| geneid | 25992 |
|---|---|
| ensemblid | ENSG00000162804.15 |
| hgncid | 24696 |
| symbol | SNED1 |
| name | sushi, nidogen and EGF like domains 1 |
| refseq_nuc | NM_001080437.3 |
| refseq_prot | NP_001073906.1 |
| ensembl_nuc | ENST00000310397.13 |
| ensembl_prot | ENSP00000308893.8 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 240998618 |
| end | 241095568 |
| strand | + |
| ver | v1.2 |
| region | chr2:240998618-241095568 |
| region5000 | chr2:240993618-241100568 |
| regionname0 | SNED1_chr2_240998618_241095568 |
| regionname5000 | SNED1_chr2_240993618_241100568 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1413 | 133 | 19 | 20 | 54 | 8 | 30 | 35 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002 | 0/0 | 1413 | 92 | 48 | 11 | 28 | 1 | 4 | 20 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003 | 0/0 | 1413 | 33 | 1 | 3 | 27 | 1 | 1 | 22 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004 | 0/0 | 1413 | 18 | 1 | 4 | 13 | 0 | 0 | 11 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005 | 0/0 | 1413 | 16 | 0 | 3 | 13 | 0 | 0 | 9 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006 | 0/0 | 1413 | 11 | 0 | 4 | 5 | 1 | 1 | 5 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007 | 0/0 | 188 | 8 | 1 | 2 | 3 | 0 | 2 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008 | 0/0 | 1413 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009 | 0/0 | 1413 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0010 | 0/0 | 1413 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0011 | 0/0 | 1413 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0012 | 0/0 | 1413 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0013 | 0/0 | 1413 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0014 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0015 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0016 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0017 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0018 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0019 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0020 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0021 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0022 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0023 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 4242 | 68 | 7 | 11 | 30 | 4 | 15 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0002 | 0/1 | 4242 | 35 | 1 | 8 | 10 | 3 | 12 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0003 | 0/0 | 4242 | 30 | 2 | 6 | 20 | 0 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0004 | 0/0 | 4242 | 24 | 0 | 1 | 22 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0005 | 0/0 | 4242 | 13 | 0 | 4 | 9 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0006 | 0/0 | 4242 | 11 | 0 | 0 | 10 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0007 | 0/0 | 4242 | 10 | 0 | 3 | 7 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0008 | 0/0 | 4242 | 9 | 3 | 2 | 2 | 1 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0009 | 0/0 | 4242 | 7 | 5 | 1 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0010 | 0/0 | 4242 | 6 | 6 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0011 | 0/0 | 4242 | 6 | 6 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0012 | 0/0 | 4242 | 5 | 0 | 3 | 1 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0013 | 0/0 | 4242 | 5 | 4 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0014 | 0/0 | 4242 | 5 | 0 | 0 | 5 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0015 | 0/0 | 4242 | 4 | 0 | 0 | 4 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0016 | 0/0 | 4242 | 4 | 4 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0017 | 0/0 | 4242 | 4 | 3 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0018 | 0/0 | 4242 | 4 | 1 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0019 | 0/0 | 4242 | 4 | 4 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0020 | 0/0 | 4242 | 3 | 0 | 1 | 1 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0021 | 0/0 | 4242 | 3 | 2 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0022 | 0/0 | 4242 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0023 | 0/0 | 4242 | 3 | 0 | 0 | 2 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0024 | 0/0 | 4242 | 3 | 0 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0025 | 0/0 | 4242 | 3 | 0 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0026 | 0/0 | 4242 | 3 | 1 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0027 | 0/0 | 4243 | 2 | 0 | 0 | 1 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0028 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0029 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0030 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0031 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0032 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0033 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0034 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0035 | 0/0 | 4242 | 2 | 0 | 2 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0036 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0037 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0038 | 0/0 | 4243 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0039 | 0/0 | 4243 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0040 | 0/0 | 4243 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0041 | 0/0 | 4243 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0042 | 0/0 | 4243 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0043 | 0/0 | 4243 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0044 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0045 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0046 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0047 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0048 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0049 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0050 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0051 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0052 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0053 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0054 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0055 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0056 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0057 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0058 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0059 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0060 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0061 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0062 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0063 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0064 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0065 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0066 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0067 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0068 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0069 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0070 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0071 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0072 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0073 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0074 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0075 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0076 | 0/0 | 4232 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0077 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0078 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0079 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0080 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0081 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0082 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0083 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| c0084 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4152 | 46 | 2 | 10 | 26 | 1 | 6 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0002 | 0/0 | 4151 | 38 | 5 | 10 | 14 | 6 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0003 | 0/0 | 4153 | 20 | 5 | 2 | 9 | 1 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0004 | 0/0 | 4065 | 20 | 4 | 3 | 11 | 1 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0005 | 0/0 | 4153 | 20 | 0 | 2 | 15 | 0 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0006 | 0/0 | 4067 | 19 | 0 | 1 | 17 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0007 | 0/0 | 4068 | 16 | 0 | 4 | 11 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0008 | 0/0 | 4068 | 14 | 0 | 5 | 9 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0009 | 0/0 | 4154 | 11 | 3 | 1 | 4 | 1 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0010 | 0/0 | 4064 | 11 | 0 | 0 | 11 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0011 | 0/0 | 4066 | 9 | 8 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0012 | 0/0 | 4066 | 8 | 1 | 4 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0013 | 0/0 | 4065 | 8 | 0 | 0 | 6 | 0 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0014 | 0/0 | 4065 | 7 | 7 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0015 | 0/0 | 4065 | 7 | 7 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0016 | 0/0 | 4064 | 7 | 7 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0017 | 0/1 | 4155 | 6 | 0 | 0 | 2 | 0 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0018 | 0/0 | 4152 | 5 | 1 | 0 | 1 | 0 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0019 | 0/0 | 4063 | 5 | 5 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0020 | 0/0 | 4150 | 5 | 2 | 0 | 1 | 1 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0021 | 0/0 | 4066 | 4 | 4 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0022 | 0/0 | 4066 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0023 | 0/0 | 4152 | 3 | 0 | 0 | 0 | 0 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0024 | 0/0 | 4065 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0025 | 0/0 | 4065 | 3 | 1 | 2 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0026 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0027 | 0/0 | 4066 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0028 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0029 | 0/0 | 4064 | 2 | 1 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0030 | 0/0 | 4066 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0031 | 0/0 | 4065 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0032 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0033 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0034 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0035 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0036 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0037 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0038 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0039 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0040 | 0/0 | 4154 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0041 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0042 | 0/0 | 4148 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0043 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0044 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0045 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0046 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0047 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0048 | 0/0 | 4152 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0049 | 0/0 | 4237 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0050 | 0/0 | 4151 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0051 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0052 | 0/0 | 4151 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0053 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0054 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0055 | 0/0 | 4150 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0056 | 0/0 | 4066 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0057 | 0/0 | 4151 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0058 | 0/0 | 4152 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0059 | 0/0 | 4152 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0060 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0061 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0062 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0063 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0064 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| t0065 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4242 | 68 | 7 | 11 | 30 | 4 | 15 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002 | 0/1 | 4242 | 35 | 1 | 8 | 10 | 3 | 12 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0006 | 0/0 | 4242 | 11 | 0 | 0 | 10 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0016 | 0/0 | 4242 | 4 | 4 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0020 | 0/0 | 4242 | 3 | 0 | 1 | 1 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0025 | 0/0 | 4242 | 3 | 0 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0037 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0045 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0050 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0057 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0060 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0068 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0071 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0074 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003 | 0/0 | 4242 | 30 | 2 | 6 | 20 | 0 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008 | 0/0 | 4242 | 9 | 3 | 2 | 2 | 1 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0009 | 0/0 | 4242 | 7 | 5 | 1 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0010 | 0/0 | 4242 | 6 | 6 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0011 | 0/0 | 4242 | 6 | 6 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0013 | 0/0 | 4242 | 5 | 4 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0018 | 0/0 | 4242 | 4 | 1 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0019 | 0/0 | 4242 | 4 | 4 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0021 | 0/0 | 4242 | 3 | 2 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0022 | 0/0 | 4242 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0034 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0036 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0052 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0055 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0058 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0061 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0064 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0073 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0075 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0080 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0082 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0083 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0084 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0004 | 0/0 | 4242 | 24 | 0 | 1 | 22 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0023 | 0/0 | 4242 | 3 | 0 | 0 | 2 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0024 | 0/0 | 4242 | 3 | 0 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0048 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0056 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0066 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0005 | 0/0 | 4242 | 13 | 0 | 4 | 9 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0026 | 0/0 | 4242 | 3 | 1 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0028 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0007 | 0/0 | 4242 | 10 | 0 | 3 | 7 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0014 | 0/0 | 4242 | 5 | 0 | 0 | 5 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0047 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0012 | 0/0 | 4242 | 5 | 0 | 3 | 1 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0015 | 0/0 | 4242 | 4 | 0 | 0 | 4 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0063 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0077 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0027 | 0/0 | 4243 | 2 | 0 | 0 | 1 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0038 | 0/0 | 4243 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0039 | 0/0 | 4243 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0040 | 0/0 | 4243 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0041 | 0/0 | 4243 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0042 | 0/0 | 4243 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0043 | 0/0 | 4243 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0032 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0033 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0051 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0069 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0081 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009c0030 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009c0031 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009c0067 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0010c0017 | 0/0 | 4242 | 4 | 3 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0011c0035 | 0/0 | 4242 | 2 | 0 | 2 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0011c0054 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0012c0049 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0012c0079 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0013c0029 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0014c0044 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0015c0046 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0016c0053 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0017c0072 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0018c0065 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0019c0070 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0020c0062 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0021c0078 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0022c0059 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0023c0076 | 0/0 | 4232 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8393 | 21 | 2 | 4 | 10 | 0 | 4 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0002 | 0/0 | 8392 | 23 | 3 | 6 | 7 | 4 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0005 | 0/0 | 8394 | 12 | 0 | 1 | 9 | 0 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0009 | 0/0 | 8395 | 2 | 0 | 0 | 1 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0017 | 0/0 | 8396 | 2 | 0 | 0 | 0 | 0 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0020 | 0/0 | 8391 | 3 | 1 | 0 | 1 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0049 | 0/0 | 8478 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0051 | 0/0 | 8394 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0052 | 0/0 | 8392 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0053 | 0/0 | 8456 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0001t0055 | 0/0 | 8391 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0001 | 0/0 | 8393 | 5 | 0 | 2 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0002 | 0/0 | 8392 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0003 | 0/0 | 8394 | 9 | 0 | 2 | 4 | 1 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0005 | 0/0 | 8394 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0009 | 0/0 | 8395 | 5 | 1 | 1 | 1 | 1 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0017 | 0/1 | 8396 | 3 | 0 | 0 | 1 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0018 | 0/0 | 8393 | 3 | 0 | 0 | 0 | 0 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0020 | 0/0 | 8391 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0023 | 0/0 | 8393 | 3 | 0 | 0 | 0 | 0 | 3 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0041 | 0/0 | 8392 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0043 | 0/0 | 8393 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0048 | 0/0 | 8393 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0002t0059 | 0/0 | 8393 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0006t0001 | 0/0 | 8393 | 5 | 0 | 0 | 4 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0006t0002 | 0/0 | 8392 | 5 | 0 | 0 | 5 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0006t0058 | 0/0 | 8393 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0016t0003 | 0/0 | 8394 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0016t0009 | 0/0 | 8395 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0020t0001 | 0/0 | 8393 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0020t0042 | 0/0 | 8389 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0020t0057 | 0/0 | 8392 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0025t0003 | 0/0 | 8394 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0025t0009 | 0/0 | 8395 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0037t0002 | 0/0 | 8392 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0037t0020 | 0/0 | 8391 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0045t0002 | 0/0 | 8392 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0050t0003 | 0/0 | 8394 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0057t0009 | 0/0 | 8395 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0060t0005 | 0/0 | 8394 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0068t0018 | 0/0 | 8393 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0071t0003 | 0/0 | 8394 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0001c0074t0002 | 0/0 | 8392 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0004 | 0/0 | 8306 | 3 | 0 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0006 | 0/0 | 8308 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0007 | 0/0 | 8309 | 3 | 0 | 1 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0008 | 0/0 | 8309 | 11 | 0 | 5 | 6 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0010 | 0/0 | 8305 | 5 | 0 | 0 | 5 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0013 | 0/0 | 8306 | 5 | 0 | 0 | 3 | 0 | 2 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0022 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0003t0062 | 0/0 | 8305 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0004 | 0/0 | 8306 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0008 | 0/0 | 8309 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0010 | 0/0 | 8305 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0012 | 0/0 | 8307 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0019 | 0/0 | 8304 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0029 | 0/0 | 8305 | 2 | 1 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0033 | 0/0 | 8309 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0008t0061 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0009t0004 | 0/0 | 8306 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0009t0012 | 0/0 | 8307 | 2 | 1 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0009t0016 | 0/0 | 8305 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0009t0046 | 0/0 | 8309 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0010t0014 | 0/0 | 8306 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0010t0016 | 0/0 | 8305 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0010t0019 | 0/0 | 8304 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0010t0044 | 0/0 | 8304 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0011t0011 | 0/0 | 8307 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0011t0015 | 0/0 | 8306 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0013t0011 | 0/0 | 8307 | 2 | 1 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0013t0015 | 0/0 | 8306 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0018t0010 | 0/0 | 8305 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0018t0013 | 0/0 | 8306 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0018t0022 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0019t0014 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0019t0026 | 0/0 | 8305 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0019t0034 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0021t0004 | 0/0 | 8306 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0021t0014 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0021t0047 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0022t0014 | 0/0 | 8306 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0022t0035 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0034t0004 | 0/0 | 8306 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0034t0006 | 0/0 | 8308 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0036t0014 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0036t0025 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0052t0011 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0055t0022 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0058t0019 | 0/0 | 8304 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0061t0008 | 0/0 | 8309 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0064t0060 | 0/0 | 8308 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0073t0063 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0075t0045 | 0/0 | 8305 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0080t0011 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0082t0039 | 0/0 | 8308 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0083t0011 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0002c0084t0037 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0004t0006 | 0/0 | 8308 | 14 | 0 | 1 | 12 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0004t0007 | 0/0 | 8309 | 7 | 0 | 0 | 7 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0004t0010 | 0/0 | 8305 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0004t0032 | 0/0 | 8309 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0004t0064 | 0/0 | 8309 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0023t0004 | 0/0 | 8306 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0023t0006 | 0/0 | 8308 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0023t0007 | 0/0 | 8309 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0024t0004 | 0/0 | 8306 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0024t0010 | 0/0 | 8305 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0048t0007 | 0/0 | 8309 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0056t0007 | 0/0 | 8309 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0003c0066t0015 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0005t0004 | 0/0 | 8306 | 5 | 0 | 2 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0005t0008 | 0/0 | 8309 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0005t0010 | 0/0 | 8305 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0005t0012 | 0/0 | 8307 | 3 | 0 | 2 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0005t0031 | 0/0 | 8306 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0005t0065 | 0/0 | 8307 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0026t0004 | 0/0 | 8306 | 2 | 1 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0026t0013 | 0/0 | 8306 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0004c0028t0012 | 0/0 | 8307 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0007t0001 | 0/0 | 8393 | 3 | 0 | 0 | 3 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0007t0002 | 0/0 | 8392 | 4 | 0 | 3 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0007t0005 | 0/0 | 8394 | 2 | 0 | 0 | 2 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0007t0054 | 0/0 | 8393 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0014t0001 | 0/0 | 8393 | 5 | 0 | 0 | 5 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0005c0047t0050 | 0/0 | 8392 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0012t0001 | 0/0 | 8393 | 3 | 0 | 2 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0012t0005 | 0/0 | 8394 | 2 | 0 | 1 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0015t0003 | 0/0 | 8394 | 4 | 0 | 0 | 4 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0063t0001 | 0/0 | 8393 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0006c0077t0003 | 0/0 | 8394 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0027t0001 | 0/0 | 8394 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0027t0002 | 0/0 | 8393 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0038t0018 | 0/0 | 8394 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0039t0001 | 0/0 | 8394 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0040t0007 | 0/0 | 8310 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0041t0007 | 0/0 | 8310 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0042t0013 | 0/0 | 8307 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0007c0043t0011 | 0/0 | 8308 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0032t0021 | 0/0 | 8307 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0033t0016 | 0/0 | 8305 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0033t0030 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0051t0021 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0069t0016 | 0/0 | 8305 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0008c0081t0021 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009c0030t0027 | 0/0 | 8307 | 2 | 2 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009c0031t0028 | 0/0 | 8308 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009c0031t0036 | 0/0 | 8309 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0009c0067t0028 | 0/0 | 8308 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0010c0017t0024 | 0/0 | 8306 | 3 | 3 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0010c0017t0056 | 0/0 | 8307 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0011c0035t0025 | 0/0 | 8306 | 2 | 0 | 2 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0011c0054t0030 | 0/0 | 8307 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0012c0049t0019 | 0/0 | 8304 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0012c0079t0016 | 0/0 | 8305 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0013c0029t0006 | 0/0 | 8308 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0013c0029t0007 | 0/0 | 8309 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0014c0044t0005 | 0/0 | 8394 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0015c0046t0040 | 0/0 | 8395 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0016c0053t0017 | 0/0 | 8396 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0017c0072t0002 | 0/0 | 8392 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0018c0065t0038 | 0/0 | 8306 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0019c0070t0019 | 0/0 | 8304 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0020c0062t0005 | 0/0 | 8394 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0021c0078t0016 | 0/0 | 8305 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0022c0059t0004 | 0/0 | 8306 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| a0023c0076t0006 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | copy fasta | chr2 | 240993618 | 241100568 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0009g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0017g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0017g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0020g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0020g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0049g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0051g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0052g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0053g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0001t0055g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0009g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0009g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0017g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0017g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0017g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0018g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0018g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0018g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0020g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0023g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0023g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0023g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0041g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0043g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0048g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0002t0059g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0006t0058g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0016t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0016t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0016t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0016t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0020t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0020t0042g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0020t0057g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0025t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0025t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0025t0009g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0037t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0037t0020g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0045t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0050t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0057t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0060t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0068t0018g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0071t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0001c0074t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0007g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0008g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0010g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0010g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0010g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0010g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0013g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0013g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0013g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0013g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0022g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0003t0062g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0008g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0010g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0012g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0019g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0029g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0029g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0033g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0008t0061g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0009t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0009t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0009t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0009t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0009t0012g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0009t0016g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0009t0046g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0010t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0010t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0010t0016g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0010t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0010t0019g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0010t0044g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0011t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0011t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0011t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0011t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0011t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0011t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0013t0011g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0013t0011g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0013t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0013t0015g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0013t0015g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0018t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0018t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0018t0013g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0018t0022g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0019t0014g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0019t0026g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0019t0026g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0019t0034g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0021t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0021t0014g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0021t0047g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0022t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0022t0014g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0022t0035g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0034t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0034t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0036t0014g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0036t0025g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0052t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0055t0022g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0058t0019g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0061t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0064t0060g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0073t0063g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0075t0045g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0080t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0082t0039g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0083t0011g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0002c0084t0037g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0032g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0004t0064g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0023t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0023t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0023t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0024t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0024t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0024t0010g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0048t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0056t0007g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0003c0066t0015g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0012g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0012g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0012g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0031g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0031g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0005t0065g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0026t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0026t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0026t0013g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0028t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0004c0028t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0007t0054g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0014t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0014t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0014t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0014t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0014t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0005c0047t0050g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0012t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0012t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0012t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0012t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0015t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0015t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0015t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0015t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0063t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0006c0077t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0027t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0027t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0038t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0039t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0040t0007g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0041t0007g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0042t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0007c0043t0011g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0008c0032t0021g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0008c0032t0021g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0008c0033t0016g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0008c0033t0030g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0008c0051t0021g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0008c0069t0016g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0008c0081t0021g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0009c0030t0027g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0009c0030t0027g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0009c0031t0028g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0009c0031t0036g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0009c0067t0028g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0010c0017t0024g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0010c0017t0024g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0010c0017t0024g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0010c0017t0056g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0011c0035t0025g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0011c0035t0025g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0011c0054t0030g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0012c0049t0019g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0012c0079t0016g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0013c0029t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0013c0029t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0014c0044t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0015c0046t0040g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0016c0053t0017g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0017c0072t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0018c0065t0038g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0019c0070t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0020c0062t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0021c0078t0016g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0022c0059t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| a0023c0076t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | GBR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00099 | hp2 | a0001 | c0002 | t0020 | g0308 | EUR | GBR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | GBR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | GBR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00423 | hp2 | a0005 | c0014 | t0001 | g0091 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00438 | hp1 | a0002 | c0003 | t0010 | g0190 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00438 | hp2 | a0001 | c0006 | t0002 | g0089 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00558 | hp1 | a0002 | c0003 | t0008 | g0066 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00558 | hp2 | a0003 | c0004 | t0006 | g0213 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00597 | hp1 | a0005 | c0014 | t0001 | g0125 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00597 | hp2 | a0002 | c0003 | t0010 | g0068 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00609 | hp1 | a0002 | c0003 | t0008 | g0259 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0134 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00621 | hp1 | a0014 | c0044 | t0005 | g0206 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00621 | hp2 | a0002 | c0003 | t0013 | g0263 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00673 | hp1 | a0001 | c0006 | t0002 | g0088 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00673 | hp2 | a0003 | c0004 | t0006 | g0292 | EAS | CHS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00738 | hp1 | a0005 | c0007 | t0002 | g0248 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00738 | hp2 | a0001 | c0002 | t0041 | g0181 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01070 | hp2 | a0006 | c0012 | t0001 | g0001 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01071 | hp2 | a0006 | c0012 | t0001 | g0001 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01081 | hp1 | a0003 | c0048 | t0007 | g0176 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01081 | hp2 | a0002 | c0003 | t0008 | g0282 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01099 | hp1 | a0006 | c0012 | t0005 | g0309 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01099 | hp2 | a0002 | c0013 | t0011 | g0214 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01167 | hp1 | a0011 | c0035 | t0025 | g0342 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0177 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01169 | hp1 | a0011 | c0035 | t0025 | g0343 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01169 | hp2 | a0001 | c0002 | t0009 | g0187 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01175 | hp1 | a0002 | c0003 | t0008 | g0285 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01175 | hp2 | a0001 | c0002 | t0048 | g0191 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01243 | hp1 | a0010 | c0017 | t0056 | g0226 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0324 | AMR | PUR | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01255 | hp1 | a0006 | c0063 | t0001 | g0242 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01255 | hp2 | a0003 | c0056 | t0007 | g0009 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01256 | hp1 | a0002 | c0003 | t0008 | g0113 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01261 | hp1 | a0002 | c0009 | t0012 | g0312 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01433 | hp1 | a0002 | c0008 | t0012 | g0186 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01433 | hp2 | a0002 | c0003 | t0008 | g0020 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01515 | hp1 | a0017 | c0072 | t0002 | g0069 | EUR | IBS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01515 | hp2 | a0001 | c0002 | t0009 | g0178 | EUR | IBS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0302 | EUR | IBS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01516 | hp2 | a0003 | c0004 | t0006 | g0135 | EUR | IBS | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01884 | hp1 | a0002 | c0010 | t0014 | g0222 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01884 | hp2 | a0002 | c0083 | t0011 | g0316 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01891 | hp1 | a0015 | c0046 | t0040 | g0336 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01891 | hp2 | a0002 | c0010 | t0044 | g0078 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01928 | hp2 | a0004 | c0005 | t0012 | g0201 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01934 | hp1 | a0007 | c0040 | t0007 | g0057 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01943 | hp1 | a0001 | c0020 | t0042 | g0154 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01943 | hp2 | a0002 | c0021 | t0004 | g0198 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01975 | hp2 | a0004 | c0005 | t0004 | g0203 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01993 | hp1 | a0007 | c0039 | t0001 | g0183 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01993 | hp2 | a0004 | c0005 | t0004 | g0202 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02015 | hp2 | a0013 | c0029 | t0006 | g0106 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02027 | hp1 | a0001 | c0025 | t0009 | g0291 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02027 | hp2 | a0001 | c0006 | t0058 | g0085 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02040 | hp1 | a0002 | c0003 | t0008 | g0070 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02040 | hp2 | a0022 | c0059 | t0004 | g0126 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02055 | hp2 | a0001 | c0002 | t0009 | g0211 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02056 | hp1 | a0001 | c0025 | t0009 | g0073 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02071 | hp1 | a0001 | c0002 | t0005 | g0115 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02071 | hp2 | a0001 | c0025 | t0003 | g0074 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02074 | hp1 | a0004 | c0005 | t0065 | g0062 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02080 | hp1 | a0003 | c0024 | t0010 | g0286 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02080 | hp2 | a0004 | c0026 | t0013 | g0048 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02083 | hp2 | a0001 | c0001 | t0009 | g0278 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02129 | hp1 | a0001 | c0001 | t0051 | g0270 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02129 | hp2 | a0002 | c0003 | t0006 | g0275 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02132 | hp1 | a0001 | c0020 | t0001 | g0105 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02135 | hp1 | a0005 | c0014 | t0001 | g0090 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02135 | hp2 | a0003 | c0004 | t0007 | g0006 | EAS | KHV | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02145 | hp1 | a0021 | c0078 | t0016 | g0035 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02155 | hp1 | a0020 | c0062 | t0005 | g0262 | EAS | CDX | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02155 | hp2 | a0001 | c0006 | t0002 | g0084 | EAS | CDX | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02165 | hp1 | a0002 | c0003 | t0010 | g0260 | EAS | CDX | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02165 | hp2 | a0003 | c0004 | t0010 | g0212 | EAS | CDX | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02257 | hp1 | a0002 | c0022 | t0014 | g0087 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02257 | hp2 | a0018 | c0065 | t0038 | g0024 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02258 | hp1 | a0002 | c0013 | t0011 | g0207 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02258 | hp2 | a0002 | c0010 | t0014 | g0038 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02273 | hp1 | a0002 | c0003 | t0007 | g0284 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02273 | hp2 | a0002 | c0003 | t0008 | g0235 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02280 | hp1 | a0008 | c0033 | t0030 | g0335 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02280 | hp2 | a0002 | c0003 | t0022 | g0023 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02293 | hp1 | a0004 | c0005 | t0012 | g0204 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02293 | hp2 | a0005 | c0007 | t0002 | g0205 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02300 | hp1 | a0005 | c0007 | t0002 | g0112 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02300 | hp2 | a0002 | c0008 | t0033 | g0287 | AMR | PEL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02451 | hp1 | a0002 | c0009 | t0004 | g0146 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02451 | hp2 | a0009 | c0031 | t0028 | g0224 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02572 | hp1 | a0002 | c0003 | t0062 | g0077 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02572 | hp2 | a0001 | c0037 | t0002 | g0314 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02602 | hp2 | a0001 | c0002 | t0018 | g0160 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02615 | hp1 | a0001 | c0016 | t0003 | g0216 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02615 | hp2 | a0002 | c0084 | t0037 | g0318 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02622 | hp1 | a0002 | c0021 | t0014 | g0233 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02622 | hp2 | a0002 | c0013 | t0015 | g0188 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02630 | hp1 | a0002 | c0019 | t0026 | g0072 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02630 | hp2 | a0010 | c0017 | t0024 | g0042 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02647 | hp1 | a0002 | c0011 | t0011 | g0234 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02647 | hp2 | a0002 | c0082 | t0039 | g0032 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02683 | hp1 | a0002 | c0003 | t0013 | g0194 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02683 | hp2 | a0003 | c0023 | t0004 | g0210 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02717 | hp1 | a0002 | c0022 | t0035 | g0037 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02717 | hp2 | a0002 | c0013 | t0015 | g0215 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02723 | hp1 | a0002 | c0009 | t0016 | g0220 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02723 | hp2 | a0008 | c0081 | t0021 | g0031 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02735 | hp1 | a0001 | c0002 | t0023 | g0179 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02735 | hp2 | a0001 | c0001 | t0017 | g0272 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02738 | hp1 | a0001 | c0006 | t0001 | g0116 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02738 | hp2 | a0001 | c0002 | t0043 | g0306 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02809 | hp2 | a0001 | c0074 | t0002 | g0086 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02886 | hp1 | a0002 | c0009 | t0004 | g0332 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02886 | hp2 | a0001 | c0016 | t0009 | g0232 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02896 | hp1 | a0001 | c0057 | t0009 | g0094 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02896 | hp2 | a0002 | c0011 | t0015 | g0028 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02897 | hp1 | a0001 | c0016 | t0003 | g0230 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02897 | hp2 | a0002 | c0011 | t0011 | g0029 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02922 | hp1 | a0002 | c0019 | t0014 | g0041 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02922 | hp2 | a0002 | c0009 | t0004 | g0040 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02965 | hp1 | a0002 | c0008 | t0019 | g0227 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02965 | hp2 | a0001 | c0071 | t0003 | g0333 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02970 | hp1 | a0004 | c0026 | t0004 | g0228 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02970 | hp2 | a0002 | c0010 | t0019 | g0195 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02976 | hp1 | a0003 | c0066 | t0015 | g0330 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02976 | hp2 | a0002 | c0052 | t0011 | g0256 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03041 | hp1 | a0002 | c0055 | t0022 | g0052 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03041 | hp2 | a0010 | c0017 | t0024 | g0225 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03098 | hp1 | a0002 | c0073 | t0063 | g0007 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03098 | hp2 | a0002 | c0075 | t0045 | g0251 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03130 | hp1 | a0001 | c0001 | t0055 | g0173 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03130 | hp2 | a0002 | c0036 | t0025 | g0022 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03139 | hp1 | a0008 | c0051 | t0021 | g0337 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03139 | hp2 | a0001 | c0068 | t0018 | g0320 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03195 | hp1 | a0002 | c0013 | t0015 | g0317 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03195 | hp2 | a0012 | c0049 | t0019 | g0050 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03209 | hp1 | a0002 | c0036 | t0014 | g0326 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03209 | hp2 | a0002 | c0019 | t0026 | g0155 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03225 | hp1 | a0019 | c0070 | t0019 | g0008 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03225 | hp2 | a0002 | c0080 | t0011 | g0124 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0175 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03453 | hp2 | a0009 | c0067 | t0028 | g0039 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03486 | hp1 | a0001 | c0016 | t0003 | g0231 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03486 | hp2 | a0002 | c0010 | t0016 | g0033 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03491 | hp2 | a0001 | c0002 | t0023 | g0246 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03492 | hp1 | a0001 | c0002 | t0023 | g0247 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03492 | hp2 | a0001 | c0001 | t0052 | g0147 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03516 | hp1 | a0002 | c0021 | t0047 | g0321 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03516 | hp2 | a0002 | c0022 | t0014 | g0327 | AFR | ESN | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03540 | hp1 | a0010 | c0017 | t0024 | g0338 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03540 | hp2 | a0009 | c0030 | t0027 | g0127 | AFR | GWD | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03579 | hp1 | a0002 | c0011 | t0011 | g0128 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03579 | hp2 | a0008 | c0069 | t0016 | g0133 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0149 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03654 | hp2 | a0007 | c0027 | t0001 | g0267 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03669 | hp1 | a0001 | c0002 | t0059 | g0053 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0169 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03710 | hp2 | a0001 | c0002 | t0018 | g0185 | SAS | PJL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0299 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0340 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03834 | hp1 | a0001 | c0020 | t0057 | g0341 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03834 | hp2 | a0002 | c0008 | t0029 | g0289 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03927 | hp1 | a0001 | c0001 | t0017 | g0273 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03942 | hp1 | a0001 | c0001 | t0049 | g0322 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03942 | hp2 | a0001 | c0001 | t0009 | g0274 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04184 | hp1 | a0001 | c0002 | t0017 | g0323 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04184 | hp2 | a0002 | c0003 | t0013 | g0307 | SAS | BEB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04199 | hp1 | a0001 | c0001 | t0020 | g0025 | SAS | STU | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04199 | hp2 | a0006 | c0077 | t0003 | g0093 | SAS | STU | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04204 | hp1 | a0007 | c0041 | t0007 | g0249 | SAS | STU | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | STU | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04228 | hp1 | a0001 | c0002 | t0009 | g0310 | SAS | STU | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG04228 | hp2 | a0001 | c0060 | t0005 | g0193 | SAS | STU | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18522 | hp1 | a0002 | c0011 | t0015 | g0036 | AFR | YRI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18522 | hp2 | a0009 | c0030 | t0027 | g0208 | AFR | YRI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18747 | hp1 | a0005 | c0007 | t0002 | g0243 | EAS | CHB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18906 | hp1 | a0002 | c0019 | t0034 | g0026 | AFR | YRI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18906 | hp2 | a0002 | c0008 | t0061 | g0168 | AFR | YRI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18940 | hp1 | a0001 | c0006 | t0001 | g0054 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18940 | hp2 | a0006 | c0015 | t0003 | g0137 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18941 | hp1 | a0003 | c0024 | t0004 | g0269 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18942 | hp1 | a0001 | c0006 | t0002 | g0076 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18942 | hp2 | a0002 | c0003 | t0008 | g0277 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18943 | hp1 | a0002 | c0003 | t0010 | g0218 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18943 | hp2 | a0005 | c0007 | t0005 | g0111 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18945 | hp2 | a0004 | c0005 | t0012 | g0016 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18947 | hp1 | a0002 | c0003 | t0013 | g0219 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18947 | hp2 | a0004 | c0026 | t0004 | g0080 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18948 | hp2 | a0006 | c0015 | t0003 | g0139 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18950 | hp1 | a0001 | c0006 | t0002 | g0276 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18951 | hp1 | a0002 | c0003 | t0010 | g0268 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18951 | hp2 | a0003 | c0023 | t0006 | g0237 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18960 | hp1 | a0002 | c0003 | t0004 | g0271 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18960 | hp2 | a0003 | c0004 | t0006 | g0097 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18963 | hp1 | a0005 | c0014 | t0001 | g0150 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18963 | hp2 | a0003 | c0004 | t0006 | g0002 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18964 | hp1 | a0001 | c0002 | t0017 | g0014 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18964 | hp2 | a0003 | c0004 | t0006 | g0119 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18970 | hp1 | a0006 | c0015 | t0003 | g0138 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18970 | hp2 | a0003 | c0004 | t0006 | g0120 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18972 | hp2 | a0002 | c0018 | t0010 | g0264 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18974 | hp1 | a0004 | c0005 | t0004 | g0047 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18974 | hp2 | a0005 | c0007 | t0001 | g0110 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18978 | hp1 | a0016 | c0053 | t0017 | g0239 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18978 | hp2 | a0003 | c0004 | t0007 | g0099 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18979 | hp1 | a0005 | c0047 | t0050 | g0130 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18979 | hp2 | a0005 | c0007 | t0001 | g0056 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18983 | hp1 | a0003 | c0004 | t0007 | g0121 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18983 | hp2 | a0005 | c0007 | t0005 | g0046 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18984 | hp1 | a0001 | c0001 | t0053 | g0013 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18984 | hp2 | a0002 | c0034 | t0006 | g0293 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18986 | hp1 | a0003 | c0004 | t0064 | g0107 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18986 | hp2 | a0002 | c0008 | t0010 | g0298 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18988 | hp1 | a0002 | c0034 | t0004 | g0083 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18989 | hp1 | a0023 | c0076 | t0006 | g0288 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18990 | hp1 | a0004 | c0005 | t0008 | g0058 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18990 | hp2 | a0003 | c0004 | t0006 | g0122 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18992 | hp2 | a0003 | c0004 | t0007 | g0017 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18993 | hp1 | a0006 | c0015 | t0003 | g0140 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18993 | hp2 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18998 | hp2 | a0003 | c0004 | t0007 | g0102 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18999 | hp1 | a0003 | c0004 | t0006 | g0118 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18999 | hp2 | a0004 | c0005 | t0004 | g0045 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19000 | hp1 | a0002 | c0003 | t0007 | g0131 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19002 | hp1 | a0003 | c0004 | t0006 | g0100 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19002 | hp2 | a0001 | c0002 | t0009 | g0109 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19003 | hp1 | a0005 | c0007 | t0001 | g0261 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19004 | hp1 | a0003 | c0004 | t0007 | g0152 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19005 | hp1 | a0004 | c0005 | t0010 | g0266 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19005 | hp2 | a0003 | c0004 | t0006 | g0101 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19007 | hp1 | a0001 | c0001 | t0020 | g0004 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19007 | hp2 | a0002 | c0003 | t0008 | g0081 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19010 | hp2 | a0003 | c0004 | t0006 | g0103 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19012 | hp1 | a0002 | c0061 | t0008 | g0253 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19012 | hp2 | a0002 | c0003 | t0007 | g0290 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19030 | hp1 | a0007 | c0043 | t0011 | g0325 | AFR | LWK | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19030 | hp2 | a0002 | c0064 | t0060 | g0250 | AFR | LWK | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19060 | hp1 | a0002 | c0003 | t0008 | g0283 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19060 | hp2 | a0001 | c0006 | t0001 | g0257 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19062 | hp1 | a0002 | c0003 | t0013 | g0049 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19062 | hp2 | a0005 | c0007 | t0054 | g0313 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19063 | hp2 | a0003 | c0004 | t0032 | g0123 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19064 | hp1 | a0003 | c0004 | t0007 | g0104 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19064 | hp2 | a0004 | c0005 | t0031 | g0059 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19065 | hp1 | a0005 | c0014 | t0001 | g0279 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19066 | hp2 | a0002 | c0008 | t0008 | g0255 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19067 | hp2 | a0003 | c0023 | t0007 | g0236 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19068 | hp2 | a0013 | c0029 | t0007 | g0153 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19070 | hp2 | a0004 | c0028 | t0012 | g0095 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19082 | hp1 | a0001 | c0006 | t0001 | g0258 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19082 | hp2 | a0003 | c0024 | t0004 | g0281 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19084 | hp2 | a0004 | c0005 | t0031 | g0061 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19085 | hp1 | a0006 | c0012 | t0005 | g0145 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19085 | hp2 | a0002 | c0003 | t0004 | g0015 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19086 | hp2 | a0007 | c0042 | t0013 | g0003 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19087 | hp2 | a0003 | c0004 | t0006 | g0114 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19088 | hp1 | a0004 | c0005 | t0004 | g0151 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19088 | hp2 | a0002 | c0018 | t0010 | g0241 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19090 | hp1 | a0002 | c0018 | t0013 | g0265 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19090 | hp2 | a0001 | c0006 | t0001 | g0108 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19091 | hp2 | a0004 | c0028 | t0012 | g0096 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19240 | hp1 | a0008 | c0033 | t0016 | g0221 | AFR | YRI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA19240 | hp2 | a0001 | c0037 | t0020 | g0030 | AFR | YRI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20752 | hp1 | a0006 | c0012 | t0001 | g0311 | EUR | TSI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20805 | hp1 | a0002 | c0008 | t0004 | g0192 | EUR | TSI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20805 | hp2 | a0001 | c0045 | t0002 | g0148 | EUR | TSI | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20905 | hp1 | a0002 | c0009 | t0046 | g0082 | SAS | GIH | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20905 | hp2 | a0001 | c0002 | t0018 | g0339 | SAS | GIH | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01123 | hp1 | a0003 | c0004 | t0006 | g0132 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0229 | AMR | CLM | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02109 | hp1 | a0002 | c0011 | t0015 | g0043 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02109 | hp2 | a0008 | c0032 | t0021 | g0328 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02486 | hp1 | a0012 | c0079 | t0016 | g0331 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02486 | hp2 | a0002 | c0058 | t0019 | g0209 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02559 | hp1 | a0002 | c0010 | t0016 | g0157 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG02559 | hp2 | a0001 | c0050 | t0003 | g0051 | AFR | ACB | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03471 | hp1 | a0009 | c0031 | t0036 | g0027 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG06807 | hp1 | a0002 | c0018 | t0022 | g0223 | AFR | USA | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| HG06807 | hp2 | a0002 | c0009 | t0012 | g0034 | AFR | USA | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18955 | hp1 | a0007 | c0038 | t0018 | g0159 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA18955 | hp2 | a0007 | c0027 | t0002 | g0012 | EAS | JPT | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20300 | hp1 | a0008 | c0032 | t0021 | g0329 | AFR | USA | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA20300 | hp2 | a0002 | c0008 | t0029 | g0162 | AFR | USA | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| NA21309 | hp2 | a0011 | c0054 | t0030 | g0319 | AFR | LWK | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0017 | g0143 | REF | REF | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0199 | REF | REF | SNED1_chr2_240993618_241100568 | SNED1 | chr2 | 240993618 | 241100568 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:240998897
|
C | CG | 1 | a0007 | 8 | HG01934.hp1 HG01993.hp1 HG03654.hp2 others(5): Show |
frameshift_variant | HIGH | c.64dupG | p.Val22fs | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/32 | 285/8394 | 65/4242 | 22/1413 | INFO_REALIGN_3_PRIME | chr2 | 240998897 | |
| chr2:241030470
|
G | A | 1 | a0014 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.400G>A | p.Val134Ile | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/32 | 620/8394 | 400/4242 | 134/1413 | chr2 | 241030470 | ||
| chr2:241040402
|
G | A | 1 | a0015 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1262G>A | p.Arg421His | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/32 | 1482/8394 | 1262/4242 | 421/1413 | chr2 | 241040402 | ||
| chr2:241062889
|
G | A | 5 | a0004a0005a0007others(2): Show | 37 | HG00423.hp2 HG00597.hp1 HG00738.hp1 others(34): Show |
missense_variant | MODERATE | c.2356G>A | p.Ala786Thr | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/32 | 2576/8394 | 2356/4242 | 786/1413 | chr2 | 241062889 | ||
| chr2:241064850
|
A | C | 1 | a0016 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.2606A>C | p.Asp869Ala | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/32 | 2826/8394 | 2606/4242 | 869/1413 | chr2 | 241064850 | ||
| chr2:241065331
|
A | G | 1 | a0012 | 2 | HG02486.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.2746A>G | p.Arg916Gly | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/32 | 2966/8394 | 2746/4242 | 916/1413 | chr2 | 241065331 | ||
| chr2:241065370
|
C | G | 1 | a0017 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2785C>G | p.Pro929Ala | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/32 | 3005/8394 | 2785/4242 | 929/1413 | chr2 | 241065370 | ||
| chr2:241065374
|
A | G | 1 | a0021 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.2789A>G | p.Asn930Ser | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/32 | 3009/8394 | 2789/4242 | 930/1413 | chr2 | 241065374 | ||
| chr2:241065469
|
C | T | 1 | a0018 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2884C>T | p.Arg962Cys | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/32 | 3104/8394 | 2884/4242 | 962/1413 | chr2 | 241065469 | ||
| chr2:241067769
|
C | T | 1 | a0007 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.3016C>T | p.Arg1006Cys | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/32 | 3236/8394 | 3016/4242 | 1006/1413 | chr2 | 241067769 | ||
| chr2:241067797
|
A | G | 1 | a0013 | 2 | HG02015.hp2 NA19068.hp2 |
missense_variant | MODERATE | c.3044A>G | p.Asn1015Ser | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/32 | 3264/8394 | 3044/4242 | 1015/1413 | chr2 | 241067797 | ||
| chr2:241067913
|
G | A | 1 | a0014 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.3160G>A | p.Asp1054Asn | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/32 | 3380/8394 | 3160/4242 | 1054/1413 | chr2 | 241067913 | ||
| chr2:241067925
|
A | G | 1 | a0016 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.3172A>G | p.Ser1058Gly | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/32 | 3392/8394 | 3172/4242 | 1058/1413 | chr2 | 241067925 | ||
| chr2:241070159
|
G | A | 1 | a0020 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.3547G>A | p.Gly1183Arg | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/32 | 3767/8394 | 3547/4242 | 1183/1413 | chr2 | 241070159 | ||
| chr2:241071651
|
C | T | 1 | a0022 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.3665C>T | p.Pro1222Leu | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 25/32 | 3885/8394 | 3665/4242 | 1222/1413 | chr2 | 241071651 | ||
| chr2:241071669
|
T | C | 5 | a0003a0006a0007others(2): Show | 48 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(45): Show |
missense_variant | MODERATE | c.3683T>C | p.Leu1228Pro | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 25/32 | 3903/8394 | 3683/4242 | 1228/1413 | chr2 | 241071669 | ||
| chr2:241071853
|
CAGCAAAG others(3): Show |
C | 1 | a0023 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.3793_3802delAGCAAA others(4): Show |
p.Ser1265fs | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/32 | 4013/8394 | 3793/4242 | 1265/1413 | chr2 | 241071853 | ||
| chr2:241071864
|
C | T | 1 | a0023 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.3803C>T | p.Ala1268Val | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/32 | 4023/8394 | 3803/4242 | 1268/1413 | chr2 | 241071864 | ||
| chr2:241071873
|
G | T | 1 | a0023 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.3812G>T | p.Arg1271Ile | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/32 | 4032/8394 | 3812/4242 | 1271/1413 | chr2 | 241071873 | ||
| chr2:241071874
|
A | C | 1 | a0023 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.3813A>C | p.Arg1271Ser | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/32 | 4033/8394 | 3813/4242 | 1271/1413 | chr2 | 241071874 | ||
| chr2:241073314
|
G | A | 2 | a0008a0009 | 12 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
missense_variant | MODERATE | c.3866G>A | p.Arg1289Gln | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/32 | 4086/8394 | 3866/4242 | 1289/1413 | chr2 | 241073314 | ||
| chr2:241073320
|
G | A | 1 | a0011 | 3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.3872G>A | p.Ser1291Asn | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/32 | 4092/8394 | 3872/4242 | 1291/1413 | chr2 | 241073320 | ||
| chr2:241073344
|
A | G | 2 | a0009a0010 | 9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
missense_variant | MODERATE | c.3896A>G | p.His1299Arg | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/32 | 4116/8394 | 3896/4242 | 1299/1413 | chr2 | 241073344 | ||
| chr2:241082318
|
G | A | 1 | a0019 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.4075G>A | p.Glu1359Lys | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/32 | 4295/8394 | 4075/4242 | 1359/1413 | chr2 | 241082318 | ||
| chr2:241082327
|
G | T | 15 | a0002a0003a0004others(12): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
missense_variant | MODERATE | c.4084G>T | p.Ala1362Ser | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/32 | 4304/8394 | 4084/4242 | 1362/1413 | chr2 | 241082327 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241033806
|
C | T | 14 | a0001c0037a0002c0009a0002c0019others(11): Show | 30 | HG00423.hp2 HG00597.hp1 HG01261.hp1 others(27): Show |
synonymous_variant | LOW | c.573C>T | p.Ile191Ile | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/32 | 793/8394 | 573/4242 | 191/1413 | chr2 | 241033806 | ||
| chr2:241033809
|
G | A | 1 | a0001c0045 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.576G>A | p.Val192Val | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/32 | 796/8394 | 576/4242 | 192/1413 | chr2 | 241033809 | ||
| chr2:241033857
|
C | T | 1 | a0002c0075 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.624C>T | p.Leu208Leu | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/32 | 844/8394 | 624/4242 | 208/1413 | chr2 | 241033857 | ||
| chr2:241034585
|
C | G | 4 | a0001c0074a0002c0011a0002c0036others(1): Show | 10 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
synonymous_variant | LOW | c.660C>G | p.Gly220Gly | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/32 | 880/8394 | 660/4242 | 220/1413 | chr2 | 241034585 | ||
| chr2:241034657
|
C | T | 1 | a0002c0084 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.732C>T | p.Asn244Asn | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/32 | 952/8394 | 732/4242 | 244/1413 | chr2 | 241034657 | ||
| chr2:241037292
|
C | T | 2 | a0002c0073a0011c0035 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.984C>T | p.His328His | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/32 | 1204/8394 | 984/4242 | 328/1413 | chr2 | 241037292 | ||
| chr2:241040133
|
T | C | 50 | a0001c0002a0001c0016a0001c0020others(47): Show | 163 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(160): Show |
synonymous_variant | LOW | c.1104T>C | p.Asn368Asn | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 7/32 | 1324/8394 | 1104/4242 | 368/1413 | chr2 | 241040133 | ||
| chr2:241040145
|
G | A | 1 | a0002c0022 | 3 | HG02257.hp1 HG02717.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1116G>A | p.Val372Val | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 7/32 | 1336/8394 | 1116/4242 | 372/1413 | chr2 | 241040145 | ||
| chr2:241040160
|
C | T | 1 | a0010c0017 | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.1131C>T | p.Ala377Ala | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 7/32 | 1351/8394 | 1131/4242 | 377/1413 | chr2 | 241040160 | ||
| chr2:241040361
|
G | T | 2 | a0001c0057a0002c0058 | 2 | HG02486.hp2 HG02896.hp1 |
synonymous_variant | LOW | c.1221G>T | p.Gly407Gly | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/32 | 1441/8394 | 1221/4242 | 407/1413 | chr2 | 241040361 | ||
| chr2:241051781
|
C | T | 1 | a0003c0056 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1773C>T | p.Asn591Asn | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 13/32 | 1993/8394 | 1773/4242 | 591/1413 | chr2 | 241051781 | ||
| chr2:241052458
|
G | A | 27 | a0001c0020a0002c0009a0002c0018others(24): Show | 101 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(98): Show |
synonymous_variant | LOW | c.2073G>A | p.Arg691Arg | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/32 | 2293/8394 | 2073/4242 | 691/1413 | chr2 | 241052458 | ||
| chr2:241053154
|
G | A | 1 | a0001c0060 | 1 | HG04228.hp2 | splice_region_variant&synonymous_variant | LOW | c.2085G>A | p.Glu695Glu | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/32 | 2305/8394 | 2085/4242 | 695/1413 | chr2 | 241053154 | ||
| chr2:241062846
|
C | T | 2 | a0001c0006a0002c0034 | 13 | HG00438.hp2 HG00673.hp1 HG02027.hp2 others(10): Show |
synonymous_variant | LOW | c.2313C>T | p.Arg771Arg | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/32 | 2533/8394 | 2313/4242 | 771/1413 | chr2 | 241062846 | ||
| chr2:241064070
|
C | T | 29 | a0001c0020a0002c0009a0002c0018others(26): Show | 104 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(101): Show |
synonymous_variant | LOW | c.2544C>T | p.Gly848Gly | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/32 | 2764/8394 | 2544/4242 | 848/1413 | chr2 | 241064070 | ||
| chr2:241064938
|
G | A | 3 | a0001c0050a0001c0057a0002c0058 | 3 | HG02486.hp2 HG02559.hp2 HG02896.hp1 |
synonymous_variant | LOW | c.2694G>A | p.Thr898Thr | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/32 | 2914/8394 | 2694/4242 | 898/1413 | chr2 | 241064938 | ||
| chr2:241065312
|
G | A | 1 | a0002c0061 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.2727G>A | p.Pro909Pro | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/32 | 2947/8394 | 2727/4242 | 909/1413 | chr2 | 241065312 | ||
| chr2:241065450
|
A | G | 51 | a0001c0016a0001c0020a0001c0068others(48): Show | 148 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(145): Show |
synonymous_variant | LOW | c.2865A>G | p.Thr955Thr | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/32 | 3085/8394 | 2865/4242 | 955/1413 | chr2 | 241065450 | ||
| chr2:241068935
|
C | T | 1 | a0015c0046 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.3219C>T | p.Tyr1073Tyr | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/32 | 3439/8394 | 3219/4242 | 1073/1413 | chr2 | 241068935 | ||
| chr2:241069939
|
C | T | 1 | a0001c0025 | 3 | HG02027.hp1 HG02056.hp1 HG02071.hp2 |
synonymous_variant | LOW | c.3327C>T | p.Asn1109Asn | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/32 | 3547/8394 | 3327/4242 | 1109/1413 | chr2 | 241069939 | ||
| chr2:241070110
|
G | A | 1 | a0009c0030 | 2 | HG03540.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.3498G>A | p.Pro1166Pro | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/32 | 3718/8394 | 3498/4242 | 1166/1413 | chr2 | 241070110 | ||
| chr2:241071610
|
G | A | 13 | a0001c0068a0001c0074a0002c0011others(10): Show | 25 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(22): Show |
synonymous_variant | LOW | c.3624G>A | p.Gln1208Gln | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 25/32 | 3844/8394 | 3624/4242 | 1208/1413 | chr2 | 241071610 | ||
| chr2:241081678
|
C | T | 1 | a0002c0064 | 1 | NA19030.hp2 | splice_region_variant&synonymous_variant | LOW | c.3918C>T | p.Asn1306Asn | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 28/32 | 4138/8394 | 3918/4242 | 1306/1413 | chr2 | 241081678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:240998651
|
C | T | 3 | a0003c0004t0064a0004c0005t0031a0004c0005t0065 | 4 | HG02074.hp1 NA18986.hp1 NA19064.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-187C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/32 | chr2 | 240998651 | ||||||
| chr2:241091675
|
G | A | 17 | a0002c0003t0006a0002c0003t0007a0002c0008t0033others(14): Show | 38 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*39G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3274 | chr2 | 241091675 | |||||
| chr2:241091692
|
G | A | 8 | a0002c0010t0014a0002c0019t0014a0002c0019t0026others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*56G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3291 | chr2 | 241091692 | |||||
| chr2:241091821
|
C | T | 8 | a0002c0003t0062a0002c0009t0016a0002c0010t0016others(5): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*185C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3420 | chr2 | 241091821 | |||||
| chr2:241091866
|
C | T | 26 | a0002c0003t0006a0002c0003t0007a0002c0008t0033others(23): Show | 49 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*230C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3465 | chr2 | 241091866 | |||||
| chr2:241091920
|
G | A | 8 | a0002c0010t0014a0002c0019t0014a0002c0019t0026others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*284G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3519 | chr2 | 241091920 | |||||
| chr2:241092152
|
C | T | 1 | a0002c0008t0061 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3751 | chr2 | 241092152 | |||||
| chr2:241092219
|
G | A | 4 | a0009c0030t0027a0009c0031t0028a0009c0031t0036others(1): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*583G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3818 | chr2 | 241092219 | |||||
| chr2:241092228
|
T | C | 1 | a0002c0003t0062 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3827 | chr2 | 241092228 | |||||
| chr2:241092229
|
A | G | 1 | a0001c0002t0059 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*593A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3828 | chr2 | 241092229 | |||||
| chr2:241092277
|
C | T | 1 | a0002c0073t0063 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*641C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3876 | chr2 | 241092277 | |||||
| chr2:241092396
|
G | A | 1 | a0002c0084t0037 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 3995 | chr2 | 241092396 | |||||
| chr2:241092533
|
CA | C | 8 | a0002c0003t0062a0002c0009t0016a0002c0010t0016others(5): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*899delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4134 | INFO_REALIGN_3_PRIME | chr2 | 241092533 | ||||
| chr2:241092791
|
C | T | 1 | a0001c0006t0058 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1155C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4390 | chr2 | 241092791 | |||||
| chr2:241092870
|
A | G | 1 | a0001c0020t0057 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4469 | chr2 | 241092870 | |||||
| chr2:241092933
|
C | T | 2 | a0010c0017t0024a0010c0017t0056 | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1297C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4532 | chr2 | 241092933 | |||||
| chr2:241093008
|
A | G | 9 | a0002c0011t0011a0002c0011t0015a0002c0013t0011others(6): Show | 16 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1372A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4607 | chr2 | 241093008 | |||||
| chr2:241093077
|
G | C | 4 | a0009c0030t0027a0009c0031t0028a0009c0031t0036others(1): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1441G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4676 | chr2 | 241093077 | |||||
| chr2:241093125
|
C | A | 125 | a0001c0001t0009a0001c0001t0017a0001c0002t0003others(122): Show | 221 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1489C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4724 | chr2 | 241093125 | |||||
| chr2:241093217
|
G | A | 5 | a0002c0003t0022a0002c0018t0022a0002c0055t0022others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1581G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4816 | chr2 | 241093217 | |||||
| chr2:241093249
|
G | A | 3 | a0008c0032t0021a0008c0051t0021a0008c0081t0021 | 4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1613G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4848 | chr2 | 241093249 | |||||
| chr2:241093253
|
A | C | 31 | a0002c0003t0008a0002c0003t0010a0002c0003t0013others(28): Show | 60 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1617A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4852 | chr2 | 241093253 | |||||
| chr2:241093259
|
G | A | 8 | a0002c0010t0014a0002c0019t0014a0002c0019t0026others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1623G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4858 | chr2 | 241093259 | |||||
| chr2:241093260
|
C | T | 1 | a0001c0001t0055 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1624C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4859 | chr2 | 241093260 | |||||
| chr2:241093294
|
C | T | 25 | a0002c0003t0004a0002c0003t0022a0002c0008t0004others(22): Show | 41 | HG01261.hp1 HG01433.hp1 HG01928.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1658C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4893 | chr2 | 241093294 | |||||
| chr2:241093316
|
C | T | 1 | a0005c0007t0054 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1680C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4915 | chr2 | 241093316 | |||||
| chr2:241093347
|
A | G | 25 | a0002c0003t0004a0002c0003t0022a0002c0008t0004others(22): Show | 41 | HG01261.hp1 HG01433.hp1 HG01928.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1711A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4946 | chr2 | 241093347 | |||||
| chr2:241093350
|
T | C | 1 | a0001c0002t0048 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1714T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 4949 | chr2 | 241093350 | |||||
| chr2:241093416
|
A | AGCCACAC others(78): Show |
1 | a0001c0001t0049 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1945_*2029dupCTTG others(81): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5265 | INFO_REALIGN_3_PRIME | chr2 | 241093416 | ||||
| chr2:241093416
|
AGCCACAC others(78): Show |
A | 32 | a0002c0003t0004a0002c0003t0022a0002c0008t0004others(29): Show | 48 | HG01261.hp1 HG01433.hp1 HG01891.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1945_*2029delCTTG others(81): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5180 | INFO_REALIGN_3_PRIME | chr2 | 241093416 | ||||
| chr2:241093462
|
TTGTGTCA others(77): Show |
T | 71 | a0002c0003t0006a0002c0003t0007a0002c0003t0008others(68): Show | 127 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1828_*1911delGTGT others(80): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5063 | INFO_REALIGN_3_PRIME | chr2 | 241093462 | ||||
| chr2:241093675
|
A | AGGACTTG others(56): Show |
1 | a0001c0001t0053 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2041_*2103dupGACT others(59): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5339 | INFO_REALIGN_3_PRIME | chr2 | 241093675 | ||||
| chr2:241093860
|
A | G | 7 | a0002c0008t0019a0002c0010t0019a0002c0010t0044others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2224A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5459 | chr2 | 241093860 | |||||
| chr2:241093975
|
T | C | 1 | a0002c0010t0044 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2339T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5574 | chr2 | 241093975 | |||||
| chr2:241093979
|
C | A | 21 | a0001c0001t0009a0001c0001t0017a0001c0002t0003others(18): Show | 45 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2343C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5578 | chr2 | 241093979 | |||||
| chr2:241093999
|
T | C | 1 | a0005c0047t0050 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2363T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5598 | chr2 | 241093999 | |||||
| chr2:241094046
|
G | C | 1 | a0001c0001t0051 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2410G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5645 | chr2 | 241094046 | |||||
| chr2:241094178
|
G | A | 33 | a0002c0003t0004a0002c0003t0022a0002c0008t0004others(30): Show | 49 | HG01261.hp1 HG01433.hp1 HG01891.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2542G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5777 | chr2 | 241094178 | |||||
| chr2:241094281
|
T | C | 41 | a0002c0003t0004a0002c0003t0022a0002c0008t0004others(38): Show | 64 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2645T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5880 | chr2 | 241094281 | |||||
| chr2:241094351
|
G | A | 1 | a0002c0008t0061 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2715G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5950 | chr2 | 241094351 | |||||
| chr2:241094355
|
T | A | 21 | a0001c0001t0009a0001c0001t0017a0001c0002t0003others(18): Show | 45 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2719T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 5954 | chr2 | 241094355 | |||||
| chr2:241094537
|
T | A | 1 | a0015c0046t0040 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2901T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6136 | chr2 | 241094537 | |||||
| chr2:241094545
|
C | T | 14 | a0002c0003t0008a0002c0003t0010a0002c0003t0013others(11): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2909C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6144 | chr2 | 241094545 | |||||
| chr2:241094651
|
G | T | 9 | a0002c0011t0011a0002c0011t0015a0002c0013t0011others(6): Show | 16 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3015G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6250 | chr2 | 241094651 | |||||
| chr2:241094688
|
G | A | 32 | a0002c0003t0004a0002c0003t0022a0002c0008t0004others(29): Show | 48 | HG01261.hp1 HG01433.hp1 HG01891.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3052G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6287 | chr2 | 241094688 | |||||
| chr2:241094734
|
C | T | 98 | a0001c0002t0043a0002c0003t0004a0002c0003t0006others(95): Show | 167 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*3098C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6333 | chr2 | 241094734 | |||||
| chr2:241094965
|
T | C | 125 | a0001c0001t0009a0001c0001t0017a0001c0002t0003others(122): Show | 221 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*3329T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6564 | chr2 | 241094965 | |||||
| chr2:241094980
|
C | T | 1 | a0002c0021t0047 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3344C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6579 | chr2 | 241094980 | |||||
| chr2:241095058
|
A | AAG | 6 | a0001c0001t0009a0001c0002t0009a0001c0016t0009others(3): Show | 12 | HG01169.hp2 HG01515.hp2 HG01891.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3422_*3423insAG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6658 | chr2 | 241095058 | |||||
| chr2:241095058
|
A | AAGC | 3 | a0001c0001t0017a0001c0002t0017a0016c0053t0017 | 6 | HG02735.hp2 HG03927.hp1 HG04184.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3422_*3423insAGC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6658 | chr2 | 241095058 | |||||
| chr2:241095059
|
C | A | 11 | a0001c0002t0003a0001c0002t0018a0001c0002t0041others(8): Show | 26 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3423C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6658 | chr2 | 241095059 | |||||
| chr2:241095060
|
G | C | 9 | a0001c0001t0009a0001c0001t0017a0001c0002t0009others(6): Show | 18 | HG01169.hp2 HG01515.hp2 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3424G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6659 | chr2 | 241095060 | |||||
| chr2:241095060
|
G | GC | 16 | a0001c0001t0005a0001c0001t0051a0001c0002t0003others(13): Show | 42 | HG00609.hp2 HG00621.hp1 HG01099.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3439dupC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6675 | INFO_REALIGN_3_PRIME | chr2 | 241095060 | ||||
| chr2:241095060
|
GC | G | 31 | a0001c0001t0002a0001c0001t0052a0001c0002t0002others(28): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3439delC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6674 | INFO_REALIGN_3_PRIME | chr2 | 241095060 | ||||
| chr2:241095060
|
GCC | G | 33 | a0001c0001t0020a0001c0001t0055a0001c0002t0020others(30): Show | 51 | HG00099.hp2 HG01099.hp2 HG01243.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3438_*3439delCC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6673 | INFO_REALIGN_3_PRIME | chr2 | 241095060 | ||||
| chr2:241095060
|
GCCC | G | 25 | a0002c0003t0013a0002c0003t0062a0002c0008t0029others(22): Show | 40 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*3437_*3439delCCC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6672 | INFO_REALIGN_3_PRIME | chr2 | 241095060 | ||||
| chr2:241095060
|
GCCCC | G | 14 | a0001c0020t0042a0002c0003t0010a0002c0008t0010others(11): Show | 20 | HG00438.hp1 HG00597.hp2 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3436_*3439delCCCC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6671 | INFO_REALIGN_3_PRIME | chr2 | 241095060 | ||||
| chr2:241095062
|
C | G | 1 | a0001c0002t0023 | 3 | HG02735.hp1 HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3426C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6661 | chr2 | 241095062 | |||||
| chr2:241095063
|
C | G | 1 | a0001c0001t0052 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3427C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6662 | chr2 | 241095063 | |||||
| chr2:241095074
|
C | A | 20 | a0001c0002t0043a0002c0003t0006a0002c0003t0007others(17): Show | 42 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3438C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6673 | chr2 | 241095074 | |||||
| chr2:241095075
|
C | A | 8 | a0002c0003t0062a0002c0009t0016a0002c0010t0016others(5): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3439C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6674 | chr2 | 241095075 | |||||
| chr2:241095075
|
C | G | 1 | a0002c0064t0060 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3439C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 6674 | chr2 | 241095075 | |||||
| chr2:241095535
|
A | T | 1 | a0003c0004t0032 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3899A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 32/32 | 7134 | chr2 | 241095535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:240999140
|
C | A | 1 | a0003c0004t0006g0002 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.213+90C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999140 | ||||||
| chr2:240999193
|
T | C | 1 | a0007c0042t0013g0003 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.213+143T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999193 | ||||||
| chr2:240999194
|
C | T | 3 | a0007c0042t0013g0003a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.213+144C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999194 | ||||||
| chr2:240999212
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0020g0004 | 2 | NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.213+162G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999212 | ||||||
| chr2:240999299
|
C | T | 3 | a0001c0001t0005g0340a0001c0002t0018g0339a0001c0020t0057g0341 | 3 | HG03831.hp2 HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.213+249C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999299 | ||||||
| chr2:240999311
|
G | C | 1 | a0003c0004t0007g0006 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.213+261G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999311 | ||||||
| chr2:240999318
|
C | G | 14 | a0001c0001t0001g0334a0001c0071t0003g0333a0002c0009t0004g0332others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.213+268C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999318 | ||||||
| chr2:240999350
|
G | A | 1 | a0007c0043t0011g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.213+300G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999350 | ||||||
| chr2:240999358
|
G | A | 2 | a0002c0073t0063g0007a0019c0070t0019g0008 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.213+308G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999358 | ||||||
| chr2:240999511
|
G | A | 1 | a0003c0056t0007g0009 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.213+461G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999511 | ||||||
| chr2:240999527
|
G | A | 1 | a0001c0001t0005g0010 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.213+477G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999527 | ||||||
| chr2:240999609
|
