Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2888 |
|---|---|
| ensemblid | ENSG00000115290.11 |
| hgncid | 4565 |
| symbol | GRB14 |
| name | growth factor receptor bound protein 14 |
| refseq_nuc | NM_004490.3 |
| refseq_prot | NP_004481.2 |
| ensembl_nuc | ENST00000263915.8 |
| ensembl_prot | ENSP00000263915.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 164492417 |
| end | 164621482 |
| strand | - |
| ver | v1.2 |
| region | chr2:164492417-164621482 |
| region5000 | chr2:164487417-164626482 |
| regionname0 | GRB14_chr2_164492417_164621482 |
| regionname5000 | GRB14_chr2_164487417_164626482 |
| 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 | 154 | 72 | 21 | 48 | 4 | 7 | 34 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0002 | 0/0 | 540 | 132 | 8 | 38 | 57 | 7 | 22 | 43 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0003 | 0/0 | 540 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0004 | 0/0 | 540 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0005 | 0/0 | 540 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0006 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0007 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0008 | 0/0 | 540 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0009 | 0/0 | 540 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| 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 | 1/1 | 1623 | 149 | 72 | 20 | 46 | 3 | 6 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0002 | 0/0 | 1623 | 132 | 8 | 38 | 57 | 7 | 22 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0003 | 0/0 | 1623 | 2 | 0 | 0 | 1 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0004 | 0/0 | 1623 | 2 | 0 | 1 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0005 | 0/0 | 1623 | 2 | 0 | 1 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0006 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0007 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0008 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0009 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0010 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0011 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| c0012 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 793 | 93 | 42 | 10 | 33 | 1 | 5 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0002 | 0/0 | 790 | 68 | 0 | 19 | 34 | 4 | 11 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0003 | 0/0 | 793 | 48 | 5 | 10 | 24 | 1 | 8 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0004 | 0/0 | 790 | 29 | 11 | 4 | 9 | 2 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0005 | 0/0 | 793 | 18 | 3 | 9 | 0 | 3 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0006 | 0/0 | 793 | 14 | 7 | 2 | 4 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0007 | 0/0 | 793 | 9 | 7 | 1 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0008 | 0/0 | 793 | 5 | 2 | 2 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0009 | 0/0 | 790 | 3 | 3 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0010 | 0/0 | 790 | 3 | 0 | 2 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0011 | 0/0 | 790 | 2 | 1 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0012 | 0/0 | 793 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| t0013 | 0/0 | 790 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| 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 | 1/1 | 1623 | 149 | 72 | 20 | 46 | 3 | 6 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0003 | 0/0 | 1623 | 2 | 0 | 0 | 1 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0005 | 0/0 | 1623 | 2 | 0 | 1 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0012 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0002c0002 | 0/0 | 1623 | 132 | 8 | 38 | 57 | 7 | 22 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0003c0004 | 0/0 | 1623 | 2 | 0 | 1 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0004c0006 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0005c0010 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0006c0011 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0007c0008 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0008c0007 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0009c0009 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2415 | 89 | 42 | 10 | 32 | 0 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0001t0004 | 0/0 | 2412 | 29 | 11 | 4 | 9 | 2 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0001t0006 | 0/0 | 2415 | 14 | 7 | 2 | 4 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0001t0007 | 0/0 | 2415 | 6 | 6 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0001t0008 | 0/0 | 2415 | 3 | 2 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0001t0009 | 0/0 | 2412 | 3 | 3 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0001t0010 | 0/0 | 2412 | 3 | 0 | 2 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0001t0011 | 0/0 | 2412 | 2 | 1 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0003t0001 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0003t0007 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0005t0001 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0005t0007 | 0/0 | 2415 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0001c0012t0001 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0002c0002t0002 | 0/0 | 2412 | 68 | 0 | 19 | 34 | 4 | 11 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0002c0002t0003 | 0/0 | 2415 | 47 | 5 | 10 | 23 | 1 | 8 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0002c0002t0005 | 0/0 | 2415 | 17 | 3 | 9 | 0 | 2 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0003c0004t0008 | 0/0 | 2415 | 2 | 0 | 1 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0004c0006t0001 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0005c0010t0012 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0006c0011t0007 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0007c0008t0013 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0008c0007t0003 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| a0009c0009t0005 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | copy fasta | chr2 | 164487417 | 164626482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0010g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0011g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0003t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0005t0007g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0012t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0003c0004t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0003c0004t0008g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0004c0006t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0005c0010t0012g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0006c0011t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0007c0008t0013g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0008c0007t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0009c0009t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0276 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0051 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0256 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0198 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00609 | hp1 | a0001 | c0003 | t0007 | g0042 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00639 | hp1 | a0001 | c0005 | t0007 | g0047 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0281 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0260 