Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6645 |
|---|---|
| ensemblid | ENSG00000168807.17 |
| hgncid | 11169 |
| symbol | SNTB2 |
| name | syntrophin beta 2 |
| refseq_nuc | NM_006750.4 |
| refseq_prot | NP_006741.1 |
| ensembl_nuc | ENST00000336278.9 |
| ensembl_prot | ENSP00000338191.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 69187164 |
| end | 69309052 |
| strand | + |
| ver | v1.2 |
| region | chr16:69187164-69309052 |
| region5000 | chr16:69182164-69314052 |
| regionname0 | SNTB2_chr16_69187164_69309052 |
| regionname5000 | SNTB2_chr16_69182164_69314052 |
| 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 | 540 | 216 | 83 | 38 | 57 | 8 | 28 | 37 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0002 | 0/0 | 232 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0003 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| 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 | 1623 | 152 | 52 | 25 | 51 | 4 | 19 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| c0002 | 0/1 | 1623 | 61 | 31 | 11 | 6 | 3 | 9 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| c0003 | 0/0 | 1623 | 3 | 0 | 2 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| c0004 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| c0005 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| 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 | 0/0 | 8132 | 40 | 18 | 8 | 11 | 1 | 2 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0002 | 1/0 | 8132 | 35 | 1 | 8 | 18 | 2 | 5 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0003 | 0/0 | 8132 | 22 | 2 | 7 | 8 | 0 | 5 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0004 | 0/0 | 8132 | 17 | 5 | 2 | 5 | 0 | 5 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0005 | 0/0 | 8132 | 13 | 5 | 2 | 4 | 1 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0006 | 0/0 | 8132 | 9 | 9 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0007 | 0/0 | 8132 | 8 | 0 | 0 | 5 | 0 | 3 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0008 | 0/0 | 8132 | 6 | 6 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0009 | 0/0 | 8133 | 6 | 5 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0010 | 0/0 | 8132 | 5 | 2 | 2 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0011 | 0/0 | 8133 | 4 | 4 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0012 | 0/0 | 8132 | 4 | 0 | 2 | 1 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0013 | 0/0 | 8133 | 3 | 3 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0014 | 0/0 | 8132 | 3 | 2 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0015 | 0/0 | 8132 | 3 | 3 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0016 | 0/0 | 8132 | 3 | 3 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0017 | 0/0 | 8132 | 2 | 0 | 0 | 0 | 0 | 2 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0018 | 0/0 | 8132 | 2 | 0 | 2 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0019 | 0/1 | 8132 | 2 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0020 | 0/0 | 8132 | 2 | 0 | 1 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0021 | 0/0 | 8133 | 2 | 2 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0022 | 0/0 | 8125 | 2 | 0 | 0 | 2 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0023 | 0/0 | 8132 | 2 | 2 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0024 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0025 | 0/0 | 8133 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0026 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0027 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0028 | 0/0 | 8132 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0029 | 0/0 | 8133 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0030 | 0/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0031 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0032 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0033 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0034 | 0/0 | 8133 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0035 | 0/0 | 8132 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0036 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0037 | 0/0 | 8133 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0038 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0039 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0040 | 0/0 | 8132 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0041 | 0/0 | 8132 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0042 | 0/0 | 8132 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0043 | 0/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0044 | 0/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0045 | 0/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| t0046 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| 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 | 1623 | 152 | 52 | 25 | 51 | 4 | 19 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002 | 0/1 | 1623 | 61 | 31 | 11 | 6 | 3 | 9 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0003 | 0/0 | 1623 | 3 | 0 | 2 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0002c0004 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0003c0005 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9754 | 39 | 18 | 8 | 10 | 1 | 2 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0002 | 1/0 | 9754 | 35 | 1 | 8 | 18 | 2 | 5 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0003 | 0/0 | 9754 | 22 | 2 | 7 | 8 | 0 | 5 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0005 | 0/0 | 9754 | 10 | 5 | 0 | 4 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0006 | 0/0 | 9754 | 9 | 9 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0007 | 0/0 | 9754 | 8 | 0 | 0 | 5 | 0 | 3 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0010 | 0/0 | 9754 | 5 | 2 | 2 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0011 | 0/0 | 9755 | 4 | 4 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0013 | 0/0 | 9755 | 3 | 3 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0016 | 0/0 | 9754 | 3 | 3 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0022 | 0/0 | 9747 | 2 | 0 | 0 | 2 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0025 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0031 | 0/0 | 9753 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0034 | 0/0 | 9755 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0035 | 0/0 | 9754 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0039 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0040 | 0/0 | 9754 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0041 | 0/0 | 9754 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0042 | 0/0 | 9754 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0043 | 0/0 | 9754 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0044 | 0/0 | 9754 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0045 | 0/0 | 9754 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0001t0046 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0004 | 0/0 | 9754 | 17 | 5 | 2 | 5 | 0 | 5 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0008 | 0/0 | 9754 | 6 | 6 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0009 | 0/0 | 9755 | 6 | 5 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0012 | 0/0 | 9754 | 4 | 0 | 2 | 1 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0014 | 0/0 | 9754 | 3 | 2 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0015 | 0/0 | 9754 | 3 | 3 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0017 | 0/0 | 9754 | 2 | 0 | 0 | 0 | 0 | 2 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0018 | 0/0 | 9754 | 2 | 0 | 2 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0019 | 0/1 | 9754 | 2 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0020 | 0/0 | 9754 | 2 | 0 | 1 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0021 | 0/0 | 9755 | 2 | 2 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0023 | 0/0 | 9754 | 2 | 2 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0024 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0026 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0027 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0028 | 0/0 | 9754 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0029 | 0/0 | 9755 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0030 | 0/0 | 9754 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0032 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0036 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0037 | 0/0 | 9755 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0002t0038 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0001c0003t0005 | 0/0 | 9754 | 3 | 0 | 2 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0002c0004t0001 | 0/0 | 9776 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| a0003c0005t0033 | 0/0 | 9754 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | copy fasta | chr16 | 69182164 | 69314052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0010g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0010g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0013g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0016g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0016g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0022g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0022g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0025g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0031g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0034g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0035g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0039g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0040g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0041g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0042g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0043g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0044g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0045g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0001t0046g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0009g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0009g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0012g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0012g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0012g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0014g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0014g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0015g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0015g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0017g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0017g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0018g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0018g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0019g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0019g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0020g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0020g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0021g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0021g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0023g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0026g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0027g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0028g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0029g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0030g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0032g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0036g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0037g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0002t0038g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0003t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0003t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0001c0003t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0002c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| a0003c0005t0033g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0020 | g0011 | EUR | GBR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00099 | hp2 | a0001 | c0001 | t0010 | g0141 | EUR | GBR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00280 | hp2 | a0001 | c0002 | t0019 | g0042 | EUR | FIN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00544 | hp2 | a0001 | c0001 | t0007 | g0153 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00597 | hp2 | a0001 | c0001 | t0040 | g0105 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00621 | hp2 | a0001 | c0001 | t0041 | g0080 | EAS | CHS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0037 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00738 | hp1 | a0001 | c0002 | t0020 | g0013 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG00738 | hp2 | a0001 | c0002 | t0009 | g0009 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0106 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01109 | hp2 | a0001 | c0002 | t0028 | g0010 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01169 | hp1 | a0001 | c0002 | t0018 | g0034 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01192 | hp1 | a0001 | c0002 | t0029 | g0012 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01243 | hp2 | a0001 | c0002 | t0012 | g0206 | AMR | PUR | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01346 | hp1 | a0001 | c0002 | t0012 | g0203 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01346 | hp2 | a0001 | c0003 | t0005 | g0214 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01361 | hp2 | a0001 | c0003 | t0005 | g0215 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0140 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01433 | hp2 | a0001 | c0002 | t0014 | g0072 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01496 | hp2 | a0001 | c0002 | t0018 | g0036 | AMR | CLM | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01517 | hp2 | a0001 | c0002 | t0012 | g0205 | EUR | IBS | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01891 | hp2 | a0001 | c0001 | t0025 | g0152 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0031 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | KHV | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02145 | hp1 | a0001 | c0002 | t0009 | g0005 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02145 | hp2 | a0001 | c0001 | t0034 | g0161 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0142 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0177 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0078 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0050 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02572 | hp2 | a0001 | c0002 | t0015 | g0066 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0040 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02602 | hp2 | a0001 | c0001 | t0044 | g0159 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0018 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0048 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02717 | hp1 | a0001 | c0002 | t0009 | g0008 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02717 | hp2 | a0001 | c0002 | t0023 | g0068 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0055 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0170 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0045 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02809 | hp1 | a0001 | c0002 | t0008 | g0017 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02809 | hp2 | a0003 | c0005 | t0033 | g0073 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0169 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02895 | hp2 | a0001 | c0002 | t0008 | g0020 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02897 | hp2 | a0001 | c0002 | t0008 | g0021 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02922 | hp2 | a0001 | c0002 | t0014 | g0071 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0051 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02965 | hp2 | a0001 | c0002 | t0009 | g0003 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02976 | hp2 | a0001 | c0002 | t0026 | g0004 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0046 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03041 | hp1 | a0001 | c0002 | t0008 | g0015 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03041 | hp2 | a0001 | c0002 | t0021 | g0075 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03130 | hp1 | a0001 | c0002 | t0014 | g0070 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03139 | hp1 | a0001 | c0002 | t0024 | g0027 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03139 | hp2 | a0001 | c0002 | t0009 | g0007 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03225 | hp1 | a0001 | c0002 | t0021 | g0074 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03225 | hp2 | a0001 | c0002 | t0032 | g0014 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03453 | hp2 | a0001 | c0002 | t0009 | g0006 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0056 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03486 | hp2 | a0001 | c0002 | t0015 | g0064 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03491 | hp2 | a0001 | c0002 | t0017 | g0043 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03492 | hp1 | a0001 | c0002 | t0017 | g0044 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03516 | hp1 | a0001 | c0002 | t0036 | g0019 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0168 | AFR | ESN | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03540 | hp1 | a0001 | c0002 | t0023 | g0067 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03654 | hp2 | a0001 | c0001 | t0045 | g0216 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0158 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0197 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03710 | hp2 | a0001 | c0002 | t0037 | g0204 | SAS | PJL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0038 | SAS | BEB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0151 | SAS | BEB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0039 | SAS | BEB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | STU | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0208 | SAS | STU | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18522 | hp1 | a0001 | c0002 | t0015 | g0065 | AFR | YRI | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0156 | EAS | CHB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | CHB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | YRI | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18964 | hp2 | a0001 | c0002 | t0012 | g0202 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18973 | hp2 | a0001 | c0001 | t0035 | g0194 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18997 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18998 | hp1 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19030 | hp1 | a0001 | c0001 | t0039 | g0053 | AFR | LWK | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19030 | hp2 | a0001 | c0001 | t0031 | g0150 | AFR | LWK | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19043 | hp1 | a0001 | c0002 | t0008 | g0016 | AFR | LWK | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19064 | hp1 | a0001 | c0001 | t0022 | g0196 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19077 | hp2 | a0001 | c0001 | t0042 | g0144 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19084 | hp1 | a0001 | c0001 | t0022 | g0195 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19087 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA19087 | hp2 | a0002 | c0004 | t0001 | g0192 | EAS | JPT | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ASW | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA20805 | hp1 | a0001 | c0003 | t0005 | g0209 | EUR | TSI | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0124 | EUR | TSI | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA20905 | hp1 | a0001 | c0001 | t0043 | g0088 | SAS | GIH | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA20905 | hp2 | a0001 | c0002 | t0030 | g0035 | SAS | GIH | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02486 | hp1 | a0001 | c0001 | t0046 | g0176 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0062 | AFR | ACB | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0059 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG06807 | hp1 | a0001 | c0002 | t0038 | g0069 | AFR | USA | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | USA | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | LWK | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| NA21309 | hp2 | a0001 | c0002 | t0027 | g0047 | AFR | LWK | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0019 | g0041 | REF | REF | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0077 | REF | REF | SNTB2_chr16_69182164_69314052 | SNTB2 | chr16 | 69182164 | 69314052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69245709
|
G | T | 1 | a0003 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.688G>T | p.Asp230Tyr | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/7 | 691/9754 | 688/1623 | 230/540 | chr16 | 69245709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69187607
|
C | G | 2 | a0001c0002a0003c0005 | 62 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(59): Show |
synonymous_variant | LOW | c.441C>G | p.Pro147Pro | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/7 | 444/9754 | 441/1623 | 147/540 | chr16 | 69187607 | ||
| chr16:69270145
|
A | G | 1 | a0001c0003 | 3 | HG01346.hp2 HG01361.hp2 NA20805.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1008A>G | p.Ala336Ala | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/7 | 1011/9754 | 1008/1623 | 336/540 | chr16 | 69270145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69300977
|
C | CA | 13 | a0001c0001t0013a0001c0001t0025a0001c0002t0004others(10): Show | 35 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*65dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 66 | INFO_REALIGN_3_PRIME | chr16 | 69300977 | ||||
| chr16:69301559
|
A | C | 1 | a0001c0001t0046 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*635A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 635 | chr16 | 69301559 | |||||
| chr16:69301685
|
A | G | 1 | a0001c0001t0016 | 3 | HG02280.hp1 HG02622.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*761A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 761 | chr16 | 69301685 | |||||
| chr16:69302045
|
G | C | 1 | a0001c0001t0010 | 5 | HG00099.hp2 HG01081.hp2 HG01433.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1121G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 1121 | chr16 | 69302045 | |||||
| chr16:69302166
|
C | T | 1 | a0001c0002t0030 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1242C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 1242 | chr16 | 69302166 | |||||
| chr16:69302201
|
A | G | 1 | a0001c0001t0045 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1277A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 1277 | chr16 | 69302201 | |||||
| chr16:69302306
|
A | G | 3 | a0001c0001t0007a0001c0001t0044a0001c0001t0045 | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1382A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 1382 | chr16 | 69302306 | |||||
| chr16:69302318
|
A | T | 6 | a0001c0001t0003a0001c0001t0010a0001c0001t0040others(3): Show | 31 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1394A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 1394 | chr16 | 69302318 | |||||
| chr16:69302626
|
A | G | 1 | a0001c0001t0039 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1702A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 1702 | chr16 | 69302626 | |||||
| chr16:69303039
|
G | A | 1 | a0001c0002t0017 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2115G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2115 | chr16 | 69303039 | |||||
| chr16:69303083
|
T | G | 1 | a0001c0002t0024 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2159T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2159 | chr16 | 69303083 | |||||
| chr16:69303147
|
G | A | 1 | a0001c0002t0017 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2223G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2223 | chr16 | 69303147 | |||||
| chr16:69303188
|
A | G | 23 | a0001c0001t0006a0001c0001t0013a0001c0001t0016others(20): Show | 71 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2264A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2264 | chr16 | 69303188 | |||||
| chr16:69303423
|
C | T | 1 | a0001c0002t0038 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2499C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2499 | chr16 | 69303423 | |||||
| chr16:69303455
|
G | A | 4 | a0001c0001t0006a0001c0001t0013a0001c0001t0016others(1): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2531G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2531 | chr16 | 69303455 | |||||
| chr16:69303500
|
C | T | 11 | a0001c0002t0004a0001c0002t0017a0001c0002t0018others(8): Show | 31 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2576C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2576 | chr16 | 69303500 | |||||
| chr16:69303540
|
G | A | 4 | a0001c0001t0005a0001c0001t0025a0001c0001t0031others(1): Show | 15 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2616G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2616 | chr16 | 69303540 | |||||
| chr16:69303541
|
G | A | 1 | a0001c0001t0040 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2617G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2617 | chr16 | 69303541 | |||||
| chr16:69303671
|
G | A | 23 | a0001c0001t0006a0001c0001t0013a0001c0001t0016others(20): Show | 71 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2747G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2747 | chr16 | 69303671 | |||||
| chr16:69303726
|
G | A | 1 | a0001c0002t0036 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2802G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2802 | chr16 | 69303726 | |||||
| chr16:69303803
|
T | A | 4 | a0001c0002t0014a0001c0002t0021a0001c0002t0032others(1): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2879T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 2879 | chr16 | 69303803 | |||||
| chr16:69304187
|
G | T | 1 | a0003c0005t0033 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3263G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 3263 | chr16 | 69304187 | |||||
| chr16:69304305
|
TAGATAAG | T | 1 | a0001c0001t0022 | 2 | NA19064.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3384_*3390delATAA others(3): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 3384 | INFO_REALIGN_3_PRIME | chr16 | 69304305 | ||||
| chr16:69304312
|
G | T | 1 | a0001c0001t0035 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3388G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 3388 | chr16 | 69304312 | |||||
| chr16:69304850
|
C | CT | 2 | a0001c0001t0034a0001c0002t0009 | 7 | HG00738.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3938dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 3939 | INFO_REALIGN_3_PRIME | chr16 | 69304850 | ||||
| chr16:69304991
|
A | G | 4 | a0001c0002t0008a0001c0002t0009a0001c0002t0032others(1): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4067A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 4067 | chr16 | 69304991 | |||||
| chr16:69304992
|
A | T | 25 | a0001c0001t0006a0001c0001t0013a0001c0001t0016others(22): Show | 73 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4068A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 4068 | chr16 | 69304992 | |||||
| chr16:69305039
|
G | A | 1 | a0001c0001t0041 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4115G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 4115 | chr16 | 69305039 | |||||
| chr16:69305066
|
C | T | 1 | a0001c0002t0020 | 2 | HG00099.hp1 HG00738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4142C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 4142 | chr16 | 69305066 | |||||
| chr16:69305067
|
G | A | 3 | a0001c0002t0014a0001c0002t0021a0003c0005t0033 | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4143G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 4143 | chr16 | 69305067 | |||||
| chr16:69305237
|
A | G | 1 | a0001c0001t0044 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4313A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 4313 | chr16 | 69305237 | |||||
| chr16:69305645
|
G | C | 1 | a0001c0002t0026 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4721G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 4721 | chr16 | 69305645 | |||||
| chr16:69306247
|
G | GT | 4 | a0001c0001t0011a0001c0002t0021a0001c0002t0029others(1): Show | 8 | HG01192.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5332dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 5333 | INFO_REALIGN_3_PRIME | chr16 | 69306247 | ||||
| chr16:69306260
|
T | C | 2 | a0001c0002t0014a0003c0005t0033 | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5336T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 5336 | chr16 | 69306260 | |||||
| chr16:69306589
|
A | G | 2 | a0001c0002t0028a0001c0002t0029 | 2 | HG01109.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5665A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 5665 | chr16 | 69306589 | |||||
| chr16:69306618
|
G | A | 1 | a0001c0002t0015 | 3 | HG02572.hp2 HG03486.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5694G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 5694 | chr16 | 69306618 | |||||
| chr16:69307424
|
A | T | 1 | a0001c0002t0014 | 3 | HG01433.hp2 HG02922.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6500A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 6500 | chr16 | 69307424 | |||||
| chr16:69307521
|
CT | C | 12 | a0001c0001t0031a0001c0002t0004a0001c0002t0017others(9): Show | 32 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*6600delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 6600 | INFO_REALIGN_3_PRIME | chr16 | 69307521 | ||||
| chr16:69307749
|
A | G | 1 | a0001c0001t0043 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6825A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 6825 | chr16 | 69307749 | |||||
| chr16:69307878
|
A | G | 47 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(44): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*6954A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 6954 | chr16 | 69307878 | |||||
| chr16:69307942
|
A | G | 1 | a0001c0001t0041 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7018A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7018 | chr16 | 69307942 | |||||
| chr16:69308197
|
C | T | 1 | a0001c0002t0019 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7273C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7273 | chr16 | 69308197 | |||||
| chr16:69308365
|
G | T | 2 | a0001c0002t0018a0001c0002t0030 | 3 | HG01169.hp1 HG01496.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7441G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7441 | chr16 | 69308365 | |||||
| chr16:69308417
|
T | C | 2 | a0001c0001t0031a0001c0002t0027 | 2 | NA19030.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7493T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7493 | chr16 | 69308417 | |||||
| chr16:69308419
|
G | A | 3 | a0001c0002t0014a0001c0002t0021a0003c0005t0033 | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7495G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7495 | chr16 | 69308419 | |||||
| chr16:69308454
|
C | T | 1 | a0001c0002t0023 | 2 | HG02717.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7530C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7530 | chr16 | 69308454 | |||||
| chr16:69308611
|
G | A | 1 | a0001c0001t0042 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7687G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7687 | chr16 | 69308611 | |||||
| chr16:69308716
|
A | G | 2 | a0001c0001t0031a0001c0002t0027 | 2 | NA19030.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7792A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7792 | chr16 | 69308716 | |||||
| chr16:69308923
|
C | T | 1 | a0001c0001t0045 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7999C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 7/7 | 7999 | chr16 | 69308923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69187741
|
T | TGGAGGGT others(15): Show |
1 | a0002c0004t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.580+4_580+25dupAGC others(19): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69187741 | |||||
| chr16:69187786
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.580+40G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69187786 | ||||||
| chr16:69187998
|
C | T | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG02129.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.580+252C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69187998 | ||||||
| chr16:69188141
|
TA | T | 9 | a0001c0001t0002g0213a0001c0001t0005g0208a0001c0001t0005g0210others(6): Show | 9 | HG01346.hp2 HG01361.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.580+409delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69188141 | |||||
| chr16:69188157
|
T | G | 8 | a0001c0001t0002g0213a0001c0001t0005g0208a0001c0001t0005g0210others(5): Show | 8 | HG01346.hp2 HG01361.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.580+411T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69188157 | ||||||
| chr16:69188223
|
T | C | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.580+477T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69188223 | ||||||
| chr16:69188239
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.580+493C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69188239 | ||||||
| chr16:69188318
|
A | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+572A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69188318 | ||||||
| chr16:69188953
|
G | A | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.580+1207G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69188953 | ||||||
| chr16:69189074
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+1328G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69189074 | ||||||
| chr16:69189597
|
C | T | 2 | a0001c0003t0005g0214a0001c0003t0005g0215 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.580+1851C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69189597 | ||||||
| chr16:69189646
|
G | A | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.580+1900G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69189646 | ||||||
| chr16:69189762
|
C | A | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.580+2016C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69189762 | ||||||
| chr16:69189827
|
C | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+2081C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69189827 | ||||||
| chr16:69189890
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.580+2144C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69189890 | ||||||
| chr16:69190317
|
A | G | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+2571A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190317 | ||||||
| chr16:69190339
|
G | C | 12 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(9): Show | 12 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580+2593G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190339 | ||||||