T | C | 11 | a0001c0001t0002g0018a0001c0001t0005g0019a0001c0001t0005g0021others(8): Show | 11 | HG01433.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+559T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999609 | ||||||
| chr2:240999891
|
C | T | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.213+841C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999891 | ||||||
| chr2:240999919
|
C | T | 1 | a0001c0002t0017g0323 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.213+869C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999919 | ||||||
| chr2:240999948
|
G | A | 1 | a0002c0036t0025g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+898G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 240999948 | ||||||
| chr2:241000138
|
C | A | 2 | a0002c0003t0022g0023a0018c0065t0038g0024 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.213+1088C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000138 | ||||||
| chr2:241000168
|
C | T | 1 | a0001c0001t0049g0322 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.213+1118C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000168 | ||||||
| chr2:241000179
|
C | T | 4 | a0001c0068t0018g0320a0002c0021t0047g0321a0002c0084t0037g0318others(1): Show | 4 | HG02615.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+1129C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000179 | ||||||
| chr2:241000192
|
A | G | 3 | a0002c0013t0015g0317a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.213+1142A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000192 | ||||||
| chr2:241000218
|
C | T | 1 | a0002c0083t0011g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.213+1168C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000218 | ||||||
| chr2:241000270
|
C | G | 1 | a0001c0002t0003g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.213+1220C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000270 | ||||||
| chr2:241000281
|
G | A | 1 | a0001c0001t0049g0322 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.213+1231G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000281 | ||||||
| chr2:241000306
|
C | T | 1 | a0001c0037t0002g0314 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.213+1256C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000306 | ||||||
| chr2:241000397
|
T | C | 1 | a0001c0001t0020g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.213+1347T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000397 | ||||||
| chr2:241000404
|
C | A | 1 | a0002c0036t0014g0326 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.213+1354C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000404 | ||||||
| chr2:241000424
|
G | A | 31 | a0001c0001t0001g0334a0001c0037t0020g0030a0001c0071t0003g0333others(28): Show | 31 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.213+1374G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000424 | ||||||
| chr2:241000439
|
A | C | 14 | a0001c0001t0001g0334a0001c0071t0003g0333a0002c0009t0004g0332others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.213+1389A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000439 | ||||||
| chr2:241000478
|
G | C | 4 | a0001c0001t0001g0044a0004c0005t0004g0045a0004c0005t0004g0047others(1): Show | 4 | NA18945.hp1 NA18974.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1428G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000478 | ||||||
| chr2:241000482
|
G | A | 4 | a0001c0068t0018g0320a0002c0021t0047g0321a0002c0084t0037g0318others(1): Show | 4 | HG02615.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+1432G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000482 | ||||||
| chr2:241000677
|
G | T | 4 | a0001c0068t0018g0320a0002c0021t0047g0321a0002c0084t0037g0318others(1): Show | 4 | HG02615.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+1627G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000677 | ||||||
| chr2:241000723
|
C | T | 1 | a0005c0007t0054g0313 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.213+1673C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000723 | ||||||
| chr2:241000869
|
G | A | 14 | a0001c0001t0001g0334a0001c0071t0003g0333a0002c0009t0004g0332others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.213+1819G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000869 | ||||||
| chr2:241000915
|
G | A | 1 | a0004c0026t0013g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.213+1865G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000915 | ||||||
| chr2:241000917
|
A | G | 165 | a0001c0001t0001g0238a0001c0001t0001g0244a0001c0001t0001g0245others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.213+1867A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000917 | ||||||
| chr2:241000985
|
A | G | 1 | a0014c0044t0005g0206 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.213+1935A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241000985 | ||||||
| chr2:241001208
|
C | T | 15 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0002g0301others(12): Show | 16 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.213+2158C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241001208 | ||||||
| chr2:241001341
|
C | T | 1 | a0001c0001t0005g0300 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.213+2291C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241001341 | ||||||
| chr2:241001573
|
G | C | 3 | a0002c0013t0011g0207a0002c0058t0019g0209a0009c0030t0027g0208 | 3 | HG02258.hp1 HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.213+2523G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241001573 | ||||||
| chr2:241001647
|
C | T | 5 | a0004c0005t0004g0202a0004c0005t0004g0203a0004c0005t0012g0201others(2): Show | 5 | HG01928.hp2 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+2597C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241001647 | ||||||
| chr2:241001983
|
G | A | 1 | a0003c0023t0004g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.213+2933G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241001983 | ||||||
| chr2:241002009
|
C | T | 1 | a0001c0020t0057g0341 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.213+2959C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002009 | ||||||
| chr2:241002123
|
C | T | 9 | a0001c0001t0001g0334a0001c0071t0003g0333a0002c0009t0004g0332others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+3073C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002123 | ||||||
| chr2:241002190
|
C | A | 4 | a0001c0001t0001g0303a0001c0001t0002g0301a0001c0001t0002g0304others(1): Show | 4 | HG00140.hp1 HG01074.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+3140C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002190 | ||||||
| chr2:241002356
|
G | A | 294 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.213+3306G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002356 | ||||||
| chr2:241002439
|
C | T | 2 | a0001c0001t0005g0021a0001c0001t0005g0299 | 2 | HG03831.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.213+3389C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002439 | ||||||
| chr2:241002573
|
C | T | 10 | a0001c0001t0001g0334a0001c0001t0002g0158a0001c0071t0003g0333others(7): Show | 10 | HG00741.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.213+3523C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002573 | ||||||
| chr2:241002694
|
C | T | 2 | a0001c0001t0005g0340a0001c0002t0018g0339 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.213+3644C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002694 | ||||||
| chr2:241002834
|
T | A | 116 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(113): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.213+3784T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002834 | ||||||
| chr2:241002909
|
C | T | 1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.213+3859C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002909 | ||||||
| chr2:241002951
|
C | T | 50 | a0001c0001t0001g0295a0001c0001t0002g0280a0001c0001t0002g0294others(47): Show | 50 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.213+3901C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002951 | ||||||
| chr2:241002984
|
G | A | 2 | a0002c0003t0022g0023a0018c0065t0038g0024 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.213+3934G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241002984 | ||||||
| chr2:241003036
|
A | C | 3 | a0001c0001t0002g0158a0002c0011t0015g0043a0002c0052t0011g0256 | 3 | HG00741.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.213+3986A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003036 | ||||||
| chr2:241003115
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+4065C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003115 | ||||||
| chr2:241003153
|
C | A | 1 | a0002c0084t0037g0318 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.213+4103C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003153 | ||||||
| chr2:241003248
|
A | G | 1 | a0003c0004t0006g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.213+4198A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003248 | ||||||
| chr2:241003304
|
T | C | 1 | a0002c0009t0016g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.213+4254T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003304 | ||||||
| chr2:241003350
|
G | T | 1 | a0002c0008t0008g0255 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.213+4300G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003350 | ||||||
| chr2:241003471
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.213+4421C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003471 | ||||||
| chr2:241003491
|
T | C | 6 | a0002c0009t0016g0220a0002c0010t0014g0222a0002c0018t0022g0223others(3): Show | 6 | HG01884.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+4441T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003491 | ||||||
| chr2:241003517
|
C | A | 2 | a0011c0035t0025g0342a0011c0035t0025g0343 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.213+4467C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003517 | ||||||
| chr2:241003783
|
G | C | 10 | a0001c0001t0001g0334a0001c0001t0002g0158a0001c0071t0003g0333others(7): Show | 10 | HG00741.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.213+4733G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003783 | ||||||
| chr2:241003836
|
C | T | 12 | a0001c0001t0001g0303a0001c0001t0002g0301a0001c0001t0002g0304others(9): Show | 13 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+4786C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003836 | ||||||
| chr2:241003897
|
G | A | 2 | a0001c0006t0001g0257a0001c0006t0001g0258 | 2 | NA19060.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.213+4847G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241003897 | ||||||
| chr2:241004033
|
A | G | 70 | a0001c0001t0001g0295a0001c0001t0001g0334a0001c0001t0002g0005others(67): Show | 70 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.213+4983A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004033 | ||||||
| chr2:241004117
|
T | C | 4 | a0002c0011t0015g0043a0002c0013t0015g0317a0002c0021t0047g0321others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+5067T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004117 | ||||||
| chr2:241004158
|
A | G | 156 | a0001c0001t0001g0238a0001c0001t0001g0244a0001c0001t0001g0245others(153): Show | 157 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.213+5108A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004158 | ||||||
| chr2:241004286
|
T | A | 1 | a0002c0003t0013g0049 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.213+5236T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004286 | ||||||
| chr2:241004314
|
G | A | 2 | a0002c0084t0037g0318a0011c0054t0030g0319 | 2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.213+5264G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004314 | ||||||
| chr2:241004475
|
T | A | 1 | a0002c0003t0013g0049 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.213+5425T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004475 | ||||||
| chr2:241004485
|
T | G | 58 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(55): Show | 58 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.213+5435T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004485 | ||||||
| chr2:241004531
|
AT | A | 66 | a0001c0001t0001g0238a0001c0001t0001g0244a0001c0001t0001g0245others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.213+5488delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241004531 | |||||
| chr2:241004585
|
AAAT | A | 25 | a0001c0037t0020g0030a0002c0009t0004g0040a0002c0009t0012g0034others(22): Show | 25 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.213+5540_213+5542d others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241004585 | |||||
| chr2:241004606
|
A | C | 1 | a0001c0020t0042g0154 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.213+5556A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004606 | ||||||
| chr2:241004722
|
TTTTG | T | 3 | a0001c0068t0018g0320a0002c0084t0037g0318a0011c0054t0030g0319 | 3 | HG02615.hp2 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.213+5684_213+5687d others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241004722 | |||||
| chr2:241004780
|
T | TG | 6 | a0002c0009t0004g0040a0002c0019t0014g0041a0002c0019t0026g0155others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+5732dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241004780 | |||||
| chr2:241004867
|
G | A | 88 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(85): Show | 88 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.213+5817G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004867 | ||||||
| chr2:241004873
|
G | C | 154 | a0001c0001t0001g0238a0001c0001t0001g0244a0001c0001t0001g0245others(151): Show | 155 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.213+5823G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241004873 | ||||||
| chr2:241005159
|
T | A | 5 | a0001c0050t0003g0051a0002c0010t0016g0157a0002c0036t0025g0022others(2): Show | 5 | HG02559.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+6109T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005159 | ||||||
| chr2:241005193
|
CTGTTTT | C | 57 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(54): Show | 57 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.213+6162_213+6167d others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241005193 | |||||
| chr2:241005297
|
G | A | 2 | a0001c0002t0059g0053a0002c0021t0047g0321 | 2 | HG03516.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.213+6247G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005297 | ||||||
| chr2:241005485
|
T | A | 1 | a0001c0006t0001g0054 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.213+6435T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005485 | ||||||
| chr2:241005561
|
T | G | 184 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(181): Show | 184 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.213+6511T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005561 | ||||||
| chr2:241005687
|
G | T | 1 | a0001c0006t0001g0054 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.213+6637G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005687 | ||||||
| chr2:241005688
|
T | G | 1 | a0001c0006t0001g0054 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.213+6638T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005688 | ||||||
| chr2:241005779
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.213+6729C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005779 | ||||||
| chr2:241005787
|
A | G | 1 | a0002c0021t0004g0198 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.213+6737A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005787 | ||||||
| chr2:241005887
|
T | C | 3 | a0001c0016t0003g0216a0002c0052t0011g0256a0002c0064t0060g0250 | 3 | HG02615.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.213+6837T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005887 | ||||||
| chr2:241005924
|
G | A | 3 | a0001c0002t0009g0211a0003c0004t0006g0132a0003c0004t0006g0135 | 3 | HG01123.hp1 HG01516.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.213+6874G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005924 | ||||||
| chr2:241005928
|
G | A | 30 | a0001c0016t0003g0216a0001c0037t0020g0030a0002c0009t0004g0040others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.213+6878G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241005928 | ||||||
| chr2:241006099
|
C | T | 88 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(85): Show | 88 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.213+7049C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006099 | ||||||
| chr2:241006148
|
A | T | 1 | a0001c0006t0001g0054 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.213+7098A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006148 | ||||||
| chr2:241006519
|
G | A | 5 | a0001c0016t0003g0216a0002c0052t0011g0256a0002c0058t0019g0209others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+7469G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006519 | ||||||
| chr2:241006613
|
A | G | 1 | a0002c0008t0010g0298 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.213+7563A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006613 | ||||||
| chr2:241006755
|
G | A | 90 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0217others(87): Show | 90 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.213+7705G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006755 | ||||||
| chr2:241006839
|
G | A | 30 | a0001c0016t0003g0216a0001c0037t0020g0030a0002c0009t0004g0040others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.213+7789G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006839 | ||||||
| chr2:241006897
|
A | G | 89 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0217others(86): Show | 89 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.213+7847A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006897 | ||||||
| chr2:241006951
|
G | T | 25 | a0001c0037t0020g0030a0002c0009t0004g0040a0002c0009t0012g0034others(22): Show | 25 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.213+7901G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006951 | ||||||
| chr2:241006980
|
G | A | 6 | a0001c0001t0002g0252a0002c0003t0008g0259a0002c0003t0010g0260others(3): Show | 6 | HG00609.hp1 HG00621.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+7930G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241006980 | ||||||
| chr2:241007116
|
G | A | 90 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0217others(87): Show | 90 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.213+8066G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007116 | ||||||
| chr2:241007308
|
G | C | 1 | a0001c0002t0003g0161 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.213+8258G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007308 | ||||||
| chr2:241007368
|
T | C | 3 | a0002c0018t0010g0264a0002c0018t0013g0265a0007c0042t0013g0003 | 3 | NA18972.hp2 NA19086.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.213+8318T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007368 | ||||||
| chr2:241007381
|
C | T | 1 | a0003c0056t0007g0009 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.213+8331C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007381 | ||||||
| chr2:241007516
|
A | G | 128 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(125): Show | 128 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.213+8466A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007516 | ||||||
| chr2:241007566
|
G | A | 2 | a0011c0035t0025g0342a0011c0035t0025g0343 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.213+8516G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007566 | ||||||
| chr2:241007582
|
T | C | 306 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.213+8532T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007582 | ||||||
| chr2:241007680
|
G | A | 2 | a0002c0011t0015g0043a0002c0021t0047g0321 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.213+8630G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007680 | ||||||
| chr2:241007705
|
G | A | 290 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(287): Show | 290 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.213+8655G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007705 | ||||||
| chr2:241007731
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.213+8681G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241007731 | ||||||
| chr2:241008052
|
G | A | 179 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(176): Show | 179 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.213+9002G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008052 | ||||||
| chr2:241008112
|
G | A | 1 | a0001c0001t0049g0322 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.213+9062G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008112 | ||||||
| chr2:241008122
|
C | T | 1 | a0019c0070t0019g0008 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.213+9072C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008122 | ||||||
| chr2:241008177
|
A | G | 60 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0217others(57): Show | 60 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.213+9127A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008177 | ||||||
| chr2:241008291
|
G | A | 1 | a0001c0020t0057g0341 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.213+9241G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008291 | ||||||
| chr2:241008302
|
G | A | 2 | a0011c0035t0025g0342a0011c0035t0025g0343 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.213+9252G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008302 | ||||||
| chr2:241008429
|
C | T | 1 | a0002c0075t0045g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+9379C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008429 | ||||||
| chr2:241008843
|
A | G | 1 | a0001c0001t0049g0322 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.213+9793A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241008843 | ||||||
| chr2:241009064
|
A | G | 303 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.213+10014A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009064 | ||||||
| chr2:241009213
|
T | C | 263 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.213+10163T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009213 | ||||||
| chr2:241009294
|
G | T | 2 | a0001c0060t0005g0193a0002c0003t0013g0194 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.213+10244G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009294 | ||||||
| chr2:241009314
|
G | A | 10 | a0001c0016t0003g0216a0001c0037t0002g0314a0002c0011t0015g0043others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+10264G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009314 | ||||||
| chr2:241009344
|
G | A | 35 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(32): Show | 35 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.213+10294G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009344 | ||||||
| chr2:241009460
|
G | C | 1 | a0002c0010t0019g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+10410G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009460 | ||||||
| chr2:241009638
|
C | T | 1 | a0002c0008t0004g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.213+10588C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009638 | ||||||
| chr2:241009682
|
C | T | 1 | a0001c0002t0048g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.213+10632C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009682 | ||||||
| chr2:241009683
|
G | A | 25 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0002g0055others(22): Show | 25 | HG00140.hp2 HG01074.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.213+10633G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009683 | ||||||
| chr2:241009689
|
G | A | 1 | a0001c0025t0003g0074 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.213+10639G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009689 | ||||||
| chr2:241009793
|
TGTCCCAT others(18): Show |
T | 42 | a0001c0002t0001g0075a0001c0016t0003g0216a0001c0037t0020g0030others(39): Show | 42 | HG01884.hp1 HG02083.hp1 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.213+10769_213+1079 others(29): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241009793 | |||||
| chr2:241009859
|
C | T | 5 | a0002c0011t0015g0036a0002c0011t0015g0043a0002c0013t0015g0317others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+10809C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009859 | ||||||
| chr2:241009860
|
G | A | 15 | a0001c0001t0001g0334a0001c0001t0002g0158a0001c0071t0003g0333others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.213+10810G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009860 | ||||||
| chr2:241009944
|
G | A | 65 | a0001c0001t0002g0005a0001c0001t0002g0158a0001c0001t0002g0252others(62): Show | 65 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.213+10894G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009944 | ||||||
| chr2:241009964
|
G | A | 4 | a0001c0001t0052g0147a0002c0003t0062g0077a0002c0009t0004g0146others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+10914G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009964 | ||||||
| chr2:241009984
|
G | A | 2 | a0001c0002t0003g0136a0001c0002t0059g0053 | 2 | HG03669.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.213+10934G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241009984 | ||||||
| chr2:241010128
|
G | A | 3 | a0001c0068t0018g0320a0002c0084t0037g0318a0011c0054t0030g0319 | 3 | HG02615.hp2 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.213+11078G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010128 | ||||||
| chr2:241010156
|
G | A | 1 | a0001c0001t0005g0200 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.213+11106G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010156 | ||||||
| chr2:241010219
|
C | CT | 4 | a0002c0008t0019g0227a0004c0026t0004g0228a0010c0017t0024g0225others(1): Show | 4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+11170dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241010219 | |||||
| chr2:241010249
|
G | A | 1 | a0002c0013t0011g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.213+11199G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010249 | ||||||
| chr2:241010286
|
T | C | 57 | a0001c0001t0001g0117a0001c0001t0001g0163a0001c0001t0001g0166others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.213+11236T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010286 | ||||||
| chr2:241010324
|
C | T | 1 | a0001c0002t0005g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.213+11274C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010324 | ||||||
| chr2:241010619
|
G | T | 3 | a0001c0068t0018g0320a0002c0084t0037g0318a0011c0054t0030g0319 | 3 | HG02615.hp2 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.213+11569G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010619 | ||||||
| chr2:241010808
|
G | C | 1 | a0014c0044t0005g0206 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.213+11758G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010808 | ||||||
| chr2:241010865
|
C | G | 1 | a0002c0011t0011g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213+11815C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241010865 | ||||||
| chr2:241011029
|
A | C | 1 | a0003c0004t0006g0114 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.213+11979A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011029 | ||||||
| chr2:241011054
|
G | GCCTGGGG others(29): Show |
71 | a0001c0001t0001g0098a0001c0001t0001g0189a0001c0001t0002g0217others(68): Show | 71 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.213+12038_213+1207 others(40): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011054 | |||||
| chr2:241011076
|
G | GGGTCTCC others(218): Show |
1 | a0002c0013t0011g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.213+12090_213+1209 others(229): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011076 | |||||
| chr2:241011076
|
G | GGGTCTCC others(56): Show |
1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.213+12073_213+1207 others(67): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011076 | |||||
| chr2:241011076
|
G | GGGTCTCC others(218): Show |
5 | a0002c0010t0044g0078a0002c0011t0011g0234a0002c0013t0011g0214others(2): Show | 5 | HG01099.hp2 HG01891.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+12073_213+1207 others(229): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011076 | |||||
| chr2:241011076
|
G | GGGTCTCC others(227): Show |
18 | a0001c0001t0001g0117a0001c0001t0001g0238a0001c0001t0002g0129others(15): Show | 18 | HG02015.hp1 HG02080.hp2 HG02273.hp2 others(15): Show |
intron_variant | MODIFIER | c.213+12073_213+1207 others(238): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011076 | |||||
| chr2:241011082
|
C | T | 1 | a0007c0041t0007g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.213+12032C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011082 | ||||||
| chr2:241011103
|
A | AGGTCTCC others(2): Show |
19 | a0001c0037t0020g0030a0002c0009t0004g0040a0002c0009t0012g0034others(16): Show | 19 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.213+12065_213+1207 others(13): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011103 | |||||
| chr2:241011103
|
A | AGGTCTCC others(65): Show |
1 | a0002c0036t0025g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+12073_213+1207 others(76): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011103 | |||||
| chr2:241011114
|
GTCTCCTG others(20): Show |
G | 63 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(60): Show | 63 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.213+12074_213+1210 others(31): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011114 | |||||
| chr2:241011139
|
G | GGGTCTCC others(11): Show |
19 | a0001c0037t0020g0030a0002c0009t0004g0040a0002c0009t0012g0034others(16): Show | 19 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.213+12090_213+1209 others(22): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011139 | |||||
| chr2:241011141
|
T | A | 24 | a0001c0001t0001g0334a0001c0001t0002g0158a0001c0016t0003g0216others(21): Show | 24 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.213+12091T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011141 | ||||||
| chr2:241011141
|
T | G | 138 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0001g0189others(135): Show | 139 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.213+12091T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011141 | ||||||
| chr2:241011163
|
G | T | 36 | a0001c0001t0002g0005a0001c0001t0002g0252a0001c0001t0002g0280others(33): Show | 36 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.213+12113G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011163 | ||||||
| chr2:241011164
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0060 | 2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.213+12114G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011164 | ||||||
| chr2:241011165
|
C | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0060 | 2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.213+12115C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011165 | ||||||
| chr2:241011166
|
AGGTCTCC others(2): Show |
A | 63 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(60): Show | 63 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.213+12137_213+1214 others(13): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011166 | |||||
| chr2:241011175
|
GGGTCTCC others(20): Show |
G | 8 | a0001c0016t0003g0216a0002c0010t0014g0038a0002c0011t0015g0036others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+12146_213+1217 others(31): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011175 | |||||
| chr2:241011211
|
GGGTCTCC others(20): Show |
G | 64 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(61): Show | 64 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.213+12185_213+1221 others(31): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011211 | |||||
| chr2:241011233
|
G | C | 1 | a0002c0008t0061g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.213+12183G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011233 | ||||||
| chr2:241011235
|
T | G | 18 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0002g0196others(15): Show | 19 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.213+12185T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011235 | ||||||
| chr2:241011238
|
A | AGGTCTCC others(20): Show |
4 | a0001c0068t0018g0320a0002c0009t0046g0082a0002c0084t0037g0318others(1): Show | 4 | HG02615.hp2 HG03139.hp2 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+12199_213+1220 others(31): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011238
|
A | AGGTCTCC others(29): Show |
109 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0001g0189others(106): Show | 109 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.213+12201_213+1223 others(40): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011238
|
A | AGGTCTCC others(182): Show |
1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.213+12235_213+1223 others(193): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011238
|
A | AGGTCTCC others(92): Show |
1 | a0002c0036t0025g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.213+12235_213+1223 others(103): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011238
|
A | AGGTCTCC others(182): Show |
1 | a0002c0010t0014g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.213+12235_213+1223 others(193): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011238
|
A | AGGTCTCC others(182): Show |
5 | a0002c0018t0022g0223a0002c0058t0019g0209a0002c0073t0063g0007others(2): Show | 5 | HG02486.hp2 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+12235_213+1223 others(193): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011238
|
A | AGGTCTCC others(218): Show |
1 | a0002c0010t0019g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+12208_213+1220 others(229): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011238
|
A | AGGTCTCC others(227): Show |
15 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0002g0301others(12): Show | 16 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.213+12208_213+1220 others(238): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011238 | |||||
| chr2:241011251
|
C | CTCCTGGG others(29): Show |
1 | a0002c0013t0011g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.213+12235_213+1227 others(40): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241011251 | |||||
| chr2:241011424
|
C | T | 22 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0002g0301others(19): Show | 23 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.213+12374C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011424 | ||||||
| chr2:241011443
|
C | T | 22 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0002g0301others(19): Show | 23 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.213+12393C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011443 | ||||||
| chr2:241011592
|
A | G | 225 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0001g0189others(222): Show | 226 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.213+12542A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011592 | ||||||
| chr2:241011793
|
C | T | 26 | a0001c0001t0001g0098a0001c0020t0001g0105a0001c0025t0009g0291others(23): Show | 26 | HG00558.hp2 HG00673.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.213+12743C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011793 | ||||||
| chr2:241011804
|
C | T | 1 | a0002c0011t0011g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.213+12754C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011804 | ||||||
| chr2:241011884
|
G | A | 1 | a0001c0002t0003g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.213+12834G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241011884 | ||||||
| chr2:241012000
|
C | T | 30 | a0001c0001t0001g0117a0001c0001t0001g0238a0001c0001t0002g0129others(27): Show | 30 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.213+12950C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012000 | ||||||
| chr2:241012007
|
C | T | 30 | a0001c0001t0001g0117a0001c0001t0001g0238a0001c0001t0002g0129others(27): Show | 30 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.213+12957C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012007 | ||||||
| chr2:241012034
|
G | A | 225 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0001g0189others(222): Show | 226 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.213+12984G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012034 | ||||||
| chr2:241012037
|
C | T | 63 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(60): Show | 63 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.213+12987C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012037 | ||||||
| chr2:241012078
|
C | G | 76 | a0001c0001t0001g0098a0001c0001t0001g0189a0001c0001t0002g0217others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.213+13028C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012078 | ||||||
| chr2:241012133
|
T | TG | 7 | a0001c0001t0001g0170a0001c0001t0002g0156a0001c0001t0005g0010others(4): Show | 7 | HG00099.hp1 HG01123.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+13089dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241012133 | |||||
| chr2:241012229
|
A | G | 1 | a0001c0016t0003g0216 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.213+13179A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012229 | ||||||
| chr2:241012271
|
C | T | 2 | a0011c0035t0025g0342a0011c0035t0025g0343 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.213+13221C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012271 | ||||||
| chr2:241012332
|
A | T | 1 | a0021c0078t0016g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+13282A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012332 | ||||||
| chr2:241012365
|
A | C | 6 | a0002c0010t0014g0038a0002c0011t0011g0128a0002c0011t0015g0036others(3): Show | 6 | HG02258.hp2 HG02717.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+13315A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012365 | ||||||
| chr2:241012405
|
G | C | 4 | a0001c0001t0051g0270a0002c0003t0010g0268a0003c0024t0004g0269others(1): Show | 4 | HG02129.hp1 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+13355G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012405 | ||||||
| chr2:241012693
|
G | A | 75 | a0001c0001t0001g0098a0001c0001t0001g0189a0001c0001t0002g0217others(72): Show | 75 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.213+13643G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012693 | ||||||
| chr2:241012824
|
T | C | 5 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0002g0301others(2): Show | 5 | HG00140.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+13774T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012824 | ||||||
| chr2:241012825
|
CT | C | 128 | a0001c0001t0001g0098a0001c0001t0001g0189a0001c0001t0001g0295others(125): Show | 128 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.213+13791delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241012825 | |||||
| chr2:241012825
|
CTT | C | 88 | a0001c0001t0001g0117a0001c0001t0001g0238a0001c0001t0001g0303others(85): Show | 89 | HG00099.hp2 HG00140.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.213+13790_213+1379 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241012825 | |||||
| chr2:241012827
|
T | C | 3 | a0002c0008t0019g0227a0010c0017t0024g0225a0010c0017t0056g0226 | 3 | HG01243.hp1 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.213+13777T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012827 | ||||||
| chr2:241012828
|
T | G | 1 | a0003c0024t0010g0286 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.213+13778T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012828 | ||||||
| chr2:241012829
|
T | G | 62 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(59): Show | 62 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.213+13779T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012829 | ||||||
| chr2:241012839
|
T | G | 1 | a0001c0006t0001g0108 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.213+13789T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241012839 | ||||||
| chr2:241013126
|
G | A | 1 | a0010c0017t0024g0338 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.213+14076G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013126 | ||||||
| chr2:241013129
|
C | T | 2 | a0001c0002t0023g0246a0001c0002t0023g0247 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.213+14079C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013129 | ||||||
| chr2:241013130
|
G | A | 14 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0002g0301others(11): Show | 15 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.213+14080G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013130 | ||||||
| chr2:241013142
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.213+14092T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013142 | ||||||
| chr2:241013478
|
C | T | 100 | a0001c0001t0001g0295a0001c0001t0001g0303a0001c0001t0001g0305others(97): Show | 101 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.213+14428C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013478 | ||||||
| chr2:241013513
|
C | A | 1 | a0002c0003t0010g0260 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.213+14463C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013513 | ||||||
| chr2:241013682
|
C | T | 1 | a0002c0061t0008g0253 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.213+14632C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013682 | ||||||
| chr2:241013834
|
G | A | 76 | a0001c0001t0001g0295a0001c0001t0001g0303a0001c0001t0001g0305others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.213+14784G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013834 | ||||||
| chr2:241013919
|
A | G | 1 | a0002c0013t0011g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.213+14869A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013919 | ||||||
| chr2:241013953
|
G | T | 1 | a0007c0027t0001g0267 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.213+14903G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241013953 | ||||||
| chr2:241014040
|
G | A | 1 | a0006c0012t0005g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.213+14990G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014040 | ||||||
| chr2:241014061
|
C | T | 154 | a0001c0001t0001g0117a0001c0001t0001g0238a0001c0001t0001g0295others(151): Show | 155 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.213+15011C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014061 | ||||||
| chr2:241014080
|
T | C | 154 | a0001c0001t0001g0117a0001c0001t0001g0238a0001c0001t0001g0295others(151): Show | 155 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.213+15030T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014080 | ||||||
| chr2:241014090
|
C | T | 60 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(57): Show | 60 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.213+15040C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014090 | ||||||
| chr2:241014248
|
A | G | 1 | a0002c0013t0011g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.213+15198A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014248 | ||||||
| chr2:241014254
|
C | G | 60 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(57): Show | 60 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.213+15204C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014254 | ||||||
| chr2:241014296
|
A | G | 1 | a0002c0011t0015g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.213+15246A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014296 | ||||||
| chr2:241014412
|
G | A | 17 | a0001c0037t0020g0030a0002c0010t0016g0033a0002c0011t0011g0029others(14): Show | 17 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.213+15362G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014412 | ||||||
| chr2:241014445
|
G | A | 23 | a0001c0001t0001g0334a0001c0001t0002g0158a0001c0071t0003g0333others(20): Show | 23 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.213+15395G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014445 | ||||||
| chr2:241014452
|
G | A | 1 | a0002c0036t0014g0326 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.213+15402G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014452 | ||||||
| chr2:241014549
|
A | G | 1 | a0003c0056t0007g0009 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.213+15499A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014549 | ||||||
| chr2:241014601
|
A | G | 7 | a0001c0016t0003g0216a0001c0068t0018g0320a0002c0009t0004g0040others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+15551A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014601 | ||||||
| chr2:241014667
|
A | G | 50 | a0001c0001t0001g0117a0001c0001t0001g0238a0001c0001t0001g0334others(47): Show | 50 | HG00741.hp2 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.213+15617A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014667 | ||||||
| chr2:241014692
|
T | A | 1 | a0002c0003t0004g0011 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.214-15592T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014692 | ||||||
| chr2:241014974
|
T | C | 2 | a0002c0003t0004g0271a0004c0005t0010g0266 | 2 | NA18960.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.214-15310T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241014974 | ||||||
| chr2:241015141
|
G | A | 1 | a0022c0059t0004g0126 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.214-15143G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015141 | ||||||
| chr2:241015231
|
G | A | 2 | a0002c0011t0011g0029a0002c0011t0015g0028 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.214-15053G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015231 | ||||||
| chr2:241015251
|
A | G | 43 | a0001c0001t0005g0092a0001c0001t0052g0147a0001c0002t0001g0075others(40): Show | 43 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.214-15033A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015251 | ||||||
| chr2:241015528
|
A | G | 1 | a0001c0002t0018g0160 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.214-14756A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015528 | ||||||
| chr2:241015543
|
C | G | 3 | a0002c0013t0011g0207a0002c0013t0015g0317a0002c0075t0045g0251 | 3 | HG02258.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.214-14741C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015543 | ||||||
| chr2:241015621
|
C | T | 12 | a0001c0001t0002g0280a0001c0001t0002g0297a0002c0003t0007g0284others(9): Show | 12 | HG01081.hp2 HG01175.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.214-14663C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015621 | ||||||
| chr2:241015628
|
C | T | 1 | a0002c0003t0008g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.214-14656C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015628 | ||||||
| chr2:241015664
|
G | A | 2 | a0001c0002t0001g0171a0001c0002t0001g0172 | 2 | HG02132.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.214-14620G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015664 | ||||||
| chr2:241015708
|
T | TGCTGGCC others(97): Show |
1 | a0004c0026t0004g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.214-14477_214-1447 others(108): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241015708 | |||||
| chr2:241015720
|
C | CCTCCAAT others(149): Show |
62 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(59): Show | 62 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.214-14517_214-1451 others(160): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241015720 | |||||
| chr2:241015720
|
C | CCTCCAAT others(149): Show |
1 | a0002c0008t0008g0255 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.214-14517_214-1451 others(160): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241015720 | |||||
| chr2:241015725
|
A | C | 1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.214-14559A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015725 | ||||||
| chr2:241015768
|
A | G | 2 | a0002c0010t0014g0038a0002c0036t0025g0022 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214-14516A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015768 | ||||||
| chr2:241015778
|
G | A | 6 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-14506G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015778 | ||||||
| chr2:241015795
|
G | A | 1 | a0008c0033t0030g0335 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.214-14489G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015795 | ||||||
| chr2:241015867
|
G | A | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.214-14417G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015867 | ||||||
| chr2:241015873
|
T | G | 7 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-14411T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015873 | ||||||
| chr2:241015922
|
T | C | 63 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(60): Show | 63 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.214-14362T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015922 | ||||||
| chr2:241015953
|
C | T | 62 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(59): Show | 63 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.214-14331C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241015953 | ||||||
| chr2:241016047
|
A | ATTAATGG others(23): Show |
97 | a0001c0001t0001g0189a0001c0001t0001g0295a0001c0001t0002g0005others(94): Show | 97 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.214-14185_214-1415 others(34): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016047 | |||||
| chr2:241016047
|
A | ATTAATGG others(53): Show |
2 | a0002c0010t0014g0038a0002c0036t0025g0022 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214-14215_214-1415 others(64): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016047 | |||||