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00642 | hp2 | a0002 | c0002 | t0005 | g0264 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0155 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0090 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0233 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0234 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0232 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0231 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0258 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01099 | hp1 | a0003 | c0004 | t0008 | g0142 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0243 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01169 | hp2 | a0002 | c0002 | t0005 | g0238 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0140 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0247 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0163 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01257 | hp1 | a0002 | c0002 | t0005 | g0275 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01257 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01258 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0164 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0171 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01346 | hp1 | a0002 | c0002 | t0005 | g0222 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0184 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0143 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0152 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0173 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01516 | hp1 | a0002 | c0002 | t0005 | g0167 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01516 | hp2 | a0002 | c0002 | t0003 | g0240 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0175 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01517 | hp2 | a0002 | c0002 | t0005 | g0181 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01884 | hp2 | a0002 | c0002 | t0005 | g0282 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01928 | hp1 | a0002 | c0002 | t0005 | g0245 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0248 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0253 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0251 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0283 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01975 | hp2 | a0002 | c0002 | t0005 | g0285 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0252 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01993 | hp2 | a0002 | c0002 | t0005 | g0265 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0250 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02056 | hp1 | a0002 | c0002 | t0003 | g0205 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0170 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02080 | hp2 | a0002 | c0002 | t0003 | g0261 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0206 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0267 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02148 | hp2 | a0002 | c0002 | t0005 | g0263 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | CDX | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | CDX | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02273 | hp1 | a0002 | c0002 | t0005 | g0278 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0279 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02293 | hp1 | a0002 | c0002 | t0003 | g0266 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0255 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0087 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0189 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0160 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02647 | hp1 | a0007 | c0008 | t0013 | g0216 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0149 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0172 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0218 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0229 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02922 | hp1 | a0002 | c0002 | t0005 | g0201 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02970 | hp1 | a0002 | c0002 | t0003 | g0202 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03017 | hp1 | a0002 | c0002 | t0005 | g0239 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0230 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0150 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0244 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0237 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03491 | hp1 | a0005 | c0010 | t0012 | g0011 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0292 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0289 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0272 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0120 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0286 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03654 | hp2 | a0003 | c0004 | t0008 | g0156 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0257 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0195 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0176 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0269 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03831 | hp2 | a0002 | c0002 | t0005 | g0193 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0254 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0168 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0273 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0079 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0284 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0074 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0290 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18940 | hp2 | a0008 | c0007 | t0003 | g0220 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18944 | hp1 | a0002 | c0002 | t0003 | g0190 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18945 | hp2 | a0002 | c0002 | t0003 | g0235 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18951 | hp1 | a0001 | c0012 | t0001 | g0139 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0219 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18970 | hp2 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18975 | hp1 | a0002 | c0002 | t0003 | g0249 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0208 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0178 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19001 | hp1 | a0002 | c0002 | t0003 | g0169 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19003 | hp2 | a0002 | c0002 | t0003 | g0287 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0241 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19030 | hp2 | a0006 | c0011 | t0007 | g0131 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0200 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19065 | hp1 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0194 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19079 | hp1 | a0002 | c0002 | t0003 | g0188 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19079 | hp2 | a0001 | c0001 | t0010 | g0147 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19081 | hp1 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0204 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19087 | hp2 | a0002 | c0002 | t0003 | g0185 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | ASW | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0101 | AFR | ASW | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20805 | hp1 | a0009 | c0009 | t0005 | g0288 | EUR | TSI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0026 | EUR | TSI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20905 | hp1 | a0002 | c0002 | t0005 | g0259 | SAS | GIH | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20905 | hp2 | a0004 | c0006 | t0001 | g0003 | SAS | GIH | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0274 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0119 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0082 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0203 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA21309 | hp1 | a0002 | c0002 | t0005 | g0162 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0058 | REF | REF | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0048 | REF | REF | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164497473