| chr16:69190363
|
G | A | 5 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+2617G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190363 | ||||||
| chr16:69190712
|
C | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0162others(142): Show | 145 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.580+2966C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190712 | ||||||
| chr16:69190727
|
G | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+2981G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190727 | ||||||
| chr16:69190735
|
T | C | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.580+2989T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190735 | ||||||
| chr16:69190973
|
G | A | 3 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072 | 3 | HG01433.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.580+3227G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190973 | ||||||
| chr16:69190993
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0162others(142): Show | 145 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.580+3247C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69190993 | ||||||
| chr16:69191221
|
T | TA | 6 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+3488dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191221 | |||||
| chr16:69191221
|
TA | T | 9 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(6): Show | 9 | HG00609.hp1 HG02896.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.580+3488delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191221 | |||||
| chr16:69191275
|
G | A | 4 | a0001c0001t0006g0049a0001c0001t0016g0048a0001c0001t0016g0050others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+3529G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69191275 | ||||||
| chr16:69191391
|
CA | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.580+3656delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191391 | |||||
| chr16:69191403
|
T | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+3657T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69191403 | ||||||
| chr16:69191412
|
C | CAATTAGC others(5118): Show |
1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5127): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5124): Show |
3 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066 | 3 | HG02572.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5133): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5124): Show |
2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5133): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5133): Show |
1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5142): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0002t0009g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5133): Show |
5 | a0001c0002t0009g0003a0001c0002t0009g0006a0001c0002t0009g0007others(2): Show | 5 | HG00738.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5142): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0006g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
10 | a0001c0001t0006g0049a0001c0001t0006g0054a0001c0001t0006g0057others(7): Show | 10 | HG02451.hp2 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0013g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0002t0024g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
3 | a0001c0002t0018g0034a0001c0002t0018g0036a0001c0002t0030g0035 | 3 | HG01169.hp1 HG01496.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
3 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0037 | 3 | HG00735.hp1 NA18968.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
11 | a0001c0002t0004g0030a0001c0002t0004g0031a0001c0002t0004g0032others(8): Show | 11 | HG00280.hp2 HG00621.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0002t0004g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0002t0004g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5137): Show |
1 | a0001c0001t0006g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5146): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0016g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5145): Show |
4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5154): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5145): Show |
1 | a0001c0002t0032g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5154): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5145): Show |
1 | a0001c0002t0008g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5154): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5145): Show |
4 | a0001c0002t0008g0016a0001c0002t0008g0017a0001c0002t0008g0018others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5154): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5146): Show |
2 | a0001c0002t0008g0020a0001c0002t0008g0021 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5155): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5133): Show |
1 | a0001c0001t0002g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5142): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
4 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5136): Show |
1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5145): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
7 | a0001c0001t0002g0213a0001c0001t0005g0210a0001c0001t0005g0211others(4): Show | 7 | HG01346.hp2 HG01361.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0007g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
8 | a0001c0001t0007g0153a0001c0001t0007g0154a0001c0001t0007g0155others(5): Show | 8 | HG00544.hp2 HG01891.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0044g0159 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0045g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0034g0161 | 3 | HG01175.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
21 | a0001c0001t0001g0002a0001c0001t0001g0164a0001c0001t0001g0165others(18): Show | 21 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0001g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0002g0181 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
13 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(10): Show | 13 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0035g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
2 | a0001c0001t0022g0195a0001c0001t0022g0196 | 2 | NA19064.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5136): Show |
1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5145): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5136): Show |
2 | a0001c0001t0003g0079a0001c0001t0041g0080 | 2 | HG00621.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5145): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0003g0081 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
1 | a0001c0001t0003g0082 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0002g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5136): Show |
3 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0086 | 3 | HG00735.hp2 NA18747.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5145): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
22 | a0001c0001t0001g0001a0001c0001t0001g0096a0001c0001t0001g0103others(19): Show | 22 | HG00544.hp1 HG01169.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5136): Show |
1 | a0001c0001t0040g0105 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5145): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
32 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0129others(29): Show | 32 | HG00280.hp1 HG00408.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
2 | a0001c0001t0002g0136a0001c0001t0002g0137 | 2 | NA18612.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5133): Show |
1 | a0001c0001t0001g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5142): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5135): Show |
4 | a0001c0001t0002g0139a0001c0001t0010g0140a0001c0001t0010g0141others(1): Show | 4 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5144): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5134): Show |
1 | a0001c0001t0016g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5143): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5464): Show |
1 | a0001c0002t0012g0202 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5473): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5464): Show |
1 | a0001c0002t0012g0203 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5473): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5452): Show |
1 | a0001c0002t0037g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5461): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5451): Show |
1 | a0001c0002t0012g0205 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5460): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5451): Show |
1 | a0001c0002t0012g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5460): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5138): Show |
1 | a0001c0002t0014g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5147): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5137): Show |
2 | a0001c0002t0014g0071a0003c0005t0033g0073 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.580+3680_580+3681i others(5146): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5138): Show |
1 | a0001c0002t0014g0072 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5147): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5130): Show |
1 | a0001c0002t0021g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5139): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191412
|
C | CAATTAGC others(5137): Show |
1 | a0001c0002t0021g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.580+3680_580+3681i others(5146): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191412 | |||||
| chr16:69191494
|
C | T | 1 | a0001c0002t0024g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580+3748C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69191494 | ||||||
| chr16:69191557
|
C | CA | 12 | a0001c0001t0001g0001a0001c0001t0002g0107a0001c0001t0003g0087others(9): Show | 12 | HG01081.hp2 HG01346.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.580+3832dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191557 | |||||
| chr16:69191557
|
CA | C | 20 | a0001c0001t0001g0135a0001c0001t0001g0199a0001c0001t0001g0201others(17): Show | 20 | HG00280.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.580+3832delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69191557 | |||||
| chr16:69191800
|
C | A | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.580+4054C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69191800 | ||||||
| chr16:69191890
|
C | T | 22 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(19): Show | 22 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.580+4144C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69191890 | ||||||
| chr16:69192036
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.580+4290G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192036 | ||||||
| chr16:69192055
|
A | G | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0002c0004t0001g0192 | 3 | HG00597.hp1 NA19060.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.580+4309A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192055 | ||||||
| chr16:69192264
|
A | T | 4 | a0001c0001t0007g0158a0001c0001t0007g0197a0001c0001t0044g0159others(1): Show | 4 | HG02602.hp2 HG03654.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+4518A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192264 | ||||||
| chr16:69192537
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+4791G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192537 | ||||||
| chr16:69192677
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.580+4931A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192677 | ||||||
| chr16:69192805
|
T | A | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+5059T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192805 | ||||||
| chr16:69192851
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+5105T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192851 | ||||||
| chr16:69192889
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.580+5143A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69192889 | ||||||
| chr16:69193004
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.580+5258A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193004 | ||||||
| chr16:69193064
|
T | C | 6 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(3): Show | 6 | HG00621.hp1 HG02004.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+5318T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193064 | ||||||
| chr16:69193079
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.580+5333A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193079 | ||||||
| chr16:69193256
|
C | T | 1 | a0001c0002t0037g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.580+5510C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193256 | ||||||
| chr16:69193274
|
T | G | 1 | a0001c0001t0003g0084 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.580+5528T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193274 | ||||||
| chr16:69193318
|
C | CT | 49 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0001t0001g0178others(46): Show | 49 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.580+5600dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69193318 | |||||
| chr16:69193318
|
C | CTT | 16 | a0001c0001t0006g0052a0001c0001t0006g0057a0001c0001t0006g0058others(13): Show | 16 | HG00621.hp1 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+5599_580+5600d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69193318 | |||||
| chr16:69193318
|
C | CTTT | 9 | a0001c0002t0004g0045a0001c0002t0004g0046a0001c0002t0017g0043others(6): Show | 9 | HG00280.hp2 HG01169.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.580+5598_580+5600d others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69193318 | |||||
| chr16:69193318
|
CT | C | 23 | a0001c0001t0001g0164a0001c0001t0001g0182a0001c0001t0002g0109others(20): Show | 23 | HG01243.hp2 HG01258.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.580+5600delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69193318 | |||||
| chr16:69193326
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.580+5580T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193326 | ||||||
| chr16:69193359
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+5613T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193359 | ||||||
| chr16:69193452
|
C | G | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.580+5706C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193452 | ||||||
| chr16:69193483
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+5737C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193483 | ||||||
| chr16:69193484
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+5738G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193484 | ||||||
| chr16:69193535
|
G | T | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+5789G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193535 | ||||||
| chr16:69193713
|
T | C | 92 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.580+5967T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193713 | ||||||
| chr16:69193876
|
G | C | 92 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.580+6130G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193876 | ||||||
| chr16:69193916
|
G | A | 10 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(7): Show | 10 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.580+6170G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69193916 | ||||||
| chr16:69194949
|
A | G | 26 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(23): Show | 26 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.580+7203A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69194949 | ||||||
| chr16:69194986
|
T | A | 14 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.580+7240T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69194986 | ||||||
| chr16:69195049
|
A | G | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+7303A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195049 | ||||||
| chr16:69195095
|
G | A | 4 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+7349G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195095 | ||||||
| chr16:69195156
|
A | G | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+7410A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195156 | ||||||
| chr16:69195230
|
G | A | 91 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.580+7484G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195230 | ||||||
| chr16:69195323
|
T | C | 1 | a0001c0001t0006g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580+7577T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195323 | ||||||
| chr16:69195443
|
A | AT | 13 | a0001c0001t0001g0002a0001c0002t0004g0045a0001c0002t0004g0046others(10): Show | 13 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.580+7712dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69195443 | |||||
| chr16:69195625
|
C | T | 1 | a0001c0001t0006g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.580+7879C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195625 | ||||||
| chr16:69195807
|
A | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+8061A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195807 | ||||||
| chr16:69195834
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+8088G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195834 | ||||||
| chr16:69195983
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.580+8237G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69195983 | ||||||
| chr16:69196058
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0179a0001c0001t0046g0176 | 3 | HG02486.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.580+8312C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196058 | ||||||
| chr16:69196163
|
C | T | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.580+8417C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196163 | ||||||
| chr16:69196219
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.580+8473A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196219 | ||||||
| chr16:69196319
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.580+8573G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196319 | ||||||
| chr16:69196360
|
TTTTTC | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0198a0001c0001t0034g0161 | 3 | HG02145.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.580+8624_580+8628d others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69196360 | |||||
| chr16:69196376
|
C | CT | 7 | a0001c0002t0004g0029a0001c0002t0004g0033a0001c0002t0014g0070others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+8646dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69196376 | |||||
| chr16:69196484
|
C | T | 2 | a0001c0001t0003g0102a0001c0001t0043g0088 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.580+8738C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196484 | ||||||
| chr16:69196569
|
T | G | 1 | a0001c0001t0040g0105 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.580+8823T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196569 | ||||||
| chr16:69196594
|
C | T | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.580+8848C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196594 | ||||||
| chr16:69196708
|
G | A | 2 | a0001c0001t0007g0153a0001c0001t0007g0154 | 2 | HG00544.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.580+8962G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196708 | ||||||
| chr16:69196888
|
G | A | 1 | a0001c0002t0004g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.580+9142G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196888 | ||||||
| chr16:69196897
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.580+9151A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196897 | ||||||
| chr16:69196899
|
G | C | 1 | a0001c0002t0004g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.580+9153G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196899 | ||||||
| chr16:69196900
|
T | A | 1 | a0001c0002t0004g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.580+9154T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69196900 | ||||||
| chr16:69197018
|
A | AT | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+9283dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69197018 | |||||
| chr16:69197347
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0010g0106 | 2 | HG01081.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.580+9601G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69197347 | ||||||
| chr16:69197349
|
A | G | 26 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(23): Show | 26 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.580+9603A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69197349 | ||||||
| chr16:69197490
|
T | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+9744T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69197490 | ||||||
| chr16:69197515
|
A | T | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.580+9769A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69197515 | ||||||
| chr16:69197866
|
G | T | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.580+10120G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69197866 | ||||||
| chr16:69197997
|
T | TA | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.580+10256dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69197997 | |||||
| chr16:69198098
|
A | AT | 10 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0002g0098others(7): Show | 10 | HG00408.hp2 HG00544.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.580+10372dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69198098 | |||||
| chr16:69198098
|
AT | A | 35 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(32): Show | 35 | HG01346.hp2 HG02004.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.580+10372delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69198098 | |||||
| chr16:69198098
|
ATT | A | 46 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(43): Show | 46 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.580+10371_580+1037 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69198098 | |||||
| chr16:69198117
|
T | G | 5 | a0001c0001t0003g0102a0001c0001t0043g0088a0001c0002t0023g0067others(2): Show | 5 | HG02717.hp2 HG03017.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+10371T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69198117 | ||||||
| chr16:69198118
|
T | G | 22 | a0001c0001t0001g0165a0001c0001t0002g0107a0001c0001t0002g0213others(19): Show | 22 | HG00280.hp2 HG01081.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.580+10372T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69198118 | ||||||
| chr16:69198189
|
A | G | 1 | a0001c0002t0009g0009 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.580+10443A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69198189 | ||||||
| chr16:69198792
|
C | T | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+11046C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69198792 | ||||||
| chr16:69198895
|
TG | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0003g0101 | 3 | HG02735.hp2 HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.580+11150delG | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69198895 | ||||||
| chr16:69198896
|
G | GT | 42 | a0001c0001t0001g0163a0001c0001t0001g0174a0001c0001t0002g0121others(39): Show | 42 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.580+11169dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69198896 | |||||
| chr16:69198896
|
GT | G | 8 | a0001c0001t0001g0166a0001c0001t0001g0183a0001c0001t0003g0102others(5): Show | 8 | HG01243.hp2 HG01256.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.580+11169delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69198896 | |||||
| chr16:69198897
|
T | G | 5 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(2): Show | 5 | HG02809.hp1 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+11151T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69198897 | ||||||
| chr16:69198985
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.580+11239C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69198985 | ||||||
| chr16:69199041
|
C | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+11295C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199041 | ||||||
| chr16:69199095
|
G | A | 92 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.580+11349G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199095 | ||||||
| chr16:69199156
|
A | G | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+11410A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199156 | ||||||
| chr16:69199174
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.580+11428C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199174 | ||||||
| chr16:69199280
|
A | G | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+11534A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199280 | ||||||
| chr16:69199386
|
C | T | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.580+11640C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199386 | ||||||
| chr16:69199514
|
G | A | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+11768G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199514 | ||||||
| chr16:69199595
|
C | CA | 16 | a0001c0001t0001g0103a0001c0001t0002g0121a0001c0001t0002g0213others(13): Show | 16 | HG01346.hp2 HG01361.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.580+11865dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAA | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+11863_580+1186 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(1): Show |
5 | a0001c0002t0009g0003a0001c0002t0009g0006a0001c0002t0009g0007others(2): Show | 5 | HG00738.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+11858_580+1186 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(4): Show |
3 | a0001c0002t0014g0070a0001c0002t0014g0071a0003c0005t0033g0073 | 3 | HG02809.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.580+11855_580+1186 others(15): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(5): Show |
1 | a0001c0002t0014g0072 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.580+11854_580+1186 others(16): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0004g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.580+11853_580+1186 others(17): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0039g0053a0001c0002t0004g0045a0001c0002t0018g0036others(1): Show | 4 | HG01496.hp2 HG02735.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(22): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0006g0061a0001c0002t0004g0046a0001c0002t0017g0043others(1): Show | 4 | HG02818.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(23): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(13): Show |
15 | a0001c0001t0006g0052a0001c0001t0006g0054a0001c0001t0006g0059others(12): Show | 15 | HG01169.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(24): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(14): Show |
5 | a0001c0001t0006g0049a0001c0001t0006g0057a0001c0001t0006g0058others(2): Show | 5 | HG02451.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(25): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(16): Show |
2 | a0001c0002t0026g0004a0001c0002t0036g0019 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.580+11865_580+1186 others(27): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(17): Show |
3 | a0001c0002t0012g0202a0001c0002t0027g0047a0001c0002t0037g0204 | 3 | HG03710.hp2 NA18964.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.580+11865_580+1186 others(28): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(18): Show |
6 | a0001c0002t0004g0029a0001c0002t0004g0031a0001c0002t0004g0032others(3): Show | 6 | HG00621.hp1 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(29): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(19): Show |
6 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025others(3): Show | 6 | HG00280.hp2 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(30): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(20): Show |
4 | a0001c0002t0004g0022a0001c0002t0004g0033a0001c0002t0004g0040others(1): Show | 4 | HG02602.hp1 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(31): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(21): Show |
4 | a0001c0002t0004g0037a0001c0002t0012g0205a0001c0002t0023g0068others(1): Show | 4 | HG00735.hp1 HG01517.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+11865_580+1186 others(32): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(22): Show |
1 | a0001c0002t0004g0030 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.580+11865_580+1186 others(33): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(27): Show |
1 | a0001c0002t0023g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.580+11865_580+1186 others(38): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(30): Show |
1 | a0001c0002t0004g0039 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.580+11865_580+1186 others(41): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(36): Show |
1 | a0001c0002t0004g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.580+11865_580+1186 others(47): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199595
|
C | CAAAAAAA others(43): Show |
1 | a0001c0002t0024g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580+11865_580+1186 others(54): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69199595 | |||||
| chr16:69199633
|
G | A | 92 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.580+11887G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199633 | ||||||
| chr16:69199772
|
A | G | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+12026A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199772 | ||||||
| chr16:69199961
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.580+12215C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199961 | ||||||
| chr16:69199977
|
C | T | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+12231C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69199977 | ||||||
| chr16:69200210
|
T | A | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.580+12464T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200210 | ||||||
| chr16:69200285
|
A | G | 1 | a0001c0001t0007g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.580+12539A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200285 | ||||||
| chr16:69200362
|
C | G | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+12616C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200362 | ||||||
| chr16:69200379
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0002g0108others(2): Show | 5 | HG01496.hp1 HG01981.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+12633C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200379 | ||||||
| chr16:69200420
|
A | T | 11 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(8): Show | 11 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.580+12674A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200420 | ||||||
| chr16:69200510
|
A | G | 1 | a0001c0001t0002g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.580+12764A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200510 | ||||||
| chr16:69200541
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+12795G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200541 | ||||||
| chr16:69200558
|
G | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+12812G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200558 | ||||||
| chr16:69200573
|
A | C | 6 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+12827A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200573 | ||||||
| chr16:69200715
|
A | G | 1 | a0001c0001t0013g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.580+12969A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200715 | ||||||
| chr16:69200791
|
A | T | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.580+13045A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200791 | ||||||
| chr16:69200817
|
G | A | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580+13071G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69200817 | ||||||
| chr16:69201014
|
A | G | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+13268A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201014 | ||||||
| chr16:69201056
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580+13310C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201056 | ||||||
| chr16:69201419
|
GAA | G | 2 | a0001c0001t0007g0153a0001c0001t0007g0154 | 2 | HG00544.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.580+13674_580+1367 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201419 | ||||||
| chr16:69201460
|
C | T | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.580+13714C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201460 | ||||||
| chr16:69201495
|
G | A | 1 | a0001c0001t0007g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.580+13749G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201495 | ||||||
| chr16:69201696
|
A | C | 5 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+13950A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201696 | ||||||
| chr16:69201799
|
A | G | 3 | a0001c0001t0013g0055a0001c0001t0013g0056a0001c0001t0013g0062 | 3 | HG02486.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.580+14053A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201799 | ||||||
| chr16:69201828
|
AT | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+14090delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69201828 | |||||
| chr16:69201893
|
A | G | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+14147A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201893 | ||||||
| chr16:69201979
|
T | C | 2 | a0001c0002t0014g0070a0001c0002t0014g0071 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.580+14233T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69201979 | ||||||
| chr16:69202187
|
C | T | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.580+14441C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69202187 | ||||||
| chr16:69202277
|
CCTCACAT others(128): Show |
C | 3 | a0001c0001t0013g0055a0001c0001t0013g0056a0001c0001t0013g0062 | 3 | HG02486.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.580+14532_580+1466 others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69202277 | ||||||
| chr16:69202358
|
C | T | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+14612C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69202358 | ||||||
| chr16:69202402
|
A | AT | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+14667dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69202402 | |||||
| chr16:69202402
|
AT | A | 21 | a0001c0002t0004g0023a0001c0002t0004g0028a0001c0002t0004g0029others(18): Show | 21 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.580+14667delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69202402 | |||||
| chr16:69202601
|
C | T | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.580+14855C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69202601 | ||||||