| chr2:241016066
|
A | AATAAAGT others(23): Show |
1 | a0002c0008t0029g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.214-14189_214-1418 others(34): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016066 | |||||
| chr2:241016177
|
T | A | 7 | a0002c0008t0061g0168a0002c0013t0011g0207a0002c0013t0011g0214others(4): Show | 7 | HG01099.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-14107T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016177 | ||||||
| chr2:241016188
|
A | AT | 50 | a0001c0001t0001g0071a0001c0001t0001g0166a0001c0001t0001g0167others(47): Show | 50 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.214-14072dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016188 | |||||
| chr2:241016188
|
AT | A | 88 | a0001c0001t0001g0098a0001c0001t0001g0141a0001c0001t0001g0189others(85): Show | 89 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.214-14072delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016188 | |||||
| chr2:241016188
|
ATT | A | 83 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(80): Show | 83 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(80): Show |
intron_variant | MODIFIER | c.214-14073_214-1407 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016188 | |||||
| chr2:241016188
|
ATTT | A | 7 | a0001c0001t0005g0134a0002c0011t0011g0029a0002c0011t0015g0028others(4): Show | 7 | HG00609.hp2 HG00738.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-14074_214-1407 others(7): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016188 | |||||
| chr2:241016239
|
G | A | 9 | a0001c0074t0002g0086a0002c0011t0015g0036a0002c0036t0014g0326others(6): Show | 9 | HG01243.hp1 HG02280.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.214-14045G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016239 | ||||||
| chr2:241016284
|
A | T | 205 | a0001c0001t0001g0098a0001c0001t0001g0170a0001c0001t0001g0189others(202): Show | 206 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.214-14000A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016284 | ||||||
| chr2:241016296
|
C | T | 53 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(50): Show | 54 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.214-13988C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016296 | ||||||
| chr2:241016484
|
CCACGCCC others(2): Show |
C | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.214-13798_214-1379 others(13): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016484 | |||||
| chr2:241016540
|
G | T | 1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214-13744G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016540 | ||||||
| chr2:241016541
|
C | T | 1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214-13743C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016541 | ||||||
| chr2:241016566
|
A | G | 7 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-13718A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016566 | ||||||
| chr2:241016600
|
C | G | 62 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(59): Show | 62 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.214-13684C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016600 | ||||||
| chr2:241016793
|
A | G | 1 | a0002c0003t0008g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.214-13491A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016793 | ||||||
| chr2:241016850
|
C | CT | 21 | a0001c0001t0001g0245a0001c0001t0001g0295a0001c0001t0002g0196others(18): Show | 21 | HG00741.hp1 HG01071.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.214-13416dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016850 | |||||
| chr2:241016850
|
CT | C | 69 | a0001c0001t0001g0144a0001c0001t0001g0170a0001c0001t0002g0129others(66): Show | 69 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(66): Show |
intron_variant | MODIFIER | c.214-13416delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241016850 | |||||
| chr2:241016878
|
G | A | 43 | a0001c0001t0001g0189a0001c0001t0005g0092a0001c0001t0009g0278others(40): Show | 43 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.214-13406G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016878 | ||||||
| chr2:241016977
|
C | T | 62 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(59): Show | 62 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.214-13307C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241016977 | ||||||
| chr2:241017003
|
C | T | 33 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0167others(30): Show | 33 | HG00423.hp1 HG01123.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.214-13281C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017003 | ||||||
| chr2:241017353
|
C | A | 62 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(59): Show | 62 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.214-12931C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017353 | ||||||
| chr2:241017367
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.214-12917A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017367 | ||||||
| chr2:241017449
|
C | G | 1 | a0006c0015t0003g0140 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.214-12835C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017449 | ||||||
| chr2:241017468
|
C | T | 3 | a0003c0066t0015g0330a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.214-12816C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017468 | ||||||
| chr2:241017548
|
C | T | 9 | a0002c0008t0061g0168a0002c0013t0011g0207a0002c0013t0011g0214others(6): Show | 9 | HG01099.hp2 HG01123.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-12736C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017548 | ||||||
| chr2:241017658
|
C | T | 4 | a0003c0004t0006g0213a0003c0004t0006g0292a0003c0004t0007g0006others(1): Show | 4 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-12626C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017658 | ||||||
| chr2:241017752
|
A | C | 1 | a0015c0046t0040g0336 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214-12532A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017752 | ||||||
| chr2:241017796
|
C | A | 1 | a0001c0002t0009g0211 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.214-12488C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017796 | ||||||
| chr2:241017809
|
G | A | 41 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(38): Show | 42 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.214-12475G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017809 | ||||||
| chr2:241017966
|
G | A | 1 | a0001c0037t0020g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.214-12318G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017966 | ||||||
| chr2:241017983
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.214-12301A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241017983 | ||||||
| chr2:241018023
|
C | A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214-12261C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018023 | ||||||
| chr2:241018057
|
C | T | 1 | a0001c0001t0005g0299 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.214-12227C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018057 | ||||||
| chr2:241018096
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.214-12188A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018096 | ||||||
| chr2:241018101
|
G | A | 3 | a0002c0011t0011g0128a0009c0030t0027g0127a0009c0030t0027g0208 | 3 | HG03540.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214-12183G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018101 | ||||||
| chr2:241018235
|
C | T | 1 | a0001c0002t0003g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.214-12049C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018235 | ||||||
| chr2:241018260
|
A | G | 62 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(59): Show | 62 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.214-12024A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018260 | ||||||
| chr2:241018267
|
T | C | 5 | a0003c0066t0015g0330a0008c0032t0021g0328a0008c0032t0021g0329others(2): Show | 5 | HG02109.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-12017T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018267 | ||||||
| chr2:241018371
|
G | C | 7 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-11913G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018371 | ||||||
| chr2:241018428
|
G | A | 5 | a0001c0001t0009g0278a0001c0002t0001g0075a0001c0006t0002g0088others(2): Show | 5 | HG00438.hp2 HG00673.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-11856G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018428 | ||||||
| chr2:241018446
|
G | A | 1 | a0004c0026t0013g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.214-11838G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018446 | ||||||
| chr2:241018529
|
G | A | 43 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(40): Show | 44 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.214-11755G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018529 | ||||||
| chr2:241018544
|
C | T | 7 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-11740C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018544 | ||||||
| chr2:241018630
|
G | A | 3 | a0002c0010t0019g0195a0008c0033t0016g0221a0009c0067t0028g0039 | 3 | HG02970.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.214-11654G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018630 | ||||||
| chr2:241018832
|
C | T | 1 | a0002c0003t0006g0275 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.214-11452C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018832 | ||||||
| chr2:241018900
|
A | G | 1 | a0001c0074t0002g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214-11384A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241018900 | ||||||
| chr2:241019055
|
A | AGGACCAG others(21): Show |
67 | a0001c0001t0001g0170a0001c0001t0001g0334a0001c0001t0049g0322others(64): Show | 67 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.214-11104_214-1107 others(32): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241019055 | |||||
| chr2:241019055
|
AGGACCAG others(21): Show |
A | 20 | a0001c0001t0002g0158a0001c0001t0002g0301a0001c0002t0001g0075others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.214-11104_214-1107 others(32): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241019055 | |||||
| chr2:241019317
|
A | G | 93 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(90): Show | 93 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.214-10967A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019317 | ||||||
| chr2:241019321
|
C | T | 1 | a0002c0084t0037g0318 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.214-10963C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019321 | ||||||
| chr2:241019322
|
G | A | 1 | a0001c0001t0020g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.214-10962G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019322 | ||||||
| chr2:241019377
|
T | A | 1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214-10907T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019377 | ||||||
| chr2:241019502
|
C | T | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.214-10782C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019502 | ||||||
| chr2:241019635
|
A | G | 250 | a0001c0001t0001g0098a0001c0001t0001g0170a0001c0001t0001g0189others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(248): Show |
intron_variant | MODIFIER | c.214-10649A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019635 | ||||||
| chr2:241019685
|
G | A | 1 | a0001c0001t0005g0299 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.214-10599G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019685 | ||||||
| chr2:241019686
|
C | T | 2 | a0011c0035t0025g0342a0011c0035t0025g0343 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.214-10598C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019686 | ||||||
| chr2:241019695
|
C | T | 6 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-10589C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019695 | ||||||
| chr2:241019838
|
C | T | 2 | a0002c0010t0014g0038a0002c0036t0025g0022 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214-10446C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241019838 | ||||||
| chr2:241020049
|
T | G | 1 | a0004c0026t0013g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.214-10235T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020049 | ||||||
| chr2:241020137
|
C | T | 1 | a0009c0031t0036g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.214-10147C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020137 | ||||||
| chr2:241020397
|
A | C | 1 | a0001c0001t0002g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.214-9887A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020397 | ||||||
| chr2:241020428
|
G | T | 65 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(62): Show | 66 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.214-9856G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020428 | ||||||
| chr2:241020448
|
C | T | 4 | a0003c0004t0006g0213a0003c0004t0006g0292a0003c0004t0007g0006others(1): Show | 4 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-9836C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020448 | ||||||
| chr2:241020596
|
C | T | 4 | a0003c0066t0015g0330a0008c0032t0021g0328a0008c0032t0021g0329others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-9688C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020596 | ||||||
| chr2:241020728
|
G | A | 3 | a0002c0011t0011g0128a0009c0030t0027g0127a0009c0030t0027g0208 | 3 | HG03540.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214-9556G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020728 | ||||||
| chr2:241020778
|
A | G | 4 | a0003c0066t0015g0330a0008c0032t0021g0328a0008c0032t0021g0329others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-9506A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020778 | ||||||
| chr2:241020803
|
C | T | 1 | a0001c0002t0005g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.214-9481C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020803 | ||||||
| chr2:241020987
|
A | G | 93 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(90): Show | 93 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.214-9297A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241020987 | ||||||
| chr2:241021209
|
G | C | 248 | a0001c0001t0001g0098a0001c0001t0001g0170a0001c0001t0001g0189others(245): Show | 249 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.214-9075G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021209 | ||||||
| chr2:241021212
|
C | G | 1 | a0002c0003t0006g0275 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.214-9072C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021212 | ||||||
| chr2:241021227
|
G | A | 1 | a0003c0023t0004g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.214-9057G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021227 | ||||||
| chr2:241021262
|
C | G | 1 | a0001c0001t0001g0334 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214-9022C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021262 | ||||||
| chr2:241021332
|
G | A | 248 | a0001c0001t0001g0098a0001c0001t0001g0170a0001c0001t0001g0189others(245): Show | 249 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.214-8952G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021332 | ||||||
| chr2:241021333
|
A | G | 1 | a0017c0072t0002g0069 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.214-8951A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021333 | ||||||
| chr2:241021361
|
G | A | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.214-8923G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021361 | ||||||
| chr2:241021401
|
C | T | 1 | a0006c0077t0003g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214-8883C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021401 | ||||||
| chr2:241021416
|
A | G | 65 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(62): Show | 66 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.214-8868A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021416 | ||||||
| chr2:241021510
|
G | A | 16 | a0001c0001t0002g0158a0001c0074t0002g0086a0002c0010t0014g0038others(13): Show | 16 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.214-8774G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021510 | ||||||
| chr2:241021661
|
T | C | 93 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(90): Show | 93 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.214-8623T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021661 | ||||||
| chr2:241021676
|
A | G | 1 | a0002c0082t0039g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.214-8608A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021676 | ||||||
| chr2:241021736
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0002g0129 | 2 | HG02015.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.214-8548T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021736 | ||||||
| chr2:241021841
|
G | A | 3 | a0001c0001t0002g0158a0002c0010t0014g0038a0002c0036t0025g0022 | 3 | HG00741.hp2 HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214-8443G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021841 | ||||||
| chr2:241021884
|
C | T | 2 | a0002c0010t0014g0038a0002c0036t0025g0022 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214-8400C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021884 | ||||||
| chr2:241021929
|
A | G | 62 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(59): Show | 63 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.214-8355A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241021929 | ||||||
| chr2:241021962
|
AG | A | 93 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(90): Show | 93 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.214-8320delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241021962 | |||||
| chr2:241022295
|
A | G | 5 | a0001c0001t0001g0245a0001c0001t0002g0018a0001c0001t0005g0019others(2): Show | 5 | NA18747.hp1 NA18948.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-7989A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022295 | ||||||
| chr2:241022300
|
A | G | 1 | a0002c0034t0006g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.214-7984A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022300 | ||||||
| chr2:241022356
|
T | C | 1 | a0002c0010t0019g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214-7928T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022356 | ||||||
| chr2:241022447
|
A | T | 1 | a0003c0023t0006g0237 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.214-7837A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022447 | ||||||
| chr2:241022464
|
C | A | 7 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-7820C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022464 | ||||||
| chr2:241022542
|
C | T | 1 | a0017c0072t0002g0069 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.214-7742C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022542 | ||||||
| chr2:241022694
|
T | C | 1 | a0009c0031t0036g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.214-7590T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022694 | ||||||
| chr2:241022945
|
T | G | 1 | a0001c0002t0001g0171 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.214-7339T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241022945 | ||||||
| chr2:241023157
|
A | G | 96 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(93): Show | 96 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.214-7127A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241023157 | ||||||
| chr2:241023215
|
A | G | 3 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043 | 3 | HG02109.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.214-7069A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241023215 | ||||||
| chr2:241023289
|
C | T | 96 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(93): Show | 96 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.214-6995C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241023289 | ||||||
| chr2:241023484
|
T | TA | 130 | a0001c0001t0001g0044a0001c0001t0001g0079a0001c0001t0001g0170others(127): Show | 130 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.214-6789dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023484 | |||||
| chr2:241023484
|
TA | T | 8 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(5): Show | 8 | HG01261.hp1 HG02027.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.214-6789delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023484 | |||||
| chr2:241023667
|
A | G | 1 | a0012c0079t0016g0331 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.214-6617A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241023667 | ||||||
| chr2:241023674
|
G | C | 2 | a0001c0006t0001g0257a0001c0006t0001g0258 | 2 | NA19060.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.214-6610G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241023674 | ||||||
| chr2:241023888
|
C | CT | 11 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0167others(8): Show | 11 | HG00423.hp1 HG01516.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.214-6377dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023888 | |||||
| chr2:241023888
|
C | CTTT | 77 | a0001c0001t0001g0170a0001c0001t0005g0092a0001c0001t0009g0278others(74): Show | 77 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.214-6379_214-6377d others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023888 | |||||
| chr2:241023888
|
C | CTTTT | 28 | a0001c0002t0002g0184a0001c0002t0003g0149a0001c0002t0003g0177others(25): Show | 28 | HG00438.hp2 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.214-6380_214-6377d others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023888 | |||||
| chr2:241023888
|
C | CTTTTT | 60 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0160others(57): Show | 61 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.214-6381_214-6377d others(7): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023888 | |||||
| chr2:241023888
|
C | CTTTTTT | 51 | a0001c0001t0001g0295a0001c0001t0002g0158a0001c0001t0002g0252others(48): Show | 51 | HG00738.hp1 HG00741.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.214-6382_214-6377d others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023888 | |||||
| chr2:241023888
|
C | CTTTTTTT | 28 | a0001c0001t0002g0005a0001c0001t0002g0296a0001c0001t0005g0134others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.214-6383_214-6377d others(9): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241023888 | |||||
| chr2:241023950
|
C | T | 5 | a0001c0001t0001g0170a0001c0002t0001g0182a0001c0002t0001g0324others(2): Show | 5 | HG01167.hp2 HG01175.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-6334C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241023950 | ||||||
| chr2:241023986
|
G | A | 248 | a0001c0001t0001g0098a0001c0001t0001g0170a0001c0001t0001g0189others(245): Show | 249 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.214-6298G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241023986 | ||||||
| chr2:241024068
|
T | C | 7 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-6216T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024068 | ||||||
| chr2:241024101
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.214-6183G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024101 | ||||||
| chr2:241024111
|
T | G | 11 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-6173T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024111 | ||||||
| chr2:241024129
|
G | A | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.214-6155G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024129 | ||||||
| chr2:241024199
|
A | G | 2 | a0001c0001t0049g0322a0001c0002t0018g0185 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.214-6085A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024199 | ||||||
| chr2:241024233
|
A | C | 1 | a0002c0010t0016g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.214-6051A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024233 | ||||||
| chr2:241024235
|
C | CT | 42 | a0001c0001t0001g0067a0001c0001t0001g0238a0001c0001t0001g0303others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(39): Show |
intron_variant | MODIFIER | c.214-6020dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024235
|
C | CTT | 46 | a0001c0001t0001g0245a0001c0001t0001g0295a0001c0001t0002g0005others(43): Show | 46 | HG00438.hp1 HG00621.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.214-6021_214-6020d others(4): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024235
|
C | CTTT | 13 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0017g0273others(10): Show | 13 | HG01433.hp2 HG02071.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-6022_214-6020d others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024235
|
C | CTTTTTTT others(7): Show |
1 | a0010c0017t0024g0225 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214-6033_214-6020d others(16): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024235
|
C | CTTTTTTT others(9): Show |
7 | a0002c0011t0015g0036a0002c0036t0014g0326a0004c0026t0004g0228others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-6035_214-6020d others(18): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024235
|
C | CTTTTTTT others(11): Show |
1 | a0002c0011t0011g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.214-6037_214-6020d others(20): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024235
|
C | CTTTTTTT others(16): Show |
1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.214-6042_214-6020d others(25): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024235
|
CT | C | 71 | a0001c0001t0001g0144a0001c0001t0001g0189a0001c0001t0002g0018others(68): Show | 71 | HG00423.hp2 HG00621.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.214-6020delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024235 | |||||
| chr2:241024236
|
T | C | 1 | a0001c0057t0009g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214-6048T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024236 | ||||||
| chr2:241024238
|
T | TA | 3 | a0003c0066t0015g0330a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.214-6046_214-6045i others(3): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024238 | ||||||
| chr2:241024464
|
G | A | 4 | a0003c0066t0015g0330a0008c0032t0021g0328a0008c0032t0021g0329others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-5820G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024464 | ||||||
| chr2:241024561
|
T | G | 3 | a0001c0001t0009g0274a0001c0001t0017g0272a0001c0001t0017g0273 | 3 | HG02735.hp2 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.214-5723T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024561 | ||||||
| chr2:241024596
|
C | T | 2 | a0002c0010t0044g0078a0002c0011t0011g0234 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.214-5688C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024596 | ||||||
| chr2:241024652
|
C | CTTATTTT others(3): Show |
54 | a0001c0001t0001g0098a0001c0001t0002g0158a0001c0002t0009g0310others(51): Show | 55 | HG00673.hp2 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.214-5610_214-5601d others(12): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024652 | |||||
| chr2:241024652
|
C | CTTATTTT others(8): Show |
41 | a0001c0001t0001g0189a0001c0001t0002g0252a0001c0002t0003g0161others(38): Show | 41 | HG00558.hp2 HG00621.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.214-5615_214-5601d others(17): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024652 | |||||
| chr2:241024652
|
C | CTTATTTT others(13): Show |
107 | a0001c0001t0001g0170a0001c0001t0002g0280a0001c0001t0002g0297others(104): Show | 107 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.214-5620_214-5601d others(22): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024652 | |||||
| chr2:241024652
|
C | CTTATTTT others(18): Show |
35 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0294others(32): Show | 35 | HG00738.hp2 HG02056.hp1 HG02056.hp2 others(32): Show |
intron_variant | MODIFIER | c.214-5625_214-5601d others(27): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024652 | |||||
| chr2:241024652
|
C | CTTATTTT others(23): Show |
6 | a0001c0006t0001g0257a0001c0006t0001g0258a0002c0003t0010g0190others(3): Show | 6 | HG00438.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-5630_214-5601d others(32): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024652 | |||||
| chr2:241024652
|
C | CTTATTTT others(1818): Show |
1 | a0002c0003t0006g0275 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.214-5601_214-5600i others(1827): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024652 | |||||
| chr2:241024817
|
G | GC | 167 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0001g0295others(164): Show | 167 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.214-5466dupC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241024817 | |||||
| chr2:241024925
|
C | G | 1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.214-5359C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241024925 | ||||||
| chr2:241025500
|
T | C | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.214-4784T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241025500 | ||||||
| chr2:241025785
|
A | G | 2 | a0011c0035t0025g0342a0011c0035t0025g0343 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.214-4499A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241025785 | ||||||
| chr2:241026009
|
C | CTTT | 80 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0002g0158others(77): Show | 80 | HG00597.hp1 HG00673.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.214-4253_214-4251d others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTT | 97 | a0001c0001t0001g0098a0001c0001t0002g0005a0001c0001t0002g0252others(94): Show | 98 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.214-4254_214-4251d others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTTT | 35 | a0001c0001t0001g0295a0001c0001t0005g0299a0001c0001t0009g0274others(32): Show | 35 | HG01175.hp1 HG01884.hp1 HG02027.hp2 others(32): Show |
intron_variant | MODIFIER | c.214-4255_214-4251d others(7): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTTTT | 6 | a0001c0006t0002g0076a0001c0037t0002g0314a0002c0010t0016g0033others(3): Show | 6 | HG02572.hp2 HG03209.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-4256_214-4251d others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0163a0001c0001t0002g0174a0001c0001t0002g0254others(2): Show | 5 | HG03130.hp1 HG03471.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-4261_214-4251d others(13): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTTTTT others(5): Show |
16 | a0001c0001t0001g0166a0001c0001t0001g0244a0001c0001t0002g0217others(13): Show | 16 | HG01123.hp2 HG02027.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-4262_214-4251d others(14): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTTTTT others(6): Show |
7 | a0001c0001t0001g0167a0001c0001t0002g0018a0001c0001t0005g0019others(4): Show | 7 | HG00423.hp1 HG03654.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-4263_214-4251d others(15): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTTTTT others(7): Show |
1 | a0006c0063t0001g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214-4264_214-4251d others(16): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0245a0001c0001t0020g0175a0003c0023t0004g0210 | 3 | HG02683.hp2 HG03453.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.214-4265_214-4251d others(17): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
CTTT | C | 11 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-4253_214-4251d others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026009
|
CTTTTTTT | C | 10 | a0001c0074t0002g0086a0002c0011t0011g0128a0002c0011t0015g0036others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-4257_214-4251d others(9): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241026009 | |||||
| chr2:241026295
|
C | A | 11 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-3989C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241026295 | ||||||
| chr2:241026296
|
G | A | 1 | a0001c0001t0049g0322 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.214-3988G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241026296 | ||||||
| chr2:241026379
|
T | C | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.214-3905T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241026379 | ||||||
| chr2:241026516
|
T | C | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.214-3768T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241026516 | ||||||
| chr2:241026582
|
A | G | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.214-3702A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241026582 | ||||||
| chr2:241026639
|
T | C | 60 | a0001c0001t0001g0098a0001c0002t0009g0310a0001c0002t0018g0339others(57): Show | 61 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.214-3645T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241026639 | ||||||
| chr2:241026770
|
A | G | 6 | a0001c0002t0003g0136a0001c0002t0003g0180a0006c0015t0003g0137others(3): Show | 6 | NA18940.hp2 NA18948.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-3514A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241026770 | ||||||
| chr2:241027084
|
C | CT | 93 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(90): Show | 93 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.214-3187dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241027084 | |||||
| chr2:241027097
|
T | A | 149 | a0001c0001t0001g0098a0001c0001t0001g0295a0001c0001t0002g0005others(146): Show | 150 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.214-3187T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027097 | ||||||
| chr2:241027097
|
T | TA | 4 | a0002c0003t0010g0218a0002c0003t0013g0219a0003c0024t0010g0286others(1): Show | 4 | HG02080.hp1 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-3184dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241027097 | |||||
| chr2:241027267
|
A | G | 286 | a0001c0001t0001g0098a0001c0001t0001g0163a0001c0001t0001g0166others(283): Show | 287 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(284): Show |
intron_variant | MODIFIER | c.214-3017A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027267 | ||||||
| chr2:241027731
|
C | CT | 3 | a0001c0001t0001g0189a0006c0015t0003g0137a0008c0033t0030g0335 | 3 | HG02074.hp2 HG02280.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.214-2552dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241027731 | |||||
| chr2:241027732
|
TG | T | 64 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0158others(61): Show | 64 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.214-2551delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027732 | ||||||
| chr2:241027733
|
G | T | 183 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0005g0092others(180): Show | 184 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.214-2551G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027733 | ||||||
| chr2:241027802
|
C | T | 1 | a0001c0002t0005g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.214-2482C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027802 | ||||||
| chr2:241027835
|
G | A | 3 | a0002c0003t0010g0190a0009c0030t0027g0127a0009c0030t0027g0208 | 3 | HG00438.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.214-2449G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027835 | ||||||
| chr2:241027854
|
C | T | 1 | a0019c0070t0019g0008 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.214-2430C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027854 | ||||||
| chr2:241027885
|
C | T | 1 | a0009c0031t0036g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.214-2399C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027885 | ||||||
| chr2:241027896
|
G | A | 1 | a0002c0008t0029g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.214-2388G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027896 | ||||||
| chr2:241027968
|
C | T | 1 | a0001c0002t0018g0160 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.214-2316C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027968 | ||||||
| chr2:241027969
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.214-2315G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241027969 | ||||||
| chr2:241028025
|
G | A | 2 | a0005c0007t0001g0110a0005c0007t0005g0111 | 2 | NA18943.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.214-2259G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028025 | ||||||
| chr2:241028028
|
G | A | 62 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0002t0020g0308others(59): Show | 63 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.214-2256G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028028 | ||||||
| chr2:241028097
|
A | G | 18 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0084others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.214-2187A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028097 | ||||||
| chr2:241028304
|
T | C | 1 | a0001c0002t0005g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.214-1980T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028304 | ||||||
| chr2:241028372
|
G | A | 1 | a0001c0006t0002g0276 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.214-1912G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028372 | ||||||
| chr2:241028469
|
G | A | 62 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0002t0020g0308others(59): Show | 63 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.214-1815G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028469 | ||||||
| chr2:241028497
|
T | A | 1 | a0002c0008t0029g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-1787T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028497 | ||||||
| chr2:241028741
|
C | T | 1 | a0005c0014t0001g0125 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.214-1543C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241028741 | ||||||
| chr2:241029180
|
G | A | 1 | a0007c0041t0007g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.214-1104G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029180 | ||||||
| chr2:241029240
|
A | G | 2 | a0002c0010t0014g0038a0002c0036t0025g0022 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214-1044A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029240 | ||||||
| chr2:241029243
|
G | T | 11 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-1041G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029243 | ||||||
| chr2:241029339
|
T | C | 1 | a0001c0002t0005g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.214-945T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029339 | ||||||
| chr2:241029540
|
T | A | 1 | a0002c0003t0004g0015 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.214-744T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029540 | ||||||
| chr2:241029562
|
A | G | 247 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0001g0295others(244): Show | 248 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.214-722A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029562 | ||||||
| chr2:241029616
|
G | T | 68 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(65): Show | 68 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.214-668G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029616 | ||||||
| chr2:241029740
|
G | A | 1 | a0002c0010t0019g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214-544G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029740 | ||||||
| chr2:241029831
|
C | T | 6 | a0003c0004t0006g0118a0003c0004t0006g0119a0003c0004t0006g0120others(3): Show | 6 | NA18964.hp2 NA18970.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-453C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029831 | ||||||
| chr2:241029839
|
A | C | 158 | a0001c0001t0001g0098a0001c0001t0001g0163a0001c0001t0001g0166others(155): Show | 158 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.214-445A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029839 | ||||||
| chr2:241029840
|
C | G | 107 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0002g0156others(104): Show | 107 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.214-444C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029840 | ||||||
| chr2:241029959
|
G | C | 1 | a0005c0014t0001g0150 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.214-325G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241029959 | ||||||
| chr2:241030051
|
T | C | 1 | a0002c0003t0008g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214-233T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241030051 | ||||||
| chr2:241030081
|
A | G | 11 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-203A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241030081 | ||||||
| chr2:241030113
|
A | G | 4 | a0003c0066t0015g0330a0008c0032t0021g0328a0008c0032t0021g0329others(1): Show | 4 | HG02109.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-171A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241030113 | ||||||
| chr2:241030139
|
G | A | 1 | a0001c0025t0003g0074 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.214-145G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241030139 | ||||||
| chr2:241030257
|
TC | T | 18 | a0001c0037t0002g0314a0001c0037t0020g0030a0001c0057t0009g0094others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.214-23delC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr2 | 241030257 | |||||
| chr2:241030262
|
G | A | 23 | a0001c0037t0002g0314a0001c0037t0020g0030a0001c0057t0009g0094others(20): Show | 23 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.214-22G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 1/31 | chr2 | 241030262 | ||||||
| chr2:241030586
|
T | C | 1 | a0003c0004t0007g0099 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.501+15T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241030586 | ||||||
| chr2:241030623
|
G | T | 1 | a0002c0010t0014g0038 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.501+52G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241030623 | ||||||
| chr2:241030901
|
T | TTCCTTGA others(41): Show |
1 | a0005c0007t0001g0110 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+331_501+378dup others(48): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr2 | 241030901 | |||||
| chr2:241031015
|
C | T | 6 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+444C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031015 | ||||||
| chr2:241031191
|
G | A | 1 | a0001c0001t0049g0322 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.501+620G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031191 | ||||||
| chr2:241031344
|
C | T | 37 | a0001c0001t0001g0189a0001c0001t0005g0092a0001c0001t0009g0278others(34): Show | 37 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.501+773C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031344 | ||||||
| chr2:241031356
|
G | T | 2 | a0002c0009t0016g0220a0012c0079t0016g0331 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.501+785G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031356 | ||||||
| chr2:241031387
|
A | T | 37 | a0001c0001t0001g0189a0001c0001t0005g0092a0001c0001t0009g0278others(34): Show | 37 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.501+816A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031387 | ||||||
| chr2:241031490
|
C | A | 56 | a0001c0001t0001g0295a0001c0001t0002g0005a0001c0001t0002g0252others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.501+919C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031490 | ||||||
| chr2:241031496
|
C | T | 37 | a0001c0001t0001g0189a0001c0001t0005g0092a0001c0001t0009g0278others(34): Show | 37 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.501+925C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031496 | ||||||
| chr2:241031522
|
G | A | 44 | a0001c0001t0001g0170a0001c0002t0001g0171a0001c0002t0001g0172others(41): Show | 44 | HG00621.hp1 HG00738.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.501+951G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031522 | ||||||
| chr2:241031650
|
G | A | 32 | a0001c0001t0001g0189a0001c0001t0005g0092a0001c0001t0009g0278others(29): Show | 32 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.501+1079G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031650 | ||||||
| chr2:241031736
|
C | T | 1 | a0003c0004t0007g0017 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.501+1165C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031736 | ||||||
| chr2:241031776
|
G | A | 1 | a0002c0019t0014g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.501+1205G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031776 | ||||||
| chr2:241031783
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.501+1212T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031783 | ||||||
| chr2:241031885
|
CAAGCGGC others(3): Show |
C | 1 | a0003c0004t0007g0017 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.501+1315_501+1324d others(12): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241031885 | ||||||
| chr2:241032205
|
C | T | 1 | a0002c0009t0012g0312 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.502-1530C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032205 | ||||||
| chr2:241032206
|
C | T | 1 | a0011c0054t0030g0319 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.502-1529C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032206 | ||||||
| chr2:241032243
|
G | A | 1 | a0001c0006t0002g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.502-1492G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032243 | ||||||
| chr2:241032306
|
T | C | 2 | a0007c0027t0001g0267a0013c0029t0006g0106 | 2 | HG02015.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.502-1429T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032306 | ||||||
| chr2:241032372
|
C | T | 7 | a0005c0007t0001g0110a0005c0007t0001g0261a0005c0007t0002g0112others(4): Show | 7 | HG00738.hp1 HG02293.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-1363C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032372 | ||||||
| chr2:241032411
|
A | G | 258 | a0001c0001t0001g0098a0001c0001t0001g0170a0001c0001t0001g0189others(255): Show | 259 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.502-1324A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032411 | ||||||
| chr2:241032483
|
G | A | 1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.502-1252G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032483 | ||||||
| chr2:241032495
|
G | A | 1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.502-1240G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032495 | ||||||
| chr2:241032497
|
T | A | 1 | a0004c0026t0013g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.502-1238T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032497 | ||||||
| chr2:241032498
|
C | G | 1 | a0004c0026t0013g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.502-1237C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032498 | ||||||
| chr2:241032511
|
G | A | 1 | a0004c0026t0013g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.502-1224G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032511 | ||||||
| chr2:241032522
|
C | T | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.502-1213C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032522 | ||||||
| chr2:241032524
|
C | T | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.502-1211C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032524 | ||||||
| chr2:241032570
|
CACATGTA others(1): Show |
C | 4 | a0001c0006t0002g0076a0002c0003t0008g0066a0002c0003t0008g0259others(1): Show | 4 | HG00558.hp1 HG00609.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-1160_502-1153d others(10): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr2 | 241032570 | |||||
| chr2:241032583
|
A | G | 7 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0043others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-1152A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032583 | ||||||
| chr2:241032872
|
T | C | 2 | a0002c0052t0011g0256a0009c0031t0036g0027 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.502-863T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032872 | ||||||
| chr2:241032895
|
C | T | 1 | a0002c0010t0014g0038 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.502-840C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032895 | ||||||
| chr2:241032912
|
G | A | 7 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0019t0014g0041others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.502-823G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032912 | ||||||
| chr2:241032918
|
G | A | 4 | a0004c0005t0031g0059a0004c0005t0031g0061a0007c0040t0007g0057others(1): Show | 4 | HG01934.hp1 HG02040.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-817G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241032918 | ||||||
| chr2:241033165
|
A | G | 8 | a0002c0052t0011g0256a0002c0073t0063g0007a0009c0030t0027g0127others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.502-570A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241033165 | ||||||
| chr2:241033326
|
G | T | 1 | a0002c0003t0007g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.502-409G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241033326 | ||||||
| chr2:241033340
|
C | T | 8 | a0002c0008t0019g0227a0002c0010t0016g0033a0002c0010t0016g0157others(5): Show | 8 | HG02109.hp2 HG02559.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-395C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241033340 | ||||||
| chr2:241033419
|
A | T | 10 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.502-316A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241033419 | ||||||
