 4 | a0001c0001t0003g0344 a0001c0001t0005g0123 a0001c0001t0005g0124 others(1): Show |
4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161+664G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005458 | |||||||
| chr10:111005644 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1161+850C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005644 | |||||||
| chr10:111005721 | A | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1161+927A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005721 | |||||||
| chr10:111005856 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0309 a0001c0001t0001g0343 |
3 | NA18966.hp2 NA18989.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1161+1062T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005856 | |||||||
| chr10:111005922 | G | A | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(323): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1161+1128G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005922 | |||||||
| chr10:111006196 | G | A | 1 | a0001c0004t0012g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1162-1335G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006196 | |||||||
| chr10:111006238 | C | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1162-1293C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006238 | |||||||
| chr10:111006394 | G | A | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1162-1137G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006394 | |||||||
| chr10:111006401 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1162-1130C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006401 | |||||||
| chr10:111006402 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1162-1129G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006402 | |||||||
| chr10:111006423 | T | G | 2 | a0001c0001t0001g0328 a0001c0001t0018g0327 |
2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1162-1108T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006423 | |||||||
| chr10:111006461 | C | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1162-1070C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006461 | |||||||
| chr10:111006516 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1162-1015G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006516 | |||||||
| chr10:111006520 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1162-1011G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006520 | |||||||
| chr10:111006572 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1162-959G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006572 | |||||||
| chr10:111006580 | C | T | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1162-951C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006580 | |||||||
| chr10:111006683 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1162-848A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006683 | |||||||
| chr10:111006731 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1162-800G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006731 | |||||||
| chr10:111006844 | T | C | 1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1162-687T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006844 | |||||||
| chr10:111006879 | G | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0167 others(7): Show |
14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1162-652G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006879 | |||||||
| chr10:111006990 | G | T | 3 | a0001c0001t0003g0333 a0001c0001t0003g0334 a0001c0001t0003g0335 |
3 | HG01168.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1162-541G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006990 | |||||||
| chr10:111007171 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1162-360T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007171 | |||||||
| chr10:111007254 | C | T | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-277C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007254 | |||||||
| chr10:111007261 | G | A | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1162-270G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007261 | |||||||
| chr10:111007278 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1162-253G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007278 | |||||||
| chr10:111007291 | C | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162-240C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007291 | |||||||
| chr10:111007401 | T | G | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1162-130T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007401 | |||||||
| chr10:111007726 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0322 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1284+73A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111007726 | |||||||
| chr10:111007938 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0322 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1284+285T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111007938 | |||||||
| chr10:111008405 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG01109.hp2 HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1284+752A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008405 | |||||||
| chr10:111008438 | T | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1284+785T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008438 | |||||||
| chr10:111008442 | C | G | 1 | a0001c0001t0002g0235 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1284+789C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008442 | |||||||
| chr10:111008535 | T | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1285-713T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008535 | |||||||
| chr10:111008592 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1285-656A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008592 | |||||||
| chr10:111008760 | C | T | 1 | a0001c0001t0009g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1285-488C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008760 | |||||||
| chr10:111008845 | T | C | 1 | a0001c0001t0016g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1285-403T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008845 | |||||||
| chr10:111008866 | TA | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
6 | NA18949.hp2 NA18973.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-379delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 111008866 | ||||||
| chr10:111008870 | T | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1285-378T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008870 | |||||||
| chr10:111009058 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0046 |
4 | HG00140.hp2 HG00639.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-190C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111009058 | |||||||
| chr10:111009060 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1285-188C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111009060 | |||||||
| chr10:111009092 | A | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1285-156A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111009092 | |||||||
| chr10:111009509 | C | T | 1 | a0001c0001t0014g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1422+124C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/8 | chr10 | 111009509 | |||||||
| chr10:111009620 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0275 |
2 | HG02257.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1423-93T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/8 | chr10 | 111009620 | |||||||
| chr10:111009706 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0226 |
2 | HG03139.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.1423-7C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/8 | chr10 | 111009706 | |||||||
| chr10:111009860 | A | T | 1 | a0001c0001t0003g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1540+30A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111009860 | |||||||
| chr10:111010286 | T | C | 1 | a0001c0001t0003g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1540+456T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010286 | |||||||
| chr10:111010541 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1540+711G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010541 | |||||||
| chr10:111010546 | G | C | 79 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1540+716G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010546 | |||||||
| chr10:111010681 | TA | T | 325 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(322): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1540+860delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 111010681 | ||||||
| chr10:111010893 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1541-717T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010893 | |||||||
| chr10:111010957 | C | T | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1541-653C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010957 | |||||||
| chr10:111011020 | T | C | 2 | a0001c0001t0005g0123 a0001c0001t0005g0124 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1541-590T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011020 | |||||||
| chr10:111011077 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0003g0333 a0001c0001t0003g0334 others(2): Show |
5 | HG01074.hp2 HG01168.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541-533A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011077 | |||||||
| chr10:111011134 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1541-476A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011134 | |||||||
| chr10:111011223 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1541-387A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011223 | |||||||
| chr10:111011581 | A | T | 10 | a0001c0001t0003g0027 a0001c0001t0003g0333 a0001c0001t0003g0334 others(7): Show |
11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541-29A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011581 |