| chr16:69203138
|
C | T | 2 | a0001c0001t0002g0119a0001c0001t0002g0128 | 2 | HG02015.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.580+15392C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203138 | ||||||
| chr16:69203178
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+15432T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203178 | ||||||
| chr16:69203237
|
C | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.580+15491C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203237 | ||||||
| chr16:69203298
|
G | C | 1 | a0001c0002t0021g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580+15552G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203298 | ||||||
| chr16:69203323
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0167 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.580+15577G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203323 | ||||||
| chr16:69203446
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0164others(3): Show | 6 | HG01109.hp1 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+15700C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203446 | ||||||
| chr16:69203540
|
C | G | 2 | a0001c0001t0002g0107a0001c0001t0010g0106 | 2 | HG01081.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.580+15794C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203540 | ||||||
| chr16:69203621
|
G | A | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.580+15875G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203621 | ||||||
| chr16:69203733
|
G | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+15987G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203733 | ||||||
| chr16:69203870
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.580+16124C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203870 | ||||||
| chr16:69203934
|
C | A | 1 | a0001c0001t0002g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.580+16188C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203934 | ||||||
| chr16:69203946
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+16200G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203946 | ||||||
| chr16:69203968
|
C | T | 1 | a0001c0001t0005g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.580+16222C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69203968 | ||||||
| chr16:69204147
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+16401T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204147 | ||||||
| chr16:69204155
|
A | AG | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.580+16409_580+1641 others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204155 | ||||||
| chr16:69204172
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+16426G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204172 | ||||||
| chr16:69204261
|
C | T | 21 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(18): Show | 21 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.580+16515C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204261 | ||||||
| chr16:69204313
|
A | G | 4 | a0001c0001t0002g0213a0001c0001t0005g0210a0001c0001t0005g0211others(1): Show | 4 | NA18957.hp2 NA18960.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+16567A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204313 | ||||||
| chr16:69204405
|
T | C | 4 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0019g0041others(1): Show | 4 | HG00280.hp2 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+16659T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204405 | ||||||
| chr16:69204413
|
T | A | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+16667T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204413 | ||||||
| chr16:69204465
|
G | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+16719G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204465 | ||||||
| chr16:69204672
|
T | G | 4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+16926T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204672 | ||||||
| chr16:69204697
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+16951T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204697 | ||||||
| chr16:69204717
|
G | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.580+16971G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204717 | ||||||
| chr16:69204857
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.580+17111A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69204857 | ||||||
| chr16:69205036
|
A | C | 1 | a0001c0002t0012g0202 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.580+17290A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69205036 | ||||||
| chr16:69205054
|
A | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18968.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.580+17308A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69205054 | ||||||
| chr16:69205112
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+17366C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69205112 | ||||||
| chr16:69205139
|
A | T | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+17393A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69205139 | ||||||
| chr16:69205158
|
C | CT | 18 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0005g0146others(15): Show | 18 | HG01346.hp1 HG01361.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.580+17427dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69205158 | |||||
| chr16:69205316
|
A | AT | 18 | a0001c0001t0001g0163a0001c0001t0001g0180a0001c0001t0007g0151others(15): Show | 18 | HG00738.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.580+17593dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69205316 | |||||
| chr16:69205316
|
AT | A | 39 | a0001c0001t0001g0138a0001c0001t0001g0160a0001c0001t0001g0164others(36): Show | 39 | HG00280.hp2 HG00621.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.580+17593delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69205316 | |||||
| chr16:69205316
|
ATT | A | 12 | a0001c0001t0025g0152a0001c0002t0004g0037a0001c0002t0004g0040others(9): Show | 12 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.580+17592_580+1759 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69205316 | |||||
| chr16:69205316
|
ATTT | A | 5 | a0001c0001t0006g0049a0001c0002t0008g0020a0001c0002t0008g0021others(2): Show | 5 | HG01109.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+17591_580+1759 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69205316 | |||||
| chr16:69205548
|
G | A | 1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.580+17802G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69205548 | ||||||
| chr16:69205730
|
G | T | 2 | a0001c0002t0012g0202a0001c0002t0012g0203 | 2 | HG01346.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.580+17984G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69205730 | ||||||
| chr16:69206024
|
C | T | 11 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(8): Show | 11 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.580+18278C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206024 | ||||||
| chr16:69206025
|
TTGCTCTG others(9): Show |
T | 1 | a0001c0001t0001g0187 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.580+18280_580+1829 others(20): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206025 | ||||||
| chr16:69206108
|
C | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+18362C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206108 | ||||||
| chr16:69206123
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.580+18377A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206123 | ||||||
| chr16:69206359
|
T | C | 1 | a0001c0002t0004g0030 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.580+18613T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206359 | ||||||
| chr16:69206404
|
A | G | 1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.580+18658A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206404 | ||||||
| chr16:69206440
|
G | T | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.580+18694G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206440 | ||||||
| chr16:69206595
|
G | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+18849G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206595 | ||||||
| chr16:69206606
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(51): Show | 54 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.580+18860G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206606 | ||||||
| chr16:69206632
|
T | G | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.580+18886T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206632 | ||||||
| chr16:69206655
|
C | T | 1 | a0001c0002t0014g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.580+18909C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206655 | ||||||
| chr16:69206691
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.580+18945C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206691 | ||||||
| chr16:69206826
|
C | T | 3 | a0001c0001t0002g0098a0001c0001t0002g0110a0001c0001t0002g0120 | 3 | HG00544.hp1 NA18973.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.580+19080C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69206826 | ||||||
| chr16:69207011
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+19265C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207011 | ||||||
| chr16:69207052
|
C | G | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.580+19306C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207052 | ||||||
| chr16:69207142
|
T | TTTTC | 57 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(54): Show | 57 | HG00544.hp2 HG01346.hp1 HG01346.hp2 others(54): Show |
intron_variant | MODIFIER | c.580+19408_580+1941 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69207142 | |||||
| chr16:69207154
|
C | CTTTCT | 28 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(25): Show | 28 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.580+19411_580+1941 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69207154 | |||||
| chr16:69207154
|
C | CTTTCTT | 15 | a0001c0002t0004g0029a0001c0002t0004g0030a0001c0002t0004g0031others(12): Show | 15 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.580+19411_580+1941 others(10): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69207154 | |||||
| chr16:69207194
|
G | A | 1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.580+19448G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207194 | ||||||
| chr16:69207216
|
G | A | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.580+19470G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207216 | ||||||
| chr16:69207235
|
A | AC | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.580+19490dupC | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69207235 | |||||
| chr16:69207270
|
C | T | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.580+19524C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207270 | ||||||
| chr16:69207365
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.580+19619C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207365 | ||||||
| chr16:69207531
|
GAA | G | 4 | a0001c0001t0002g0213a0001c0001t0005g0210a0001c0001t0005g0211others(1): Show | 4 | NA18957.hp2 NA18960.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+19788_580+1978 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69207531 | |||||
| chr16:69207695
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+19949G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207695 | ||||||
| chr16:69207829
|
CA | C | 14 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.580+20084delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207829 | ||||||
| chr16:69207911
|
C | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+20165C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207911 | ||||||
| chr16:69207954
|
C | CAAAAATT others(310): Show |
5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+20223_580+2022 others(321): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69207954 | |||||
| chr16:69207984
|
T | C | 92 | a0001c0001t0002g0213a0001c0001t0005g0146a0001c0001t0005g0147others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.580+20238T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69207984 | ||||||
| chr16:69208108
|
C | CA | 38 | a0001c0001t0001g0162a0001c0001t0001g0187a0001c0001t0002g0121others(35): Show | 38 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.580+20379dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208108 | |||||
| chr16:69208108
|
CA | C | 13 | a0001c0001t0002g0145a0001c0001t0007g0151a0001c0001t0007g0153others(10): Show | 13 | HG00544.hp2 HG01496.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.580+20379delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208108 | |||||
| chr16:69208354
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+20608C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69208354 | ||||||
| chr16:69208533
|
T | C | 1 | a0001c0001t0003g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.580+20787T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69208533 | ||||||
| chr16:69208839
|
CA | C | 79 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(76): Show | 79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.580+21106delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208839 | |||||
| chr16:69208971
|
A | AGT | 10 | a0001c0001t0003g0079a0001c0001t0003g0081a0001c0001t0003g0082others(7): Show | 10 | HG00609.hp2 HG01243.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.580+21244_580+2124 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208971 | |||||
| chr16:69208971
|
A | AGTGTGTG others(27): Show |
1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.580+21245_580+2124 others(38): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208971 | |||||
| chr16:69208971
|
A | AGTGTGTG others(29): Show |
2 | a0001c0002t0014g0071a0001c0002t0014g0072 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.580+21245_580+2124 others(40): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208971 | |||||
| chr16:69208990
|
G | GTGTGTGT others(19): Show |
1 | a0001c0002t0021g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.580+21245_580+2124 others(30): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208990 | |||||
| chr16:69208990
|
G | GTGTGTGT others(17): Show |
1 | a0001c0002t0021g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580+21245_580+2124 others(28): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69208990 | |||||
| chr16:69208991
|
T | TGTGTGTG others(30): Show |
1 | a0001c0002t0014g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.580+21245_580+2124 others(41): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69208991 | ||||||
| chr16:69209132
|
C | T | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+21386C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209132 | ||||||
| chr16:69209213
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+21467C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209213 | ||||||
| chr16:69209218
|
G | A | 1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.580+21472G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209218 | ||||||
| chr16:69209390
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+21644G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209390 | ||||||
| chr16:69209797
|
G | C | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+22051G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209797 | ||||||
| chr16:69209838
|
G | A | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.580+22092G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209838 | ||||||
| chr16:69209868
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0164others(3): Show | 6 | HG01109.hp1 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+22122A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209868 | ||||||
| chr16:69209961
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+22215T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69209961 | ||||||
| chr16:69210019
|
A | AT | 10 | a0001c0001t0002g0124a0001c0002t0004g0028a0001c0002t0008g0015others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.580+22297dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69210019 | |||||
| chr16:69210019
|
A | T | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+22273A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210019 | ||||||
| chr16:69210019
|
AT | A | 20 | a0001c0001t0001g0138a0001c0001t0001g0188a0001c0001t0001g0198others(17): Show | 20 | HG01433.hp2 HG01884.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.580+22297delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69210019 | |||||
| chr16:69210019
|
ATT | A | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.580+22296_580+2229 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69210019 | |||||
| chr16:69210022
|
T | A | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+22276T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210022 | ||||||
| chr16:69210027
|
T | A | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+22281T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210027 | ||||||
| chr16:69210031
|
T | A | 6 | a0001c0001t0006g0049a0001c0001t0006g0054a0001c0001t0006g0063others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+22285T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210031 | ||||||
| chr16:69210048
|
G | T | 1 | a0001c0001t0002g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.580+22302G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210048 | ||||||
| chr16:69210231
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.580+22485G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210231 | ||||||
| chr16:69210354
|
C | T | 1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.580+22608C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210354 | ||||||
| chr16:69210861
|
C | T | 1 | a0001c0001t0002g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.580+23115C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210861 | ||||||
| chr16:69210986
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.580+23240G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69210986 | ||||||
| chr16:69211054
|
C | T | 1 | a0001c0001t0011g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.580+23308C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69211054 | ||||||
| chr16:69211167
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+23421T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69211167 | ||||||
| chr16:69211531
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.580+23785C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69211531 | ||||||
| chr16:69211536
|
G | GA | 31 | a0001c0001t0001g0163a0001c0001t0001g0167a0001c0001t0002g0111others(28): Show | 31 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.580+23807dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69211536 | |||||
| chr16:69211718
|
G | C | 2 | a0001c0002t0017g0043a0001c0002t0017g0044 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.580+23972G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69211718 | ||||||
| chr16:69211827
|
C | T | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.580+24081C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69211827 | ||||||
| chr16:69211854
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.580+24108C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69211854 | ||||||
| chr16:69212234
|
T | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+24488T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69212234 | ||||||
| chr16:69212284
|
C | T | 1 | a0001c0002t0032g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.580+24538C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69212284 | ||||||
| chr16:69212328
|
G | GTATT | 23 | a0001c0001t0002g0139a0001c0001t0010g0140a0001c0001t0010g0142others(20): Show | 23 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.580+24608_580+2461 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69212328 | |||||
| chr16:69212328
|
GTATTTAT others(1): Show |
G | 2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.580+24604_580+2461 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69212328 | |||||
| chr16:69212698
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+24952G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69212698 | ||||||
| chr16:69212711
|
C | T | 19 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0180others(16): Show | 19 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.580+24965C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69212711 | ||||||
| chr16:69212715
|
A | T | 1 | a0001c0001t0001g0001 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.580+24969A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69212715 | ||||||
| chr16:69212742
|
C | T | 5 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0018others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+24996C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69212742 | ||||||
| chr16:69212885
|
G | A | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.580+25139G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69212885 | ||||||
| chr16:69213101
|
A | G | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+25355A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213101 | ||||||
| chr16:69213419
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+25673C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213419 | ||||||
| chr16:69213506
|
AT | A | 106 | a0001c0001t0002g0113a0001c0001t0002g0145a0001c0001t0002g0213others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.580+25771delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69213506 | |||||
| chr16:69213626
|
A | G | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+25880A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213626 | ||||||
| chr16:69213645
|
G | A | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.580+25899G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213645 | ||||||
| chr16:69213663
|
C | G | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.580+25917C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213663 | ||||||
| chr16:69213712
|
C | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+25966C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213712 | ||||||
| chr16:69213811
|
A | G | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+26065A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213811 | ||||||
| chr16:69213822
|
C | CT | 54 | a0001c0001t0001g0198a0001c0001t0002g0109a0001c0001t0002g0124others(51): Show | 54 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.580+26098dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69213822 | |||||
| chr16:69213822
|
C | CTT | 17 | a0001c0001t0006g0063a0001c0001t0013g0056a0001c0001t0013g0062others(14): Show | 17 | HG00099.hp1 HG00738.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.580+26097_580+2609 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69213822 | |||||
| chr16:69213822
|
CTT | C | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+26097_580+2609 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69213822 | |||||
| chr16:69213984
|
G | T | 2 | a0001c0001t0003g0079a0001c0001t0003g0082 | 2 | HG00609.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.580+26238G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213984 | ||||||
| chr16:69213997
|
T | G | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.580+26251T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69213997 | ||||||
| chr16:69214127
|
A | AT | 17 | a0001c0001t0001g0138a0001c0001t0002g0108a0001c0001t0002g0113others(14): Show | 17 | HG01346.hp2 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.580+26395dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69214127 | |||||
| chr16:69214131
|
T | A | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+26385T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214131 | ||||||
| chr16:69214134
|
T | A | 7 | a0001c0002t0004g0032a0001c0002t0015g0064a0001c0002t0015g0065others(4): Show | 7 | HG00621.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+26388T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214134 | ||||||
| chr16:69214136
|
T | A | 2 | a0001c0001t0013g0055a0001c0001t0013g0056 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.580+26390T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214136 | ||||||
| chr16:69214142
|
A | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+26396A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214142 | ||||||
| chr16:69214161
|
C | T | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.580+26415C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214161 | ||||||
| chr16:69214288
|
G | T | 6 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(3): Show | 6 | HG00621.hp1 HG02004.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+26542G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214288 | ||||||
| chr16:69214290
|
C | T | 6 | a0001c0001t0006g0052a0001c0001t0006g0057a0001c0001t0006g0058others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+26544C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214290 | ||||||
| chr16:69214349
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+26603T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214349 | ||||||
| chr16:69214440
|
A | G | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+26694A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214440 | ||||||
| chr16:69214671
|
C | T | 7 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(4): Show | 7 | HG00621.hp1 HG02004.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.580+26925C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214671 | ||||||
| chr16:69214778
|
C | T | 1 | a0001c0002t0036g0019 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580+27032C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214778 | ||||||
| chr16:69214893
|
G | C | 1 | a0001c0002t0004g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.580+27147G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214893 | ||||||
| chr16:69214972
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.580+27226T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69214972 | ||||||
| chr16:69215074
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.580+27328C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69215074 | ||||||
| chr16:69215278
|
G | A | 2 | a0001c0002t0004g0037a0001c0002t0004g0040 | 2 | HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.580+27532G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69215278 | ||||||
| chr16:69215470
|
G | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+27724G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69215470 | ||||||
| chr16:69215968
|
A | G | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.580+28222A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69215968 | ||||||
| chr16:69216088
|
T | C | 4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+28342T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69216088 | ||||||
| chr16:69216091
|
A | G | 3 | a0001c0003t0005g0209a0001c0003t0005g0214a0001c0003t0005g0215 | 3 | HG01346.hp2 HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.580+28345A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69216091 | ||||||
| chr16:69216152
|
G | T | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.580+28406G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69216152 | ||||||
| chr16:69216339
|
ATCTTCAT others(29): Show |
A | 1 | a0001c0001t0001g0187 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.580+28595_580+2863 others(40): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69216339 | |||||
| chr16:69216499
|
G | A | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.580+28753G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69216499 | ||||||
| chr16:69216523
|
T | TA | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+28792dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69216523 | |||||
| chr16:69216694
|
A | C | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-28908A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69216694 | ||||||
| chr16:69216881
|
C | A | 1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.581-28721C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69216881 | ||||||
| chr16:69217028
|
T | C | 2 | a0001c0002t0004g0038a0001c0002t0004g0039 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.581-28574T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69217028 | ||||||
| chr16:69217037
|
T | A | 60 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.581-28565T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69217037 | ||||||
| chr16:69217038
|
A | T | 1 | a0001c0002t0037g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.581-28564A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69217038 | ||||||
| chr16:69217168
|
T | C | 1 | a0001c0001t0003g0084 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.581-28434T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69217168 | ||||||
| chr16:69217371
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.581-28231G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69217371 | ||||||
| chr16:69217421
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.581-28181T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69217421 | ||||||
| chr16:69218008
|
A | G | 4 | a0001c0001t0006g0049a0001c0001t0016g0048a0001c0001t0016g0050others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-27594A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218008 | ||||||
| chr16:69218123
|
C | G | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.581-27479C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218123 | ||||||
| chr16:69218289
|
A | G | 1 | a0001c0001t0002g0133 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.581-27313A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218289 | ||||||
| chr16:69218423
|
CT | C | 9 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0005g0112others(6): Show | 9 | HG01175.hp2 HG01346.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.581-27166delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69218423 | |||||
| chr16:69218567
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0002c0004t0001g0192 | 3 | HG00597.hp1 NA19060.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.581-27035G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218567 | ||||||
| chr16:69218606
|
A | G | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-26996A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218606 | ||||||
| chr16:69218611
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-26991C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218611 | ||||||
| chr16:69218684
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-26918G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218684 | ||||||
| chr16:69218716
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-26886T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218716 | ||||||
| chr16:69218746
|
C | G | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-26856C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69218746 | ||||||
| chr16:69219036
|
G | C | 6 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-26566G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69219036 | ||||||
| chr16:69219582
|
GA | G | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-26017delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219582 | |||||
| chr16:69219713
|
ATTTTATT others(3): Show |
A | 13 | a0001c0001t0006g0049a0001c0001t0006g0054a0001c0001t0006g0063others(10): Show | 13 | HG01433.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.581-25884_581-2587 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219713 | |||||
| chr16:69219713
|
ATTTTATT others(8): Show |
A | 6 | a0001c0001t0006g0052a0001c0001t0006g0057a0001c0001t0006g0058others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-25884_581-2587 others(19): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219713 | |||||
| chr16:69219718
|
A | ATTTTG | 39 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0002g0114others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.581-25839_581-2583 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219718 | |||||
| chr16:69219718
|
A | ATTTTGTT others(3): Show |
1 | a0001c0002t0004g0039 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.581-25844_581-2583 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219718 | |||||
| chr16:69219718
|
A | G | 3 | a0001c0002t0015g0065a0001c0002t0021g0074a0001c0002t0021g0075 | 3 | HG03041.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.581-25884A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69219718 | ||||||
| chr16:69219718
|
ATTTTG | A | 4 | a0001c0002t0009g0006a0001c0002t0018g0034a0001c0002t0018g0036others(1): Show | 4 | HG01169.hp1 HG01496.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-25839_581-2583 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219718 | |||||
| chr16:69219718
|
ATTTTGTT others(3): Show |
A | 15 | a0001c0001t0001g0173a0001c0001t0002g0098a0001c0001t0003g0100others(12): Show | 15 | HG00099.hp1 HG00544.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.581-25844_581-2583 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219718 | |||||
| chr16:69219718
|
ATTTTGTT others(8): Show |
A | 6 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0003g0093others(3): Show | 6 | HG02258.hp1 HG02886.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-25849_581-2583 others(19): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69219718 | |||||
| chr16:69220154
|
A | AT | 29 | a0001c0001t0001g0138a0001c0001t0001g0163a0001c0001t0001g0166others(26): Show | 29 | HG00621.hp2 HG01361.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.581-25422dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69220154 | |||||
| chr16:69220154
|
A | ATTT | 19 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(16): Show | 19 | HG00099.hp1 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.581-25424_581-2542 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69220154 | |||||
| chr16:69220154
|
A | ATTTT | 7 | a0001c0001t0006g0063a0001c0001t0013g0055a0001c0001t0039g0053others(4): Show | 7 | HG00738.hp1 HG01517.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-25425_581-2542 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69220154 | |||||
| chr16:69220154
|
AT | A | 10 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0002g0133others(7): Show | 10 | HG01109.hp1 HG01433.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-25422delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69220154 | |||||
| chr16:69220158
|
T | G | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-25444T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220158 | ||||||
| chr16:69220280
|
G | T | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.581-25322G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220280 | ||||||
| chr16:69220534
|
G | GT | 5 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-25057dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69220534 | |||||
| chr16:69220544
|