| chr2:241033481
|
A | G | 40 | a0001c0037t0002g0314a0001c0037t0020g0030a0001c0074t0002g0086others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.502-254A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241033481 | ||||||
| chr2:241033598
|
G | A | 1 | a0002c0003t0062g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.502-137G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 2/31 | chr2 | 241033598 | ||||||
| chr2:241033879
|
G | A | 16 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(13): Show | 16 | HG00621.hp1 HG02083.hp1 HG02132.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.642+4G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241033879 | ||||||
| chr2:241033934
|
G | C | 1 | a0001c0002t0059g0053 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.642+59G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241033934 | ||||||
| chr2:241033961
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.642+86C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241033961 | ||||||
| chr2:241033968
|
T | C | 1 | a0001c0002t0001g0182 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.642+93T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241033968 | ||||||
| chr2:241034016
|
A | G | 1 | a0021c0078t0016g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.642+141A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034016 | ||||||
| chr2:241034057
|
C | T | 2 | a0002c0010t0014g0222a0002c0018t0022g0223 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.642+182C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034057 | ||||||
| chr2:241034063
|
C | T | 3 | a0002c0073t0063g0007a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.642+188C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034063 | ||||||
| chr2:241034126
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.642+251G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034126 | ||||||
| chr2:241034131
|
A | T | 47 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0002t0020g0308others(44): Show | 48 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+256A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034131 | ||||||
| chr2:241034194
|
C | A | 3 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0082t0039g0032 | 3 | HG02572.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.642+319C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034194 | ||||||
| chr2:241034256
|
G | A | 1 | a0001c0060t0005g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.643-312G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034256 | ||||||
| chr2:241034320
|
C | A | 30 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0009t0004g0040others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.643-248C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034320 | ||||||
| chr2:241034560
|
A | G | 20 | a0001c0001t0002g0005a0001c0001t0020g0004a0001c0006t0001g0054others(17): Show | 20 | HG01891.hp2 HG02027.hp2 HG02155.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.643-8A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 3/31 | chr2 | 241034560 | ||||||
| chr2:241034825
|
C | T | 3 | a0006c0012t0001g0001a0006c0012t0001g0311a0006c0012t0005g0309 | 4 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+95C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241034825 | ||||||
| chr2:241034872
|
G | A | 238 | a0001c0001t0001g0334a0001c0001t0002g0005a0001c0001t0002g0252others(235): Show | 239 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.805+142G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241034872 | ||||||
| chr2:241034894
|
G | T | 1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805+164G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241034894 | ||||||
| chr2:241034933
|
ACACACAC others(54): Show |
A | 2 | a0009c0030t0027g0127a0009c0030t0027g0208 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.805+217_805+277del others(61): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241034933 | |||||
| chr2:241034947
|
C | G | 3 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.805+217C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241034947 | ||||||
| chr2:241034947
|
CTGGGTTG others(54): Show |
C | 1 | a0011c0054t0030g0319 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.805+246_805+306del others(61): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241034947 | |||||
| chr2:241034979
|
C | T | 1 | a0002c0018t0022g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805+249C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241034979 | ||||||
| chr2:241035091
|
A | G | 248 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0117others(245): Show | 249 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.805+361A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035091 | ||||||
| chr2:241035260
|
G | A | 1 | a0001c0002t0023g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.805+530G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035260 | ||||||
| chr2:241035269
|
A | T | 133 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(130): Show | 134 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.805+539A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035269 | ||||||
| chr2:241035406
|
G | A | 1 | a0002c0003t0008g0020 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.805+676G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035406 | ||||||
| chr2:241035442
|
G | A | 30 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0009t0012g0312others(27): Show | 30 | HG00423.hp2 HG00597.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.805+712G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035442 | ||||||
| chr2:241035485
|
T | TG | 3 | a0006c0012t0001g0001a0006c0012t0001g0311a0006c0012t0005g0309 | 4 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+759dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241035485 | |||||
| chr2:241035621
|
G | C | 1 | a0002c0018t0022g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805+891G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035621 | ||||||
| chr2:241035644
|
G | C | 2 | a0001c0001t0001g0334a0001c0071t0003g0333 | 2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.805+914G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035644 | ||||||
| chr2:241035674
|
G | C | 3 | a0002c0003t0004g0271a0002c0003t0006g0275a0002c0003t0010g0190 | 3 | HG00438.hp1 HG02129.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.805+944G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035674 | ||||||
| chr2:241035712
|
C | CG | 7 | a0001c0068t0018g0320a0002c0010t0014g0038a0002c0010t0044g0078others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+986dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241035712 | |||||
| chr2:241035712
|
C | CGGGGTGC others(223): Show |
1 | a0001c0001t0001g0071 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.806-946_806-945ins others(230): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241035712 | |||||
| chr2:241035890
|
C | T | 3 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.806-900C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035890 | ||||||
| chr2:241035911
|
C | T | 2 | a0002c0008t0008g0255a0016c0053t0017g0239 | 2 | NA18978.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.806-879C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035911 | ||||||
| chr2:241035951
|
C | CGGGGTTG others(47): Show |
1 | a0001c0006t0002g0076 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.806-835_806-782dup others(54): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241035951 | |||||
| chr2:241035975
|
G | GGGGTGGG others(115): Show |
1 | a0001c0001t0001g0170 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(122): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241035975 | |||||
| chr2:241035979
|
T | TGGGGGGC others(73): Show |
3 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.806-787_806-786ins others(80): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241035979 | |||||
| chr2:241035992
|
C | CGCGTCAC others(86): Show |
1 | a0002c0003t0007g0290 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(93): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241035992 | |||||
| chr2:241035994
|
C | T | 25 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0009t0004g0040others(22): Show | 25 | HG00597.hp1 HG01261.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.806-796C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241035994 | ||||||
| chr2:241036009
|
AGTGGGGG others(22): Show |
A | 1 | a0005c0007t0001g0056 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.806-758_806-730del others(29): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036009 | |||||
| chr2:241036010
|
G | GTGGGGGG others(25): Show |
1 | a0001c0001t0002g0304 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.806-751_806-750ins others(32): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036010 | |||||
| chr2:241036014
|
G | C | 1 | a0005c0014t0001g0279 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.806-776G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036014 | ||||||
| chr2:241036017
|
G | T | 18 | a0001c0037t0002g0314a0001c0037t0020g0030a0001c0050t0003g0051others(15): Show | 18 | HG02145.hp1 HG02486.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.806-773G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036017 | ||||||
| chr2:241036035
|
GT | G | 3 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0082t0039g0032 | 3 | HG02572.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.806-754delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036035 | ||||||
| chr2:241036039
|
G | GGGT | 49 | a0001c0002t0017g0143a0001c0002t0018g0339a0001c0002t0020g0308others(46): Show | 50 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.806-751_806-750ins others(3): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036039 | ||||||
| chr2:241036039
|
G | GGGTTGGG others(28): Show |
1 | a0001c0006t0002g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.806-751_806-750ins others(35): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036039 | ||||||
| chr2:241036039
|
G | GTGGGGGG others(25): Show |
1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.806-730_806-729ins others(32): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036039 | |||||
| chr2:241036042
|
G | GGGGGCGG others(43): Show |
4 | a0002c0009t0004g0332a0002c0010t0016g0033a0002c0010t0016g0157others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-744_806-743ins others(50): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036042 | |||||
| chr2:241036046
|
G | A | 1 | a0002c0011t0011g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.806-744G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036046 | ||||||
| chr2:241036050
|
A | G | 4 | a0002c0009t0004g0332a0002c0010t0016g0033a0002c0010t0016g0157others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-740A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036050 | ||||||
| chr2:241036053
|
T | C | 4 | a0002c0009t0004g0332a0002c0010t0016g0033a0002c0010t0016g0157others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-737T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036053 | ||||||
| chr2:241036053
|
T | TGCGTCAC others(43): Show |
2 | a0001c0001t0001g0305a0001c0001t0002g0018 | 2 | HG01070.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.806-706_806-705ins others(50): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(11): Show |
7 | a0001c0001t0052g0147a0001c0002t0017g0143a0002c0011t0011g0128others(4): Show | 7 | HG02109.hp2 HG02976.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.806-730_806-729ins others(18): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(44): Show |
1 | a0001c0001t0005g0164 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.806-730_806-729ins others(51): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(43): Show |
230 | a0001c0001t0001g0098a0001c0001t0001g0163a0001c0001t0001g0166others(227): Show | 231 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.806-730_806-729ins others(50): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(44): Show |
2 | a0001c0002t0009g0211a0003c0004t0007g0006 | 2 | HG02055.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.806-730_806-729ins others(51): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(75): Show |
1 | a0004c0028t0012g0096 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(82): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(168): Show |
1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(175): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(42): Show |
1 | a0005c0007t0001g0110 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(49): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(40): Show |
1 | a0003c0004t0006g0002 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(47): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036053
|
T | TGCGTCAC others(101): Show |
1 | a0002c0022t0014g0327 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(108): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036053 | |||||
| chr2:241036056
|
G | GTCACGGG others(43): Show |
1 | a0008c0081t0021g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806-730_806-729ins others(50): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036056 | |||||
| chr2:241036061
|
A | G | 5 | a0001c0001t0001g0334a0001c0002t0048g0191a0001c0006t0001g0258others(2): Show | 5 | HG00673.hp1 HG01099.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-729A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036061 | ||||||
| chr2:241036065
|
T | TGGGGGTT others(44): Show |
2 | a0001c0002t0048g0191a0001c0006t0001g0258 | 2 | HG01175.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.806-720_806-719ins others(51): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036065 | |||||
| chr2:241036070
|
G | GTTGGGGG others(46): Show |
1 | a0006c0012t0005g0309 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.806-720_806-719ins others(53): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036070 | ||||||
| chr2:241036071
|
G | T | 2 | a0001c0001t0001g0334a0001c0001t0002g0196 | 2 | HG01071.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.806-719G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036071 | ||||||
| chr2:241036072
|
T | G | 1 | a0006c0012t0005g0309 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.806-718T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036072 | ||||||
| chr2:241036072
|
T | TG | 124 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(121): Show | 125 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.806-712dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036072 | |||||
| chr2:241036072
|
T | TGGGGGGT others(45): Show |
1 | a0001c0001t0001g0334 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.806-706_806-705ins others(52): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036072 | |||||
| chr2:241036072
|
T | TGGGGGGT others(76): Show |
1 | a0001c0001t0002g0196 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.806-706_806-705ins others(83): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036072 | |||||
| chr2:241036088
|
A | G | 1 | a0003c0066t0015g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.806-702A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036088 | ||||||
| chr2:241036117
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.806-673C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036117 | ||||||
| chr2:241036154
|
G | C | 4 | a0002c0011t0011g0029a0002c0011t0015g0028a0002c0011t0015g0036others(1): Show | 4 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-636G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036154 | ||||||
| chr2:241036203
|
A | G | 4 | a0001c0001t0001g0334a0001c0071t0003g0333a0002c0073t0063g0007others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-587A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036203 | ||||||
| chr2:241036289
|
A | C | 1 | a0001c0002t0017g0143 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.806-501A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036289 | ||||||
| chr2:241036377
|
C | G | 1 | a0002c0021t0004g0198 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.806-413C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036377 | ||||||
| chr2:241036415
|
C | G | 1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.806-375C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036415 | ||||||
| chr2:241036554
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.806-236C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036554 | ||||||
| chr2:241036588
|
C | T | 7 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0019t0014g0041others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.806-202C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036588 | ||||||
| chr2:241036599
|
G | GCCCCTGC others(1): Show |
12 | a0001c0002t0001g0172a0001c0002t0005g0115a0002c0003t0007g0131others(9): Show | 12 | HG00738.hp1 HG01255.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-172_806-165dup others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr2 | 241036599 | |||||
| chr2:241036666
|
T | C | 1 | a0006c0012t0005g0309 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.806-124T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036666 | ||||||
| chr2:241036706
|
G | A | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.806-84G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036706 | ||||||
| chr2:241036780
|
A | G | 1 | a0002c0008t0019g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.806-10A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 4/31 | chr2 | 241036780 | ||||||
| chr2:241036998
|
G | A | 1 | a0001c0002t0017g0143 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.931+83G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241036998 | ||||||
| chr2:241037055
|
G | C | 1 | a0002c0003t0004g0015 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.931+140G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037055 | ||||||
| chr2:241037104
|
G | C | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.932-136G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037104 | ||||||
| chr2:241037106
|
C | G | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.932-134C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037106 | ||||||
| chr2:241037106
|
C | T | 3 | a0006c0015t0003g0137a0006c0015t0003g0138a0006c0015t0003g0139 | 3 | NA18940.hp2 NA18948.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.932-134C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037106 | ||||||
| chr2:241037108
|
G | A | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.932-132G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037108 | ||||||
| chr2:241037157
|
G | A | 1 | a0003c0004t0006g0118 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.932-83G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037157 | ||||||
| chr2:241037160
|
C | G | 10 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.932-80C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037160 | ||||||
| chr2:241037198
|
C | T | 1 | a0002c0022t0014g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.932-42C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | chr2 | 241037198 | ||||||
| chr2:241037198
|
CG | C | 66 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(63): Show | 66 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.932-39delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr2 | 241037198 | |||||
| chr2:241037369
|
C | T | 2 | a0008c0069t0016g0133a0012c0079t0016g0331 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1045+16C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241037369 | ||||||
| chr2:241037394
|
G | A | 2 | a0001c0002t0003g0177a0001c0002t0009g0187 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1045+41G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241037394 | ||||||
| chr2:241037582
|
G | A | 3 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037 | 3 | HG02257.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1045+229G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241037582 | ||||||
| chr2:241037719
|
A | G | 105 | a0001c0001t0002g0297a0001c0002t0009g0310a0001c0002t0018g0339others(102): Show | 106 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1045+366A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241037719 | ||||||
| chr2:241037743
|
C | T | 3 | a0002c0073t0063g0007a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1045+390C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241037743 | ||||||
| chr2:241037811
|
C | T | 3 | a0002c0073t0063g0007a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1045+458C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241037811 | ||||||
| chr2:241038013
|
G | A | 15 | a0001c0020t0001g0105a0003c0004t0006g0002a0003c0004t0006g0100others(12): Show | 15 | HG02015.hp2 HG02132.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1045+660G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038013 | ||||||
| chr2:241038069
|
A | AC | 30 | a0001c0001t0001g0238a0001c0001t0002g0005a0001c0001t0005g0164others(27): Show | 30 | HG01175.hp2 HG01243.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.1045+725dupC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr2 | 241038069 | |||||
| chr2:241038069
|
A | ACC | 53 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(50): Show | 53 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1045+724_1045+725d others(4): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr2 | 241038069 | |||||
| chr2:241038125
|
G | A | 1 | a0003c0004t0006g0100 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1045+772G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038125 | ||||||
| chr2:241038248
|
A | G | 238 | a0001c0001t0002g0005a0001c0001t0002g0252a0001c0001t0002g0280others(235): Show | 239 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.1045+895A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038248 | ||||||
| chr2:241038379
|
G | C | 1 | a0008c0033t0016g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1045+1026G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038379 | ||||||
| chr2:241038600
|
T | C | 66 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(63): Show | 66 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.1045+1247T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038600 | ||||||
| chr2:241038665
|
G | A | 1 | a0006c0015t0003g0140 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1045+1312G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038665 | ||||||
| chr2:241038684
|
G | T | 45 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(42): Show | 45 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1045+1331G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038684 | ||||||
| chr2:241038739
|
G | A | 2 | a0002c0010t0014g0038a0002c0010t0044g0078 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1046-1336G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038739 | ||||||
| chr2:241038775
|
A | T | 65 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(62): Show | 65 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.1046-1300A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038775 | ||||||
| chr2:241038814
|
T | C | 47 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0002t0020g0308others(44): Show | 48 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1046-1261T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038814 | ||||||
| chr2:241038832
|
C | T | 1 | a0002c0003t0062g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1046-1243C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038832 | ||||||
| chr2:241038840
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1046-1235C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038840 | ||||||
| chr2:241038906
|
G | A | 1 | a0001c0037t0020g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1046-1169G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038906 | ||||||
| chr2:241038958
|
C | A | 1 | a0003c0066t0015g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1046-1117C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241038958 | ||||||
| chr2:241039039
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1046-1036C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039039 | ||||||
| chr2:241039055
|
A | G | 241 | a0001c0001t0001g0334a0001c0001t0002g0005a0001c0001t0002g0252others(238): Show | 242 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.1046-1020A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039055 | ||||||
| chr2:241039102
|
G | A | 1 | a0004c0005t0008g0058 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1046-973G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039102 | ||||||
| chr2:241039172
|
G | A | 3 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037 | 3 | HG02257.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1046-903G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039172 | ||||||
| chr2:241039217
|
G | A | 46 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(43): Show | 46 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1046-858G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039217 | ||||||
| chr2:241039279
|
C | T | 1 | a0001c0001t0052g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1046-796C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039279 | ||||||
| chr2:241039538
|
G | T | 1 | a0001c0002t0017g0143 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1046-537G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039538 | ||||||
| chr2:241039568
|
C | G | 8 | a0002c0052t0011g0256a0002c0073t0063g0007a0009c0030t0027g0127others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1046-507C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039568 | ||||||
| chr2:241039641
|
C | G | 41 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0002t0020g0308others(38): Show | 42 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.1046-434C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039641 | ||||||
| chr2:241039847
|
C | T | 78 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0002t0020g0308others(75): Show | 79 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1046-228C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 6/31 | chr2 | 241039847 | ||||||
| chr2:241040189
|
G | T | 1 | a0003c0004t0007g0099 | 1 | NA18978.hp2 | splice_donor_variant&intron_variant | HIGH | c.1159+1G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 7/31 | chr2 | 241040189 | ||||||
| chr2:241040206
|
G | T | 4 | a0002c0052t0011g0256a0009c0030t0027g0127a0009c0031t0036g0027others(1): Show | 4 | HG02976.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+18G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 7/31 | chr2 | 241040206 | ||||||
| chr2:241040209
|
T | C | 1 | a0002c0052t0011g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1159+21T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 7/31 | chr2 | 241040209 | ||||||
| chr2:241040469
|
A | G | 4 | a0002c0052t0011g0256a0009c0030t0027g0127a0009c0030t0027g0208others(1): Show | 4 | HG02976.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+56A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040469 | ||||||
| chr2:241040653
|
T | C | 5 | a0002c0052t0011g0256a0009c0030t0027g0127a0009c0030t0027g0208others(2): Show | 5 | HG02976.hp2 HG03471.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+240T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040653 | ||||||
| chr2:241040676
|
C | G | 20 | a0002c0009t0004g0040a0002c0009t0004g0146a0002c0009t0004g0332others(17): Show | 20 | HG00423.hp2 HG00597.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+263C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040676 | ||||||
| chr2:241040706
|
A | G | 90 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0002t0020g0308others(87): Show | 91 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1273+293A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040706 | ||||||
| chr2:241040817
|
T | C | 3 | a0006c0012t0001g0001a0006c0012t0001g0311a0006c0012t0005g0309 | 4 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+404T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040817 | ||||||
| chr2:241040846
|
T | C | 3 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1273+433T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040846 | ||||||
| chr2:241040888
|
G | A | 3 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1273+475G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040888 | ||||||
| chr2:241040895
|
G | A | 1 | a0003c0048t0007g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1273+482G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040895 | ||||||
| chr2:241040953
|
G | A | 1 | a0004c0005t0012g0201 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1273+540G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241040953 | ||||||
| chr2:241041011
|
G | A | 1 | a0001c0002t0005g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1273+598G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041011 | ||||||
| chr2:241041034
|
G | A | 3 | a0001c0001t0001g0334a0001c0071t0003g0333a0008c0033t0030g0335 | 3 | HG02145.hp2 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1273+621G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041034 | ||||||
| chr2:241041120
|
G | A | 2 | a0009c0030t0027g0127a0009c0030t0027g0208 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1273+707G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041120 | ||||||
| chr2:241041351
|
G | A | 5 | a0002c0010t0016g0033a0002c0010t0016g0157a0002c0010t0019g0195others(2): Show | 5 | HG02559.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1273+938G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041351 | ||||||
| chr2:241041444
|
G | A | 69 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(66): Show | 69 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.1273+1031G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041444 | ||||||
| chr2:241041483
|
A | G | 160 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(157): Show | 161 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.1273+1070A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041483 | ||||||
| chr2:241041578
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1273+1165G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041578 | ||||||
| chr2:241041653
|
C | T | 2 | a0002c0010t0014g0222a0002c0018t0022g0223 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1273+1240C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041653 | ||||||
| chr2:241041660
|
G | A | 2 | a0002c0003t0008g0283a0003c0024t0004g0281 | 2 | NA19060.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1273+1247G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041660 | ||||||
| chr2:241041688
|
A | G | 5 | a0002c0052t0011g0256a0009c0030t0027g0127a0009c0030t0027g0208others(2): Show | 5 | HG02976.hp2 HG03471.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+1275A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041688 | ||||||
| chr2:241041732
|
G | A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1273+1319G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041732 | ||||||
| chr2:241041842
|
C | G | 1 | a0014c0044t0005g0206 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1273+1429C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041842 | ||||||
| chr2:241041975
|
C | T | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1562C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241041975 | ||||||
| chr2:241042151
|
G | A | 2 | a0001c0002t0003g0177a0001c0002t0009g0187 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1273+1738G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241042151 | ||||||
| chr2:241042400
|
C | G | 7 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0019t0014g0041others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273+1987C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241042400 | ||||||
| chr2:241042429
|
A | C | 1 | a0001c0025t0003g0074 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1273+2016A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241042429 | ||||||
| chr2:241042489
|
A | G | 48 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(45): Show | 49 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.1273+2076A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241042489 | ||||||
| chr2:241042532
|
C | A | 1 | a0001c0002t0009g0109 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1273+2119C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241042532 | ||||||
| chr2:241042650
|
GA | G | 13 | a0001c0001t0002g0005a0001c0001t0020g0004a0001c0001t0053g0013others(10): Show | 13 | HG02027.hp2 HG02155.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1273+2244delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241042650 | |||||
| chr2:241042869
|
C | T | 5 | a0002c0052t0011g0256a0009c0030t0027g0127a0009c0030t0027g0208others(2): Show | 5 | HG02976.hp2 HG03471.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+2456C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241042869 | ||||||
| chr2:241042948
|
C | T | 80 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(77): Show | 81 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1273+2535C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241042948 | ||||||
| chr2:241043006
|
T | C | 90 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(87): Show | 91 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.1273+2593T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043006 | ||||||
| chr2:241043061
|
G | A | 1 | a0005c0014t0001g0091 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1273+2648G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043061 | ||||||
| chr2:241043188
|
A | G | 10 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1273+2775A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043188 | ||||||
| chr2:241043204
|
A | G | 7 | a0001c0002t0003g0161a0001c0002t0003g0180a0001c0002t0003g0315others(4): Show | 7 | NA18954.hp1 NA18955.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273+2791A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043204 | ||||||
| chr2:241043292
|
C | G | 65 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(62): Show | 65 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.1273+2879C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043292 | ||||||
| chr2:241043427
|
T | C | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1273+3014T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043427 | ||||||
| chr2:241043490
|
T | G | 32 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0009t0004g0040others(29): Show | 32 | HG00423.hp2 HG00597.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1273+3077T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043490 | ||||||
| chr2:241043551
|
A | G | 32 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0009t0004g0040others(29): Show | 32 | HG00423.hp2 HG00597.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1273+3138A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043551 | ||||||
| chr2:241043605
|
G | A | 45 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(42): Show | 45 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1273+3192G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043605 | ||||||
| chr2:241043661
|
C | T | 66 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(63): Show | 66 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.1273+3248C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043661 | ||||||
| chr2:241043710
|
A | G | 5 | a0001c0002t0003g0136a0006c0015t0003g0137a0006c0015t0003g0138others(2): Show | 5 | NA18940.hp2 NA18948.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1273+3297A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043710 | ||||||
| chr2:241043745
|
T | C | 6 | a0004c0005t0004g0151a0004c0005t0031g0059a0004c0005t0031g0061others(3): Show | 6 | HG01934.hp1 HG02040.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273+3332T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043745 | ||||||
| chr2:241043760
|
A | G | 2 | a0002c0010t0014g0038a0002c0010t0044g0078 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1273+3347A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241043760 | ||||||
| chr2:241044080
|
C | T | 86 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(83): Show | 87 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1273+3667C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044080 | ||||||
| chr2:241044117
|
A | G | 65 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(62): Show | 65 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.1273+3704A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044117 | ||||||
| chr2:241044158
|
G | A | 49 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(46): Show | 50 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1273+3745G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044158 | ||||||
| chr2:241044174
|
T | C | 3 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1273+3761T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044174 | ||||||
| chr2:241044176
|
G | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1273+3763G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044176 | ||||||
| chr2:241044204
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1273+3791T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044204 | ||||||
| chr2:241044271
|
T | C | 80 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(77): Show | 81 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1273+3858T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044271 | ||||||
| chr2:241044314
|
C | CT | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+3902dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241044314 | |||||
| chr2:241044327
|
C | T | 1 | a0001c0002t0001g0171 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1273+3914C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044327 | ||||||
| chr2:241044337
|
T | C | 2 | a0002c0003t0008g0020a0002c0003t0008g0113 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1273+3924T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044337 | ||||||
| chr2:241044618
|
G | A | 1 | a0008c0033t0016g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1274-3697G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044618 | ||||||
| chr2:241044696
|
C | T | 3 | a0002c0073t0063g0007a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1274-3619C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044696 | ||||||
| chr2:241044880
|
G | A | 2 | a0002c0010t0014g0038a0002c0010t0044g0078 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1274-3435G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241044880 | ||||||
| chr2:241045084
|
T | G | 1 | a0006c0012t0005g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1274-3231T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045084 | ||||||
| chr2:241045183
|
T | C | 1 | a0003c0004t0006g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1274-3132T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045183 | ||||||
| chr2:241045186
|
T | A | 10 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1274-3129T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045186 | ||||||
| chr2:241045207
|
G | A | 45 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(42): Show | 45 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1274-3108G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045207 | ||||||
| chr2:241045223
|
T | C | 1 | a0002c0003t0004g0011 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1274-3092T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045223 | ||||||
| chr2:241045353
|
T | C | 1 | a0002c0013t0015g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1274-2962T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045353 | ||||||
| chr2:241045713
|
C | CA | 77 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(74): Show | 77 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(74): Show |
intron_variant | MODIFIER | c.1274-2588dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241045713 | |||||
| chr2:241045727
|
AT | A | 3 | a0002c0073t0063g0007a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1274-2585delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241045727 | |||||
| chr2:241045728
|
T | A | 8 | a0002c0008t0061g0168a0002c0013t0011g0207a0002c0013t0011g0214others(5): Show | 8 | HG01099.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1274-2587T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045728 | ||||||
| chr2:241045890
|
G | A | 1 | a0002c0018t0022g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1274-2425G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045890 | ||||||
| chr2:241045922
|
T | G | 2 | a0003c0024t0004g0269a0003c0024t0010g0286 | 2 | HG02080.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1274-2393T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045922 | ||||||
| chr2:241045994
|
A | G | 1 | a0005c0014t0001g0125 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1274-2321A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241045994 | ||||||
| chr2:241046111
|
C | T | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1274-2204C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241046111 | ||||||
| chr2:241046343
|
A | C | 10 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1274-1972A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241046343 | ||||||
| chr2:241046613
|
A | C | 66 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(63): Show | 66 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.1274-1702A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241046613 | ||||||
| chr2:241046850
|
A | G | 28 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(25): Show | 28 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1274-1465A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241046850 | ||||||
| chr2:241046870
|
C | T | 80 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(77): Show | 81 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1274-1445C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241046870 | ||||||
| chr2:241046872
|
T | C | 61 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(58): Show | 61 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1274-1443T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241046872 | ||||||
| chr2:241046960
|
G | T | 141 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(138): Show | 142 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1274-1355G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241046960 | ||||||
| chr2:241047102
|
G | T | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1274-1213G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047102 | ||||||
| chr2:241047146
|
C | CA | 17 | a0001c0001t0001g0067a0001c0001t0002g0018a0001c0001t0002g0063others(14): Show | 17 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1274-1146dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047146 | |||||
| chr2:241047146
|
CA | C | 13 | a0001c0001t0001g0305a0001c0074t0002g0086a0002c0011t0011g0029others(10): Show | 13 | HG01070.hp1 HG02647.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1274-1146delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047146 | |||||
| chr2:241047164
|
AAAAAAGT | A | 39 | a0001c0037t0002g0314a0001c0037t0020g0030a0001c0068t0018g0320others(36): Show | 39 | HG00423.hp2 HG00597.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1274-1147_1274-114 others(11): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047164 | |||||
| chr2:241047165
|
AAAAAGT | A | 55 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(52): Show | 55 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1274-1146_1274-114 others(10): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047165 | |||||
| chr2:241047167
|
AAAGT | A | 6 | a0001c0002t0017g0323a0002c0008t0061g0168a0003c0004t0032g0123others(3): Show | 6 | HG04184.hp1 NA18906.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1274-1145_1274-114 others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047167 | |||||
| chr2:241047168
|
AAGT | A | 43 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(40): Show | 44 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1274-1145_1274-114 others(7): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047168 | |||||
| chr2:241047169
|
AGT | A | 4 | a0003c0004t0006g0103a0003c0004t0006g0114a0003c0004t0007g0099others(1): Show | 4 | HG01081.hp1 NA18978.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1274-1145_1274-114 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047169 | ||||||
| chr2:241047170
|
GTAAAT | G | 59 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(56): Show | 59 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.1274-1142_1274-113 others(9): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047170 | |||||
| chr2:241047171
|
T | A | 1 | a0007c0041t0007g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1274-1144T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047171 | ||||||
| chr2:241047175
|
T | G | 149 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(146): Show | 150 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.1274-1140T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047175 | ||||||
| chr2:241047253
|
C | T | 3 | a0002c0073t0063g0007a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1274-1062C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047253 | ||||||
| chr2:241047290
|
G | A | 2 | a0001c0006t0001g0108a0001c0006t0002g0076 | 2 | NA18942.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1274-1025G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047290 | ||||||
| chr2:241047510
|
C | A | 1 | a0001c0001t0005g0240 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1274-805C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047510 | ||||||
| chr2:241047581
|
AG | A | 4 | a0002c0009t0016g0220a0008c0081t0021g0031a0012c0079t0016g0331others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1274-732delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047581 | |||||
| chr2:241047621
|
T | C | 57 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(54): Show | 57 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1274-694T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047621 | ||||||
| chr2:241047785
|
GTC | G | 59 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(56): Show | 59 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1274-524_1274-523d others(4): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047785 | |||||
| chr2:241047813
|
T | A | 49 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(46): Show | 50 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1274-502T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047813 | ||||||
| chr2:241047818
|
A | G | 49 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(46): Show | 50 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1274-497A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047818 | ||||||
| chr2:241047944
|
T | C | 9 | a0002c0010t0014g0222a0002c0018t0022g0223a0003c0004t0006g0097others(6): Show | 9 | HG01884.hp1 HG06807.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1274-371T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047944 | ||||||
| chr2:241047944
|
T | TGGTGCTT others(31): Show |
3 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329 | 3 | HG02109.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1274-334_1274-333i others(40): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047944 | |||||
| chr2:241047982
|
T | C | 85 | a0001c0002t0009g0310a0001c0002t0018g0339a0001c0020t0001g0105others(82): Show | 86 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1274-333T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241047982 | ||||||
| chr2:241047982
|
T | TGGTGCTT others(31): Show |
9 | a0001c0068t0018g0320a0002c0010t0016g0033a0002c0010t0016g0157others(6): Show | 9 | HG02559.hp1 HG02970.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1274-262_1274-225d others(40): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047982 | |||||
| chr2:241047982
|
T | TGGTGCTT others(69): Show |
45 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(42): Show | 45 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1274-300_1274-225d others(78): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241047982 | |||||
| chr2:241048003
|
A | ATCCTGGG others(31): Show |
2 | a0002c0010t0014g0222a0002c0018t0022g0223 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1274-275_1274-274i others(40): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr2 | 241048003 | |||||
| chr2:241048137
|
G | A | 68 | a0001c0002t0001g0075a0001c0002t0001g0171a0001c0002t0001g0172others(65): Show | 68 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(65): Show |
intron_variant | MODIFIER | c.1274-178G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241048137 | ||||||
| chr2:241048146
|
G | A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1274-169G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241048146 | ||||||
| chr2:241048264
|
C | T | 2 | a0001c0006t0002g0088a0001c0006t0002g0089 | 2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1274-51C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 8/31 | chr2 | 241048264 | ||||||
| chr2:241048788
|
C | A | 1 | a0008c0033t0016g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1504+22C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 10/31 | chr2 | 241048788 | ||||||
| chr2:241048830
|
G | A | 1 | a0001c0001t0005g0300 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1504+64G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 10/31 | chr2 | 241048830 | ||||||
| chr2:241048842
|
G | A | 3 | a0002c0073t0063g0007a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1504+76G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 10/31 | chr2 | 241048842 | ||||||
| chr2:241048858
|
G | A | 1 | a0002c0013t0011g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1504+92G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 10/31 | chr2 | 241048858 | ||||||
| chr2:241048973
|
G | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1505-49G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 10/31 | chr2 | 241048973 | ||||||
| chr2:241048975
|
T | C | 40 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(37): Show | 40 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1505-47T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 10/31 | chr2 | 241048975 | ||||||
| chr2:241049146
|
C | T | 11 | a0001c0074t0002g0086a0002c0003t0022g0023a0002c0011t0011g0029others(8): Show | 11 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1618+11C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 11/31 | chr2 | 241049146 | ||||||
| chr2:241049383
|
T | A | 1 | a0002c0075t0045g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1618+248T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 11/31 | chr2 | 241049383 | ||||||
| chr2:241049456
|
C | T | 1 | a0001c0002t0020g0308 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1618+321C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 11/31 | chr2 | 241049456 | ||||||
| chr2:241049981
|
G | T | 2 | a0001c0060t0005g0193a0002c0003t0013g0194 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1735+48G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241049981 | ||||||
| chr2:241050011
|
G | C | 1 | a0002c0011t0015g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1735+78G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050011 | ||||||
| chr2:241050284
|
G | T | 1 | a0003c0066t0015g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1735+351G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050284 | ||||||
| chr2:241050306
|
T | C | 71 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(68): Show | 71 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1735+373T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050306 | ||||||
| chr2:241050397
|
A | G | 1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1735+464A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050397 | ||||||
| chr2:241050534
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0002g0065 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1735+601G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050534 | ||||||
| chr2:241050791
|
C | G | 4 | a0003c0004t0007g0099a0003c0004t0010g0212a0003c0023t0006g0237others(1): Show | 4 | HG02165.hp2 NA18951.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735+858C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050791 | ||||||
| chr2:241050828
|
A | AG | 67 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(64): Show | 67 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1735+897dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr2 | 241050828 | |||||
| chr2:241050830
|
GT | G | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735+898delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050830 | ||||||
| chr2:241050831
|
T | G | 254 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(251): Show | 255 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.1735+898T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050831 | ||||||
| chr2:241050836
|
G | T | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735+903G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050836 | ||||||
| chr2:241050857
|
C | T | 3 | a0008c0032t0021g0328a0008c0032t0021g0329a0008c0081t0021g0031 | 3 | HG02109.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1736-887C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050857 | ||||||
| chr2:241050971
|
C | T | 3 | a0002c0010t0016g0033a0002c0010t0016g0157a0002c0036t0014g0326 | 3 | HG02559.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1736-773C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050971 | ||||||
| chr2:241050995
|
G | C | 1 | a0007c0027t0001g0267 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1736-749G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241050995 | ||||||
| chr2:241051020
|
G | C | 1 | a0003c0066t0015g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1736-724G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051020 | ||||||
| chr2:241051022
|
C | T | 1 | a0002c0018t0022g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1736-722C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051022 | ||||||
| chr2:241051034
|
G | C | 8 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0010t0044g0078others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1736-710G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051034 | ||||||
| chr2:241051055
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1736-689C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051055 | ||||||
| chr2:241051179
|
T | G | 2 | a0002c0003t0010g0218a0002c0003t0013g0219 | 2 | NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1736-565T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051179 | ||||||
| chr2:241051210
|
G | A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1736-534G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051210 | ||||||
| chr2:241051282
|
G | A | 36 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(33): Show | 36 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1736-462G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051282 | ||||||
| chr2:241051310
|
C | T | 63 | a0001c0002t0001g0182a0001c0002t0001g0324a0001c0002t0002g0184others(60): Show | 63 | HG00738.hp2 HG01099.hp2 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.1736-434C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051310 | ||||||
| chr2:241051369
|
G | A | 3 | a0001c0037t0002g0314a0001c0037t0020g0030a0002c0082t0039g0032 | 3 | HG02572.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1736-375G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051369 | ||||||
| chr2:241051437
|
G | A | 36 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(33): Show | 36 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1736-307G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051437 | ||||||
| chr2:241051441
|
G | A | 2 | a0002c0003t0008g0020a0002c0003t0008g0113 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1736-303G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051441 | ||||||
| chr2:241051443
|
T | G | 1 | a0001c0002t0048g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1736-301T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051443 | ||||||
| chr2:241051507
|
A | G | 1 | a0008c0033t0030g0335 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1736-237A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051507 | ||||||
| chr2:241051604
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1736-140C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051604 | ||||||
| chr2:241051612
|
A | G | 252 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(249): Show | 253 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.1736-132A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051612 | ||||||
| chr2:241051702
|
C | A | 1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1736-42C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051702 | ||||||
| chr2:241051728
|
C | T | 9 | a0001c0001t0001g0098a0001c0001t0001g0163a0001c0001t0001g0166others(6): Show | 9 | HG00423.hp1 HG02056.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1736-16C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 12/31 | chr2 | 241051728 | ||||||
| chr2:241052479
|
CAG | C | 15 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(12): Show | 15 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2083+12_2083+13del others(2): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052479 | ||||||
| chr2:241052486
|
A | G | 70 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(67): Show | 70 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2083+18A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052486 | ||||||
| chr2:241052506
|
T | C | 1 | a0002c0075t0045g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2083+38T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052506 | ||||||
| chr2:241052507
|
A | G | 1 | a0002c0075t0045g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2083+39A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052507 | ||||||
| chr2:241052510
|
A | G | 1 | a0002c0075t0045g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2083+42A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052510 | ||||||
| chr2:241052526
|
G | C | 4 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2083+58G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052526 | ||||||
| chr2:241052528
|
T | G | 7 | a0002c0010t0016g0033a0002c0010t0016g0157a0002c0010t0019g0195others(4): Show | 7 | HG02280.hp1 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2083+60T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052528 | ||||||
| chr2:241052533
|
A | AG | 17 | a0001c0006t0001g0116a0001c0068t0018g0320a0002c0010t0014g0038others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2083+68dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052533 | |||||
| chr2:241052533
|
AGGGCCCA others(263): Show |
A | 1 | a0002c0003t0008g0259 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2083+90_2084-326de others(1): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052533 | |||||
| chr2:241052537
|
C | G | 17 | a0001c0006t0001g0116a0001c0068t0018g0320a0002c0010t0014g0038others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2083+69C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052537 | ||||||
| chr2:241052550
|
C | T | 16 | a0001c0006t0001g0116a0001c0068t0018g0320a0002c0010t0014g0038others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2083+82C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052550 | ||||||
| chr2:241052579
|
G | T | 16 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(13): Show | 16 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2083+111G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052579 | ||||||
| chr2:241052583
|
CAGGGGGC others(211): Show |
C | 3 | a0001c0006t0001g0116a0008c0033t0016g0221a0008c0033t0030g0335 | 3 | HG02280.hp1 HG02738.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2083+116_2083+333d others(2): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052583 | ||||||
| chr2:241052584
|
AG | A | 15 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(12): Show | 15 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2083+121delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052584 | |||||
| chr2:241052585
|
G | GGGCCCAA others(43): Show |
1 | a0002c0003t0007g0284 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2083+119_2083+120i others(52): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052585 | |||||
| chr2:241052589
|
G | C | 16 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(13): Show | 16 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2083+121G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052589 | ||||||
| chr2:241052599
|
A | G | 249 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(246): Show | 250 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(247): Show |
intron_variant | MODIFIER | c.2083+131A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052599 | ||||||
| chr2:241052600
|
T | C | 1 | a0001c0025t0009g0291 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2083+132T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052600 | ||||||
| chr2:241052602
|
T | C | 16 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(13): Show | 16 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2083+134T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052602 | ||||||
| chr2:241052634
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2083+166C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052634 | ||||||
| chr2:241052635
|
CGGGGGGC others(159): Show |
C | 5 | a0001c0006t0001g0257a0001c0006t0002g0076a0001c0006t0002g0084others(2): Show | 5 | HG02027.hp2 HG02155.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2083+173_2083+338d others(2): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052635 | |||||
| chr2:241052636
|
G | A | 193 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(190): Show | 194 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(191): Show |
intron_variant | MODIFIER | c.2083+168G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052636 | ||||||
| chr2:241052641
|
G | C | 7 | a0001c0006t0001g0054a0001c0006t0001g0108a0001c0006t0001g0258others(4): Show | 7 | HG00438.hp2 HG00673.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2083+173G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052641 | ||||||
| chr2:241052642
|
CCAAGCAG others(56): Show |
C | 14 | a0001c0001t0005g0299a0001c0001t0009g0278a0001c0001t0017g0272others(11): Show | 14 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.2083+193_2083+255d others(65): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052642 | |||||
| chr2:241052654
|
C | T | 14 | a0001c0068t0018g0320a0002c0010t0014g0038a0002c0010t0014g0222others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2083+186C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052654 | ||||||
| chr2:241052661
|
C | T | 15 | a0001c0068t0018g0320a0002c0010t0014g0038a0002c0010t0014g0222others(12): Show | 15 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2083+193C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052661 | ||||||
| chr2:241052664
|
C | T | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2083+196C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052664 | ||||||
| chr2:241052665
|
G | A | 26 | a0001c0006t0001g0054a0001c0006t0001g0108a0001c0006t0001g0258others(23): Show | 26 | HG00438.hp2 HG00673.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.2083+197G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052665 | ||||||
| chr2:241052669
|
C | T | 21 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(18): Show | 21 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2083+201C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052669 | ||||||
| chr2:241052669
|
CCAGGCAG others(159): Show |
C | 12 | a0001c0001t0009g0274a0001c0006t0001g0054a0001c0006t0001g0108others(9): Show | 12 | HG00438.hp2 HG00673.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2083+215_2084-305d others(2): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052669 | |||||
| chr2:241052686
|
T | C | 31 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(28): Show | 31 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2083+218T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052686 | ||||||
| chr2:241052687
|
CGGCGGGG others(3): Show |
C | 1 | a0002c0003t0007g0284 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2083+222_2083+231d others(12): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052687 | |||||
| chr2:241052687
|
CGGCGGGG others(4): Show |
C | 14 | a0001c0068t0018g0320a0002c0010t0014g0038a0002c0010t0014g0222others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2083+222_2083+232d others(13): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052687 | |||||
| chr2:241052688
|
G | A | 5 | a0002c0003t0007g0131a0002c0003t0008g0283a0002c0008t0033g0287others(2): Show | 5 | HG02300.hp2 HG03098.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.2083+220G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052688 | ||||||
| chr2:241052690
|
C | CG | 44 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(41): Show | 44 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.2083+236dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052690 | |||||
| chr2:241052690
|
C | G | 14 | a0001c0001t0002g0252a0001c0001t0005g0134a0002c0003t0004g0011others(11): Show | 14 | HG00609.hp2 HG00621.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.2083+222C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052690 | ||||||
| chr2:241052690
|
CG | C | 46 | a0001c0020t0042g0154a0001c0074t0002g0086a0002c0009t0012g0312others(43): Show | 46 | HG00738.hp1 HG01099.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.2083+236delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052690 | |||||
| chr2:241052690
|
CGG | C | 73 | a0001c0002t0009g0109a0001c0002t0009g0211a0001c0002t0023g0247others(70): Show | 74 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.2083+235_2083+236d others(4): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052690 | |||||
| chr2:241052690
|
CGGG | C | 57 | a0001c0002t0001g0182a0001c0002t0001g0324a0001c0002t0002g0184others(54): Show | 57 | HG00738.hp2 HG01099.hp2 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.2083+234_2083+236d others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052690 | |||||
| chr2:241052693
|
G | GCCAAGCA others(290): Show |
1 | a0002c0003t0004g0011 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2083+225_2083+226i others(299): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052693 | ||||||
| chr2:241052693
|
G | GCCAAGCA others(705): Show |
5 | a0001c0001t0002g0252a0002c0003t0010g0260a0002c0003t0013g0049others(2): Show | 5 | HG00621.hp2 HG02155.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.2083+225_2083+226i others(714): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052693 | ||||||
| chr2:241052693
|
G | GCCAAGCA others(446): Show |
1 | a0002c0003t0010g0268 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2083+225_2083+226i others(455): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052693 | ||||||
| chr2:241052693
|
G | GCCAAGCA others(551): Show |
1 | a0002c0061t0008g0253 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2083+225_2083+226i others(560): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052693 | ||||||
| chr2:241052693
|
G | GCCAAGCA others(498): Show |
1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2083+225_2083+226i others(507): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052693 | ||||||
| chr2:241052693
|
G | GCCAAGCA others(34): Show |
1 | a0002c0075t0045g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2083+225_2083+226i others(43): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052693 | ||||||
| chr2:241052694
|
G | C | 1 | a0002c0003t0008g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2083+226G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052694 | ||||||
| chr2:241052694
|
G | GTCAAGCA others(345): Show |
1 | a0002c0008t0033g0287 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2083+226_2083+227i others(354): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052694 | ||||||
| chr2:241052694
|
G | GTCAAGCA others(86): Show |
1 | a0002c0003t0008g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2083+226_2083+227i others(95): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052694 | ||||||
| chr2:241052694
|
G | GTCAAGCA others(137): Show |
1 | a0003c0024t0004g0281 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2083+226_2083+227i others(146): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052694 | ||||||
| chr2:241052694
|
G | GTCAAGCA others(395): Show |
1 | a0002c0003t0007g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2083+226_2083+227i others(404): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052694 | ||||||
| chr2:241052695
|
G | GCCAAGCA others(138): Show |
6 | a0001c0001t0002g0280a0002c0003t0008g0020a0002c0003t0008g0113others(3): Show | 6 | HG01081.hp2 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2083+227_2083+228i others(147): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052695 | ||||||
| chr2:241052695
|
G | GCCAAGCA others(191): Show |
1 | a0001c0001t0002g0297 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2083+227_2083+228i others(200): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052695 | ||||||
| chr2:241052695
|
G | T | 1 | a0003c0024t0004g0281 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2083+227G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052695 | ||||||
| chr2:241052696
|
G | A | 1 | a0002c0003t0007g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2083+228G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052696 | ||||||
| chr2:241052697
|
G | C | 10 | a0001c0001t0002g0252a0001c0001t0005g0134a0002c0003t0004g0011others(7): Show | 10 | HG00609.hp2 HG00621.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.2083+229G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052697 | ||||||
| chr2:241052698
|
G | A | 2 | a0002c0003t0007g0284a0002c0008t0033g0287 | 2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2083+230G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052698 | ||||||
| chr2:241052698
|
G | C | 19 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(16): Show | 19 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2083+230G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052698 | ||||||
| chr2:241052699
|
G | A | 24 | a0001c0001t0002g0252a0001c0001t0005g0134a0001c0068t0018g0320others(21): Show | 24 | HG00609.hp2 HG00621.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.2083+231G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052699 | ||||||
| chr2:241052699
|
G | C | 9 | a0001c0001t0002g0280a0001c0001t0002g0297a0002c0003t0008g0020others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.2083+231G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052699 | ||||||
| chr2:241052699
|
G | T | 2 | a0009c0031t0028g0224a0009c0031t0036g0027 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2083+231G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052699 | ||||||
| chr2:241052700
|
G | A | 9 | a0001c0001t0002g0280a0001c0001t0002g0297a0002c0003t0008g0020others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.2083+232G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052700 | ||||||
| chr2:241052702
|
G | C | 1 | a0015c0046t0040g0336 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2083+234G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052702 | ||||||
| chr2:241052704
|
G | C | 9 | a0001c0001t0002g0280a0001c0001t0002g0297a0002c0003t0008g0020others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.2083+236G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052704 | ||||||
| chr2:241052705
|
T | C | 34 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(31): Show | 34 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.2083+237T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052705 | ||||||
| chr2:241052717
|
C | T | 41 | a0001c0001t0002g0252a0001c0001t0005g0134a0001c0001t0005g0299others(38): Show | 41 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.2083+249C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052717 | ||||||
| chr2:241052724
|
T | C | 2 | a0002c0003t0007g0284a0002c0008t0033g0287 | 2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2083+256T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052724 | ||||||
| chr2:241052728
|
A | G | 1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2083+260A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052728 | ||||||
| chr2:241052746
|
G | T | 1 | a0002c0003t0008g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2083+278G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052746 | ||||||
| chr2:241052748
|
G | A | 1 | a0002c0003t0062g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2083+280G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052748 | ||||||
| chr2:241052749
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2083+281C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052749 | ||||||
| chr2:241052750
|
CGGGGGGC others(44): Show |
C | 6 | a0001c0068t0018g0320a0002c0010t0016g0033a0002c0010t0016g0157others(3): Show | 6 | HG02559.hp1 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2083+288_2083+338d others(53): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052750 | |||||
| chr2:241052751
|
G | A | 8 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0010t0044g0078others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2083+283G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052751 | ||||||
| chr2:241052752
|
G | A | 1 | a0002c0003t0008g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2083+284G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052752 | ||||||
| chr2:241052756
|
G | C | 1 | a0002c0003t0008g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2083+288G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052756 | ||||||
| chr2:241052756
|
G | GCCAAGCA others(95): Show |
1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2084-309_2084-308i others(104): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052756 | |||||
| chr2:241052756
|
G | GCCAAGCA others(94): Show |
62 | a0001c0002t0001g0182a0001c0002t0001g0324a0001c0002t0002g0184others(59): Show | 62 | HG00738.hp2 HG01099.hp2 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.2084-309_2084-308i others(103): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052756 | |||||
| chr2:241052757
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2083+289C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052757 | ||||||
| chr2:241052758
|
C | T | 1 | a0002c0008t0033g0287 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2083+290C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052758 | ||||||
| chr2:241052759
|
A | G | 1 | a0002c0008t0033g0287 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2083+291A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052759 | ||||||
| chr2:241052769
|
C | T | 8 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0010t0044g0078others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2083+301C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052769 | ||||||
| chr2:241052776
|
T | C | 34 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(31): Show | 34 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2083+308T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052776 | ||||||
| chr2:241052777
|
G | A | 44 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(41): Show | 44 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2083+309G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052777 | ||||||
| chr2:241052779
|
T | C | 44 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(41): Show | 44 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2083+311T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052779 | ||||||
| chr2:241052780
|
G | A | 10 | a0002c0003t0008g0283a0002c0010t0014g0038a0002c0010t0014g0222others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2083+312G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052780 | ||||||
| chr2:241052784
|
T | C | 10 | a0002c0003t0008g0283a0002c0010t0014g0038a0002c0010t0014g0222others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2083+316T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052784 | ||||||
| chr2:241052793
|
T | TGAG | 44 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(41): Show | 44 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2083+325_2083+326i others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052793 | ||||||
| chr2:241052795
|
A | G | 44 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(41): Show | 44 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2083+327A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052795 | ||||||
| chr2:241052798
|
C | T | 13 | a0001c0001t0005g0299a0001c0001t0009g0278a0001c0001t0017g0272others(10): Show | 13 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.2083+330C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052798 | ||||||
| chr2:241052799
|
CTG | C | 31 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(28): Show | 31 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2083+332_2083+333d others(4): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052799 | ||||||
| chr2:241052800
|
T | A | 13 | a0001c0001t0005g0299a0001c0001t0009g0278a0001c0001t0017g0272others(10): Show | 13 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.2083+332T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052800 | ||||||
| chr2:241052806
|
GC | G | 13 | a0001c0001t0005g0299a0001c0001t0009g0278a0001c0001t0017g0272others(10): Show | 13 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.2083+341delC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr2 | 241052806 | |||||
| chr2:241052807
|
C | G | 23 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(20): Show | 23 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.2083+339C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052807 | ||||||
| chr2:241052808
|
C | T | 13 | a0001c0001t0005g0299a0001c0001t0009g0278a0001c0001t0017g0272others(10): Show | 13 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.2083+340C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052808 | ||||||
| chr2:241052827
|
T | C | 57 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(54): Show | 57 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2084-326T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052827 | ||||||
| chr2:241052828
|
G | A | 57 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(54): Show | 57 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2084-325G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052828 | ||||||
| chr2:241052829
|
C | T | 1 | a0005c0007t0001g0056 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2084-324C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052829 | ||||||
| chr2:241052831
|
G | A | 56 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.2084-322G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052831 | ||||||
| chr2:241052835
|
T | C | 56 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(53): Show | 56 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.2084-318T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052835 | ||||||
| chr2:241052836
|
C | G | 68 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(65): Show | 68 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2084-317C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052836 | ||||||
| chr2:241052849
|
T | G | 1 | a0002c0003t0008g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2084-304T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052849 | ||||||
| chr2:241052861
|
C | T | 65 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(62): Show | 65 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.2084-292C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052861 | ||||||
| chr2:241052862
|
G | A | 1 | a0002c0003t0008g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2084-291G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052862 | ||||||
| chr2:241052975
|
G | A | 1 | a0001c0002t0009g0178 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2084-178G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241052975 | ||||||
| chr2:241053080
|
G | A | 3 | a0002c0010t0016g0033a0002c0010t0016g0157a0002c0036t0014g0326 | 3 | HG02559.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2084-73G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241053080 | ||||||
| chr2:241053095
|
G | A | 1 | a0001c0068t0018g0320 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2084-58G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241053095 | ||||||
| chr2:241053125
|
G | C | 1 | a0004c0005t0004g0203 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2084-28G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 15/31 | chr2 | 241053125 | ||||||
| chr2:241053402
|
G | A | 1 | a0003c0056t0007g0009 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2257+76G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241053402 | ||||||
| chr2:241053610
|
C | T | 309 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0079others(306): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2257+284C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241053610 | ||||||
| chr2:241053761
|
A | T | 4 | a0002c0009t0016g0220a0012c0049t0019g0050a0012c0079t0016g0331others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+435A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241053761 | ||||||
| chr2:241053979
|
A | G | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2257+653A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241053979 | ||||||
| chr2:241054141
|
A | AG | 257 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(254): Show | 258 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(255): Show |
intron_variant | MODIFIER | c.2257+817dupG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241054141 | |||||
| chr2:241054182
|
A | G | 15 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(12): Show | 15 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2257+856A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241054182 | ||||||
| chr2:241054207
|
C | T | 2 | a0009c0031t0028g0224a0009c0031t0036g0027 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2257+881C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241054207 | ||||||
| chr2:241054225
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2257+899A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241054225 | ||||||
| chr2:241054529
|
CTG | C | 4 | a0002c0003t0008g0066a0002c0003t0008g0259a0002c0003t0008g0277others(1): Show | 4 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+1205_2257+120 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241054529 | |||||
| chr2:241054607
|
G | A | 15 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(12): Show | 15 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2257+1281G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241054607 | ||||||
| chr2:241054680
|
G | A | 21 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(18): Show | 21 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2257+1354G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241054680 | ||||||
| chr2:241054829
|
T | C | 1 | a0001c0068t0018g0320 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2257+1503T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241054829 | ||||||
| chr2:241054973
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2257+1647C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241054973 | ||||||
| chr2:241055048
|
C | T | 1 | a0001c0037t0002g0314 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2257+1722C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055048 | ||||||
| chr2:241055116
|
CA | C | 72 | a0001c0001t0001g0117a0001c0001t0002g0252a0001c0001t0002g0280others(69): Show | 72 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.2257+1802delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241055116 | |||||
| chr2:241055225
|
G | A | 1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2257+1899G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055225 | ||||||
| chr2:241055337
|
G | A | 1 | a0008c0033t0016g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2257+2011G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055337 | ||||||
| chr2:241055567
|
C | T | 4 | a0002c0009t0016g0220a0012c0049t0019g0050a0012c0079t0016g0331others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+2241C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055567 | ||||||
| chr2:241055597
|
G | T | 259 | a0001c0001t0001g0141a0001c0001t0002g0129a0001c0001t0002g0252others(256): Show | 260 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(257): Show |
intron_variant | MODIFIER | c.2257+2271G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055597 | ||||||
| chr2:241055624
|
T | C | 4 | a0002c0009t0016g0220a0012c0049t0019g0050a0012c0079t0016g0331others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+2298T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055624 | ||||||
| chr2:241055808
|
G | C | 18 | a0001c0071t0003g0333a0001c0074t0002g0086a0002c0011t0011g0029others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2257+2482G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055808 | ||||||
| chr2:241055955
|
G | A | 1 | a0003c0004t0007g0099 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2257+2629G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241055955 | ||||||
| chr2:241056041
|
G | GAAGCAAG others(323): Show |
3 | a0002c0008t0019g0227a0008c0032t0021g0329a0008c0081t0021g0031 | 3 | HG02723.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2257+2727_2257+272 others(334): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056041 | |||||
| chr2:241056041
|
G | GAAGCAAG others(324): Show |
1 | a0008c0032t0021g0328 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2257+2727_2257+272 others(335): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056041 | |||||
| chr2:241056261
|
G | A | 1 | a0002c0008t0008g0255 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2257+2935G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241056261 | ||||||
| chr2:241056282
|
T | C | 70 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(67): Show | 70 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2257+2956T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241056282 | ||||||
| chr2:241056453
|
C | T | 1 | a0001c0045t0002g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2257+3127C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241056453 | ||||||
| chr2:241056580
|
A | ATTTTTT | 40 | a0001c0020t0001g0105a0001c0020t0042g0154a0001c0020t0057g0341others(37): Show | 41 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.2257+3267_2257+327 others(10): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056580 | |||||
| chr2:241056580
|
A | ATTTTTTT | 11 | a0002c0018t0010g0264a0002c0022t0014g0087a0002c0022t0014g0327others(8): Show | 11 | HG01516.hp2 HG01884.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.2257+3266_2257+327 others(11): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056580 | |||||
| chr2:241056580
|
A | ATTTTTTT others(1): Show |
22 | a0001c0001t0002g0252a0001c0071t0003g0333a0001c0074t0002g0086others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2257+3265_2257+327 others(12): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056580 | |||||
| chr2:241056580
|
A | ATTTTTTT others(2): Show |
45 | a0001c0001t0002g0280a0001c0001t0002g0297a0001c0001t0005g0134others(42): Show | 45 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2257+3264_2257+327 others(13): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056580 | |||||
| chr2:241056580
|
A | ATTTTTTT others(3): Show |
104 | a0001c0001t0001g0141a0001c0001t0005g0299a0001c0002t0002g0184others(101): Show | 104 | HG00423.hp2 HG00597.hp1 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.2257+3263_2257+327 others(14): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056580 | |||||
| chr2:241056580
|
A | ATTTTTTT others(4): Show |
29 | a0001c0001t0009g0274a0001c0001t0017g0273a0001c0002t0001g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.2257+3262_2257+327 others(15): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056580 | |||||
| chr2:241056580
|
A | ATTTTTTT others(5): Show |
6 | a0001c0002t0003g0149a0001c0006t0001g0108a0001c0006t0002g0089others(3): Show | 6 | HG00438.hp2 HG01928.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2257+3261_2257+327 others(16): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241056580 | |||||
| chr2:241056681
|
C | T | 1 | a0003c0004t0006g0002 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2257+3355C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241056681 | ||||||
| chr2:241056726
|
G | A | 1 | a0008c0033t0030g0335 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2257+3400G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241056726 | ||||||
| chr2:241056781
|
C | G | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+3455C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241056781 | ||||||
| chr2:241056917
|
C | T | 1 | a0003c0004t0006g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2257+3591C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241056917 | ||||||
| chr2:241057018
|
T | C | 3 | a0002c0010t0016g0033a0002c0010t0016g0157a0002c0036t0014g0326 | 3 | HG02559.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2257+3692T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057018 | ||||||
| chr2:241057057
|
A | G | 4 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+3731A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057057 | ||||||
| chr2:241057110
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2257+3784G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057110 | ||||||
| chr2:241057149
|
T | G | 18 | a0001c0071t0003g0333a0001c0074t0002g0086a0002c0011t0011g0029others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2257+3823T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057149 | ||||||
| chr2:241057247
|
T | C | 257 | a0001c0001t0001g0141a0001c0001t0002g0252a0001c0001t0002g0280others(254): Show | 258 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(255): Show |
intron_variant | MODIFIER | c.2257+3921T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057247 | ||||||
| chr2:241057360
|
C | T | 21 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(18): Show | 21 | HG00609.hp2 HG00621.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2257+4034C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057360 | ||||||
| chr2:241057380
|
A | AAAAAAAA others(15): Show |
1 | a0002c0010t0019g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2257+4055_2257+405 others(26): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AAT | 22 | a0001c0001t0001g0067a0001c0001t0001g0189a0001c0001t0001g0238others(19): Show | 22 | HG00741.hp1 HG01071.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.2257+4085_2257+408 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATAT | 17 | a0001c0001t0002g0018a0001c0001t0002g0280a0001c0001t0005g0092others(14): Show | 17 | HG00621.hp1 HG01081.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2257+4083_2257+408 others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATAT | 8 | a0001c0001t0001g0071a0001c0001t0001g0334a0001c0001t0005g0240others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.2257+4081_2257+408 others(10): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(3): Show |
1 | a0002c0010t0014g0038 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2257+4077_2257+408 others(14): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(7): Show |
15 | a0001c0006t0001g0257a0001c0006t0002g0084a0001c0006t0002g0089others(12): Show | 15 | HG00438.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2257+4073_2257+408 others(18): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(9): Show |
6 | a0001c0001t0002g0254a0001c0006t0001g0054a0002c0010t0016g0157others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2257+4071_2257+408 others(20): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(11): Show |
4 | a0002c0003t0007g0284a0002c0036t0014g0326a0008c0033t0016g0221others(1): Show | 4 | HG02155.hp1 HG02273.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+4069_2257+408 others(22): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(13): Show |
6 | a0001c0006t0001g0108a0001c0006t0002g0076a0002c0003t0010g0260others(3): Show | 6 | HG02165.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2257+4067_2257+408 others(24): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(15): Show |
6 | a0001c0001t0002g0297a0001c0001t0005g0134a0001c0006t0001g0258others(3): Show | 6 | HG00609.hp2 HG00673.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.2257+4065_2257+408 others(26): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(19): Show |
3 | a0001c0006t0001g0116a0002c0003t0010g0268a0002c0008t0033g0287 | 3 | HG02300.hp2 HG02738.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.2257+4061_2257+408 others(30): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(21): Show |
3 | a0002c0003t0004g0011a0002c0003t0008g0283a0002c0003t0013g0263 | 3 | HG00621.hp2 NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2257+4059_2257+408 others(32): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | AATATATA others(23): Show |
3 | a0001c0001t0002g0252a0002c0003t0007g0131a0002c0061t0008g0253 | 3 | NA18954.hp2 NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2257+4057_2257+408 others(34): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
A | ATATATAT others(22): Show |
1 | a0003c0024t0004g0281 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2257+4054_2257+405 others(33): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057380 | ||||||
| chr2:241057380
|
AATAT | A | 17 | a0001c0001t0009g0274a0001c0001t0017g0272a0001c0001t0017g0273others(14): Show | 17 | HG01243.hp2 HG01261.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.2257+4083_2257+408 others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
AATATAT | A | 115 | a0001c0001t0001g0141a0001c0001t0005g0299a0001c0001t0009g0278others(112): Show | 115 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2257+4081_2257+408 others(10): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
AATATATA others(1): Show |
A | 44 | a0001c0020t0001g0105a0001c0020t0042g0154a0002c0018t0010g0241others(41): Show | 45 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.2257+4079_2257+408 others(12): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057380
|
AATATATA others(3): Show |
A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2257+4077_2257+408 others(14): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057380 | |||||
| chr2:241057391
|
A | T | 1 | a0003c0004t0007g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2257+4065A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057391 | ||||||
| chr2:241057412
|
T | TATATATA others(29): Show |
1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2257+4086_2257+408 others(40): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057412 | ||||||
| chr2:241057412
|
T | TATATGC | 5 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(2): Show | 5 | HG02809.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2257+4086_2257+408 others(10): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057412 | ||||||
| chr2:241057412
|
T | TGC | 3 | a0002c0011t0015g0043a0002c0083t0011g0316a0007c0043t0011g0325 | 3 | HG01884.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2257+4087_2257+408 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057412 | |||||
| chr2:241057434
|
A | C | 37 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(34): Show | 37 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2257+4108A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057434 | ||||||
| chr2:241057436
|
A | G | 30 | a0001c0006t0001g0054a0001c0006t0001g0108a0001c0006t0001g0116others(27): Show | 30 | HG00438.hp2 HG00673.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.2257+4110A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057436 | ||||||
| chr2:241057439
|
A | ATCCCAGC others(4): Show |
37 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(34): Show | 37 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2257+4114_2257+411 others(15): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241057439 | |||||
| chr2:241057561
|
G | A | 1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2257+4235G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057561 | ||||||
| chr2:241057570
|
A | G | 1 | a0003c0056t0007g0009 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2257+4244A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057570 | ||||||
| chr2:241057934
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2257+4608T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241057934 | ||||||
| chr2:241058125
|
A | T | 1 | a0003c0004t0006g0292 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2258-4666A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058125 | ||||||
| chr2:241058206
|
C | T | 1 | a0003c0004t0006g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2258-4585C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058206 | ||||||
| chr2:241058210
|
A | G | 47 | a0001c0020t0001g0105a0001c0020t0042g0154a0001c0020t0057g0341others(44): Show | 48 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.2258-4581A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058210 | ||||||
| chr2:241058218
|
T | A | 1 | a0002c0003t0008g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2258-4573T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058218 | ||||||
| chr2:241058313
|
A | C | 100 | a0001c0020t0001g0105a0001c0020t0042g0154a0001c0020t0057g0341others(97): Show | 101 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.2258-4478A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058313 | ||||||
| chr2:241058495
|
T | C | 34 | a0001c0006t0001g0054a0001c0006t0001g0108a0001c0006t0001g0116others(31): Show | 34 | HG00438.hp2 HG00673.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.2258-4296T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058495 | ||||||
| chr2:241058566
|
G | A | 4 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258-4225G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058566 | ||||||
| chr2:241058688
|
T | C | 37 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(34): Show | 37 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2258-4103T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058688 | ||||||
| chr2:241058698
|
C | T | 64 | a0001c0001t0001g0141a0001c0002t0001g0182a0001c0002t0001g0324others(61): Show | 64 | HG00738.hp2 HG01099.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.2258-4093C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058698 | ||||||
| chr2:241058716
|
C | T | 5 | a0002c0008t0019g0227a0008c0032t0021g0328a0008c0032t0021g0329others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2258-4075C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058716 | ||||||
| chr2:241058784
|
A | G | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2258-4007A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058784 | ||||||
| chr2:241058823
|
G | A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2258-3968G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058823 | ||||||