T | C | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-25058T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220544 | ||||||
| chr16:69220580
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-25022T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220580 | ||||||
| chr16:69220582
|
C | T | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-25020C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220582 | ||||||
| chr16:69220583
|
G | A | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.581-25019G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220583 | ||||||
| chr16:69220810
|
G | A | 20 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(17): Show | 20 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.581-24792G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220810 | ||||||
| chr16:69220812
|
A | G | 11 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(8): Show | 11 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.581-24790A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220812 | ||||||
| chr16:69220883
|
T | G | 1 | a0001c0001t0011g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.581-24719T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220883 | ||||||
| chr16:69220963
|
A | T | 1 | a0001c0002t0036g0019 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.581-24639A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69220963 | ||||||
| chr16:69221049
|
G | A | 1 | a0001c0001t0007g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.581-24553G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69221049 | ||||||
| chr16:69221205
|
G | A | 1 | a0001c0002t0008g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.581-24397G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69221205 | ||||||
| chr16:69221220
|
C | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-24382C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69221220 | ||||||
| chr16:69221420
|
A | G | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-24182A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69221420 | ||||||
| chr16:69221502
|
G | A | 12 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(9): Show | 12 | HG01346.hp2 HG01361.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.581-24100G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69221502 | ||||||
| chr16:69221683
|
C | T | 2 | a0001c0001t0002g0110a0001c0001t0002g0120 | 2 | NA18973.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.581-23919C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69221683 | ||||||
| chr16:69221721
|
A | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-23881A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69221721 | ||||||
| chr16:69222166
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-23436C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69222166 | ||||||
| chr16:69222186
|
A | G | 1 | a0001c0002t0028g0010 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.581-23416A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69222186 | ||||||
| chr16:69222400
|
C | T | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.581-23202C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69222400 | ||||||
| chr16:69222509
|
C | G | 1 | a0002c0004t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.581-23093C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69222509 | ||||||
| chr16:69222592
|
C | CA | 5 | a0001c0001t0001g0172a0001c0001t0001g0188a0001c0001t0002g0134others(2): Show | 5 | HG01981.hp2 HG02055.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-22994dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69222592 | |||||
| chr16:69222619
|
G | A | 2 | a0001c0002t0020g0011a0001c0002t0020g0013 | 2 | HG00099.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.581-22983G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69222619 | ||||||
| chr16:69223023
|
A | T | 7 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(4): Show | 7 | HG00621.hp1 HG02004.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-22579A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223023 | ||||||
| chr16:69223169
|
A | G | 3 | a0001c0001t0022g0195a0001c0001t0022g0196a0001c0001t0035g0194 | 3 | NA18973.hp2 NA19064.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.581-22433A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223169 | ||||||
| chr16:69223191
|
A | AT | 6 | a0001c0001t0002g0121a0001c0001t0022g0195a0001c0001t0034g0161others(3): Show | 6 | HG02145.hp2 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-22393dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69223191 | |||||
| chr16:69223191
|
AT | A | 29 | a0001c0001t0003g0090a0001c0001t0006g0049a0001c0001t0006g0052others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.581-22393delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69223191 | |||||
| chr16:69223315
|
C | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-22287C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223315 | ||||||
| chr16:69223579
|
C | T | 1 | a0001c0001t0007g0155 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.581-22023C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223579 | ||||||
| chr16:69223636
|
G | GT | 12 | a0001c0001t0001g0138a0001c0001t0001g0201a0001c0001t0003g0093others(9): Show | 12 | HG01433.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.581-21956dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69223636 | |||||
| chr16:69223790
|
G | A | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-21812G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223790 | ||||||
| chr16:69223839
|
C | T | 1 | a0001c0001t0045g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.581-21763C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223839 | ||||||
| chr16:69223890
|
G | A | 39 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(36): Show | 39 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.581-21712G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223890 | ||||||
| chr16:69223974
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-21628T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69223974 | ||||||
| chr16:69224210
|
A | AT | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.581-21373dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69224210 | |||||
| chr16:69224210
|
A | ATT | 9 | a0001c0001t0001g0162a0001c0001t0002g0121a0001c0001t0013g0062others(6): Show | 9 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.581-21374_581-2137 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69224210 | |||||
| chr16:69224235
|
G | A | 1 | a0001c0001t0007g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.581-21367G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224235 | ||||||
| chr16:69224389
|
C | T | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.581-21213C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224389 | ||||||
| chr16:69224401
|
C | T | 1 | a0001c0001t0003g0085 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.581-21201C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224401 | ||||||
| chr16:69224454
|
G | A | 27 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.581-21148G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224454 | ||||||
| chr16:69224535
|
A | T | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-21067A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224535 | ||||||
| chr16:69224588
|
T | G | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.581-21014T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224588 | ||||||
| chr16:69224601
|
T | G | 92 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.581-21001T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224601 | ||||||
| chr16:69224632
|
G | T | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.581-20970G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224632 | ||||||
| chr16:69224742
|
A | G | 3 | a0001c0001t0003g0086a0001c0001t0003g0092a0001c0001t0003g0097 | 3 | HG00735.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.581-20860A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69224742 | ||||||
| chr16:69225467
|
G | A | 1 | a0001c0001t0006g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.581-20135G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69225467 | ||||||
| chr16:69225655
|
C | G | 1 | a0001c0001t0003g0090 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.581-19947C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69225655 | ||||||
| chr16:69225853
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0178 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.581-19749C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69225853 | ||||||
| chr16:69225917
|
G | A | 1 | a0001c0002t0036g0019 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.581-19685G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69225917 | ||||||
| chr16:69226020
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.581-19582G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69226020 | ||||||
| chr16:69226090
|
G | A | 3 | a0001c0001t0003g0076a0001c0001t0003g0104a0001c0001t0040g0105 | 3 | HG00597.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.581-19512G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69226090 | ||||||
| chr16:69226133
|
G | A | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.581-19469G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69226133 | ||||||
| chr16:69226279
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0178 | 3 | HG02451.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.581-19323C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69226279 | ||||||
| chr16:69226338
|
T | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-19264T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69226338 | ||||||
| chr16:69226386
|
T | TA | 6 | a0001c0001t0001g0138a0001c0001t0002g0123a0001c0001t0039g0053others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-19200dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69226386 | |||||
| chr16:69226664
|
G | C | 2 | a0001c0002t0004g0028a0001c0002t0004g0029 | 2 | NA18968.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.581-18938G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69226664 | ||||||
| chr16:69226948
|
A | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-18654A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69226948 | ||||||
| chr16:69227078
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-18524C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227078 | ||||||
| chr16:69227091
|
C | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-18511C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227091 | ||||||
| chr16:69227174
|
A | G | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-18428A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227174 | ||||||
| chr16:69227181
|
T | G | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.581-18421T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227181 | ||||||
| chr16:69227250
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.581-18352C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227250 | ||||||
| chr16:69227289
|
G | C | 1 | a0001c0002t0008g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.581-18313G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227289 | ||||||
| chr16:69227445
|
A | T | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-18157A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227445 | ||||||
| chr16:69227545
|
G | T | 1 | a0001c0001t0003g0081 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.581-18057G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227545 | ||||||
| chr16:69227720
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-17882G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69227720 | ||||||
| chr16:69227841
|
A | AT | 50 | a0001c0001t0001g0163a0001c0001t0001g0191a0001c0001t0003g0079others(47): Show | 50 | HG00597.hp1 HG00735.hp2 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.581-17736dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69227841 | |||||
| chr16:69227841
|
A | ATT | 14 | a0001c0001t0006g0063a0001c0001t0007g0153a0001c0001t0007g0155others(11): Show | 14 | HG00099.hp1 HG00544.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.581-17737_581-1773 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69227841 | |||||
| chr16:69227841
|
AT | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0096a0001c0001t0001g0103others(48): Show | 51 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.581-17736delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69227841 | |||||
| chr16:69227841
|
ATT | A | 8 | a0001c0001t0002g0127a0001c0001t0002g0145a0001c0002t0014g0070others(5): Show | 8 | HG00408.hp2 HG01433.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-17737_581-1773 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69227841 | |||||
| chr16:69227841
|
ATTTTTTT | A | 19 | a0001c0002t0004g0029a0001c0002t0004g0030a0001c0002t0004g0031others(16): Show | 19 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.581-17742_581-1773 others(11): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69227841 | |||||
| chr16:69227841
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-17745_581-1773 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69227841 | |||||
| chr16:69228006
|
C | T | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-17596C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228006 | ||||||
| chr16:69228227
|
C | T | 1 | a0001c0001t0005g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.581-17375C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228227 | ||||||
| chr16:69228404
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-17198G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228404 | ||||||
| chr16:69228431
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.581-17171G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228431 | ||||||
| chr16:69228458
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.581-17144A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228458 | ||||||
| chr16:69228505
|
C | CA | 37 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0179others(34): Show | 37 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.581-17075dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69228505 | |||||
| chr16:69228505
|
C | CAA | 8 | a0001c0001t0006g0063a0001c0002t0014g0070a0001c0002t0014g0071others(5): Show | 8 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-17076_581-1707 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69228505 | |||||
| chr16:69228505
|
CA | C | 15 | a0001c0001t0002g0126a0001c0001t0005g0148a0001c0001t0007g0197others(12): Show | 15 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.581-17075delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69228505 | |||||
| chr16:69228630
|
A | G | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-16972A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228630 | ||||||
| chr16:69228836
|
A | G | 92 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.581-16766A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228836 | ||||||
| chr16:69228994
|
C | T | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.581-16608C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69228994 | ||||||
| chr16:69229259
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.581-16343A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69229259 | ||||||
| chr16:69229473
|
A | AT | 17 | a0001c0001t0001g0163a0001c0001t0003g0104a0001c0001t0006g0049others(14): Show | 17 | HG01346.hp1 HG01361.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.581-16109dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69229473 | |||||
| chr16:69229473
|
AT | A | 16 | a0001c0001t0001g0189a0001c0001t0006g0060a0001c0002t0008g0015others(13): Show | 16 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-16109delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69229473 | |||||
| chr16:69229568
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.581-16034G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69229568 | ||||||
| chr16:69229670
|
C | T | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.581-15932C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69229670 | ||||||
| chr16:69229842
|
C | CA | 6 | a0001c0001t0044g0159a0001c0002t0020g0011a0001c0002t0020g0013others(3): Show | 6 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-15744dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69229842 | |||||
| chr16:69229842
|
CA | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0096a0001c0001t0001g0115others(37): Show | 40 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.581-15744delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69229842 | |||||
| chr16:69229878
|
C | T | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-15724C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69229878 | ||||||
| chr16:69230012
|
C | T | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.581-15590C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69230012 | ||||||
| chr16:69230099
|
TTTAAG | T | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-15498_581-1549 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69230099 | |||||
| chr16:69230223
|
A | G | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-15379A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69230223 | ||||||
| chr16:69230338
|
C | T | 1 | a0001c0001t0013g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.581-15264C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69230338 | ||||||
| chr16:69230361
|
CT | C | 7 | a0001c0001t0001g0138a0001c0002t0014g0070a0001c0002t0014g0071others(4): Show | 7 | HG01433.hp2 HG01884.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-15229delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69230361 | |||||
| chr16:69230581
|
T | TC | 4 | a0001c0001t0005g0112a0001c0001t0005g0210a0001c0001t0005g0211others(1): Show | 4 | NA18957.hp2 NA18960.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-15019dupC | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69230581 | |||||
| chr16:69230704
|
G | A | 2 | a0001c0002t0004g0038a0001c0002t0004g0039 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.581-14898G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69230704 | ||||||
| chr16:69230747
|
C | CT | 28 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0003g0076others(25): Show | 28 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.581-14840dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69230747 | |||||
| chr16:69230756
|
T | TG | 5 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-14846_581-1484 others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69230756 | ||||||
| chr16:69230857
|
C | T | 3 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066 | 3 | HG02572.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.581-14745C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69230857 | ||||||
| chr16:69230929
|
G | C | 1 | a0001c0001t0005g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.581-14673G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69230929 | ||||||
| chr16:69231450
|
A | G | 1 | a0001c0001t0005g0211 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.581-14152A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69231450 | ||||||
| chr16:69231493
|
G | A | 1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.581-14109G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69231493 | ||||||
| chr16:69231816
|
C | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-13786C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69231816 | ||||||
| chr16:69231821
|
C | G | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-13781C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69231821 | ||||||
| chr16:69231942
|
A | G | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-13660A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69231942 | ||||||
| chr16:69231975
|
T | C | 1 | a0001c0002t0004g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.581-13627T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69231975 | ||||||
| chr16:69231997
|
G | A | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-13605G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69231997 | ||||||
| chr16:69232126
|
C | T | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-13476C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232126 | ||||||
| chr16:69232127
|
G | A | 5 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-13475G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232127 | ||||||
| chr16:69232151
|
C | CT | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-13443dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232151 | |||||
| chr16:69232163
|
G | A | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.581-13439G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232163 | ||||||
| chr16:69232164
|
G | T | 2 | a0001c0002t0004g0038a0001c0002t0004g0039 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.581-13438G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232164 | ||||||
| chr16:69232208
|
CT | C | 63 | a0001c0001t0002g0124a0001c0001t0002g0143a0001c0001t0005g0112others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.581-13379delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232208 | |||||
| chr16:69232306
|
C | T | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-13296C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232306 | ||||||
| chr16:69232330
|
C | T | 4 | a0001c0001t0007g0151a0001c0001t0007g0155a0001c0001t0007g0156others(1): Show | 4 | HG03927.hp1 NA18747.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-13272C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232330 | ||||||
| chr16:69232373
|
T | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-13229T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232373 | ||||||
| chr16:69232502
|
C | CT | 65 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0162others(62): Show | 65 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.581-13073dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232502 | |||||
| chr16:69232502
|
C | CTT | 12 | a0001c0001t0001g0186a0001c0001t0001g0201a0001c0001t0005g0147others(9): Show | 12 | HG00735.hp1 HG00738.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.581-13074_581-1307 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232502 | |||||
| chr16:69232502
|
C | CTTTTTTT others(6): Show |
2 | a0001c0002t0012g0202a0001c0002t0012g0205 | 2 | HG01517.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.581-13085_581-1307 others(17): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232502 | |||||
| chr16:69232502
|
C | CTTTTTTT others(29): Show |
1 | a0001c0002t0037g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.581-13073_581-1307 others(40): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232502 | |||||
| chr16:69232502
|
CT | C | 10 | a0001c0001t0001g0167a0001c0002t0004g0030a0001c0002t0004g0033others(7): Show | 10 | HG00738.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.581-13073delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232502 | |||||
| chr16:69232502
|
CTT | C | 5 | a0001c0001t0001g0164a0001c0002t0004g0028a0001c0002t0004g0029others(2): Show | 5 | HG00621.hp1 HG02004.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-13074_581-1307 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232502 | |||||
| chr16:69232502
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0012g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.581-13084_581-1307 others(16): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69232502 | |||||
| chr16:69232544
|
G | A | 11 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(8): Show | 11 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.581-13058G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232544 | ||||||
| chr16:69232553
|
C | T | 60 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.581-13049C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69232553 | ||||||
| chr16:69233306
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0160others(142): Show | 145 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.581-12296G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69233306 | ||||||
| chr16:69233568
|
A | G | 1 | a0001c0001t0042g0144 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.581-12034A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69233568 | ||||||
| chr16:69233664
|
G | A | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.581-11938G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69233664 | ||||||
| chr16:69233784
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.581-11818G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69233784 | ||||||
| chr16:69233857
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.581-11745G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69233857 | ||||||
| chr16:69233898
|
G | A | 27 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.581-11704G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69233898 | ||||||
| chr16:69234061
|
G | A | 3 | a0001c0001t0003g0093a0001c0001t0003g0102a0001c0001t0043g0088 | 3 | HG03017.hp2 NA20129.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.581-11541G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69234061 | ||||||
| chr16:69234199
|
G | A | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.581-11403G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69234199 | ||||||
| chr16:69234672
|
C | G | 4 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-10930C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69234672 | ||||||
| chr16:69234702
|
A | AT | 18 | a0001c0001t0001g0115a0001c0001t0006g0049a0001c0001t0006g0052others(15): Show | 18 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.581-10883dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69234702 | |||||
| chr16:69234702
|
A | T | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-10900A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69234702 | ||||||
| chr16:69234702
|
AT | A | 10 | a0001c0001t0001g0198a0001c0001t0002g0145a0001c0001t0025g0152others(7): Show | 10 | HG01433.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-10883delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69234702 | |||||
| chr16:69234751
|
G | A | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-10851G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69234751 | ||||||
| chr16:69234753
|
A | G | 1 | a0001c0002t0032g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.581-10849A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69234753 | ||||||
| chr16:69234995
|
G | A | 2 | a0001c0002t0004g0037a0001c0002t0004g0040 | 2 | HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.581-10607G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69234995 | ||||||
| chr16:69235126
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-10476C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235126 | ||||||
| chr16:69235160
|
C | T | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-10442C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235160 | ||||||
| chr16:69235178
|
AT | A | 6 | a0001c0001t0002g0145a0001c0002t0012g0202a0001c0002t0012g0203others(3): Show | 6 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-10409delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69235178 | |||||
| chr16:69235240
|
A | G | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.581-10362A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235240 | ||||||
| chr16:69235249
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-10353C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235249 | ||||||
| chr16:69235299
|
G | A | 4 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-10303G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235299 | ||||||
| chr16:69235334
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.581-10268G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235334 | ||||||
| chr16:69235586
|
G | T | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.581-10016G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235586 | ||||||
| chr16:69235624
|
G | A | 2 | a0001c0002t0015g0064a0001c0002t0015g0066 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.581-9978G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69235624 | ||||||
| chr16:69236263
|
A | G | 3 | a0001c0001t0003g0076a0001c0001t0003g0104a0001c0001t0040g0105 | 3 | HG00597.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.581-9339A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69236263 | ||||||
| chr16:69236375
|
ATCAGT | A | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-9225_581-9221d others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69236375 | |||||
| chr16:69236499
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0002g0108others(2): Show | 5 | HG01496.hp1 HG01981.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-9103G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69236499 | ||||||
| chr16:69236674
|
C | CA | 8 | a0001c0001t0031g0150a0001c0002t0014g0070a0001c0002t0014g0071others(5): Show | 8 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-8914dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69236674 | |||||
| chr16:69236731
|
C | T | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.581-8871C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69236731 | ||||||
| chr16:69236894
|
C | T | 1 | a0001c0001t0003g0085 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.581-8708C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69236894 | ||||||
| chr16:69236908
|
A | G | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-8694A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69236908 | ||||||
| chr16:69237085
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.581-8517G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69237085 | ||||||
| chr16:69237232
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.581-8370T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69237232 | ||||||
| chr16:69237245
|
A | AG | 7 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(4): Show | 7 | HG00621.hp1 HG02004.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-8356dupG | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69237245 | |||||
| chr16:69237587
|
C | T | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.581-8015C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69237587 | ||||||
| chr16:69237603
|
C | CT | 19 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0172others(16): Show | 19 | HG01346.hp2 HG01361.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.581-7982dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69237603 | |||||
| chr16:69237603
|
C | CTT | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG01433.hp2 HG02615.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.581-7983_581-7982d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69237603 | |||||
| chr16:69237603
|
C | CTTTTTT | 29 | a0001c0002t0004g0022a0001c0002t0004g0024a0001c0002t0004g0025others(26): Show | 29 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.581-7987_581-7982d others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69237603 | |||||
| chr16:69237605
|
T | TTC | 22 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(19): Show | 22 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.581-7996_581-7995i others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69237605 | |||||
| chr16:69237606
|
T | TC | 10 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(7): Show | 10 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-7996_581-7995i others(3): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69237606 | ||||||
| chr16:69237609
|
T | C | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-7993T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69237609 | ||||||
| chr16:69237696
|
C | T | 27 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.581-7906C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69237696 | ||||||
| chr16:69237855
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.581-7747G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69237855 | ||||||
| chr16:69238138
|
G | T | 1 | a0001c0001t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.581-7464G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69238138 | ||||||
| chr16:69238350
|
A | G | 1 | a0001c0001t0005g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.581-7252A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69238350 | ||||||
| chr16:69238384
|
C | T | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.581-7218C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69238384 | ||||||
| chr16:69238914
|
C | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-6688C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69238914 | ||||||
| chr16:69238994
|
G | A | 13 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.581-6608G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69238994 | ||||||
| chr16:69239068
|
G | A | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.581-6534G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69239068 | ||||||
| chr16:69239209
|
C | T | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-6393C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69239209 | ||||||
| chr16:69239313
|
G | A | 1 | a0001c0003t0005g0209 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.581-6289G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69239313 | ||||||
| chr16:69239480
|
C | G | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.581-6122C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69239480 | ||||||
| chr16:69239693
|
C | T | 1 | a0001c0002t0018g0034 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.581-5909C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69239693 | ||||||
| chr16:69239719
|
T | A | 101 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.581-5883T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69239719 | ||||||
| chr16:69240361
|
A | G | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.581-5241A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69240361 | ||||||
| chr16:69240647
|
T | C | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-4955T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69240647 | ||||||
| chr16:69240858
|
GTTTA | G | 25 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(22): Show | 25 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.581-4740_581-4737d others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69240858 | |||||
| chr16:69240953
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-4649C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69240953 | ||||||
| chr16:69241057
|
G | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0122 | 2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.581-4545G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241057 | ||||||
| chr16:69241106
|
CG | C | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.581-4495delG | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241106 | ||||||
| chr16:69241108
|
C | A | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.581-4494C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241108 | ||||||