| chr2:241058896
|
G | A | 1 | a0001c0068t0018g0320 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2258-3895G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241058896 | ||||||
| chr2:241059051
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0049g0322 | 2 | HG03942.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2258-3740G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241059051 | ||||||
| chr2:241059180
|
T | G | 1 | a0001c0002t0043g0306 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2258-3611T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241059180 | ||||||
| chr2:241059503
|
T | A | 1 | a0001c0001t0005g0019 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2258-3288T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241059503 | ||||||
| chr2:241059521
|
A | G | 2 | a0002c0009t0046g0082a0006c0077t0003g0093 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2258-3270A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241059521 | ||||||
| chr2:241059632
|
T | TA | 37 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(34): Show | 37 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2258-3157dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241059632 | |||||
| chr2:241060105
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2258-2686C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060105 | ||||||
| chr2:241060187
|
C | CT | 27 | a0001c0001t0005g0299a0001c0006t0001g0108a0001c0006t0001g0116others(24): Show | 27 | HG00438.hp2 HG00673.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.2258-2589dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241060187 | |||||
| chr2:241060187
|
C | CTT | 6 | a0002c0008t0019g0227a0002c0010t0016g0033a0002c0010t0016g0157others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2258-2590_2258-258 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241060187 | |||||
| chr2:241060462
|
G | A | 3 | a0001c0002t0001g0182a0001c0002t0001g0324a0001c0002t0048g0191 | 3 | HG01175.hp2 HG01243.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2258-2329G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060462 | ||||||
| chr2:241060532
|
T | C | 1 | a0002c0003t0007g0284 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2258-2259T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060532 | ||||||
| chr2:241060623
|
TTAAAGAC others(1): Show |
T | 27 | a0001c0006t0001g0054a0001c0006t0001g0108a0001c0006t0001g0116others(24): Show | 27 | HG00438.hp2 HG00673.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.2258-2163_2258-215 others(12): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241060623 | |||||
| chr2:241060644
|
TA | T | 37 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(34): Show | 37 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2258-2138delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241060644 | |||||
| chr2:241060825
|
G | A | 64 | a0001c0001t0001g0141a0001c0002t0001g0182a0001c0002t0001g0324others(61): Show | 64 | HG00738.hp2 HG01099.hp2 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.2258-1966G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060825 | ||||||
| chr2:241060856
|
G | A | 1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2258-1935G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060856 | ||||||
| chr2:241060889
|
C | T | 17 | a0001c0001t0009g0274a0001c0006t0001g0054a0001c0006t0001g0108others(14): Show | 17 | HG00438.hp2 HG00673.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2258-1902C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060889 | ||||||
| chr2:241060928
|
T | A | 1 | a0001c0001t0005g0019 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2258-1863T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060928 | ||||||
| chr2:241060929
|
C | A | 1 | a0001c0001t0005g0019 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2258-1862C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060929 | ||||||
| chr2:241060929
|
C | CA | 35 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(32): Show | 35 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2258-1853dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241060929 | |||||
| chr2:241060951
|
A | G | 35 | a0001c0001t0009g0274a0001c0006t0001g0054a0001c0006t0001g0108others(32): Show | 35 | HG00438.hp2 HG00673.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.2258-1840A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241060951 | ||||||
| chr2:241061231
|
G | A | 3 | a0001c0001t0002g0055a0001c0001t0002g0060a0001c0001t0002g0158 | 3 | HG00140.hp2 HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2258-1560G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061231 | ||||||
| chr2:241061281
|
A | G | 35 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(32): Show | 35 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2258-1510A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061281 | ||||||
| chr2:241061364
|
C | T | 36 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(33): Show | 36 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2258-1427C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061364 | ||||||
| chr2:241061365
|
G | A | 1 | a0002c0034t0006g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2258-1426G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061365 | ||||||
| chr2:241061382
|
A | G | 1 | a0002c0018t0022g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2258-1409A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061382 | ||||||
| chr2:241061465
|
A | G | 1 | a0002c0022t0014g0327 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2258-1326A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061465 | ||||||
| chr2:241061661
|
C | T | 8 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0010t0044g0078others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2258-1130C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061661 | ||||||
| chr2:241061758
|
G | A | 10 | a0001c0001t0001g0170a0001c0001t0001g0303a0001c0001t0001g0305others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(7): Show |
intron_variant | MODIFIER | c.2258-1033G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061758 | ||||||
| chr2:241061854
|
C | A | 19 | a0001c0071t0003g0333a0001c0074t0002g0086a0002c0011t0011g0029others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2258-937C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061854 | ||||||
| chr2:241061855
|
A | C | 9 | a0001c0001t0002g0174a0001c0001t0020g0175a0001c0001t0055g0173others(6): Show | 9 | HG01261.hp1 HG03130.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258-936A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241061855 | ||||||
| chr2:241061872
|
AAAAG | A | 4 | a0003c0004t0006g0213a0003c0004t0006g0292a0003c0004t0007g0006others(1): Show | 4 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.2258-915_2258-912d others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr2 | 241061872 | |||||
| chr2:241062121
|
T | A | 4 | a0002c0003t0008g0066a0002c0003t0008g0259a0002c0003t0008g0277others(1): Show | 4 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.2258-670T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241062121 | ||||||
| chr2:241062229
|
C | T | 1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2258-562C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241062229 | ||||||
| chr2:241062361
|
A | G | 1 | a0009c0030t0027g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2258-430A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241062361 | ||||||
| chr2:241062471
|
G | A | 1 | a0019c0070t0019g0008 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2258-320G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241062471 | ||||||
| chr2:241062518
|
C | T | 1 | a0002c0083t0011g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2258-273C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241062518 | ||||||
| chr2:241062574
|
A | G | 253 | a0001c0001t0001g0141a0001c0001t0002g0252a0001c0001t0002g0280others(250): Show | 254 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(251): Show |
intron_variant | MODIFIER | c.2258-217A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241062574 | ||||||
| chr2:241062777
|
C | T | 1 | a0001c0006t0002g0276 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2258-14C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 16/31 | chr2 | 241062777 | ||||||
| chr2:241063027
|
G | A | 45 | a0001c0020t0001g0105a0001c0020t0042g0154a0001c0020t0057g0341others(42): Show | 46 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.2371+123G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063027 | ||||||
| chr2:241063142
|
G | C | 76 | a0001c0002t0002g0184a0001c0002t0003g0136a0001c0002t0003g0161others(73): Show | 76 | HG00423.hp2 HG00597.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.2371+238G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063142 | ||||||
| chr2:241063190
|
C | G | 121 | a0001c0001t0002g0129a0001c0002t0002g0184a0001c0002t0003g0136others(118): Show | 122 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.2371+286C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063190 | ||||||
| chr2:241063190
|
C | T | 13 | a0001c0006t0001g0054a0001c0006t0001g0108a0001c0006t0001g0116others(10): Show | 13 | HG00438.hp2 HG00673.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.2371+286C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063190 | ||||||
| chr2:241063220
|
G | C | 1 | a0001c0002t0009g0211 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2371+316G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063220 | ||||||
| chr2:241063279
|
G | A | 1 | a0001c0002t0020g0308 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2372-308G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063279 | ||||||
| chr2:241063284
|
C | G | 215 | a0001c0001t0001g0098a0001c0001t0001g0141a0001c0001t0001g0163others(212): Show | 216 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(213): Show |
intron_variant | MODIFIER | c.2372-303C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063284 | ||||||
| chr2:241063307
|
G | A | 41 | a0001c0001t0001g0141a0001c0002t0001g0182a0001c0002t0001g0324others(38): Show | 41 | HG01099.hp2 HG01123.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.2372-280G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063307 | ||||||
| chr2:241063357
|
G | A | 3 | a0001c0016t0003g0230a0001c0016t0003g0231a0001c0016t0009g0232 | 3 | HG02886.hp2 HG02897.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2372-230G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063357 | ||||||
| chr2:241063411
|
C | T | 252 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(249): Show | 253 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.2372-176C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063411 | ||||||
| chr2:241063418
|
C | T | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2372-169C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063418 | ||||||
| chr2:241063520
|
A | G | 1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2372-67A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 17/31 | chr2 | 241063520 | ||||||
| chr2:241063712
|
C | T | 15 | a0001c0071t0003g0333a0001c0074t0002g0086a0002c0011t0011g0029others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2485+12C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 18/31 | chr2 | 241063712 | ||||||
| chr2:241063740
|
G | A | 2 | a0002c0010t0019g0195a0019c0070t0019g0008 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2485+40G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 18/31 | chr2 | 241063740 | ||||||
| chr2:241064137
|
GGCCTGCC others(15): Show |
G | 4 | a0002c0010t0016g0033a0002c0010t0016g0157a0002c0036t0014g0326others(1): Show | 4 | HG02559.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+16_2599+37del others(22): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr2 | 241064137 | |||||
| chr2:241064141
|
T | C | 258 | a0001c0001t0001g0141a0001c0001t0002g0018a0001c0001t0002g0252others(255): Show | 259 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.2599+16T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064141 | ||||||
| chr2:241064169
|
C | G | 1 | a0002c0036t0025g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2599+44C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064169 | ||||||
| chr2:241064186
|
G | A | 1 | a0001c0016t0003g0216 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2599+61G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064186 | ||||||
| chr2:241064210
|
C | G | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2599+85C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064210 | ||||||
| chr2:241064265
|
T | G | 80 | a0001c0001t0001g0166a0001c0001t0002g0252a0001c0001t0002g0280others(77): Show | 80 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.2599+140T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064265 | ||||||
| chr2:241064599
|
C | A | 5 | a0001c0001t0002g0252a0002c0003t0010g0260a0002c0003t0013g0049others(2): Show | 5 | HG00621.hp2 HG02155.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.2600-245C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064599 | ||||||
| chr2:241064626
|
G | A | 1 | a0004c0005t0008g0058 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2600-218G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064626 | ||||||
| chr2:241064635
|
C | T | 17 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(14): Show | 17 | HG00621.hp2 HG01081.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2600-209C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064635 | ||||||
| chr2:241064782
|
G | C | 245 | a0001c0001t0001g0141a0001c0001t0002g0252a0001c0001t0002g0280others(242): Show | 246 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(243): Show |
intron_variant | MODIFIER | c.2600-62G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 19/31 | chr2 | 241064782 | ||||||
| chr2:241064968
|
A | G | 1 | a0002c0061t0008g0253 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2713+11A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241064968 | ||||||
| chr2:241065000
|
T | C | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2713+43T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065000 | ||||||
| chr2:241065117
|
C | T | 1 | a0003c0004t0007g0099 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2713+160C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065117 | ||||||
| chr2:241065121
|
C | G | 2 | a0010c0017t0024g0225a0010c0017t0056g0226 | 2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2713+164C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065121 | ||||||
| chr2:241065154
|
C | T | 59 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(56): Show | 59 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.2714-145C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065154 | ||||||
| chr2:241065186
|
G | A | 15 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0001t0009g0278others(12): Show | 15 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2714-113G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065186 | ||||||
| chr2:241065216
|
C | T | 3 | a0002c0009t0016g0220a0012c0049t0019g0050a0012c0079t0016g0331 | 3 | HG02486.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2714-83C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065216 | ||||||
| chr2:241065217
|
G | A | 11 | a0001c0071t0003g0333a0001c0074t0002g0086a0002c0011t0011g0029others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2714-82G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065217 | ||||||
| chr2:241065229
|
G | A | 1 | a0003c0004t0007g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2714-70G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 20/31 | chr2 | 241065229 | ||||||
| chr2:241065608
|
G | A | 2 | a0009c0030t0027g0127a0009c0030t0027g0208 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3010+13G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241065608 | ||||||
| chr2:241065685
|
C | T | 5 | a0002c0052t0011g0256a0009c0030t0027g0127a0009c0030t0027g0208others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3010+90C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241065685 | ||||||
| chr2:241065893
|
G | C | 4 | a0001c0002t0002g0184a0001c0002t0023g0179a0001c0002t0023g0246others(1): Show | 4 | HG01934.hp2 HG02735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.3010+298G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241065893 | ||||||
| chr2:241065916
|
G | C | 10 | a0001c0071t0003g0333a0001c0074t0002g0086a0002c0011t0011g0029others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.3010+321G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241065916 | ||||||
| chr2:241065956
|
G | T | 3 | a0001c0001t0001g0067a0001c0001t0002g0065a0001c0002t0009g0310 | 3 | HG02055.hp1 HG04228.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3010+361G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241065956 | ||||||
| chr2:241066124
|
C | T | 1 | a0001c0020t0001g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3010+529C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066124 | ||||||
| chr2:241066208
|
C | T | 1 | a0001c0001t0005g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3010+613C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066208 | ||||||
| chr2:241066263
|
G | A | 25 | a0001c0016t0003g0216a0001c0016t0003g0230a0001c0016t0003g0231others(22): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.3010+668G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066263 | ||||||
| chr2:241066283
|
C | T | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3010+688C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066283 | ||||||
| chr2:241066391
|
C | T | 1 | a0006c0063t0001g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3010+796C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066391 | ||||||
| chr2:241066456
|
C | T | 12 | a0001c0001t0005g0299a0001c0001t0009g0278a0001c0060t0005g0193others(9): Show | 12 | HG00438.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.3010+861C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066456 | ||||||
| chr2:241066503
|
A | G | 1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3010+908A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066503 | ||||||
| chr2:241066546
|
G | A | 1 | a0002c0010t0016g0157 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3010+951G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066546 | ||||||
| chr2:241066631
|
T | C | 8 | a0001c0016t0003g0216a0001c0016t0003g0230a0001c0016t0003g0231others(5): Show | 8 | HG02280.hp1 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3010+1036T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066631 | ||||||
| chr2:241066634
|
A | G | 63 | a0001c0001t0001g0141a0001c0001t0009g0274a0001c0001t0017g0272others(60): Show | 63 | HG00738.hp2 HG01099.hp2 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.3010+1039A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066634 | ||||||
| chr2:241066696
|
G | A | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3011-1068G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066696 | ||||||
| chr2:241066754
|
G | A | 44 | a0001c0020t0001g0105a0001c0020t0042g0154a0001c0020t0057g0341others(41): Show | 45 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.3011-1010G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066754 | ||||||
| chr2:241066948
|
T | A | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3011-816T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066948 | ||||||
| chr2:241066949
|
C | T | 1 | a0001c0001t0051g0270 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3011-815C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241066949 | ||||||
| chr2:241067015
|
G | A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3011-749G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067015 | ||||||
| chr2:241067074
|
C | T | 5 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0055g0173others(2): Show | 5 | HG00741.hp1 HG01071.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3011-690C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067074 | ||||||
| chr2:241067129
|
C | T | 4 | a0003c0004t0006g0213a0003c0004t0006g0292a0003c0004t0007g0006others(1): Show | 4 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.3011-635C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067129 | ||||||
| chr2:241067321
|
T | C | 132 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(129): Show | 133 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(130): Show |
intron_variant | MODIFIER | c.3011-443T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067321 | ||||||
| chr2:241067341
|
T | C | 46 | a0001c0001t0009g0274a0001c0001t0017g0272a0001c0001t0017g0273others(43): Show | 46 | HG01099.hp2 HG01123.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.3011-423T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067341 | ||||||
| chr2:241067437
|
C | T | 1 | a0009c0031t0028g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3011-327C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067437 | ||||||
| chr2:241067523
|
G | A | 3 | a0008c0081t0021g0031a0011c0035t0025g0342a0011c0035t0025g0343 | 3 | HG01167.hp1 HG01169.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3011-241G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067523 | ||||||
| chr2:241067566
|
T | C | 9 | a0001c0001t0001g0334a0001c0001t0020g0175a0002c0013t0015g0317others(6): Show | 9 | HG01884.hp2 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3011-198T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067566 | ||||||
| chr2:241067618
|
A | G | 13 | a0001c0001t0002g0252a0002c0003t0004g0011a0002c0003t0008g0235others(10): Show | 13 | HG00621.hp2 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.3011-146A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067618 | ||||||
| chr2:241067657
|
T | C | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0002g0296others(1): Show | 4 | NA18988.hp1 NA18992.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.3011-107T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067657 | ||||||
| chr2:241067665
|
G | A | 1 | a0001c0001t0051g0270 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3011-99G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 21/31 | chr2 | 241067665 | ||||||
| chr2:241068002
|
G | A | 2 | a0009c0030t0027g0127a0009c0030t0027g0208 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3194+55G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068002 | ||||||
| chr2:241068050
|
AC | A | 139 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(136): Show | 139 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(136): Show |
intron_variant | MODIFIER | c.3194+105delC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr2 | 241068050 | |||||
| chr2:241068085
|
G | T | 1 | a0002c0003t0008g0235 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3194+138G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068085 | ||||||
| chr2:241068126
|
C | T | 36 | a0001c0020t0042g0154a0001c0020t0057g0341a0002c0075t0045g0251others(33): Show | 37 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.3194+179C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068126 | ||||||
| chr2:241068176
|
T | A | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3194+229T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068176 | ||||||
| chr2:241068177
|
A | T | 2 | a0009c0031t0028g0224a0009c0031t0036g0027 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3194+230A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068177 | ||||||
| chr2:241068242
|
A | C | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3194+295A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068242 | ||||||
| chr2:241068253
|
G | GCCCCTCA others(65): Show |
35 | a0001c0001t0001g0334a0002c0009t0004g0040a0002c0009t0004g0146others(32): Show | 35 | HG01123.hp1 HG01261.hp1 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.3194+384_3194+455d others(74): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr2 | 241068253 | |||||
| chr2:241068253
|
GCCCCTCA others(65): Show |
G | 22 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(19): Show | 22 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.3194+384_3194+455d others(74): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr2 | 241068253 | |||||
| chr2:241068270
|
G | A | 2 | a0002c0008t0061g0168a0003c0066t0015g0330 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3194+323G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068270 | ||||||
| chr2:241068342
|
G | A | 1 | a0001c0050t0003g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3194+395G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068342 | ||||||
| chr2:241068371
|
G | A | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3194+424G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068371 | ||||||
| chr2:241068389
|
C | T | 4 | a0002c0003t0008g0066a0002c0003t0008g0259a0002c0003t0008g0277others(1): Show | 4 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.3194+442C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068389 | ||||||
| chr2:241068424
|
G | A | 54 | a0001c0002t0002g0184a0001c0002t0003g0136a0001c0002t0003g0149others(51): Show | 54 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.3194+477G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068424 | ||||||
| chr2:241068440
|
C | T | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3195-471C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068440 | ||||||
| chr2:241068467
|
A | G | 1 | a0002c0008t0061g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3195-444A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068467 | ||||||
| chr2:241068515
|
T | A | 19 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(16): Show | 19 | HG00621.hp2 HG01081.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.3195-396T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068515 | ||||||
| chr2:241068519
|
G | A | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3195-392G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068519 | ||||||
| chr2:241068592
|
C | G | 1 | a0009c0031t0036g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3195-319C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068592 | ||||||
| chr2:241068594
|
G | A | 54 | a0001c0002t0002g0184a0001c0002t0003g0136a0001c0002t0003g0149others(51): Show | 54 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.3195-317G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068594 | ||||||
| chr2:241068677
|
G | T | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3195-234G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 22/31 | chr2 | 241068677 | ||||||
| chr2:241069046
|
C | T | 1 | a0002c0008t0029g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3307+23C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069046 | ||||||
| chr2:241069161
|
C | T | 2 | a0002c0008t0061g0168a0002c0073t0063g0007 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3307+138C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069161 | ||||||
| chr2:241069246
|
G | C | 1 | a0007c0042t0013g0003 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3307+223G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069246 | ||||||
| chr2:241069459
|
G | A | 81 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(78): Show | 81 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.3307+436G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069459 | ||||||
| chr2:241069516
|
G | A | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3308-404G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069516 | ||||||
| chr2:241069571
|
G | A | 2 | a0008c0033t0016g0221a0008c0033t0030g0335 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3308-349G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069571 | ||||||
| chr2:241069589
|
G | C | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3308-331G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069589 | ||||||
| chr2:241069640
|
C | T | 160 | a0001c0001t0001g0334a0001c0001t0002g0252a0001c0001t0002g0280others(157): Show | 161 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(158): Show |
intron_variant | MODIFIER | c.3308-280C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069640 | ||||||
| chr2:241069724
|
G | A | 38 | a0001c0020t0042g0154a0001c0020t0057g0341a0002c0008t0019g0227others(35): Show | 39 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.3308-196G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069724 | ||||||
| chr2:241069777
|
G | A | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3308-143G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069777 | ||||||
| chr2:241069845
|
C | G | 85 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(82): Show | 85 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.3308-75C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069845 | ||||||
| chr2:241069858
|
G | T | 55 | a0001c0001t0009g0274a0001c0001t0017g0272a0001c0001t0017g0273others(52): Show | 55 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.3308-62G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 23/31 | chr2 | 241069858 | ||||||
| chr2:241070234
|
C | G | 85 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(82): Show | 85 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.3589+33C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070234 | ||||||
| chr2:241070375
|
A | G | 3 | a0002c0018t0022g0223a0002c0055t0022g0052a0002c0082t0039g0032 | 3 | HG02647.hp2 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3589+174A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070375 | ||||||
| chr2:241070501
|
G | A | 3 | a0001c0002t0003g0177a0001c0002t0009g0178a0001c0002t0009g0187 | 3 | HG01168.hp1 HG01169.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.3589+300G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070501 | ||||||
| chr2:241070512
|
C | T | 2 | a0002c0013t0011g0214a0002c0013t0015g0215 | 2 | HG01099.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3589+311C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070512 | ||||||
| chr2:241070688
|
C | T | 75 | a0001c0001t0001g0334a0001c0020t0042g0154a0001c0020t0057g0341others(72): Show | 76 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.3589+487C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070688 | ||||||
| chr2:241070754
|
G | A | 1 | a0006c0012t0001g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3589+553G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070754 | ||||||
| chr2:241070831
|
C | T | 2 | a0001c0001t0001g0189a0002c0003t0013g0263 | 2 | HG00621.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3589+630C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070831 | ||||||
| chr2:241070878
|
T | C | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3589+677T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070878 | ||||||
| chr2:241070880
|
C | T | 66 | a0001c0001t0009g0274a0001c0001t0017g0272a0001c0001t0017g0273others(63): Show | 66 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(63): Show |
intron_variant | MODIFIER | c.3589+679C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070880 | ||||||
| chr2:241070912
|
C | G | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3590-664C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070912 | ||||||
| chr2:241070940
|
T | C | 19 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(16): Show | 19 | HG00621.hp2 HG01081.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.3590-636T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241070940 | ||||||
| chr2:241071121
|
G | A | 1 | a0002c0008t0061g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3590-455G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071121 | ||||||
| chr2:241071169
|
T | G | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3590-407T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071169 | ||||||
| chr2:241071170
|
G | T | 1 | a0016c0053t0017g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3590-406G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071170 | ||||||
| chr2:241071188
|
C | T | 1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3590-388C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071188 | ||||||
| chr2:241071226
|
T | C | 39 | a0001c0020t0042g0154a0001c0020t0057g0341a0002c0008t0019g0227others(36): Show | 40 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.3590-350T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071226 | ||||||
| chr2:241071251
|
C | T | 22 | a0002c0009t0016g0220a0002c0010t0014g0038a0002c0010t0014g0222others(19): Show | 22 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.3590-325C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071251 | ||||||
| chr2:241071288
|
C | T | 1 | a0005c0007t0002g0243 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3590-288C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071288 | ||||||
| chr2:241071389
|
G | A | 1 | a0001c0006t0001g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3590-187G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071389 | ||||||
| chr2:241071447
|
C | T | 1 | a0001c0060t0005g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3590-129C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 24/31 | chr2 | 241071447 | ||||||
| chr2:241071736
|
A | G | 342 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3734+16A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 25/31 | chr2 | 241071736 | ||||||
| chr2:241071780
|
C | T | 27 | a0001c0001t0001g0117a0001c0001t0002g0129a0001c0001t0002g0252others(24): Show | 27 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.3735-16C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 25/31 | chr2 | 241071780 | ||||||
| chr2:241071882
|
A | G | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | splice_region_variant&intron_variant | LOW | c.3817+4A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071882 | ||||||
| chr2:241071883
|
G | C | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | splice_region_variant&intron_variant | LOW | c.3817+5G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071883 | ||||||
| chr2:241071888
|
A | G | 7 | a0002c0003t0004g0271a0002c0003t0010g0190a0002c0003t0013g0307others(4): Show | 7 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.3817+10A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071888 | ||||||
| chr2:241071888
|
A | T | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+10A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071888 | ||||||
| chr2:241071892
|
C | A | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+14C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071892 | ||||||
| chr2:241071892
|
C | T | 3 | a0011c0035t0025g0342a0011c0035t0025g0343a0011c0054t0030g0319 | 3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3817+14C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071892 | ||||||
| chr2:241071893
|
C | G | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+15C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071893 | ||||||
| chr2:241071894
|
T | G | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+16T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071894 | ||||||
| chr2:241071903
|
A | G | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+25A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071903 | ||||||
| chr2:241071904
|
C | A | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+26C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071904 | ||||||
| chr2:241071906
|
T | C | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+28T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071906 | ||||||
| chr2:241071910
|
T | C | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+32T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071910 | ||||||
| chr2:241071912
|
G | C | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+34G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071912 | ||||||
| chr2:241071913
|
C | T | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+35C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071913 | ||||||
| chr2:241071915
|
C | A | 190 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0117others(187): Show | 190 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.3817+37C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071915 | ||||||
| chr2:241071922
|
G | T | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+44G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071922 | ||||||
| chr2:241071935
|
C | G | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+57C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071935 | ||||||
| chr2:241071938
|
T | C | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+60T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071938 | ||||||
| chr2:241071945
|
G | C | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+67G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071945 | ||||||
| chr2:241071949
|
T | A | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+71T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071949 | ||||||
| chr2:241071951
|
T | A | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+73T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071951 | ||||||
| chr2:241071982
|
A | T | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+104A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071982 | ||||||
| chr2:241071989
|
T | G | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+111T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071989 | ||||||
| chr2:241071990
|
C | G | 1 | a0023c0076t0006g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3817+112C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241071990 | ||||||
| chr2:241072029
|
C | T | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3817+151C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072029 | ||||||
| chr2:241072037
|
G | A | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3817+159G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072037 | ||||||
| chr2:241072042
|
C | G | 3 | a0002c0018t0022g0223a0002c0055t0022g0052a0002c0082t0039g0032 | 3 | HG02647.hp2 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3817+164C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072042 | ||||||
| chr2:241072046
|
C | T | 1 | a0004c0005t0012g0201 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3817+168C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072046 | ||||||
| chr2:241072063
|
A | G | 1 | a0002c0084t0037g0318 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3817+185A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072063 | ||||||
| chr2:241072116
|
G | A | 45 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(42): Show | 45 | HG00621.hp2 HG01081.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.3817+238G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072116 | ||||||
| chr2:241072180
|
G | A | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3817+302G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072180 | ||||||
| chr2:241072219
|
T | C | 20 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(17): Show | 20 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.3817+341T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072219 | ||||||
| chr2:241072338
|
G | A | 45 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(42): Show | 46 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.3817+460G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072338 | ||||||
| chr2:241072447
|
G | A | 45 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(42): Show | 46 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.3817+569G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072447 | ||||||
| chr2:241072452
|
C | T | 3 | a0011c0035t0025g0342a0011c0035t0025g0343a0011c0054t0030g0319 | 3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3817+574C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072452 | ||||||
| chr2:241072650
|
C | T | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3818-616C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072650 | ||||||
| chr2:241072927
|
G | A | 5 | a0003c0004t0006g0002a0003c0004t0006g0100a0003c0004t0006g0101others(2): Show | 5 | NA18963.hp2 NA18992.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.3818-339G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072927 | ||||||
| chr2:241072976
|
G | A | 18 | a0001c0001t0005g0299a0001c0020t0001g0105a0001c0060t0005g0193others(15): Show | 18 | HG00438.hp1 HG02080.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.3818-290G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241072976 | ||||||
| chr2:241073215
|
T | A | 1 | a0002c0003t0062g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3818-51T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241073215 | ||||||
| chr2:241073219
|
G | A | 1 | a0001c0002t0009g0178 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3818-47G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241073219 | ||||||
| chr2:241073235
|
C | T | 1 | a0011c0054t0030g0319 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3818-31C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241073235 | ||||||
| chr2:241073244
|
G | A | 2 | a0008c0033t0016g0221a0008c0033t0030g0335 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3818-22G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 26/31 | chr2 | 241073244 | ||||||
| chr2:241073367
|
G | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.3916+3G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073367 | ||||||
| chr2:241073450
|
C | T | 1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3916+86C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073450 | ||||||
| chr2:241073489
|
G | A | 18 | a0001c0001t0005g0299a0001c0020t0001g0105a0001c0060t0005g0193others(15): Show | 18 | HG00438.hp1 HG02080.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.3916+125G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073489 | ||||||
| chr2:241073509
|
G | A | 1 | a0002c0003t0013g0307 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3916+145G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073509 | ||||||
| chr2:241073510
|
G | C | 9 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3916+146G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073510 | ||||||
| chr2:241073630
|
T | C | 1 | a0007c0043t0011g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3916+266T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073630 | ||||||
| chr2:241073658
|
G | A | 2 | a0008c0033t0016g0221a0008c0033t0030g0335 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3916+294G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073658 | ||||||
| chr2:241073861
|
C | T | 2 | a0002c0018t0022g0223a0002c0082t0039g0032 | 2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3916+497C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073861 | ||||||
| chr2:241073938
|
T | C | 4 | a0001c0002t0017g0323a0001c0002t0018g0185a0001c0002t0041g0181others(1): Show | 4 | HG00738.hp2 HG02738.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3916+574T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073938 | ||||||
| chr2:241073972
|
C | T | 56 | a0001c0001t0009g0278a0001c0002t0002g0184a0001c0002t0003g0136others(53): Show | 56 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.3916+608C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241073972 | ||||||
| chr2:241074070
|
C | T | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3916+706C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074070 | ||||||
| chr2:241074104
|
T | C | 9 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3916+740T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074104 | ||||||
| chr2:241074213
|
A | G | 59 | a0001c0001t0009g0274a0001c0001t0009g0278a0001c0001t0017g0272others(56): Show | 59 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.3916+849A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074213 | ||||||
| chr2:241074266
|
C | G | 1 | a0001c0002t0059g0053 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3916+902C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074266 | ||||||
| chr2:241074287
|
TC | T | 222 | a0001c0001t0002g0060a0001c0001t0002g0252a0001c0001t0002g0280others(219): Show | 223 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(220): Show |
intron_variant | MODIFIER | c.3916+932delC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241074287 | |||||
| chr2:241074395
|
T | G | 9 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3916+1031T>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074395 | ||||||
| chr2:241074405
|
C | T | 4 | a0008c0032t0021g0328a0008c0032t0021g0329a0008c0051t0021g0337others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3916+1041C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074405 | ||||||
| chr2:241074610
|
G | C | 1 | a0002c0021t0047g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3916+1246G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074610 | ||||||
| chr2:241074641
|
C | T | 16 | a0002c0009t0016g0220a0002c0010t0014g0038a0002c0010t0014g0222others(13): Show | 16 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.3916+1277C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074641 | ||||||
| chr2:241074938
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3916+1574G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074938 | ||||||
| chr2:241074949
|
C | T | 222 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(219): Show | 223 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(220): Show |
intron_variant | MODIFIER | c.3916+1585C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241074949 | ||||||
| chr2:241075006
|
T | C | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3916+1642T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075006 | ||||||
| chr2:241075357
|
G | A | 1 | a0001c0016t0003g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3916+1993G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075357 | ||||||
| chr2:241075523
|
C | T | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3916+2159C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075523 | ||||||
| chr2:241075632
|
G | T | 1 | a0001c0001t0001g0295 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3916+2268G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075632 | ||||||
| chr2:241075633
|
T | A | 1 | a0001c0001t0001g0295 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3916+2269T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075633 | ||||||
| chr2:241075634
|
A | C | 1 | a0001c0001t0001g0295 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3916+2270A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075634 | ||||||
| chr2:241075815
|
A | G | 4 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3916+2451A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075815 | ||||||
| chr2:241075855
|
C | CTG | 96 | a0001c0074t0002g0086a0002c0003t0006g0275a0002c0003t0007g0131others(93): Show | 97 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.3916+2502_3916+250 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241075855 | |||||
| chr2:241075996
|
C | T | 32 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(29): Show | 32 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3916+2632C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075996 | ||||||
| chr2:241075998
|
G | A | 95 | a0001c0074t0002g0086a0002c0003t0006g0275a0002c0003t0007g0131others(92): Show | 96 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(93): Show |
intron_variant | MODIFIER | c.3916+2634G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241075998 | ||||||
| chr2:241076017
|
G | T | 4 | a0006c0015t0003g0137a0006c0015t0003g0138a0006c0015t0003g0139others(1): Show | 4 | NA18940.hp2 NA18948.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3916+2653G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076017 | ||||||
| chr2:241076021
|
C | T | 1 | a0009c0067t0028g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3916+2657C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076021 | ||||||
| chr2:241076122
|
G | C | 1 | a0001c0001t0002g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3916+2758G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076122 | ||||||
| chr2:241076183
|
G | A | 3 | a0002c0018t0010g0264a0002c0018t0013g0265a0007c0042t0013g0003 | 3 | NA18972.hp2 NA19086.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3916+2819G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076183 | ||||||
| chr2:241076235
|
T | C | 148 | a0001c0001t0002g0252a0001c0001t0002g0280a0001c0001t0002g0297others(145): Show | 149 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(146): Show |
intron_variant | MODIFIER | c.3916+2871T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076235 | ||||||
| chr2:241076422
|
G | T | 1 | a0003c0066t0015g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3916+3058G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076422 | ||||||
| chr2:241076438
|
A | T | 1 | a0009c0031t0036g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3916+3074A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076438 | ||||||
| chr2:241076775
|
CGCCTGTA others(47): Show |
C | 3 | a0003c0004t0006g0120a0003c0004t0006g0122a0003c0004t0032g0123 | 3 | NA18970.hp2 NA18990.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.3916+3423_3916+347 others(58): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241076775 | |||||
| chr2:241076829
|
G | C | 113 | a0001c0074t0002g0086a0002c0003t0006g0275a0002c0003t0007g0131others(110): Show | 114 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(111): Show |
intron_variant | MODIFIER | c.3916+3465G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076829 | ||||||
| chr2:241076907
|
G | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3916+3543G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076907 | ||||||
| chr2:241076952
|
G | C | 1 | a0006c0077t0003g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3916+3588G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076952 | ||||||
| chr2:241076961
|
C | T | 7 | a0002c0009t0016g0220a0002c0010t0016g0033a0002c0010t0016g0157others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3916+3597C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241076961 | ||||||
| chr2:241077004
|
G | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3916+3640G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077004 | ||||||
| chr2:241077044
|
A | C | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3916+3680A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077044 | ||||||
| chr2:241077078
|
C | CA | 89 | a0001c0074t0002g0086a0002c0003t0006g0275a0002c0003t0007g0131others(86): Show | 90 | HG00558.hp2 HG00673.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.3916+3729dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241077078 | |||||
| chr2:241077078
|
CA | C | 9 | a0001c0001t0001g0117a0001c0002t0001g0182a0001c0002t0003g0169others(6): Show | 9 | HG00738.hp2 HG01256.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3916+3729delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241077078 | |||||
| chr2:241077159
|
C | T | 59 | a0001c0001t0009g0274a0001c0001t0009g0278a0001c0001t0017g0272others(56): Show | 59 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.3916+3795C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077159 | ||||||
| chr2:241077264
|
C | T | 1 | a0002c0084t0037g0318 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3916+3900C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077264 | ||||||
| chr2:241077361
|
T | C | 1 | a0001c0001t0002g0297 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3916+3997T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077361 | ||||||
| chr2:241077401
|
C | G | 2 | a0001c0002t0041g0181a0001c0002t0043g0306 | 2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.3916+4037C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077401 | ||||||
| chr2:241077530
|
C | T | 3 | a0001c0001t0009g0274a0001c0001t0017g0272a0001c0001t0017g0273 | 3 | HG02735.hp2 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3917-4147C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077530 | ||||||
| chr2:241077843
|
G | A | 1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3917-3834G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077843 | ||||||
| chr2:241077964
|
G | C | 218 | a0001c0001t0002g0297a0001c0001t0005g0299a0001c0001t0009g0274others(215): Show | 219 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(216): Show |
intron_variant | MODIFIER | c.3917-3713G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077964 | ||||||
| chr2:241077991
|
AT | A | 3 | a0002c0036t0025g0022a0008c0033t0016g0221a0008c0033t0030g0335 | 3 | HG02280.hp1 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3917-3685delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241077991 | ||||||
| chr2:241078071
|
C | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0254 | 2 | HG03491.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.3917-3606C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078071 | ||||||
| chr2:241078080
|
A | G | 6 | a0001c0002t0009g0109a0002c0003t0010g0260a0002c0003t0010g0268others(3): Show | 6 | HG00621.hp2 HG02165.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.3917-3597A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078080 | ||||||
| chr2:241078091
|
G | A | 1 | a0003c0004t0006g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3917-3586G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078091 | ||||||
| chr2:241078106
|
C | T | 18 | a0001c0074t0002g0086a0002c0010t0014g0038a0002c0011t0011g0029others(15): Show | 18 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.3917-3571C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078106 | ||||||
| chr2:241078107
|
G | A | 1 | a0002c0003t0008g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3917-3570G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078107 | ||||||
| chr2:241078111
|
G | A | 5 | a0002c0064t0060g0250a0008c0032t0021g0328a0008c0032t0021g0329others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-3566G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078111 | ||||||
| chr2:241078122
|
CGCCTGTA others(722): Show |
C | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-3527_3917-279 others(4): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241078122 | |||||
| chr2:241078125
|
C | T | 1 | a0002c0003t0008g0113 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3917-3552C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078125 | ||||||
| chr2:241078144
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3917-3533G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078144 | ||||||
| chr2:241078151
|
G | A | 21 | a0001c0060t0005g0193a0002c0003t0004g0011a0002c0003t0004g0271others(18): Show | 21 | HG00438.hp1 HG00621.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.3917-3526G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078151 | ||||||
| chr2:241078156
|
G | A | 4 | a0002c0008t0019g0227a0002c0010t0019g0195a0002c0075t0045g0251others(1): Show | 4 | HG02965.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3917-3521G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078156 | ||||||
| chr2:241078176
|
C | A | 2 | a0002c0058t0019g0209a0012c0049t0019g0050 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3917-3501C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078176 | ||||||
| chr2:241078186
|
A | C | 2 | a0002c0058t0019g0209a0012c0049t0019g0050 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3917-3491A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078186 | ||||||
| chr2:241078189
|
T | C | 2 | a0002c0058t0019g0209a0012c0049t0019g0050 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3917-3488T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078189 | ||||||
| chr2:241078239
|
T | C | 22 | a0001c0001t0005g0299a0001c0001t0009g0274a0001c0002t0003g0169others(19): Show | 22 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.3917-3438T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078239 | ||||||
| chr2:241078252
|
G | A | 3 | a0002c0003t0010g0218a0002c0003t0013g0219a0004c0026t0013g0048 | 3 | HG02080.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.3917-3425G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078252 | ||||||
| chr2:241078253
|
G | C | 3 | a0002c0003t0010g0218a0002c0003t0013g0219a0004c0026t0013g0048 | 3 | HG02080.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.3917-3424G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078253 | ||||||
| chr2:241078254
|
G | A | 3 | a0002c0003t0010g0218a0002c0003t0013g0219a0004c0026t0013g0048 | 3 | HG02080.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.3917-3423G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078254 | ||||||
| chr2:241078256
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3917-3421G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078256 | ||||||
| chr2:241078263
|
G | A | 8 | a0001c0001t0002g0304a0001c0002t0001g0171a0001c0002t0001g0172others(5): Show | 8 | HG00140.hp1 HG02071.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.3917-3414G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078263 | ||||||
| chr2:241078272
|
C | A | 1 | a0001c0001t0002g0304 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3917-3405C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078272 | ||||||
| chr2:241078362
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3917-3315G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078362 | ||||||
| chr2:241078382
|
C | CA | 18 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(15): Show | 18 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.3917-3279dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241078382 | |||||
| chr2:241078382
|
CA | C | 208 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0071others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3917-3279delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241078382 | |||||
| chr2:241078453
|
C | T | 145 | a0001c0001t0001g0189a0001c0001t0005g0299a0001c0001t0009g0274others(142): Show | 145 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.3917-3224C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078453 | ||||||
| chr2:241078562
|
C | T | 17 | a0001c0074t0002g0086a0002c0011t0011g0029a0002c0011t0011g0128others(14): Show | 17 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.3917-3115C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078562 | ||||||
| chr2:241078618
|
G | A | 1 | a0007c0040t0007g0057 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3917-3059G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078618 | ||||||
| chr2:241078619
|
G | C | 5 | a0002c0009t0004g0040a0002c0009t0004g0146a0002c0009t0004g0332others(2): Show | 5 | HG02451.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3917-3058G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078619 | ||||||
| chr2:241078635
|
G | A | 2 | a0001c0002t0009g0211a0001c0002t0017g0143 | 2 | HG02055.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3917-3042G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078635 | ||||||
| chr2:241078769
|
T | C | 1 | a0002c0010t0044g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3917-2908T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241078769 | ||||||
| chr2:241079068
|
C | T | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-2609C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079068 | ||||||
| chr2:241079069
|
G | A | 4 | a0003c0004t0006g0213a0003c0004t0006g0292a0003c0004t0007g0006others(1): Show | 4 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.3917-2608G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079069 | ||||||
| chr2:241079113
|
C | CA | 146 | a0001c0001t0001g0295a0001c0001t0009g0274a0001c0001t0009g0278others(143): Show | 146 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.3917-2547dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241079113 | |||||
| chr2:241079113
|
C | CAA | 9 | a0001c0002t0003g0177a0001c0002t0009g0178a0001c0016t0003g0216others(6): Show | 9 | HG01168.hp1 HG01261.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.3917-2548_3917-254 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241079113 | |||||
| chr2:241079178
|
C | T | 5 | a0002c0009t0004g0040a0002c0009t0004g0146a0002c0009t0004g0332others(2): Show | 5 | HG02451.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3917-2499C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079178 | ||||||
| chr2:241079190
|
A | G | 1 | a0019c0070t0019g0008 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3917-2487A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079190 | ||||||
| chr2:241079390
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3917-2287C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079390 | ||||||
| chr2:241079411
|
C | CA | 10 | a0001c0006t0001g0258a0002c0003t0062g0077a0002c0009t0016g0220others(7): Show | 10 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.3917-2249dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241079411 | |||||
| chr2:241079411
|
CA | C | 7 | a0001c0001t0002g0280a0001c0001t0005g0200a0002c0003t0013g0049others(4): Show | 7 | HG01243.hp1 HG01975.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3917-2249delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241079411 | |||||
| chr2:241079527
|
CTAA | C | 7 | a0002c0008t0061g0168a0002c0036t0025g0022a0002c0064t0060g0250others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3917-2146_3917-214 others(7): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241079527 | |||||
| chr2:241079579
|
G | C | 46 | a0001c0001t0009g0274a0001c0001t0009g0278a0001c0001t0017g0272others(43): Show | 46 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.3917-2098G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079579 | ||||||
| chr2:241079588
|
G | A | 36 | a0002c0003t0008g0020a0002c0003t0008g0066a0002c0003t0008g0070others(33): Show | 36 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.3917-2089G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079588 | ||||||
| chr2:241079608
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3917-2069T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079608 | ||||||
| chr2:241079748
|
AT | A | 5 | a0002c0003t0010g0260a0002c0003t0010g0268a0002c0003t0013g0049others(2): Show | 5 | HG00621.hp2 HG02165.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-1928delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079748 | ||||||
| chr2:241079823
|
G | A | 7 | a0002c0008t0019g0227a0002c0010t0019g0195a0002c0010t0044g0078others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3917-1854G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079823 | ||||||
| chr2:241079829
|
G | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-1848G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079829 | ||||||
| chr2:241079873
|
C | T | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.3917-1804C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241079873 | ||||||
| chr2:241080043
|
G | T | 1 | a0002c0003t0013g0049 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3917-1634G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080043 | ||||||
| chr2:241080154
|
C | T | 3 | a0011c0035t0025g0342a0011c0035t0025g0343a0011c0054t0030g0319 | 3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3917-1523C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080154 | ||||||
| chr2:241080156
|
C | T | 3 | a0002c0010t0014g0222a0002c0019t0014g0041a0002c0021t0014g0233 | 3 | HG01884.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3917-1521C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080156 | ||||||
| chr2:241080232
|
T | C | 176 | a0001c0001t0005g0200a0002c0003t0004g0011a0002c0003t0004g0015others(173): Show | 176 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(173): Show |
intron_variant | MODIFIER | c.3917-1445T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080232 | ||||||
| chr2:241080240
|
C | T | 1 | a0007c0043t0011g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3917-1437C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080240 | ||||||
| chr2:241080283
|
C | T | 5 | a0001c0001t0002g0174a0001c0001t0002g0196a0001c0001t0002g0197others(2): Show | 5 | HG00741.hp1 HG01071.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-1394C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080283 | ||||||
| chr2:241080293
|
A | AAAT | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-1381_3917-137 others(7): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241080293 | |||||
| chr2:241080376
|
G | A | 1 | a0005c0007t0005g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3917-1301G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080376 | ||||||
| chr2:241080402
|
T | C | 1 | a0001c0057t0009g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3917-1275T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080402 | ||||||
| chr2:241080416
|
G | A | 1 | a0005c0014t0001g0125 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3917-1261G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080416 | ||||||
| chr2:241080441
|
G | A | 13 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0010t0019g0195others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3917-1236G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080441 | ||||||
| chr2:241080679
|
C | T | 5 | a0001c0016t0003g0216a0001c0016t0003g0230a0001c0016t0003g0231others(2): Show | 5 | HG02559.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3917-998C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080679 | ||||||
| chr2:241080689
|
C | T | 1 | a0002c0018t0010g0264 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3917-988C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080689 | ||||||
| chr2:241080706
|
T | C | 1 | a0002c0018t0010g0241 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3917-971T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080706 | ||||||
| chr2:241080790
|
G | A | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3917-887G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080790 | ||||||
| chr2:241080847
|
G | A | 2 | a0002c0036t0025g0022a0008c0033t0030g0335 | 2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3917-830G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080847 | ||||||
| chr2:241080936
|
G | A | 5 | a0001c0006t0001g0108a0001c0006t0002g0076a0001c0006t0002g0088others(2): Show | 5 | HG00438.hp2 HG00673.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-741G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080936 | ||||||
| chr2:241080937
|
A | T | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.3917-740A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080937 | ||||||
| chr2:241080993
|
C | G | 3 | a0001c0002t0023g0179a0001c0002t0023g0246a0001c0002t0023g0247 | 3 | HG02735.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3917-684C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241080993 | ||||||
| chr2:241081108
|
C | T | 46 | a0001c0001t0009g0274a0001c0001t0009g0278a0001c0001t0017g0272others(43): Show | 46 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.3917-569C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081108 | ||||||
| chr2:241081216
|
A | C | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3917-461A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081216 | ||||||
| chr2:241081321
|
G | A | 2 | a0002c0010t0019g0195a0002c0075t0045g0251 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3917-356G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081321 | ||||||
| chr2:241081326
|
G | A | 1 | a0021c0078t0016g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3917-351G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081326 | ||||||
| chr2:241081364
|
C | T | 48 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(45): Show | 48 | HG01261.hp1 HG01433.hp1 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.3917-313C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081364 | ||||||
| chr2:241081401
|
T | C | 39 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(36): Show | 39 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.3917-276T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081401 | ||||||
| chr2:241081410
|
CCTT | C | 7 | a0002c0008t0061g0168a0002c0036t0025g0022a0002c0064t0060g0250others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3917-266_3917-264d others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081410 | ||||||
| chr2:241081423
|
T | A | 1 | a0012c0079t0016g0331 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3917-254T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081423 | ||||||
| chr2:241081457
|
G | C | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3917-220G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081457 | ||||||
| chr2:241081549
|
C | T | 11 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0019t0014g0041others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3917-128C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081549 | ||||||
| chr2:241081585
|
A | ATCAGG | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.3917-88_3917-84dup others(5): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | 241081585 | |||||
| chr2:241081596
|
A | G | 78 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(75): Show | 78 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.3917-81A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 27/31 | chr2 | 241081596 | ||||||
| chr2:241081801
|
G | A | 48 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(45): Show | 48 | HG01261.hp1 HG01433.hp1 HG01891.hp2 others(45): Show |
splice_region_variant&intron_variant | LOW | c.4033+8G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 28/31 | chr2 | 241081801 | ||||||
| chr2:241081940
|
A | C | 11 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0019t0014g0041others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4033+147A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 28/31 | chr2 | 241081940 | ||||||
| chr2:241082023
|
G | A | 1 | a0002c0011t0011g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4033+230G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 28/31 | chr2 | 241082023 | ||||||
| chr2:241082095
|
T | C | 3 | a0011c0035t0025g0342a0011c0035t0025g0343a0011c0054t0030g0319 | 3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4034-182T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 28/31 | chr2 | 241082095 | ||||||
| chr2:241082137
|
C | T | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4034-140C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 28/31 | chr2 | 241082137 | ||||||
| chr2:241082273
|
G | A | 1 | a0001c0002t0009g0211 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.4034-4G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 28/31 | chr2 | 241082273 | ||||||
| chr2:241082374
|
T | C | 2 | a0001c0002t0023g0246a0001c0002t0023g0247 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4121+10T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082374 | ||||||
| chr2:241082394
|
G | A | 11 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0019t0014g0041others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4121+30G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082394 | ||||||
| chr2:241082414
|
AC | A | 6 | a0002c0008t0061g0168a0002c0036t0025g0022a0008c0033t0030g0335others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.4121+51delC | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082414 | ||||||
| chr2:241082450
|
C | T | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4121+86C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082450 | ||||||
| chr2:241082456
|
G | A | 1 | a0003c0004t0006g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4121+92G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082456 | ||||||
| chr2:241082463
|
C | T | 13 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0019t0014g0041others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.4121+99C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082463 | ||||||
| chr2:241082606
|
G | GGTCCCCA others(8): Show |
1 | a0003c0023t0006g0237 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4121+244_4121+258d others(17): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241082606 | |||||
| chr2:241082623
|
G | A | 97 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(94): Show | 97 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.4121+259G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082623 | ||||||
| chr2:241082696
|
T | C | 97 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(94): Show | 97 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.4121+332T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082696 | ||||||
| chr2:241082750
|
C | T | 1 | a0008c0069t0016g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4121+386C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082750 | ||||||
| chr2:241082864
|
C | T | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4121+500C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082864 | ||||||
| chr2:241082904
|
CACCTGCT others(45): Show |
C | 2 | a0001c0002t0003g0177a0001c0002t0009g0187 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4121+564_4121+615d others(54): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241082904 | |||||
| chr2:241082956
|
T | C | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.4121+592T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082956 | ||||||
| chr2:241082971
|
G | A | 1 | a0002c0003t0006g0275 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4121+607G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241082971 | ||||||
| chr2:241083002
|
G | C | 1 | a0002c0061t0008g0253 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.4121+638G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083002 | ||||||
| chr2:241083062
|
AACAG | A | 38 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(35): Show | 38 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.4121+703_4121+706d others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241083062 | |||||
| chr2:241083063
|
A | G | 7 | a0002c0008t0019g0227a0002c0010t0019g0195a0002c0010t0044g0078others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4121+699A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083063 | ||||||
| chr2:241083115
|
G | C | 73 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(70): Show | 73 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.4121+751G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083115 | ||||||
| chr2:241083138
|
C | T | 2 | a0002c0058t0019g0209a0012c0049t0019g0050 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4121+774C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083138 | ||||||
| chr2:241083161
|
G | C | 1 | a0003c0066t0015g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4121+797G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083161 | ||||||
| chr2:241083237
|
C | T | 11 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0019t0014g0041others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4121+873C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083237 | ||||||
| chr2:241083238
|
A | G | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.4121+874A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083238 | ||||||
| chr2:241083252
|
G | T | 3 | a0002c0009t0016g0220a0012c0079t0016g0331a0021c0078t0016g0035 | 3 | HG02145.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4121+888G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083252 | ||||||
| chr2:241083321
|
G | T | 10 | a0002c0003t0008g0020a0002c0003t0008g0081a0002c0003t0008g0113others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.4121+957G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083321 | ||||||
| chr2:241083340
|
T | A | 11 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0019t0014g0041others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4121+976T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083340 | ||||||
| chr2:241083370
|
TG | T | 42 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(39): Show | 42 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.4121+1008delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241083370 | |||||
| chr2:241083382
|
G | A | 1 | a0018c0065t0038g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4121+1018G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083382 | ||||||
| chr2:241083393
|
GGGA | G | 221 | a0001c0001t0009g0274a0001c0001t0009g0278a0001c0001t0017g0272others(218): Show | 221 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(218): Show |
intron_variant | MODIFIER | c.4121+1034_4121+103 others(7): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241083393 | |||||
| chr2:241083474
|
G | A | 1 | a0002c0008t0061g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4121+1110G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083474 | ||||||
| chr2:241083480
|
G | A | 16 | a0002c0011t0011g0029a0002c0011t0011g0128a0002c0011t0011g0234others(13): Show | 16 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4121+1116G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083480 | ||||||
| chr2:241083611
|
A | G | 73 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(70): Show | 73 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.4121+1247A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083611 | ||||||
| chr2:241083665
|
A | T | 1 | a0002c0003t0062g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4121+1301A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083665 | ||||||
| chr2:241083736
|
T | C | 1 | a0002c0080t0011g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4121+1372T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083736 | ||||||
| chr2:241083909
|
G | GTTTTCTA others(18): Show |
6 | a0002c0003t0022g0023a0002c0018t0022g0223a0002c0055t0022g0052others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4121+1547_4121+157 others(29): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241083909 | |||||
| chr2:241083909
|
G | GTTTTCTA others(15): Show |
35 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(32): Show | 35 | HG01261.hp1 HG01433.hp1 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.4121+1564_4121+156 others(26): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241083909 | |||||
| chr2:241083937
|
T | C | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4121+1573T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241083937 | ||||||
| chr2:241084083
|
A | G | 69 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(66): Show | 69 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.4121+1719A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241084083 | ||||||
| chr2:241084134
|
A | AT | 91 | a0001c0001t0001g0244a0001c0001t0001g0295a0001c0001t0002g0294others(88): Show | 91 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(88): Show |
intron_variant | MODIFIER | c.4121+1789dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241084134 | |||||
| chr2:241084134
|
A | ATTTT | 12 | a0002c0003t0062g0077a0002c0009t0016g0220a0002c0010t0016g0157others(9): Show | 12 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.4121+1786_4121+178 others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241084134 | |||||
| chr2:241084134
|
A | ATTTTT | 40 | a0002c0003t0006g0275a0002c0003t0007g0284a0002c0003t0007g0290others(37): Show | 40 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.4121+1785_4121+178 others(9): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241084134 | |||||
| chr2:241084134
|
A | ATTTTTT | 20 | a0002c0003t0007g0131a0002c0008t0061g0168a0002c0010t0014g0222others(17): Show | 20 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.4121+1784_4121+178 others(10): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241084134 | |||||
| chr2:241084134
|
AT | A | 22 | a0002c0011t0011g0029a0002c0011t0011g0128a0002c0011t0011g0234others(19): Show | 22 | HG00621.hp1 HG01099.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.4121+1789delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241084134 | |||||
| chr2:241084262
|
G | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4121+1898G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241084262 | ||||||
| chr2:241084352
|
C | T | 3 | a0002c0010t0016g0033a0002c0010t0016g0157a0008c0033t0016g0221 | 3 | HG02559.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4121+1988C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241084352 | ||||||
| chr2:241084475
|
T | A | 2 | a0002c0036t0025g0022a0008c0033t0030g0335 | 2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4121+2111T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241084475 | ||||||
| chr2:241084481
|
T | C | 49 | a0002c0003t0008g0020a0002c0003t0008g0066a0002c0003t0008g0070others(46): Show | 49 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.4121+2117T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241084481 | ||||||
| chr2:241084712
|
C | G | 1 | a0002c0084t0037g0318 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4121+2348C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241084712 | ||||||
| chr2:241084869
|
T | C | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4121+2505T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241084869 | ||||||
| chr2:241085014
|
G | GT | 9 | a0002c0003t0062g0077a0002c0009t0016g0220a0002c0010t0016g0033others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.4122-2377dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085014 | |||||
| chr2:241085165
|
G | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4122-2227G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241085165 | ||||||
| chr2:241085346
|
T | C | 1 | a0003c0004t0007g0099 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4122-2046T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241085346 | ||||||
| chr2:241085386
|
A | G | 16 | a0002c0011t0011g0029a0002c0011t0011g0128a0002c0011t0011g0234others(13): Show | 16 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4122-2006A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241085386 | ||||||
| chr2:241085486
|
A | G | 4 | a0008c0032t0021g0328a0008c0032t0021g0329a0008c0051t0021g0337others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4122-1906A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241085486 | ||||||
| chr2:241085490
|
C | A | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4122-1902C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241085490 | ||||||
| chr2:241085548
|
T | C | 2 | a0001c0001t0017g0272a0001c0001t0017g0273 | 2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.4122-1844T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241085548 | ||||||
| chr2:241085697
|
ATTTG | A | 7 | a0002c0022t0014g0087a0002c0022t0014g0327a0002c0022t0035g0037others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4122-1679_4122-167 others(8): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085697 | |||||
| chr2:241085697
|
ATTTGTTT others(1): Show |
A | 4 | a0008c0032t0021g0328a0008c0032t0021g0329a0008c0051t0021g0337others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4122-1683_4122-167 others(12): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085697 | |||||
| chr2:241085860
|
C | CT | 106 | a0001c0001t0001g0141a0001c0001t0001g0244a0001c0001t0001g0334others(103): Show | 106 | HG00558.hp2 HG00673.hp2 HG00741.hp2 others(103): Show |
intron_variant | MODIFIER | c.4122-1508dupT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085860 | |||||
| chr2:241085860
|
C | CTT | 13 | a0002c0003t0007g0131a0002c0003t0007g0290a0002c0003t0062g0077others(10): Show | 13 | HG01928.hp2 HG02040.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.4122-1509_4122-150 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085860 | |||||
| chr2:241085860
|
CT | C | 51 | a0001c0002t0001g0182a0001c0002t0005g0115a0001c0002t0018g0160others(48): Show | 51 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.4122-1508delT | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085860 | |||||
| chr2:241085860
|
CTTTTTTT others(5): Show |
C | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4122-1519_4122-150 others(16): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085860 | |||||
| chr2:241085860
|
CTTTTTTT others(8): Show |
C | 1 | a0019c0070t0019g0008 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4122-1522_4122-150 others(19): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241085860 | |||||
| chr2:241086367
|
A | ACT | 304 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0079others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.4122-1024_4122-102 others(6): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr2 | 241086367 | |||||
| chr2:241086467
|
A | G | 74 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(71): Show | 74 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.4122-925A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241086467 | ||||||
| chr2:241086505
|
C | G | 1 | a0002c0084t0037g0318 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4122-887C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241086505 | ||||||
| chr2:241086733
|
T | C | 2 | a0002c0058t0019g0209a0012c0049t0019g0050 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4122-659T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241086733 | ||||||
| chr2:241086763
|
A | T | 1 | a0002c0036t0014g0326 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4122-629A>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241086763 | ||||||
| chr2:241086844
|
T | C | 33 | a0002c0003t0008g0020a0002c0003t0008g0066a0002c0003t0008g0070others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.4122-548T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241086844 | ||||||
| chr2:241086855
|
G | C | 41 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(38): Show | 41 | HG01261.hp1 HG01433.hp1 HG01928.hp2 others(38): Show |
intron_variant | MODIFIER | c.4122-537G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241086855 | ||||||
| chr2:241086948
|
G | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4122-444G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241086948 | ||||||
| chr2:241087193
|
A | G | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.4122-199A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241087193 | ||||||
| chr2:241087234
|
A | G | 74 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(71): Show | 74 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.4122-158A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241087234 | ||||||
| chr2:241087260
|
G | A | 1 | a0002c0003t0013g0194 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4122-132G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 29/31 | chr2 | 241087260 | ||||||
| chr2:241087542
|
G | GC | 74 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(71): Show | 74 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.4205+67_4205+68ins others(1): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241087542 | ||||||
| chr2:241087609
|
C | T | 1 | a0001c0006t0001g0257 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4205+134C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241087609 | ||||||
| chr2:241087616
|
G | A | 1 | a0001c0002t0009g0211 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4205+141G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241087616 | ||||||
| chr2:241087871
|
G | A | 1 | a0001c0002t0048g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4205+396G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241087871 | ||||||
| chr2:241088061
|
G | A | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4206-304G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241088061 | ||||||
| chr2:241088070
|
T | C | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4206-295T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241088070 | ||||||
| chr2:241088110
|
A | G | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.4206-255A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241088110 | ||||||
| chr2:241088208
|
A | C | 3 | a0006c0012t0001g0001a0006c0012t0001g0311a0006c0012t0005g0309 | 4 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.4206-157A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241088208 | ||||||
| chr2:241088220
|
G | A | 1 | a0004c0005t0031g0059 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4206-145G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 30/31 | chr2 | 241088220 | ||||||
| chr2:241088451
|
G | T | 9 | a0002c0003t0062g0077a0002c0009t0016g0220a0002c0010t0016g0033others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.*1+49G>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088451 | ||||||
| chr2:241088511
|
T | A | 97 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(94): Show | 97 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.*1+109T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088511 | ||||||
| chr2:241088666
|
C | G | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+264C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088666 | ||||||
| chr2:241088676
|
G | A | 1 | a0002c0003t0008g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.*1+274G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088676 | ||||||
| chr2:241088710
|
A | G | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+308A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088710 | ||||||
| chr2:241088792
|
G | A | 16 | a0002c0011t0011g0029a0002c0011t0011g0128a0002c0011t0011g0234others(13): Show | 16 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.*1+390G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088792 | ||||||
| chr2:241088832
|
A | G | 1 | a0002c0084t0037g0318 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*1+430A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088832 | ||||||
| chr2:241088867
|
C | T | 175 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(172): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.*1+465C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088867 | ||||||
| chr2:241088956
|
T | C | 3 | a0002c0010t0016g0033a0002c0010t0016g0157a0008c0033t0016g0221 | 3 | HG02559.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*1+554T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088956 | ||||||
| chr2:241088991
|
G | A | 39 | a0001c0001t0001g0170a0002c0003t0006g0275a0002c0003t0007g0131others(36): Show | 39 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.*1+589G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241088991 | ||||||
| chr2:241089157
|
A | G | 1 | a0006c0077t0003g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.*1+755A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089157 | ||||||
| chr2:241089264
|
C | T | 1 | a0001c0006t0058g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.*1+862C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089264 | ||||||
| chr2:241089326
|
A | G | 46 | a0001c0001t0009g0274a0001c0001t0009g0278a0001c0001t0017g0272others(43): Show | 46 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.*1+924A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089326 | ||||||
| chr2:241089347
|
T | C | 33 | a0002c0003t0008g0020a0002c0003t0008g0066a0002c0003t0008g0070others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.*1+945T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089347 | ||||||
| chr2:241089367
|
TA | T | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+972delA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241089367 | |||||
| chr2:241089496
|
C | A | 1 | a0001c0002t0003g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.*1+1094C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089496 | ||||||
| chr2:241089532
|
T | C | 4 | a0008c0032t0021g0328a0008c0032t0021g0329a0008c0051t0021g0337others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1+1130T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089532 | ||||||
| chr2:241089565
|
CG | C | 69 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(66): Show | 69 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.*1+1165delG | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241089565 | |||||
| chr2:241089572
|
G | A | 4 | a0010c0017t0024g0042a0010c0017t0024g0225a0010c0017t0024g0338others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.*1+1170G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089572 | ||||||
| chr2:241089581
|
C | G | 7 | a0002c0008t0019g0227a0002c0010t0019g0195a0002c0010t0044g0078others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.*1+1179C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089581 | ||||||
| chr2:241089616
|
G | C | 1 | a0001c0001t0002g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.*1+1214G>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089616 | ||||||
| chr2:241089711
|
A | G | 6 | a0002c0008t0061g0168a0002c0036t0025g0022a0008c0033t0030g0335others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*1+1309A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089711 | ||||||
| chr2:241089822
|
C | T | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+1420C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089822 | ||||||
| chr2:241089826
|
C | T | 6 | a0002c0008t0061g0168a0002c0036t0025g0022a0008c0033t0030g0335others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*1+1424C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089826 | ||||||
| chr2:241089944
|
A | G | 70 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(67): Show | 70 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.*1+1542A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241089944 | ||||||
| chr2:241090011
|
G | A | 38 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(35): Show | 38 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.*1+1609G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090011 | ||||||
| chr2:241090137
|
A | G | 1 | a0002c0073t0063g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*2-1501A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090137 | ||||||
| chr2:241090138
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.*2-1500A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090138 | ||||||
| chr2:241090154
|
C | T | 1 | a0002c0064t0060g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*2-1484C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090154 | ||||||
| chr2:241090322
|
G | A | 46 | a0001c0001t0009g0274a0001c0001t0009g0278a0001c0001t0017g0272others(43): Show | 46 | HG00738.hp2 HG01123.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.*2-1316G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090322 | ||||||
| chr2:241090420
|
A | C | 1 | a0003c0004t0032g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*2-1218A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090420 | ||||||
| chr2:241090421
|
C | T | 1 | a0003c0004t0032g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*2-1217C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090421 | ||||||
| chr2:241090422
|
T | A | 5 | a0009c0030t0027g0127a0009c0030t0027g0208a0009c0031t0028g0224others(2): Show | 5 | HG02451.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.*2-1216T>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090422 | ||||||
| chr2:241090453
|
AAAT | A | 3 | a0002c0010t0016g0033a0002c0010t0016g0157a0008c0033t0016g0221 | 3 | HG02559.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*2-1181_*2-1179del others(3): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241090453 | |||||
| chr2:241090518
|
T | C | 38 | a0002c0003t0006g0275a0002c0003t0007g0131a0002c0003t0007g0284others(35): Show | 38 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.*2-1120T>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090518 | ||||||
| chr2:241090772
|
C | T | 15 | a0002c0011t0011g0029a0002c0011t0011g0128a0002c0011t0011g0234others(12): Show | 15 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.*2-866C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090772 | ||||||
| chr2:241090868
|
C | CA | 36 | a0001c0006t0001g0257a0002c0003t0006g0275a0002c0003t0007g0131others(33): Show | 36 | HG00558.hp2 HG00673.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.*2-754dupA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241090868 | |||||
| chr2:241090878
|
A | G | 11 | a0001c0001t0001g0098a0001c0001t0001g0163a0001c0001t0001g0166others(8): Show | 11 | HG00423.hp1 HG02056.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.*2-760A>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090878 | ||||||
| chr2:241090903
|
G | A | 4 | a0008c0032t0021g0328a0008c0032t0021g0329a0008c0051t0021g0337others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-735G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090903 | ||||||
| chr2:241090954
|
C | T | 2 | a0002c0022t0014g0087a0002c0036t0014g0326 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.*2-684C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241090954 | ||||||
| chr2:241091090
|
C | T | 1 | a0001c0025t0009g0073 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.*2-548C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241091090 | ||||||
| chr2:241091120
|
A | C | 1 | a0003c0004t0006g0002 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.*2-518A>C | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241091120 | ||||||
| chr2:241091141
|
T | TTA | 101 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(98): Show | 101 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.*2-494_*2-493dupTA | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241091141 | |||||
| chr2:241091203
|
C | A | 1 | a0002c0003t0007g0290 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.*2-435C>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241091203 | ||||||
| chr2:241091380
|
C | G | 1 | a0001c0002t0020g0308 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.*2-258C>G | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241091380 | ||||||
| chr2:241091399
|
C | T | 33 | a0002c0003t0008g0020a0002c0003t0008g0066a0002c0003t0008g0070others(30): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.*2-239C>T | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241091399 | ||||||
| chr2:241091412
|
C | CCCTCCCC others(48): Show |
1 | a0002c0008t0061g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*2-192_*2-191insAG others(53): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241091412 | |||||
| chr2:241091412
|
C | CCCTCCCC others(48): Show |
161 | a0002c0003t0004g0011a0002c0003t0004g0015a0002c0003t0004g0271others(158): Show | 161 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.*2-176_*2-122dupCG others(53): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241091412 | |||||
| chr2:241091412
|
C | CCCTCCCC others(158): Show |
1 | a0002c0011t0011g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.*2-122_*2-121insCG others(163): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241091412 | |||||
| chr2:241091412
|
CCCTCCCC others(48): Show |
C | 1 | a0001c0001t0020g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*2-176_*2-122delCG others(53): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241091412 | |||||
| chr2:241091471
|
C | CCCCGTGT others(47): Show |
1 | a0003c0004t0032g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*2-122_*2-121insCG others(52): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr2 | 241091471 | |||||
| chr2:241091516
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.*2-122G>A | SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241091516 | ||||||
| chr2:241091516
|
G | GCGGGGTC others(103): Show |
11 | a0002c0010t0014g0038a0002c0010t0014g0222a0002c0019t0014g0041others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.*2-122_*2-121insCG others(108): Show |
SNED1 | ENSG00000162804.15 | transcript | ENST00000310397.13 | protein_coding | 31/31 | chr2 | 241091516 |