| chr16:69241109
|
C | T | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.581-4493C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241109 | ||||||
| chr16:69241168
|
C | CT | 50 | a0001c0001t0001g0103a0001c0001t0001g0160a0001c0001t0001g0162others(47): Show | 50 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.581-4408dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69241168 | |||||
| chr16:69241168
|
C | CTT | 7 | a0001c0001t0003g0087a0001c0001t0003g0104a0001c0001t0005g0146others(4): Show | 7 | HG01361.hp2 HG01981.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-4409_581-4408d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69241168 | |||||
| chr16:69241168
|
CT | C | 46 | a0001c0001t0002g0126a0001c0001t0003g0089a0001c0001t0006g0049others(43): Show | 46 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.581-4408delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69241168 | |||||
| chr16:69241168
|
CTT | C | 16 | a0001c0002t0004g0023a0001c0002t0004g0045a0001c0002t0012g0202others(13): Show | 16 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-4409_581-4408d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69241168 | |||||
| chr16:69241168
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.581-4417_581-4408d others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69241168 | |||||
| chr16:69241326
|
G | A | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-4276G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241326 | ||||||
| chr16:69241510
|
C | T | 1 | a0001c0001t0005g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.581-4092C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241510 | ||||||
| chr16:69241552
|
C | T | 1 | a0001c0001t0006g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.581-4050C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241552 | ||||||
| chr16:69241695
|
C | T | 11 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(8): Show | 11 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.581-3907C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241695 | ||||||
| chr16:69241928
|
CA | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(102): Show | 105 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.581-3650delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69241928 | |||||
| chr16:69241928
|
CAA | C | 20 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(17): Show | 20 | HG00280.hp2 HG02055.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.581-3651_581-3650d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69241928 | |||||
| chr16:69241998
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18968.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.581-3604C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69241998 | ||||||
| chr16:69242144
|
C | G | 77 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.581-3458C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242144 | ||||||
| chr16:69242165
|
C | G | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.581-3437C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242165 | ||||||
| chr16:69242264
|
A | G | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-3338A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242264 | ||||||
| chr16:69242590
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-3012T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242590 | ||||||
| chr16:69242620
|
C | G | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.581-2982C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242620 | ||||||
| chr16:69242632
|
T | C | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.581-2970T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242632 | ||||||
| chr16:69242729
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.581-2873G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242729 | ||||||
| chr16:69242744
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-2858G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242744 | ||||||
| chr16:69242817
|
C | T | 1 | a0001c0001t0011g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.581-2785C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242817 | ||||||
| chr16:69242848
|
C | T | 1 | a0001c0002t0024g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.581-2754C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242848 | ||||||
| chr16:69242849
|
G | A | 3 | a0001c0001t0005g0112a0001c0001t0005g0210a0001c0001t0005g0212 | 3 | NA18957.hp2 NA18960.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.581-2753G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242849 | ||||||
| chr16:69242894
|
G | A | 6 | a0001c0002t0004g0045a0001c0002t0004g0046a0001c0002t0017g0043others(3): Show | 6 | HG01496.hp2 HG02735.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-2708G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69242894 | ||||||
| chr16:69243020
|
T | TA | 6 | a0001c0001t0002g0108a0001c0001t0002g0111a0001c0001t0007g0158others(3): Show | 6 | HG01175.hp1 HG02145.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-2561dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69243020 | |||||
| chr16:69243020
|
TAAAAAAA others(2): Show |
T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-2569_581-2561d others(11): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | 69243020 | |||||
| chr16:69243056
|
G | A | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.581-2546G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69243056 | ||||||
| chr16:69243170
|
T | C | 12 | a0001c0002t0004g0037a0001c0002t0004g0038a0001c0002t0004g0039others(9): Show | 12 | HG00280.hp2 HG00735.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.581-2432T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69243170 | ||||||
| chr16:69243491
|
G | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0122 | 2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.581-2111G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69243491 | ||||||
| chr16:69243669
|
A | G | 4 | a0001c0001t0001g0201a0001c0001t0011g0168a0001c0001t0011g0169others(1): Show | 4 | HG02258.hp1 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-1933A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69243669 | ||||||
| chr16:69243887
|
TA | T | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.581-1714delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69243887 | ||||||
| chr16:69244078
|
T | G | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-1524T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69244078 | ||||||
| chr16:69244225
|
A | G | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-1377A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69244225 | ||||||
| chr16:69244512
|
C | G | 39 | a0001c0001t0001g0166a0001c0001t0001g0172a0001c0001t0001g0174others(36): Show | 39 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.581-1090C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69244512 | ||||||
| chr16:69244810
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.581-792G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69244810 | ||||||
| chr16:69244900
|
A | G | 5 | a0001c0001t0003g0079a0001c0002t0020g0011a0001c0002t0020g0013others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-702A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69244900 | ||||||
| chr16:69244987
|
A | G | 33 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.581-615A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69244987 | ||||||
| chr16:69244989
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.581-613T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69244989 | ||||||
| chr16:69245350
|
C | T | 3 | a0001c0001t0003g0076a0001c0001t0003g0104a0001c0001t0040g0105 | 3 | HG00597.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.581-252C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69245350 | ||||||
| chr16:69245416
|
A | T | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-186A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69245416 | ||||||
| chr16:69245500
|
C | T | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.581-102C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69245500 | ||||||
| chr16:69245572
|
A | G | 4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.581-30A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69245572 | ||||||
| chr16:69245583
|
T | C | 2 | a0001c0002t0004g0037a0001c0002t0004g0040 | 2 | HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.581-19T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | chr16 | 69245583 | ||||||
| chr16:69245870
|
T | C | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+55T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69245870 | ||||||
| chr16:69245928
|
G | T | 1 | a0001c0001t0002g0109 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.794+113G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69245928 | ||||||
| chr16:69245979
|
A | G | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+164A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69245979 | ||||||
| chr16:69246105
|
C | G | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+290C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69246105 | ||||||
| chr16:69246420
|
T | C | 70 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.794+605T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69246420 | ||||||
| chr16:69246619
|
T | C | 2 | a0001c0001t0006g0054a0001c0001t0006g0063 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.794+804T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69246619 | ||||||
| chr16:69246805
|
G | C | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+990G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69246805 | ||||||
| chr16:69246903
|
TGGGGGGA | T | 6 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(3): Show | 6 | HG00621.hp1 HG02004.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+1099_794+1105d others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69246903 | |||||
| chr16:69247048
|
TA | T | 7 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0021g0074others(4): Show | 7 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+1241delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69247048 | |||||
| chr16:69247055
|
A | T | 6 | a0001c0001t0042g0144a0001c0002t0004g0022a0001c0002t0004g0023others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.794+1240A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69247055 | ||||||
| chr16:69247056
|
AT | A | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+1242delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69247056 | ||||||
| chr16:69247057
|
T | A | 6 | a0001c0001t0001g0165a0001c0001t0011g0170a0001c0002t0015g0064others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+1242T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69247057 | ||||||
| chr16:69247070
|
TA | T | 13 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(10): Show | 13 | HG01433.hp2 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.794+1267delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69247070 | |||||
| chr16:69247070
|
TAA | T | 11 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(8): Show | 11 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+1266_794+1267d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69247070 | |||||
| chr16:69247490
|
C | G | 1 | a0001c0002t0004g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.794+1675C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69247490 | ||||||
| chr16:69247692
|
C | A | 1 | a0001c0002t0004g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.794+1877C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69247692 | ||||||
| chr16:69247866
|
T | C | 101 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.794+2051T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69247866 | ||||||
| chr16:69247965
|
A | T | 1 | a0001c0002t0036g0019 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.794+2150A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69247965 | ||||||
| chr16:69248069
|
G | A | 1 | a0001c0001t0006g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.794+2254G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248069 | ||||||
| chr16:69248371
|
C | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+2556C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248371 | ||||||
| chr16:69248588
|
C | T | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+2773C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248588 | ||||||
| chr16:69248589
|
G | A | 7 | a0001c0001t0005g0112a0001c0001t0005g0208a0001c0001t0005g0210others(4): Show | 7 | HG01346.hp2 HG01361.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+2774G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248589 | ||||||
| chr16:69248590
|
C | A | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+2775C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248590 | ||||||
| chr16:69248631
|
C | CAAATA | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+2834_794+2838d others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69248631 | |||||
| chr16:69248757
|
T | C | 1 | a0001c0002t0018g0034 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.794+2942T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248757 | ||||||
| chr16:69248869
|
CT | C | 28 | a0001c0001t0001g0096a0001c0001t0001g0199a0001c0001t0002g0108others(25): Show | 28 | HG00280.hp2 HG01496.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.794+3072delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69248869 | |||||
| chr16:69248937
|
A | G | 1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.794+3122A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248937 | ||||||
| chr16:69248974
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.794+3159G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69248974 | ||||||
| chr16:69249023
|
C | CT | 14 | a0001c0001t0003g0079a0001c0001t0007g0151a0001c0001t0007g0153others(11): Show | 14 | HG00544.hp2 HG02027.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.794+3227dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69249023 | |||||
| chr16:69249023
|
CT | C | 77 | a0001c0001t0002g0108a0001c0001t0002g0117a0001c0001t0005g0112others(74): Show | 77 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.794+3227delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69249023 | |||||
| chr16:69249023
|
CTT | C | 5 | a0001c0001t0005g0210a0001c0001t0016g0051a0001c0002t0020g0013others(2): Show | 5 | HG00738.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+3226_794+3227d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69249023 | |||||
| chr16:69249169
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+3354G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249169 | ||||||
| chr16:69249232
|
C | T | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+3417C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249232 | ||||||
| chr16:69249265
|
A | G | 2 | a0001c0001t0003g0079a0001c0001t0003g0082 | 2 | HG00609.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.794+3450A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249265 | ||||||
| chr16:69249304
|
G | T | 6 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.794+3489G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249304 | ||||||
| chr16:69249306
|
A | G | 1 | a0001c0002t0032g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.794+3491A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249306 | ||||||
| chr16:69249421
|
G | A | 17 | a0001c0001t0001g0180a0001c0001t0006g0049a0001c0001t0006g0052others(14): Show | 17 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.794+3606G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249421 | ||||||
| chr16:69249427
|
G | A | 1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.794+3612G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249427 | ||||||
| chr16:69249520
|
C | A | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+3705C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249520 | ||||||
| chr16:69249599
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.794+3784G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249599 | ||||||
| chr16:69249745
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.794+3930G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69249745 | ||||||
| chr16:69250088
|
T | A | 19 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(16): Show | 19 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.794+4273T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250088 | ||||||
| chr16:69250092
|
T | A | 41 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(38): Show | 41 | HG00544.hp2 HG01243.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.794+4277T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250092 | ||||||
| chr16:69250134
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.794+4319A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250134 | ||||||
| chr16:69250140
|
T | G | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.794+4325T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250140 | ||||||
| chr16:69250196
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.794+4381C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250196 | ||||||
| chr16:69250288
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.794+4473T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250288 | ||||||
| chr16:69250316
|
A | G | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+4501A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250316 | ||||||
| chr16:69250668
|
G | C | 25 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(22): Show | 25 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.794+4853G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250668 | ||||||
| chr16:69250981
|
G | GT | 20 | a0001c0001t0001g0187a0001c0001t0002g0108a0001c0001t0003g0100others(17): Show | 20 | HG00597.hp2 HG01433.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.794+5181dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69250981 | |||||
| chr16:69250984
|
T | G | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.794+5169T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250984 | ||||||
| chr16:69250985
|
T | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.794+5170T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69250985 | ||||||
| chr16:69251009
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.794+5194C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251009 | ||||||
| chr16:69251017
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+5202C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251017 | ||||||
| chr16:69251124
|
T | G | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.794+5309T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251124 | ||||||
| chr16:69251213
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.794+5398C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251213 | ||||||
| chr16:69251270
|
A | G | 77 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.794+5455A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251270 | ||||||
| chr16:69251430
|
T | C | 77 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.794+5615T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251430 | ||||||
| chr16:69251468
|
T | TA | 21 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(18): Show | 21 | HG00280.hp1 HG00609.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.794+5678dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69251468 | |||||
| chr16:69251468
|
TA | T | 60 | a0001c0001t0002g0126a0001c0001t0002g0143a0001c0001t0006g0049others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.794+5678delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69251468 | |||||
| chr16:69251468
|
TAA | T | 11 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(8): Show | 11 | HG00738.hp2 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.794+5677_794+5678d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69251468 | |||||
| chr16:69251569
|
A | G | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+5754A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251569 | ||||||
| chr16:69251591
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.794+5776C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251591 | ||||||
| chr16:69251607
|
C | T | 1 | a0001c0002t0012g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.794+5792C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251607 | ||||||
| chr16:69251671
|
G | A | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.794+5856G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251671 | ||||||
| chr16:69251702
|
C | T | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.794+5887C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251702 | ||||||
| chr16:69251734
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(183): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.794+5919T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251734 | ||||||
| chr16:69251893
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.794+6078C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251893 | ||||||
| chr16:69251901
|
C | G | 1 | a0001c0001t0003g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.794+6086C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251901 | ||||||
| chr16:69251934
|
C | A | 101 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.794+6119C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69251934 | ||||||
| chr16:69252475
|
G | A | 1 | a0001c0002t0008g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.794+6660G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69252475 | ||||||
| chr16:69252509
|
C | A | 1 | a0001c0001t0041g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.794+6694C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69252509 | ||||||
| chr16:69252510
|
A | G | 1 | a0001c0001t0041g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.794+6695A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69252510 | ||||||
| chr16:69252838
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.794+7023G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69252838 | ||||||
| chr16:69252903
|
G | GT | 15 | a0001c0001t0001g0207a0001c0001t0002g0181a0001c0001t0003g0082others(12): Show | 15 | HG00280.hp2 HG00609.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.794+7106dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69252903 | |||||
| chr16:69252903
|
GT | G | 9 | a0001c0001t0001g0188a0001c0002t0014g0070a0001c0002t0014g0071others(6): Show | 9 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.794+7106delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69252903 | |||||
| chr16:69252993
|
G | A | 10 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(7): Show | 10 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.795-7057G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69252993 | ||||||
| chr16:69252994
|
G | A | 1 | a0001c0001t0013g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.795-7056G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69252994 | ||||||
| chr16:69253048
|
T | C | 70 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.795-7002T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69253048 | ||||||
| chr16:69253179
|
G | A | 1 | a0001c0001t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.795-6871G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69253179 | ||||||
| chr16:69253282
|
T | A | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.795-6768T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69253282 | ||||||
| chr16:69253371
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.795-6679C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69253371 | ||||||
| chr16:69253413
|
A | G | 77 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.795-6637A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69253413 | ||||||
| chr16:69253566
|
G | A | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-6484G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69253566 | ||||||
| chr16:69253580
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.795-6470C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69253580 | ||||||
| chr16:69254112
|
G | T | 25 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(22): Show | 25 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.795-5938G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254112 | ||||||
| chr16:69254121
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.795-5929A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254121 | ||||||
| chr16:69254323
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.795-5727C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254323 | ||||||
| chr16:69254324
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-5726G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254324 | ||||||
| chr16:69254341
|
C | T | 6 | a0001c0001t0006g0049a0001c0001t0006g0054a0001c0001t0006g0063others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-5709C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254341 | ||||||
| chr16:69254676
|
G | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0122 | 2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.795-5374G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254676 | ||||||
| chr16:69254819
|
A | T | 63 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.795-5231A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254819 | ||||||
| chr16:69254820
|
T | A | 25 | a0001c0001t0001g0116a0001c0001t0001g0162a0001c0001t0001g0182others(22): Show | 25 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.795-5230T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69254820 | ||||||
| chr16:69255015
|
A | G | 11 | a0001c0001t0003g0081a0001c0001t0007g0151a0001c0001t0007g0153others(8): Show | 11 | HG00544.hp2 HG01993.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.795-5035A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255015 | ||||||
| chr16:69255303
|
CTGTAACC others(38): Show |
C | 1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.795-4745_795-4701d others(47): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69255303 | |||||
| chr16:69255349
|
T | A | 1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.795-4701T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255349 | ||||||
| chr16:69255388
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.795-4662C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255388 | ||||||
| chr16:69255485
|
G | C | 3 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0025 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.795-4565G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255485 | ||||||
| chr16:69255511
|
G | A | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.795-4539G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255511 | ||||||
| chr16:69255570
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.795-4480A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255570 | ||||||
| chr16:69255573
|
AG | A | 56 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(53): Show | 56 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.795-4476delG | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255573 | ||||||
| chr16:69255574
|
G | A | 18 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(15): Show | 18 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.795-4476G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255574 | ||||||
| chr16:69255644
|
G | C | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-4406G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255644 | ||||||
| chr16:69255711
|
A | T | 91 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.795-4339A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255711 | ||||||
| chr16:69255754
|
C | G | 91 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.795-4296C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69255754 | ||||||
| chr16:69255877
|
C | CA | 22 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(19): Show | 22 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.795-4158dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69255877 | |||||
| chr16:69256128
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-3922G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256128 | ||||||
| chr16:69256249
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.795-3801G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256249 | ||||||
| chr16:69256252
|
T | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-3798T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256252 | ||||||
| chr16:69256386
|
T | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-3664T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256386 | ||||||
| chr16:69256446
|
G | C | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.795-3604G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256446 | ||||||
| chr16:69256471
|
G | A | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-3579G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256471 | ||||||
| chr16:69256788
|
A | C | 6 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.795-3262A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256788 | ||||||
| chr16:69256894
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.795-3156G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256894 | ||||||
| chr16:69256962
|
G | A | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-3088G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69256962 | ||||||
| chr16:69257149
|
C | T | 1 | a0001c0002t0032g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.795-2901C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69257149 | ||||||
| chr16:69257169
|
C | CA | 53 | a0001c0001t0002g0121a0001c0001t0006g0049a0001c0001t0006g0052others(50): Show | 53 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.795-2864dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69257169 | |||||
| chr16:69257169
|
C | CAA | 7 | a0001c0002t0004g0033a0001c0002t0015g0064a0001c0002t0015g0065others(4): Show | 7 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-2865_795-2864d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69257169 | |||||
| chr16:69257169
|
CA | C | 7 | a0001c0001t0031g0150a0001c0002t0008g0015a0001c0002t0008g0016others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-2864delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69257169 | |||||
| chr16:69257414
|
C | CTTAT | 9 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0002g0107others(6): Show | 9 | HG00597.hp2 HG00621.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-2593_795-2590d others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69257414 | |||||
| chr16:69257414
|
CTTAT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0162others(108): Show | 111 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.795-2593_795-2590d others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69257414 | |||||
| chr16:69257414
|
CTTATTTA others(1): Show |
C | 15 | a0001c0001t0005g0146a0001c0002t0004g0022a0001c0002t0004g0023others(12): Show | 15 | HG00738.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.795-2597_795-2590d others(10): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69257414 | |||||
| chr16:69257414
|
CTTATTTA others(5): Show |
C | 17 | a0001c0001t0001g0116a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.795-2601_795-2590d others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69257414 | |||||
| chr16:69257463
|
T | C | 2 | a0001c0003t0005g0214a0001c0003t0005g0215 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.795-2587T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69257463 | ||||||
| chr16:69257487
|
C | G | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.795-2563C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69257487 | ||||||
| chr16:69257498
|
G | A | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-2552G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69257498 | ||||||
| chr16:69257693
|
C | T | 4 | a0001c0001t0005g0112a0001c0001t0005g0210a0001c0001t0005g0211others(1): Show | 4 | NA18957.hp2 NA18960.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-2357C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69257693 | ||||||
| chr16:69257696
|
C | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-2354C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69257696 | ||||||
| chr16:69257833
|
T | A | 4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-2217T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69257833 | ||||||
| chr16:69258319
|
T | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-1731T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69258319 | ||||||
| chr16:69258342
|
TTTGA | T | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-1703_795-1700d others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69258342 | |||||
| chr16:69258605
|
C | CT | 26 | a0001c0001t0001g0116a0001c0001t0001g0163a0001c0001t0001g0164others(23): Show | 26 | HG01109.hp1 HG01256.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.795-1421dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69258605 | |||||
| chr16:69258605
|
CT | C | 33 | a0001c0001t0002g0213a0001c0001t0016g0051a0001c0002t0004g0022others(30): Show | 33 | HG00280.hp2 HG00738.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.795-1421delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69258605 | |||||
| chr16:69258651
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.795-1399G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69258651 | ||||||
| chr16:69258746
|
G | A | 19 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(16): Show | 19 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.795-1304G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69258746 | ||||||
| chr16:69258760
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.795-1290T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69258760 | ||||||
| chr16:69259160
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-890C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259160 | ||||||
| chr16:69259203
|
A | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-847A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259203 | ||||||
| chr16:69259236
|
A | AT | 54 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0116others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.795-786dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69259236 | |||||
| chr16:69259236
|
AT | A | 33 | a0001c0001t0001g0160a0001c0001t0001g0199a0001c0001t0016g0051others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.795-786delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69259236 | |||||
| chr16:69259236
|
ATTT | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-788_795-786del others(3): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69259236 | |||||
| chr16:69259236
|
ATTTTTTT others(4): Show |
A | 1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.795-796_795-786del others(11): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69259236 | |||||
| chr16:69259291
|
G | T | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-759G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259291 | ||||||
| chr16:69259314
|
C | T | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.795-736C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259314 | ||||||
| chr16:69259359
|
A | C | 1 | a0001c0001t0002g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.795-691A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259359 | ||||||
| chr16:69259360
|
G | A | 4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-690G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259360 | ||||||
| chr16:69259376
|
G | A | 1 | a0001c0002t0012g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.795-674G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259376 | ||||||
| chr16:69259381
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.795-669C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259381 | ||||||
| chr16:69259407
|
G | A | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.795-643G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259407 | ||||||
| chr16:69259602
|
C | CT | 15 | a0001c0001t0001g0163a0001c0001t0005g0146a0001c0001t0005g0147others(12): Show | 15 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.795-429dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69259602 | |||||
| chr16:69259602
|
CT | C | 12 | a0001c0001t0002g0213a0001c0001t0003g0102a0001c0001t0006g0058others(9): Show | 12 | HG02451.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.795-429delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr16 | 69259602 | |||||
| chr16:69259643
|
G | A | 2 | a0001c0001t0002g0130a0003c0005t0033g0073 | 2 | HG01256.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.795-407G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259643 | ||||||
| chr16:69259769
|
C | A | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795-281C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259769 | ||||||
| chr16:69259784
|
T | C | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-266T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2/6 | chr16 | 69259784 | ||||||
| chr16:69260867
|
G | T | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1005+607G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69260867 | ||||||
| chr16:69260889
|
A | G | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1005+629A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69260889 | ||||||
| chr16:69261076
|
G | T | 1 | a0001c0002t0030g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1005+816G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261076 | ||||||
| chr16:69261239
|
C | G | 1 | a0001c0001t0003g0076 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1005+979C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261239 | ||||||
| chr16:69261322
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1005+1062T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261322 | ||||||
| chr16:69261345
|
A | G | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | HG02735.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1005+1085A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261345 | ||||||
| chr16:69261394
|
G | A | 4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+1134G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261394 | ||||||
| chr16:69261688
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1005+1428C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261688 | ||||||
| chr16:69261709
|
C | T | 1 | a0001c0001t0040g0105 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1005+1449C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261709 | ||||||
| chr16:69261796
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1005+1536G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261796 | ||||||
| chr16:69261880
|
A | G | 2 | a0001c0002t0018g0036a0001c0002t0030g0035 | 2 | HG01496.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1005+1620A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261880 | ||||||
| chr16:69261948
|
C | G | 3 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066 | 3 | HG02572.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1005+1688C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261948 | ||||||
| chr16:69261988
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1005+1728C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69261988 | ||||||
| chr16:69262361
|
G | A | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG02129.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1005+2101G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69262361 | ||||||
| chr16:69262390
|
C | T | 4 | a0001c0001t0007g0151a0001c0001t0007g0155a0001c0001t0007g0156others(1): Show | 4 | HG03927.hp1 NA18747.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+2130C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69262390 | ||||||
| chr16:69262791
|
C | G | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1005+2531C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69262791 | ||||||
| chr16:69262867
|
G | C | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1005+2607G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69262867 | ||||||
| chr16:69263029
|
A | T | 2 | a0001c0002t0004g0038a0001c0002t0004g0039 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1005+2769A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69263029 | ||||||
| chr16:69263279
|
A | T | 1 | a0001c0002t0037g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1005+3019A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69263279 | ||||||
| chr16:69263496
|
A | T | 2 | a0001c0001t0001g0198a0001c0001t0034g0161 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1005+3236A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69263496 | ||||||
| chr16:69263499
|
A | C | 4 | a0001c0002t0020g0011a0001c0002t0020g0013a0001c0002t0028g0010others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+3239A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69263499 | ||||||
| chr16:69263568
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1005+3308G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69263568 | ||||||
| chr16:69263971
|
A | T | 5 | a0001c0001t0011g0170a0001c0001t0013g0055a0001c0001t0013g0056others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1005+3711A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69263971 | ||||||
| chr16:69264101
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1005+3841C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69264101 | ||||||
| chr16:69264125
|
G | A | 2 | a0001c0001t0002g0083a0001c0001t0002g0113 | 2 | NA18998.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1005+3865G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69264125 | ||||||
| chr16:69264140
|
G | A | 1 | a0001c0002t0008g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1005+3880G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69264140 | ||||||
| chr16:69264193
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1005+3933G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69264193 | ||||||
| chr16:69264958
|
T | G | 2 | a0001c0003t0005g0214a0001c0003t0005g0215 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1005+4698T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69264958 | ||||||
| chr16:69265020
|
C | T | 32 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1005+4760C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69265020 | ||||||
| chr16:69265032
|
A | G | 70 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1005+4772A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69265032 | ||||||
| chr16:69265211
|
T | C | 6 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(3): Show | 6 | HG00621.hp1 HG02004.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-4932T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69265211 | ||||||
| chr16:69265309
|
C | G | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1006-4834C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69265309 | ||||||
| chr16:69265430
|
C | T | 1 | a0001c0001t0005g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1006-4713C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69265430 | ||||||
| chr16:69265830
|
GAA | G | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-4296_1006-429 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr16 | 69265830 | |||||
| chr16:69265976
|
C | T | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1006-4167C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69265976 | ||||||
| chr16:69266236
|
C | T | 6 | a0001c0001t0006g0052a0001c0001t0006g0057a0001c0001t0006g0058others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006-3907C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69266236 | ||||||
| chr16:69266332
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-3811C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69266332 | ||||||
| chr16:69266364
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1006-3759_1006-375 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr16 | 69266364 | |||||
| chr16:69266389
|
C | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-3754C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69266389 | ||||||
| chr16:69266423
|
G | T | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006-3720G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69266423 | ||||||
| chr16:69266467
|
A | AGGGAAAA others(324): Show |
1 | a0001c0001t0005g0149 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1006-3659_1006-365 others(335): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr16 | 69266467 | |||||
| chr16:69266866
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1006-3277A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69266866 | ||||||
| chr16:69266985
|
A | C | 2 | a0001c0001t0002g0091a0001c0001t0002g0122 | 2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1006-3158A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69266985 | ||||||
| chr16:69267030
|
CT | C | 8 | a0001c0001t0002g0122a0001c0001t0002g0145a0001c0002t0004g0023others(5): Show | 8 | HG01169.hp1 HG02717.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-3097delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr16 | 69267030 | |||||
| chr16:69267059
|
C | T | 37 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0001g0129others(34): Show | 37 | HG00408.hp2 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1006-3084C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267059 | ||||||
| chr16:69267173
|
G | A | 4 | a0001c0001t0007g0151a0001c0001t0007g0155a0001c0001t0007g0156others(1): Show | 4 | HG03927.hp1 NA18747.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-2970G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267173 | ||||||
| chr16:69267231
|
A | G | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-2912A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267231 | ||||||
| chr16:69267419
|
G | A | 2 | a0001c0002t0019g0041a0001c0002t0019g0042 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1006-2724G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267419 | ||||||
| chr16:69267545
|
T | G | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-2598T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267545 | ||||||
| chr16:69267591
|
A | G | 1 | a0001c0001t0003g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1006-2552A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267591 | ||||||
| chr16:69267666
|
A | C | 1 | a0001c0001t0003g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1006-2477A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267666 | ||||||
| chr16:69267727
|
C | T | 1 | a0001c0001t0003g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1006-2416C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267727 | ||||||
| chr16:69267806
|
T | C | 1 | a0001c0002t0032g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1006-2337T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267806 | ||||||
| chr16:69267880
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0002g0108others(2): Show | 5 | HG01496.hp1 HG01981.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006-2263G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69267880 | ||||||
| chr16:69268155
|
T | C | 2 | a0001c0001t0003g0086a0001c0001t0003g0092 | 2 | HG00735.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1006-1988T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268155 | ||||||
| chr16:69268240
|
G | A | 3 | a0001c0001t0003g0079a0001c0001t0003g0082a0001c0001t0041g0080 | 3 | HG00609.hp2 HG00621.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1006-1903G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268240 | ||||||
| chr16:69268419
|
G | A | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-1724G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268419 | ||||||
| chr16:69268483
|
A | T | 36 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1006-1660A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268483 | ||||||
| chr16:69268590
|
C | T | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-1553C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268590 | ||||||
| chr16:69268662
|
C | T | 4 | a0001c0001t0007g0151a0001c0001t0007g0155a0001c0001t0007g0156others(1): Show | 4 | HG03927.hp1 NA18747.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-1481C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268662 | ||||||
| chr16:69268725
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006-1418C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268725 | ||||||
| chr16:69268820
|
G | A | 1 | a0001c0002t0018g0034 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1006-1323G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268820 | ||||||
| chr16:69268956
|
G | C | 16 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-1187G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268956 | ||||||
| chr16:69268995
|
C | T | 6 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006-1148C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69268995 | ||||||
| chr16:69269115
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1006-1028G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269115 | ||||||
| chr16:69269187
|
A | T | 2 | a0001c0001t0003g0102a0001c0001t0043g0088 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1006-956A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269187 | ||||||
| chr16:69269250
|
G | C | 2 | a0001c0002t0012g0202a0001c0002t0012g0203 | 2 | HG01346.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1006-893G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269250 | ||||||
| chr16:69269353
|
C | G | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-790C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269353 | ||||||
| chr16:69269431
|
T | C | 102 | a0001c0001t0001g0180a0001c0001t0005g0112a0001c0001t0005g0146others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1006-712T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269431 | ||||||
| chr16:69269468
|
G | A | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006-675G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269468 | ||||||
| chr16:69269515
|
GA | G | 8 | a0001c0001t0005g0112a0001c0001t0005g0208a0001c0001t0005g0210others(5): Show | 8 | HG01346.hp2 HG01361.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-617delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr16 | 69269515 | |||||
| chr16:69269578
|
G | C | 3 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072 | 3 | HG01433.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1006-565G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269578 | ||||||
| chr16:69269640
|
T | G | 1 | a0001c0002t0008g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1006-503T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269640 | ||||||
| chr16:69269750
|
C | A | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1006-393C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269750 | ||||||
| chr16:69269785
|
T | C | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-358T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269785 | ||||||
| chr16:69269968
|
C | A | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006-175C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69269968 | ||||||
| chr16:69270040
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006-103G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69270040 | ||||||
| chr16:69270043
|
A | G | 1 | a0001c0002t0004g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1006-100A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 3/6 | chr16 | 69270043 | ||||||
| chr16:69270339
|
A | G | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148+54A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69270339 | ||||||
| chr16:69270494
|
T | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | NA18950.hp1 NA18968.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1148+209T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69270494 | ||||||
| chr16:69270574
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1148+289T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69270574 | ||||||
| chr16:69270646
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1148+361G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69270646 | ||||||
| chr16:69270802
|
G | C | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1148+517G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69270802 | ||||||
| chr16:69270829
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1148+544T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69270829 | ||||||
| chr16:69270969
|
G | A | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1148+684G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69270969 | ||||||
| chr16:69271532
|
T | C | 7 | a0001c0002t0009g0003a0001c0002t0009g0005a0001c0002t0009g0006others(4): Show | 7 | HG00738.hp2 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148+1247T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69271532 | ||||||
| chr16:69271659
|
G | T | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1148+1374G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69271659 | ||||||
| chr16:69271776
|
A | C | 1 | a0001c0001t0006g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1148+1491A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69271776 | ||||||
| chr16:69271782
|
G | A | 1 | a0001c0001t0003g0090 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1148+1497G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69271782 | ||||||
| chr16:69271976
|
G | A | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1148+1691G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69271976 | ||||||
| chr16:69272011
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1148+1726A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272011 | ||||||
| chr16:69272135
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1148+1850T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272135 | ||||||
| chr16:69272196
|
G | T | 3 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072 | 3 | HG01433.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1148+1911G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272196 | ||||||
| chr16:69272432
|
C | T | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1148+2147C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272432 | ||||||
| chr16:69272502
|
G | A | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1148+2217G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272502 | ||||||
| chr16:69272521
|
C | T | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1148+2236C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272521 | ||||||
| chr16:69272539
|
C | CA | 17 | a0001c0001t0001g0163a0001c0001t0001g0189a0001c0001t0006g0049others(14): Show | 17 | HG02015.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1148+2273dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69272539 | |||||
| chr16:69272611
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0178 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1148+2326G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272611 | ||||||
| chr16:69272855
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1148+2570A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272855 | ||||||
| chr16:69272879
|
G | T | 1 | a0001c0001t0007g0197 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1148+2594G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69272879 | ||||||
| chr16:69272889
|
C | CA | 59 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0172others(56): Show | 59 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(56): Show |
intron_variant | MODIFIER | c.1148+2623dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69272889 | |||||
| chr16:69272889
|
C | CAA | 47 | a0001c0001t0002g0134a0001c0001t0006g0049a0001c0001t0006g0052others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1148+2622_1148+262 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69272889 | |||||
| chr16:69272889
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0015g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1148+2611_1148+262 others(17): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69272889 | |||||
| chr16:69273277
|
G | A | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1148+2992G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69273277 | ||||||
| chr16:69273295
|
A | G | 1 | a0001c0002t0014g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1148+3010A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69273295 | ||||||
| chr16:69273501
|
A | G | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1148+3216A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69273501 | ||||||
| chr16:69273605
|
T | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148+3320T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69273605 | ||||||
| chr16:69274096
|
G | T | 1 | a0001c0001t0002g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1148+3811G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274096 | ||||||
| chr16:69274196
|
C | T | 36 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1148+3911C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274196 | ||||||
| chr16:69274276
|
C | T | 3 | a0001c0001t0003g0086a0001c0001t0003g0092a0001c0001t0003g0097 | 3 | HG00735.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1148+3991C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274276 | ||||||
| chr16:69274311
|
C | CA | 17 | a0001c0001t0003g0076a0001c0001t0003g0104a0001c0001t0006g0049others(14): Show | 17 | HG01981.hp2 HG02055.hp2 HG02273.hp1 others(14): Show |
intron_variant | MODIFIER | c.1148+4041dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69274311 | |||||
| chr16:69274394
|
C | T | 3 | a0001c0001t0022g0195a0001c0001t0022g0196a0001c0001t0035g0194 | 3 | NA18973.hp2 NA19064.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1148+4109C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274394 | ||||||
| chr16:69274421
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1148+4136C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274421 | ||||||
| chr16:69274453
|
A | G | 1 | a0001c0001t0006g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1148+4168A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274453 | ||||||
| chr16:69274591
|
C | T | 2 | a0001c0002t0018g0036a0001c0002t0030g0035 | 2 | HG01496.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1148+4306C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274591 | ||||||
| chr16:69274652
|
C | CA | 23 | a0001c0001t0001g0207a0001c0001t0002g0098a0001c0001t0002g0132others(20): Show | 23 | HG00544.hp1 HG00544.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1148+4385dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69274652 | |||||
| chr16:69274915
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1148+4630C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69274915 | ||||||
| chr16:69275010
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1148+4725C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275010 | ||||||
| chr16:69275077
|
C | G | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1148+4792C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275077 | ||||||
| chr16:69275177
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1148+4892A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275177 | ||||||
| chr16:69275236
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1148+4951T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275236 | ||||||
| chr16:69275381
|
T | A | 2 | a0001c0002t0018g0036a0001c0002t0030g0035 | 2 | HG01496.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1148+5096T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275381 | ||||||
| chr16:69275528
|
G | C | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1148+5243G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275528 | ||||||
| chr16:69275568
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1148+5283G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275568 | ||||||
| chr16:69275643
|
A | G | 4 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0019g0041others(1): Show | 4 | HG00280.hp2 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+5358A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275643 | ||||||
| chr16:69275800
|
T | C | 6 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(3): Show | 6 | HG00621.hp1 HG02004.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+5515T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275800 | ||||||
| chr16:69275844
|
G | A | 1 | a0001c0002t0012g0205 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1148+5559G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275844 | ||||||
| chr16:69275954
|
C | T | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1148+5669C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69275954 | ||||||
| chr16:69276202
|
CA | C | 82 | a0001c0001t0002g0098a0001c0001t0002g0110a0001c0001t0002g0120others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1148+5931delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69276202 | |||||
| chr16:69276233
|
A | G | 8 | a0001c0001t0003g0086a0001c0001t0003g0092a0001c0001t0003g0093others(5): Show | 8 | HG00735.hp2 HG01169.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1148+5948A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69276233 | ||||||
| chr16:69276306
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0011g0168a0001c0001t0011g0169others(1): Show | 4 | HG02258.hp1 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+6021T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69276306 | ||||||
| chr16:69276328
|
G | C | 2 | a0001c0002t0028g0010a0001c0002t0029g0012 | 2 | HG01109.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1148+6043G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69276328 | ||||||
| chr16:69276456
|
G | A | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+6171G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69276456 | ||||||
| chr16:69276522
|
C | G | 2 | a0001c0002t0019g0041a0001c0002t0019g0042 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1148+6237C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69276522 | ||||||
| chr16:69276807
|
G | A | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1148+6522G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69276807 | ||||||
| chr16:69277136
|
G | A | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148+6851G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69277136 | ||||||
| chr16:69277200
|
A | G | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-6848A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69277200 | ||||||
| chr16:69277362
|
C | G | 2 | a0001c0002t0019g0041a0001c0002t0019g0042 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1149-6686C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69277362 | ||||||
| chr16:69277457
|
A | G | 1 | a0001c0001t0041g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1149-6591A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69277457 | ||||||
| chr16:69277603
|
G | A | 77 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1149-6445G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69277603 | ||||||
| chr16:69277608
|
G | C | 77 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1149-6440G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69277608 | ||||||
| chr16:69277781
|
A | T | 1 | a0001c0001t0003g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1149-6267A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69277781 | ||||||
| chr16:69278044
|
C | T | 1 | a0001c0002t0008g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1149-6004C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278044 | ||||||
| chr16:69278048
|
G | A | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-6000G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278048 | ||||||
| chr16:69278052
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1149-5996C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278052 | ||||||
| chr16:69278152
|
A | G | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1149-5896A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278152 | ||||||
| chr16:69278431
|
A | G | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-5617A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278431 | ||||||
| chr16:69278457
|
G | GT | 19 | a0001c0001t0001g0115a0001c0001t0002g0083a0001c0001t0002g0121others(16): Show | 19 | HG00597.hp2 HG00738.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1149-5575dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278457 | |||||
| chr16:69278457
|
GT | G | 22 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(19): Show | 22 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1149-5575delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278457 | |||||
| chr16:69278458
|
T | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-5590T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278458 | ||||||
| chr16:69278478
|
C | T | 5 | a0001c0001t0003g0076a0001c0002t0014g0070a0001c0002t0014g0071others(2): Show | 5 | HG01433.hp2 HG02273.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-5570C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278478 | ||||||
| chr16:69278479
|
G | A | 1 | a0001c0002t0015g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1149-5569G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278479 | ||||||
| chr16:69278627
|
T | C | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1149-5421T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278627 | ||||||
| chr16:69278802
|
G | C | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-5246G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278802 | ||||||
| chr16:69278811
|
G | A | 1 | a0001c0002t0032g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1149-5237G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278811 | ||||||
| chr16:69278837
|
C | T | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-5211C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278837 | ||||||
| chr16:69278889
|
A | AGT | 39 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0160others(36): Show | 39 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1149-5116_1149-511 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
A | AGTGT | 30 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0198others(27): Show | 30 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1149-5118_1149-511 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
A | AGTGTGT | 6 | a0001c0001t0046g0176a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG00621.hp1 HG01884.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-5120_1149-511 others(10): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0001g0179a0001c0001t0001g0201a0001c0001t0011g0168others(1): Show | 4 | HG02258.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-5122_1149-511 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGT | A | 18 | a0001c0001t0001g0103a0001c0001t0001g0135a0001c0001t0001g0138others(15): Show | 18 | HG00280.hp1 HG01884.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.1149-5116_1149-511 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGTGT | A | 47 | a0001c0001t0001g0116a0001c0001t0001g0129a0001c0001t0001g0180others(44): Show | 47 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1149-5118_1149-511 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGTGTGT | A | 15 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(12): Show | 15 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1149-5120_1149-511 others(10): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGTGTGTG others(1): Show |
A | 9 | a0001c0001t0006g0054a0001c0001t0006g0063a0001c0001t0016g0048others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149-5122_1149-511 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGTGTGTG others(3): Show |
A | 3 | a0001c0001t0011g0170a0001c0001t0013g0056a0001c0001t0013g0062 | 3 | HG02486.hp2 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1149-5124_1149-511 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0001a0001c0001t0006g0049 | 2 | HG02273.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1149-5126_1149-511 others(16): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGTGTGTG others(7): Show |
A | 2 | a0001c0002t0004g0038a0001c0002t0004g0039 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1149-5128_1149-511 others(18): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278889
|
AGTGTGTG others(21): Show |
A | 1 | a0001c0002t0004g0030 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1149-5142_1149-511 others(32): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69278889 | |||||
| chr16:69278962
|
G | A | 7 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(4): Show | 7 | HG00621.hp1 HG02004.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149-5086G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69278962 | ||||||
| chr16:69279515
|
C | CT | 40 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0162others(37): Show | 40 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1149-4505dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTT | 13 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0001g0174others(10): Show | 13 | HG00280.hp1 HG00738.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-4506_1149-450 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT | 6 | a0001c0001t0006g0060a0001c0001t0006g0063a0001c0001t0013g0062others(3): Show | 6 | HG02055.hp2 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149-4511_1149-450 others(11): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0006g0057a0001c0001t0006g0058a0001c0001t0006g0059others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149-4512_1149-450 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(3): Show |
5 | a0001c0002t0004g0038a0001c0002t0015g0064a0001c0002t0015g0065others(2): Show | 5 | HG02717.hp2 HG03486.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149-4514_1149-450 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(4): Show |
3 | a0001c0002t0004g0039a0001c0002t0017g0043a0001c0002t0019g0042 | 3 | HG00280.hp2 HG03491.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1149-4515_1149-450 others(15): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(5): Show |
8 | a0001c0002t0004g0040a0001c0002t0004g0045a0001c0002t0004g0046others(5): Show | 8 | HG01496.hp2 HG02602.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149-4516_1149-450 others(16): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(6): Show |
4 | a0001c0002t0004g0029a0001c0002t0004g0033a0001c0002t0004g0037others(1): Show | 4 | HG00735.hp1 HG01109.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-4517_1149-450 others(17): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(7): Show |
3 | a0001c0002t0004g0028a0001c0002t0004g0030a0001c0002t0029g0012 | 3 | HG01192.hp1 NA18998.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1149-4518_1149-450 others(18): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0004g0032 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1149-4519_1149-450 others(19): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
C | CTTTTTTT others(11): Show |
1 | a0001c0002t0024g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1149-4522_1149-450 others(22): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
CT | C | 22 | a0001c0001t0002g0098a0001c0001t0002g0120a0001c0001t0002g0127others(19): Show | 22 | HG00408.hp2 HG00544.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1149-4505delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279515
|
CTT | C | 5 | a0001c0002t0014g0071a0001c0002t0014g0072a0001c0002t0021g0074others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-4506_1149-450 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279515 | |||||
| chr16:69279550
|
G | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0122 | 2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1149-4498G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279550 | ||||||
| chr16:69279575
|
G | C | 1 | a0001c0002t0004g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1149-4473G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279575 | ||||||
| chr16:69279688
|
G | C | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-4360G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279688 | ||||||
| chr16:69279701
|
AT | A | 99 | a0001c0001t0002g0108a0001c0001t0005g0146a0001c0001t0005g0147others(96): Show | 99 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1149-4339delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279701 | |||||
| chr16:69279839
|
A | AT | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(183): Show | 186 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1149-4201dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279839 | |||||
| chr16:69279846
|
TTAA | T | 29 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1149-4200_1149-419 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279846 | |||||
| chr16:69279860
|
A | T | 10 | a0001c0001t0003g0100a0001c0001t0006g0057a0001c0001t0022g0196others(7): Show | 10 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1149-4188A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279860 | ||||||
| chr16:69279864
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(113): Show | 116 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.1149-4184A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279864 | ||||||
| chr16:69279868
|
A | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(176): Show | 179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1149-4180A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279868 | ||||||
| chr16:69279869
|
AT | A | 30 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1149-4176delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279869 | |||||
| chr16:69279874
|
T | A | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1149-4174T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279874 | ||||||
| chr16:69279878
|
T | A | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1149-4170T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279878 | ||||||
| chr16:69279884
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1149-4164G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279884 | ||||||
| chr16:69279967
|
TGAACAAA others(21): Show |
T | 1 | a0001c0001t0002g0118 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1149-4079_1149-405 others(32): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69279967 | |||||
| chr16:69279992
|
T | G | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1149-4056T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69279992 | ||||||
| chr16:69280202
|
A | C | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1149-3846A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280202 | ||||||
| chr16:69280234
|
A | C | 30 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1149-3814A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280234 | ||||||
| chr16:69280297
|
A | G | 1 | a0001c0002t0030g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1149-3751A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280297 | ||||||
| chr16:69280318
|
C | A | 1 | a0001c0001t0002g0083 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1149-3730C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280318 | ||||||
| chr16:69280464
|
G | A | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-3584G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280464 | ||||||
| chr16:69280516
|
T | C | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1149-3532T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280516 | ||||||
| chr16:69280528
|
CCGGGCGG others(10): Show |
C | 8 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0172others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149-3518_1149-350 others(21): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69280528 | |||||
| chr16:69280533
|
C | T | 3 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066 | 3 | HG02572.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1149-3515C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280533 | ||||||
| chr16:69280561
|
C | T | 1 | a0001c0001t0040g0105 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1149-3487C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280561 | ||||||
| chr16:69280579
|
G | A | 1 | a0001c0001t0005g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149-3469G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280579 | ||||||
| chr16:69280582
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1149-3466C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280582 | ||||||
| chr16:69280593
|
A | AC | 7 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(4): Show | 7 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-3449dupC | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69280593 | |||||
| chr16:69280615
|
G | C | 3 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072 | 3 | HG01433.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1149-3433G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280615 | ||||||
| chr16:69280727
|
A | AT | 3 | a0001c0003t0005g0209a0001c0003t0005g0214a0001c0003t0005g0215 | 3 | HG01346.hp2 HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1149-3317dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69280727 | |||||
| chr16:69280742
|
C | G | 1 | a0001c0002t0018g0034 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1149-3306C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280742 | ||||||
| chr16:69280783
|
G | A | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1149-3265G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280783 | ||||||
| chr16:69280802
|
C | CT | 6 | a0001c0001t0002g0128a0001c0002t0004g0022a0001c0002t0004g0023others(3): Show | 6 | HG01884.hp1 HG02015.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-3233dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69280802 | |||||
| chr16:69280802
|
C | CTTT | 22 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1149-3235_1149-323 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69280802 | |||||
| chr16:69280802
|
CT | C | 6 | a0001c0001t0002g0143a0001c0002t0012g0202a0001c0002t0012g0203others(3): Show | 6 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-3233delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69280802 | |||||
| chr16:69280823
|
A | T | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-3225A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280823 | ||||||
| chr16:69280843
|
G | C | 1 | a0001c0003t0005g0209 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1149-3205G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280843 | ||||||
| chr16:69280859
|
G | T | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1149-3189G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280859 | ||||||
| chr16:69280860
|
C | T | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1149-3188C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69280860 | ||||||
| chr16:69281062
|
T | C | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-2986T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281062 | ||||||
| chr16:69281075
|
A | G | 30 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1149-2973A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281075 | ||||||
| chr16:69281233
|
A | AT | 7 | a0001c0001t0002g0134a0001c0002t0004g0040a0001c0002t0014g0070others(4): Show | 7 | HG01433.hp2 HG02602.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-2800dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281233 | |||||
| chr16:69281233
|
AT | A | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-2800delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281233 | |||||
| chr16:69281336
|
A | C | 1 | a0001c0002t0004g0030 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1149-2712A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281336 | ||||||
| chr16:69281485
|
G | GT | 6 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149-2550dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281485 | |||||
| chr16:69281485
|
G | GTT | 19 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.1149-2551_1149-255 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281485 | |||||
| chr16:69281485
|
G | T | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1149-2563G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281485 | ||||||
| chr16:69281485
|
GT | G | 17 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0005g0171others(14): Show | 17 | HG01346.hp2 HG01361.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1149-2550delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281485 | |||||
| chr16:69281495
|
T | TG | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-2553_1149-255 others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281495 | ||||||
| chr16:69281496
|
T | G | 1 | a0001c0001t0003g0218 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1149-2552T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281496 | ||||||
| chr16:69281503
|
T | G | 1 | a0001c0002t0027g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1149-2545T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281503 | ||||||
| chr16:69281505
|
T | G | 23 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(20): Show | 23 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1149-2543T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281505 | ||||||
| chr16:69281588
|
C | T | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-2460C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281588 | ||||||
| chr16:69281744
|
AAGAC | A | 2 | a0001c0001t0003g0102a0001c0001t0043g0088 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1149-2301_1149-229 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281744 | |||||
| chr16:69281805
|
T | C | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1149-2243T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281805 | ||||||
| chr16:69281905
|
C | CT | 21 | a0001c0001t0001g0001a0001c0001t0002g0118a0001c0001t0002g0120others(18): Show | 21 | HG01243.hp2 HG01346.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1149-2126dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281905 | |||||
| chr16:69281905
|
C | CTT | 42 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1149-2127_1149-212 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281905 | |||||
| chr16:69281905
|
C | CTTT | 11 | a0001c0001t0006g0057a0001c0001t0039g0053a0001c0002t0004g0046others(8): Show | 11 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149-2128_1149-212 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69281905 | |||||
| chr16:69281908
|
T | C | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1149-2140T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281908 | ||||||
| chr16:69281933
|
C | T | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-2115C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69281933 | ||||||
| chr16:69282015
|
C | A | 1 | a0001c0001t0003g0099 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1149-2033C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69282015 | ||||||
| chr16:69282015
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-2033C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69282015 | ||||||
| chr16:69282209
|
C | A | 1 | a0001c0002t0004g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1149-1839C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69282209 | ||||||
| chr16:69282277
|
A | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-1771A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69282277 | ||||||
| chr16:69282306
|
C | CA | 16 | a0001c0001t0002g0133a0001c0002t0008g0015a0001c0002t0008g0016others(13): Show | 16 | HG00738.hp2 HG01346.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1149-1729dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69282306 | |||||
| chr16:69282353
|
G | A | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149-1695G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69282353 | ||||||
| chr16:69282673
|
CACCTAAA others(32): Show |
C | 71 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(68): Show | 71 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1149-1371_1149-133 others(43): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr16 | 69282673 | |||||
| chr16:69282738
|
A | G | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1149-1310A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69282738 | ||||||
| chr16:69283020
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1149-1028T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69283020 | ||||||
| chr16:69283087
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0096others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1149-961A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69283087 | ||||||
| chr16:69283431
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0002g0139 | 2 | HG01081.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1149-617C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69283431 | ||||||
| chr16:69283432
|
G | A | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-616G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69283432 | ||||||
| chr16:69283904
|
G | C | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1149-144G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 4/6 | chr16 | 69283904 | ||||||
| chr16:69284459
|
T | TA | 7 | a0001c0001t0001g0001a0001c0001t0002g0124a0001c0001t0002g0137others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345+248dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
T | TAAAAAA | 5 | a0001c0002t0014g0071a0001c0002t0014g0072a0001c0002t0021g0074others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+243_1345+248d others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
TA | T | 52 | a0001c0001t0001g0103a0001c0001t0001g0135a0001c0001t0001g0138others(49): Show | 52 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1345+248delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
TAA | T | 29 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0172others(26): Show | 29 | HG01169.hp2 HG01258.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.1345+247_1345+248d others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
TAAA | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0160others(27): Show | 30 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1345+246_1345+248d others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
TAAAA | T | 17 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG00735.hp1 HG01258.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1345+245_1345+248d others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
TAAAAA | T | 25 | a0001c0001t0006g0049a0001c0001t0006g0058a0001c0001t0006g0059others(22): Show | 25 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1345+244_1345+248d others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
TAAAAAA | T | 32 | a0001c0001t0013g0055a0001c0002t0004g0028a0001c0002t0004g0029others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1345+243_1345+248d others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284459
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0006g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1345+233_1345+248d others(18): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69284459 | |||||
| chr16:69284464
|
A | G | 13 | a0001c0001t0006g0054a0001c0001t0006g0057a0001c0001t0006g0061others(10): Show | 13 | HG00735.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1345+220A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69284464 | ||||||
| chr16:69284465
|
A | G | 20 | a0001c0001t0006g0049a0001c0001t0006g0058a0001c0001t0006g0059others(17): Show | 20 | HG00738.hp2 HG01884.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1345+221A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69284465 | ||||||
| chr16:69284466
|
A | G | 32 | a0001c0001t0013g0055a0001c0002t0004g0028a0001c0002t0004g0029others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1345+222A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69284466 | ||||||
| chr16:69284476
|
A | G | 1 | a0001c0001t0006g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1345+232A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69284476 | ||||||
| chr16:69284493
|
T | G | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1345+249T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69284493 | ||||||
| chr16:69285207
|
G | C | 1 | a0001c0002t0020g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1345+963G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69285207 | ||||||
| chr16:69285356
|
C | CT | 14 | a0001c0001t0001g0138a0001c0001t0001g0189a0001c0001t0002g0083others(11): Show | 14 | HG00544.hp2 HG01884.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1345+1131dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285356 | |||||
| chr16:69285356
|
CT | C | 12 | a0001c0001t0001g0183a0001c0001t0001g0198a0001c0001t0002g0130others(9): Show | 12 | HG01256.hp1 HG01256.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1345+1131delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285356 | |||||
| chr16:69285356
|
CTTTTTTT others(1): Show |
C | 64 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1345+1124_1345+113 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285356 | |||||
| chr16:69285453
|
C | CTATT | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0115others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1345+1248_1345+125 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285453 | |||||
| chr16:69285453
|
C | CTATTTAT others(1): Show |
10 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0167others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345+1244_1345+125 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285453 | |||||
| chr16:69285453
|
CTATT | C | 23 | a0001c0001t0005g0112a0001c0001t0005g0208a0001c0001t0005g0210others(20): Show | 23 | HG00738.hp2 HG01346.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1345+1248_1345+125 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285453 | |||||
| chr16:69285453
|
CTATTTAT others(1): Show |
C | 5 | a0001c0001t0002g0134a0001c0002t0014g0070a0001c0002t0014g0071others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+1244_1345+125 others(12): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285453 | |||||
| chr16:69285496
|
A | C | 3 | a0001c0002t0004g0046a0001c0002t0017g0043a0001c0002t0017g0044 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1345+1252A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69285496 | ||||||
| chr16:69285617
|
C | T | 19 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(16): Show | 19 | HG02055.hp2 HG02451.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1345+1373C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69285617 | ||||||
| chr16:69285658
|
A | AT | 8 | a0001c0001t0016g0048a0001c0001t0016g0050a0001c0001t0016g0051others(5): Show | 8 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345+1426dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285658 | |||||
| chr16:69285658
|
AT | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+1426delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69285658 | |||||
| chr16:69285684
|
C | A | 1 | a0001c0002t0024g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1345+1440C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69285684 | ||||||
| chr16:69285685
|
C | T | 2 | a0001c0001t0006g0057a0001c0001t0006g0060 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1345+1441C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69285685 | ||||||
| chr16:69285800
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0034g0161 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1345+1556T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69285800 | ||||||
| chr16:69285831
|
C | T | 31 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1345+1587C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69285831 | ||||||
| chr16:69286054
|
G | A | 6 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+1810G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286054 | ||||||
| chr16:69286090
|
T | C | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1345+1846T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286090 | ||||||
| chr16:69286102
|
C | T | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1345+1858C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286102 | ||||||
| chr16:69286114
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1345+1870G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286114 | ||||||
| chr16:69286227
|
A | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+1983A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286227 | ||||||
| chr16:69286500
|
G | A | 103 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1345+2256G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286500 | ||||||
| chr16:69286683
|
C | T | 4 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(1): Show | 4 | HG00621.hp1 NA18968.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+2439C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286683 | ||||||
| chr16:69286713
|
G | GA | 8 | a0001c0001t0002g0108a0001c0001t0002g0137a0001c0001t0003g0218others(5): Show | 8 | HG00735.hp1 HG02129.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345+2484dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69286713 | |||||
| chr16:69286713
|
GA | G | 12 | a0001c0001t0001g0179a0001c0002t0012g0202a0001c0002t0012g0203others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1345+2484delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69286713 | |||||
| chr16:69286915
|
C | T | 3 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066 | 3 | HG02572.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1345+2671C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69286915 | ||||||
| chr16:69287232
|
T | A | 1 | a0001c0002t0004g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1345+2988T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287232 | ||||||
| chr16:69287259
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+3015G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287259 | ||||||
| chr16:69287298
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1345+3054G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287298 | ||||||
| chr16:69287470
|
C | T | 14 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(11): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1345+3226C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287470 | ||||||
| chr16:69287523
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0011g0168a0001c0001t0011g0169others(1): Show | 4 | HG02258.hp1 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+3279T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287523 | ||||||
| chr16:69287530
|
A | C | 1 | a0001c0002t0037g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1345+3286A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287530 | ||||||
| chr16:69287633
|
AG | A | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1345+3391delG | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69287633 | |||||
| chr16:69287688
|
G | A | 3 | a0001c0001t0013g0055a0001c0001t0013g0056a0001c0001t0013g0062 | 3 | HG02486.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1345+3444G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287688 | ||||||
| chr16:69287863
|
A | AAT | 18 | a0001c0001t0001g0116a0001c0001t0001g0182a0001c0001t0001g0183others(15): Show | 18 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.1345+3636_1345+363 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69287863 | |||||
| chr16:69287865
|
T | A | 23 | a0001c0001t0002g0134a0001c0001t0006g0049a0001c0001t0006g0054others(20): Show | 23 | HG01433.hp2 HG02055.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1345+3621T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287865 | ||||||
| chr16:69287867
|
T | A | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+3623T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69287867 | ||||||
| chr16:69288014
|
G | GA | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+3780dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69288014 | |||||
| chr16:69288071
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1345+3827G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288071 | ||||||
| chr16:69288083
|
C | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+3839C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288083 | ||||||
| chr16:69288098
|
A | G | 2 | a0001c0002t0004g0037a0001c0002t0004g0040 | 2 | HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1345+3854A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288098 | ||||||
| chr16:69288123
|
G | A | 10 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154others(7): Show | 10 | HG00544.hp2 HG02602.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1345+3879G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288123 | ||||||
| chr16:69288307
|
G | C | 6 | a0001c0002t0004g0028a0001c0002t0004g0029a0001c0002t0004g0030others(3): Show | 6 | HG00621.hp1 HG02004.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+4063G>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288307 | ||||||
| chr16:69288515
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1345+4271T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288515 | ||||||
| chr16:69288679
|
T | C | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1345+4435T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288679 | ||||||
| chr16:69288684
|
T | C | 3 | a0001c0002t0009g0005a0001c0002t0009g0007a0001c0002t0009g0008 | 3 | HG02145.hp1 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1345+4440T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288684 | ||||||
| chr16:69288826
|
G | A | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+4582G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69288826 | ||||||
| chr16:69289045
|
G | A | 52 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1345+4801G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289045 | ||||||
| chr16:69289101
|
C | G | 1 | a0001c0001t0007g0154 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1345+4857C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289101 | ||||||
| chr16:69289173
|
G | A | 15 | a0001c0001t0001g0180a0001c0001t0005g0112a0001c0001t0005g0146others(12): Show | 15 | HG01346.hp2 HG01361.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1345+4929G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289173 | ||||||
| chr16:69289264
|
C | T | 14 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(11): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1345+5020C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289264 | ||||||
| chr16:69289269
|
C | CA | 80 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0005g0112others(77): Show | 80 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1345+5045dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69289269 | |||||
| chr16:69289269
|
C | CAA | 24 | a0001c0001t0005g0171a0001c0001t0005g0210a0001c0001t0006g0049others(21): Show | 24 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.1345+5044_1345+504 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69289269 | |||||
| chr16:69289345
|
G | A | 52 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1345+5101G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289345 | ||||||
| chr16:69289484
|
A | G | 30 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1345+5240A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289484 | ||||||
| chr16:69289556
|
T | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+5312T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289556 | ||||||
| chr16:69289766
|
T | A | 77 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1345+5522T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289766 | ||||||
| chr16:69289934
|
G | A | 78 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1345+5690G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69289934 | ||||||
| chr16:69290446
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+6202C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69290446 | ||||||
| chr16:69290590
|
TC | T | 30 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1345+6347delC | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69290590 | ||||||
| chr16:69291032
|
T | G | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+6788T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69291032 | ||||||
| chr16:69291042
|
G | A | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+6798G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69291042 | ||||||
| chr16:69291111
|
C | G | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345+6867C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69291111 | ||||||
| chr16:69291239
|
G | T | 102 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1345+6995G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69291239 | ||||||
| chr16:69291377
|
C | T | 29 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1345+7133C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69291377 | ||||||
| chr16:69291437
|
C | T | 5 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+7193C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69291437 | ||||||
| chr16:69291990
|
T | C | 93 | a0001c0001t0001g0180a0001c0001t0005g0112a0001c0001t0005g0146others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1346-7600T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69291990 | ||||||
| chr16:69292160
|
C | T | 4 | a0001c0001t0007g0151a0001c0001t0007g0155a0001c0001t0007g0156others(1): Show | 4 | HG03927.hp1 NA18747.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-7430C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292160 | ||||||
| chr16:69292225
|
A | G | 14 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(11): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1346-7365A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292225 | ||||||
| chr16:69292349
|
ATT | A | 9 | a0001c0001t0001g0200a0001c0001t0007g0151a0001c0001t0007g0155others(6): Show | 9 | HG00609.hp1 HG03041.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.1346-7236_1346-723 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292349 | |||||
| chr16:69292352
|
TTTTATAT others(3): Show |
T | 19 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(16): Show | 19 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1346-7236_1346-722 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292352 | |||||
| chr16:69292354
|
T | A | 76 | a0001c0001t0002g0120a0001c0001t0002g0122a0001c0001t0005g0112others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1346-7236T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292354 | ||||||
| chr16:69292354
|
TTA | T | 37 | a0001c0001t0001g0116a0001c0001t0001g0135a0001c0001t0001g0160others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.1346-7212_1346-721 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292354 | |||||
| chr16:69292354
|
TTATA | T | 4 | a0001c0001t0001g0162a0001c0001t0003g0085a0001c0001t0003g0089others(1): Show | 4 | HG01175.hp2 HG03669.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-7214_1346-721 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292354 | |||||
| chr16:69292358
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1346-7232A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292358 | ||||||
| chr16:69292360
|
ATATATAT others(23): Show |
A | 9 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0002g0108others(6): Show | 9 | HG00642.hp2 HG01496.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1346-7212_1346-718 others(34): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292360 | |||||
| chr16:69292362
|
ATATATAT others(21): Show |
A | 21 | a0001c0001t0001g0129a0001c0001t0002g0083a0001c0001t0002g0098others(18): Show | 21 | HG00544.hp1 HG01256.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1346-7171_1346-714 others(32): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292362 | |||||
| chr16:69292364
|
A | ATATAATA others(31): Show |
1 | a0001c0002t0015g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1346-7222_1346-722 others(42): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292364 | |||||
| chr16:69292364
|
ATATATAT others(19): Show |
A | 3 | a0001c0001t0001g0178a0001c0001t0002g0091a0001c0001t0002g0139 | 3 | HG01081.hp1 HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1346-7210_1346-718 others(30): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292364 | |||||
| chr16:69292365
|
TATA | T | 2 | a0001c0001t0007g0153a0001c0001t0007g0154 | 2 | HG00544.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1346-7224_1346-722 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292365 | ||||||
| chr16:69292366
|
AT | A | 4 | a0001c0001t0011g0168a0001c0001t0011g0169a0001c0001t0011g0170others(1): Show | 4 | HG02258.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-7223delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292366 | ||||||
| chr16:69292366
|
ATAT | A | 14 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(11): Show | 14 | HG01346.hp2 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1346-7223_1346-722 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292366 | ||||||
| chr16:69292366
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346-7223_1346-719 others(35): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292366 | ||||||
| chr16:69292367
|
T | A | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1346-7223T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292367 | ||||||
| chr16:69292367
|
T | TA | 44 | a0001c0001t0013g0055a0001c0001t0013g0056a0001c0001t0013g0062others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1346-7222dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292367 | |||||
| chr16:69292367
|
TATATATA others(48): Show |
T | 3 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072 | 3 | HG01433.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1346-7222_1346-716 others(59): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292367 | ||||||
| chr16:69292367
|
TATATATA others(50): Show |
T | 1 | a0003c0005t0033g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1346-7222_1346-716 others(61): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292367 | ||||||
| chr16:69292369
|
T | A | 40 | a0001c0001t0013g0055a0001c0001t0013g0056a0001c0001t0013g0062others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1346-7221T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292369 | ||||||
| chr16:69292369
|
T | TA | 5 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0018others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-7220dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292369 | |||||
| chr16:69292377
|
T | A | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1346-7213T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292377 | ||||||
| chr16:69292377
|
TATTATAT others(12): Show |
T | 4 | a0001c0001t0001g0163a0001c0001t0003g0081a0001c0001t0010g0142others(1): Show | 4 | HG00621.hp2 HG01993.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-7212_1346-719 others(23): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292377 | ||||||
| chr16:69292378
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1346-7212A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292378 | ||||||
| chr16:69292378
|
ATTATATA others(22): Show |
A | 1 | a0001c0001t0002g0134 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1346-7210_1346-718 others(33): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292378 | |||||
| chr16:69292379
|
T | A | 26 | a0001c0001t0001g0115a0001c0001t0001g0198a0001c0001t0006g0049others(23): Show | 26 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.1346-7211T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292379 | ||||||
| chr16:69292380
|
T | A | 28 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0172others(25): Show | 28 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1346-7210T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292380 | ||||||
| chr16:69292381
|
ATATATAT others(282): Show |
A | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1346-7207_1346-691 others(4): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292381 | |||||
| chr16:69292383
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1346-7199_1346-717 others(28): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292383 | |||||
| chr16:69292390
|
T | TTA | 5 | a0001c0001t0001g0198a0001c0001t0003g0086a0001c0001t0003g0092others(2): Show | 5 | HG00735.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-7184_1346-718 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292390 | |||||
| chr16:69292390
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0042g0144 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1346-7192_1346-718 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292390 | |||||
| chr16:69292390
|
TTA | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0190 | 2 | HG00642.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1346-7184_1346-718 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292390 | |||||
| chr16:69292390
|
TTATATAT others(40): Show |
T | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1346-7189_1346-714 others(51): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292390 | |||||
| chr16:69292391
|
T | A | 7 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(4): Show | 7 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1346-7199T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292391 | ||||||
| chr16:69292391
|
T | C | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-7199T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292391 | ||||||
| chr16:69292392
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0138 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1346-7185_1346-718 others(28): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292392 | |||||
| chr16:69292392
|
A | T | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-7198A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292392 | ||||||
| chr16:69292392
|
ATATATAT others(19): Show |
A | 11 | a0001c0001t0002g0127a0001c0001t0007g0151a0001c0001t0007g0153others(8): Show | 11 | HG00408.hp2 HG00544.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1346-7182_1346-715 others(30): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292392 | |||||
| chr16:69292394
|
ATATATAT others(6): Show |
A | 1 | a0001c0002t0009g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1346-7184_1346-717 others(17): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292394 | |||||
| chr16:69292394
|
ATATATAT others(17): Show |
A | 20 | a0001c0001t0001g0179a0001c0001t0003g0079a0001c0001t0003g0082others(17): Show | 20 | HG00099.hp2 HG00609.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1346-7182_1346-715 others(28): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292394 | |||||
| chr16:69292395
|
T | TATATATT others(41): Show |
2 | a0001c0002t0015g0064a0001c0002t0015g0066 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1346-7189_1346-718 others(52): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292395 | |||||
| chr16:69292396
|
ATATATAT others(15): Show |
A | 8 | a0001c0001t0003g0076a0001c0001t0003g0102a0001c0001t0003g0104others(5): Show | 8 | HG00597.hp2 HG01981.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1346-7182_1346-716 others(26): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292396 | |||||
| chr16:69292396
|
ATATATAT others(32): Show |
A | 1 | a0001c0001t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1346-7182_1346-714 others(43): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292396 | |||||
| chr16:69292398
|
ATATATAT others(13): Show |
A | 3 | a0001c0001t0011g0169a0001c0001t0011g0170a0001c0002t0004g0031 | 3 | HG02004.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1346-7182_1346-716 others(24): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292398 | |||||
| chr16:69292400
|
ATATATAT | A | 2 | a0001c0002t0004g0026a0001c0002t0019g0041 | 2 | NA18906.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1346-7182_1346-717 others(11): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292400 | |||||
| chr16:69292400
|
ATATATAT others(11): Show |
A | 8 | a0001c0002t0004g0029a0001c0002t0004g0030a0001c0002t0004g0032others(5): Show | 8 | HG00621.hp1 HG00735.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1346-7182_1346-716 others(22): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292400 | |||||
| chr16:69292402
|
A | AT | 9 | a0001c0001t0013g0056a0001c0001t0013g0062a0001c0002t0009g0003others(6): Show | 9 | HG00738.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346-7187dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292402 | |||||
| chr16:69292402
|
ATATAT | A | 6 | a0001c0001t0006g0049a0001c0001t0016g0048a0001c0001t0016g0050others(3): Show | 6 | HG00280.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-7182_1346-717 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292402 | |||||
| chr16:69292402
|
ATATATTA others(9): Show |
A | 4 | a0001c0001t0001g0160a0001c0002t0004g0028a0001c0002t0018g0036others(1): Show | 4 | HG01496.hp2 HG02818.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-7182_1346-716 others(20): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292402 | |||||
| chr16:69292403
|
TA | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-7186delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292403 | ||||||
| chr16:69292404
|
ATAT | A | 8 | a0001c0001t0006g0052a0001c0001t0006g0054a0001c0001t0006g0057others(5): Show | 8 | HG02055.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346-7182_1346-718 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292404 | |||||
| chr16:69292404
|
ATATTATA others(7): Show |
A | 4 | a0001c0002t0004g0025a0001c0002t0020g0011a0001c0002t0020g0013others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-7182_1346-716 others(18): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292404 | |||||
| chr16:69292404
|
ATATTATA others(24): Show |
A | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1346-7182_1346-715 others(35): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292404 | |||||
| chr16:69292405
|
TATTATAT others(16): Show |
T | 16 | a0001c0001t0001g0116a0001c0001t0001g0162a0001c0001t0001g0182others(13): Show | 16 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.1346-7184_1346-716 others(27): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292405 | ||||||
| chr16:69292406
|
A | T | 2 | a0001c0001t0002g0123a0001c0001t0039g0053 | 2 | HG03710.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346-7184A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292406 | ||||||
| chr16:69292406
|
AT | A | 25 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(22): Show | 25 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1346-7182delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292406 | |||||
| chr16:69292406
|
ATTATATA others(5): Show |
A | 6 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0038others(3): Show | 6 | HG01169.hp1 HG01192.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-7182_1346-717 others(16): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292406 | |||||
| chr16:69292406
|
ATTATATA others(22): Show |
A | 2 | a0001c0001t0001g0001a0001c0001t0001g0115 | 2 | HG02273.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1346-7182_1346-715 others(33): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292406 | |||||
| chr16:69292407
|
T | A | 3 | a0001c0001t0002g0123a0001c0001t0039g0053a0001c0002t0015g0065 | 3 | HG03710.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346-7183T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292407 | ||||||
| chr16:69292407
|
T | TA | 3 | a0001c0001t0013g0055a0001c0001t0013g0056a0001c0001t0013g0062 | 3 | HG02486.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1346-7183_1346-718 others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292407 | ||||||
| chr16:69292407
|
T | TATATAAT others(12): Show |
1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1346-7183_1346-718 others(23): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292407 | ||||||
| chr16:69292407
|
T | TTATA | 6 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-7175_1346-717 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292407 | |||||
| chr16:69292407
|
TTATATAT others(3): Show |
T | 7 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0002t0004g0022others(4): Show | 7 | HG01109.hp1 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1346-7181_1346-717 others(14): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292407 | |||||
| chr16:69292407
|
TTATATAT others(20): Show |
T | 8 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0172others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1346-7181_1346-715 others(31): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292407 | |||||
| chr16:69292408
|
T | A | 6 | a0001c0001t0001g0178a0001c0001t0001g0198a0001c0001t0002g0136others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-7182T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292408 | ||||||
| chr16:69292412
|
TATATATT others(18): Show |
T | 13 | a0001c0001t0005g0112a0001c0001t0005g0146a0001c0001t0005g0147others(10): Show | 13 | HG01346.hp2 HG01361.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1346-7177_1346-715 others(29): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292412 | ||||||
| chr16:69292415
|
ATAT | A | 4 | a0001c0001t0001g0163a0001c0001t0003g0081a0001c0001t0010g0142others(1): Show | 4 | HG00621.hp2 HG01993.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-7171_1346-716 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292415 | |||||
| chr16:69292417
|
AT | A | 6 | a0001c0001t0001g0201a0001c0001t0006g0059a0001c0002t0004g0026others(3): Show | 6 | HG00280.hp2 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-7171delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292417 | |||||
| chr16:69292418
|
T | A | 7 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0002t0004g0022others(4): Show | 7 | HG01109.hp1 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1346-7172T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292418 | ||||||
| chr16:69292418
|
T | TA | 6 | a0001c0001t0013g0055a0001c0001t0013g0056a0001c0001t0013g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-7172_1346-717 others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292418 | ||||||
| chr16:69292419
|
T | A | 12 | a0001c0001t0002g0111a0001c0001t0006g0049a0001c0001t0006g0052others(9): Show | 12 | HG01175.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1346-7171T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292419 | ||||||
| chr16:69292420
|
A | T | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1346-7170A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292420 | ||||||
| chr16:69292421
|
TATATATA others(20): Show |
T | 1 | a0001c0001t0002g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1346-7168_1346-714 others(31): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292421 | ||||||
| chr16:69292424
|
ATATATAT others(4): Show |
A | 11 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1346-7154_1346-714 others(15): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292424 | |||||
| chr16:69292428
|
AT | A | 3 | a0001c0001t0006g0059a0001c0001t0013g0055a0001c0001t0039g0053 | 3 | HG02723.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1346-7161delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292428 | ||||||
| chr16:69292429
|
T | TA | 2 | a0001c0001t0013g0056a0001c0001t0013g0062 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1346-7160dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292429 | |||||
| chr16:69292430
|
A | ATAT | 2 | a0001c0001t0001g0186a0001c0001t0001g0190 | 2 | HG00642.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1346-7159_1346-715 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292430 | |||||
| chr16:69292430
|
ATATAT | A | 5 | a0001c0001t0001g0002a0001c0002t0012g0202a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01517.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-7154_1346-715 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292430 | |||||
| chr16:69292434
|
A | T | 14 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(11): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1346-7156A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292434 | ||||||
| chr16:69292434
|
AT | A | 93 | a0001c0001t0001g0116a0001c0001t0001g0160a0001c0001t0001g0162others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1346-7154delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292434 | |||||
| chr16:69292435
|
T | A | 22 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0172others(19): Show | 22 | HG00738.hp2 HG01891.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1346-7155T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292435 | ||||||
| chr16:69292435
|
T | TA | 5 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0190others(2): Show | 5 | HG00642.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-7155_1346-715 others(5): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292435 | ||||||
| chr16:69292435
|
T | TATA | 2 | a0001c0001t0001g0198a0001c0001t0034g0161 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1346-7155_1346-715 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292435 | ||||||
| chr16:69292435
|
T | TATATA | 3 | a0001c0001t0003g0086a0001c0001t0003g0092a0001c0001t0003g0097 | 3 | HG00735.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1346-7155_1346-715 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292435 | ||||||
| chr16:69292435
|
T | TATATATA others(2): Show |
3 | a0001c0001t0042g0144a0001c0002t0015g0065a0001c0002t0038g0069 | 3 | HG06807.hp1 NA18522.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1346-7155_1346-715 others(13): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292435 | ||||||
| chr16:69292435
|
T | TATATATT others(36): Show |
1 | a0001c0001t0001g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1346-7155_1346-715 others(47): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292435 | ||||||
| chr16:69292436
|
T | A | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346-7154T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292436 | ||||||
| chr16:69292437
|
A | T | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346-7153A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292437 | ||||||
| chr16:69292446
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1346-7144T>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292446 | ||||||
| chr16:69292608
|
A | AT | 68 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0001g0129others(65): Show | 68 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1346-6966dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292608 | |||||
| chr16:69292608
|
A | ATT | 14 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0191others(11): Show | 14 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.1346-6967_1346-696 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292608 | |||||
| chr16:69292608
|
AT | A | 10 | a0001c0001t0005g0112a0001c0001t0005g0208a0001c0001t0005g0210others(7): Show | 10 | HG01346.hp2 HG01361.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1346-6966delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69292608 | |||||
| chr16:69292622
|
T | G | 8 | a0001c0001t0005g0112a0001c0001t0005g0208a0001c0001t0005g0210others(5): Show | 8 | HG01346.hp2 HG01361.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.1346-6968T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292622 | ||||||
| chr16:69292676
|
C | T | 1 | a0001c0001t0005g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1346-6914C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292676 | ||||||
| chr16:69292744
|
C | T | 29 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1346-6846C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292744 | ||||||
| chr16:69292785
|
G | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-6805G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292785 | ||||||
| chr16:69292892
|
C | T | 1 | a0001c0001t0006g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1346-6698C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292892 | ||||||
| chr16:69292989
|
G | A | 1 | a0001c0001t0031g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346-6601G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69292989 | ||||||
| chr16:69293043
|
A | G | 17 | a0001c0001t0001g0116a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1346-6547A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69293043 | ||||||
| chr16:69293118
|
A | G | 1 | a0001c0002t0038g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1346-6472A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69293118 | ||||||
| chr16:69293445
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1346-6145G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69293445 | ||||||
| chr16:69293768
|
A | G | 4 | a0001c0001t0011g0168a0001c0001t0011g0169a0001c0001t0011g0170others(1): Show | 4 | HG02258.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-5822A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69293768 | ||||||
| chr16:69294126
|
T | G | 30 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0024others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1346-5464T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69294126 | ||||||
| chr16:69294539
|
T | C | 163 | a0001c0001t0001g0116a0001c0001t0001g0162a0001c0001t0001g0163others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1346-5051T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69294539 | ||||||
| chr16:69294599
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1346-4991G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69294599 | ||||||
| chr16:69294642
|
A | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-4948A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69294642 | ||||||
| chr16:69294818
|
A | AT | 11 | a0001c0001t0001g0103a0001c0001t0001g0167a0001c0001t0001g0198others(8): Show | 11 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1346-4758dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69294818 | |||||
| chr16:69294872
|
G | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-4718G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69294872 | ||||||
| chr16:69294929
|
C | T | 14 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(11): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1346-4661C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69294929 | ||||||
| chr16:69295107
|
C | T | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-4483C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69295107 | ||||||
| chr16:69295230
|
A | AT | 26 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0001g0172others(23): Show | 26 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1346-4329dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295230
|
A | ATT | 9 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0179others(6): Show | 9 | HG00544.hp1 HG02027.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1346-4330_1346-432 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295230
|
AT | A | 9 | a0001c0001t0001g0198a0001c0001t0002g0126a0001c0001t0002g0130others(6): Show | 9 | HG01169.hp2 HG01256.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346-4329delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295230
|
ATTT | A | 12 | a0001c0001t0005g0208a0001c0001t0006g0052a0001c0001t0006g0057others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1346-4331_1346-432 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295230
|
ATTTT | A | 21 | a0001c0001t0005g0112a0001c0001t0005g0210a0001c0001t0005g0211others(18): Show | 21 | HG01169.hp1 HG01346.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.1346-4332_1346-432 others(8): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295230
|
ATTTTT | A | 23 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(20): Show | 23 | HG00738.hp2 HG01243.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1346-4333_1346-432 others(9): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295230
|
ATTTTTT | A | 26 | a0001c0001t0002g0120a0001c0002t0004g0022a0001c0002t0004g0024others(23): Show | 26 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1346-4334_1346-432 others(10): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295230
|
ATTTTTTT | A | 9 | a0001c0001t0001g0138a0001c0002t0004g0023a0001c0002t0014g0070others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346-4335_1346-432 others(11): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69295230 | |||||
| chr16:69295365
|
T | G | 69 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1346-4225T>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69295365 | ||||||
| chr16:69295493
|
C | T | 1 | a0001c0001t0013g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1346-4097C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69295493 | ||||||
| chr16:69295687
|
G | A | 75 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1346-3903G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69295687 | ||||||
| chr16:69295920
|
G | A | 4 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(1): Show | 4 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-3670G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69295920 | ||||||
| chr16:69296003
|
G | A | 14 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(11): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1346-3587G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296003 | ||||||
| chr16:69296276
|
G | A | 6 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-3314G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296276 | ||||||
| chr16:69296290
|
A | AT | 4 | a0001c0001t0006g0049a0001c0001t0016g0048a0001c0001t0016g0050others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-3292dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69296290 | |||||
| chr16:69296290
|
A | T | 1 | a0001c0002t0004g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1346-3300A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296290 | ||||||
| chr16:69296299
|
A | T | 14 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(11): Show | 14 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1346-3291A>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296299 | ||||||
| chr16:69296521
|
G | A | 64 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1346-3069G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296521 | ||||||
| chr16:69296659
|
T | C | 6 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(3): Show | 6 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-2931T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296659 | ||||||
| chr16:69296661
|
G | T | 3 | a0001c0003t0005g0209a0001c0003t0005g0214a0001c0003t0005g0215 | 3 | HG01346.hp2 HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1346-2929G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296661 | ||||||
| chr16:69296719
|
C | CA | 8 | a0001c0001t0001g0163a0001c0001t0002g0134a0001c0002t0009g0003others(5): Show | 8 | HG00738.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1346-2857dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69296719 | |||||
| chr16:69296719
|
CA | C | 6 | a0001c0001t0001g0183a0001c0002t0012g0202a0001c0002t0012g0203others(3): Show | 6 | HG01243.hp2 HG01256.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-2857delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69296719 | |||||
| chr16:69296734
|
G | T | 4 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(1): Show | 4 | HG02572.hp2 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-2856G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296734 | ||||||
| chr16:69296735
|
A | C | 4 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(1): Show | 4 | HG02572.hp2 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-2855A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296735 | ||||||
| chr16:69296738
|
A | G | 5 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0018others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-2852A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69296738 | ||||||
| chr16:69297103
|
A | G | 76 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1346-2487A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69297103 | ||||||
| chr16:69297173
|
G | A | 2 | a0001c0002t0023g0067a0001c0002t0023g0068 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1346-2417G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69297173 | ||||||
| chr16:69297306
|
C | CA | 5 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(2): Show | 5 | HG01361.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-2256dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69297306 | |||||
| chr16:69297306
|
CA | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0096a0001c0001t0001g0116others(112): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1346-2256delA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69297306 | |||||
| chr16:69297306
|
CAA | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0135others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1346-2257_1346-225 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69297306 | |||||
| chr16:69297306
|
CAAA | C | 25 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(22): Show | 25 | HG01346.hp1 HG01433.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.1346-2258_1346-225 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69297306 | |||||
| chr16:69297306
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1346-2267_1346-225 others(16): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69297306 | |||||
| chr16:69297342
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1346-2248G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69297342 | ||||||
| chr16:69297391
|
G | A | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1346-2199G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69297391 | ||||||
| chr16:69297485
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1346-2105G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69297485 | ||||||
| chr16:69297535
|
T | C | 1 | a0001c0001t0039g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1346-2055T>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69297535 | ||||||
| chr16:69297616
|
C | CA | 77 | a0001c0001t0001g0178a0001c0001t0006g0049a0001c0001t0006g0052others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1346-1963dupA | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69297616 | |||||
| chr16:69297973
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1346-1617C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69297973 | ||||||
| chr16:69298012
|
C | A | 3 | a0001c0001t0007g0151a0001c0001t0007g0156a0001c0001t0007g0157 | 3 | HG03927.hp1 NA18747.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1346-1578C>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298012 | ||||||
| chr16:69298512
|
C | CT | 27 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0001g0174others(24): Show | 27 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1346-1052dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69298512 | |||||
| chr16:69298512
|
C | CTT | 34 | a0001c0001t0006g0049a0001c0001t0006g0057a0001c0001t0006g0058others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1346-1053_1346-105 others(6): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69298512 | |||||
| chr16:69298512
|
C | CTTT | 13 | a0001c0001t0006g0052a0001c0001t0006g0054a0001c0001t0013g0055others(10): Show | 13 | HG00621.hp1 HG01109.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1346-1054_1346-105 others(7): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69298512 | |||||
| chr16:69298512
|
CT | C | 20 | a0001c0001t0003g0093a0001c0001t0005g0112a0001c0001t0005g0146others(17): Show | 20 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1346-1052delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69298512 | |||||
| chr16:69298512
|
CTTTTTT | C | 11 | a0001c0002t0008g0015a0001c0002t0008g0018a0001c0002t0008g0020others(8): Show | 11 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1346-1057_1346-105 others(10): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69298512 | |||||
| chr16:69298606
|
C | G | 1 | a0001c0002t0026g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1346-984C>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298606 | ||||||
| chr16:69298711
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1346-879G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298711 | ||||||
| chr16:69298734
|
C | T | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1346-856C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298734 | ||||||
| chr16:69298736
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1346-854A>G | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298736 | ||||||
| chr16:69298760
|
G | A | 5 | a0001c0002t0014g0070a0001c0002t0014g0071a0001c0002t0014g0072others(2): Show | 5 | HG01433.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-830G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298760 | ||||||
| chr16:69298777
|
C | T | 2 | a0001c0001t0003g0102a0001c0001t0043g0088 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1346-813C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298777 | ||||||
| chr16:69298792
|
G | T | 13 | a0001c0002t0008g0015a0001c0002t0008g0016a0001c0002t0008g0017others(10): Show | 13 | HG00738.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1346-798G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298792 | ||||||
| chr16:69298967
|
A | C | 20 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(17): Show | 20 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1346-623A>C | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69298967 | ||||||
| chr16:69299035
|
C | T | 4 | a0001c0002t0015g0064a0001c0002t0015g0065a0001c0002t0015g0066others(1): Show | 4 | HG02572.hp2 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-555C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69299035 | ||||||
| chr16:69299146
|
C | CT | 11 | a0001c0001t0011g0177a0001c0001t0016g0048a0001c0001t0016g0050others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1346-428dupT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr16 | 69299146 | |||||
| chr16:69299213
|
G | T | 5 | a0001c0001t0005g0146a0001c0001t0005g0147a0001c0001t0005g0148others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-377G>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69299213 | ||||||
| chr16:69299383
|
C | T | 5 | a0001c0002t0012g0202a0001c0002t0012g0203a0001c0002t0012g0205others(2): Show | 5 | HG01243.hp2 HG01346.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-207C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69299383 | ||||||
| chr16:69299390
|
C | T | 2 | a0001c0002t0021g0074a0001c0002t0021g0075 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1346-200C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 5/6 | chr16 | 69299390 | ||||||
| chr16:69299966
|
C | T | 1 | a0001c0001t0010g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1530+192C>T | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 6/6 | chr16 | 69299966 | ||||||
| chr16:69300019
|
G | A | 1 | a0001c0002t0018g0036 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1530+245G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 6/6 | chr16 | 69300019 | ||||||
| chr16:69300063
|
AT | A | 76 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1530+295delT | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr16 | 69300063 | |||||
| chr16:69300274
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1530+500G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 6/6 | chr16 | 69300274 | ||||||
| chr16:69300307
|
G | A | 1 | a0001c0001t0025g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1531-525G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 6/6 | chr16 | 69300307 | ||||||
| chr16:69300376
|
G | A | 61 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1531-456G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 6/6 | chr16 | 69300376 | ||||||
| chr16:69300398
|
G | A | 48 | a0001c0001t0006g0049a0001c0001t0006g0052a0001c0001t0006g0054others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1531-434G>A | SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 6/6 | chr16 | 69300398 |