|
A | T | 1 | a0007 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1122T>A | p.Asn374Lys | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 10/14 | 1295/2415 | 1122/1623 | 374/540 | chr2 | 164497473 | ||
| chr2:164525008
|
A | G | 1 | a0008 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.674T>C | p.Leu225Ser | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/14 | 847/2415 | 674/1623 | 225/540 | chr2 | 164525008 | ||
| chr2:164525032
|
C | A | 2 | a0003a0009 | 3 | HG01099.hp1 HG03654.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.650G>T | p.Gly217Val | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/14 | 823/2415 | 650/1623 | 217/540 | chr2 | 164525032 | ||
| chr2:164547710
|
A | G | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.431T>C | p.Ile144Thr | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/14 | 604/2415 | 431/1623 | 144/540 | chr2 | 164547710 | ||
| chr2:164547749
|
C | T | 1 | a0005 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.392G>A | p.Arg131Gln | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/14 | 565/2415 | 392/1623 | 131/540 | chr2 | 164547749 | ||
| chr2:164619743
|
A | T | 4 | a0002a0007a0008others(1): Show | 135 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
missense_variant | MODERATE | c.268T>A | p.Phe90Ile | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/14 | 441/2415 | 268/1623 | 90/540 | chr2 | 164619743 | ||
| chr2:164621134
|
C | T | 1 | a0004 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.176G>A | p.Gly59Asp | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 349/2415 | 176/1623 | 59/540 | chr2 | 164621134 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164527056
|
A | G | 1 | a0001c0003 | 2 | HG00609.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.561T>C | p.Phe187Phe | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/14 | 734/2415 | 561/1623 | 187/540 | chr2 | 164527056 | ||
| chr2:164527116
|
G | A | 1 | a0001c0005 | 2 | HG00639.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.501C>T | p.His167His | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/14 | 674/2415 | 501/1623 | 167/540 | chr2 | 164527116 | ||
| chr2:164621238
|
G | A | 1 | a0001c0012 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.72C>T | p.Ala24Ala | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 245/2415 | 72/1623 | 24/540 | chr2 | 164621238 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164492493
|
G | A | 2 | a0001c0001t0009a0007c0008t0013 | 4 | HG02486.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 543 | chr2 | 164492493 | |||||
| chr2:164492538
|
C | T | 14 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(11): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*498G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 498 | chr2 | 164492538 | |||||
| chr2:164492539
|
G | A | 1 | a0005c0010t0012 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 497 | chr2 | 164492539 | |||||
| chr2:164492609
|
GTTA | G | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0010others(3): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*424_*426delTAA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 424 | chr2 | 164492609 | |||||
| chr2:164492630
|
A | G | 1 | a0001c0001t0011 | 2 | HG00735.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*406T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 406 | chr2 | 164492630 | |||||
| chr2:164492712
|
T | C | 14 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(11): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*324A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 324 | chr2 | 164492712 | |||||
| chr2:164492724
|
T | C | 1 | a0001c0001t0011 | 2 | HG00735.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 312 | chr2 | 164492724 | |||||
| chr2:164492949
|
G | A | 14 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(11): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*87C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 87 | chr2 | 164492949 | |||||
| chr2:164492953
|
T | C | 8 | a0001c0001t0007a0001c0001t0008a0001c0003t0007others(5): Show | 32 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*83A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 83 | chr2 | 164492953 | |||||
| chr2:164621326
|
G | A | 4 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(1): Show | 22 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-17C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 17 | chr2 | 164621326 | |||||
| chr2:164621393
|
G | C | 6 | a0002c0002t0002a0002c0002t0003a0002c0002t0005others(3): Show | 135 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 84 | chr2 | 164621393 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164493258
|
T | C | 1 | a0002c0002t0003g0229 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1477-76A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493258 | ||||||
| chr2:164493330
|
GT | G | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1477-149delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493330 | ||||||
| chr2:164493352
|
T | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0055others(24): Show | 27 | HG01261.hp2 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1477-170A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493352 | ||||||
| chr2:164493392
|
C | T | 145 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0102others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1477-210G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493392 | ||||||
| chr2:164493424
|
TTC | T | 21 | a0001c0001t0007g0082a0001c0001t0007g0091a0001c0001t0007g0134others(18): Show | 21 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1477-244_1477-243d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493424 | ||||||
| chr2:164493492
|
T | C | 28 | a0001c0001t0007g0082a0001c0001t0007g0091a0001c0001t0007g0113others(25): Show | 28 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1477-310A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493492 | ||||||
| chr2:164493783
|
G | A | 4 | a0001c0001t0009g0111a0001c0001t0009g0119a0001c0001t0009g0120others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-601C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493783 | ||||||
| chr2:164493791
|
A | AATT | 21 | a0001c0001t0007g0082a0001c0001t0007g0091a0001c0001t0007g0134others(18): Show | 21 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1477-612_1477-610d others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493791 | ||||||
| chr2:164493915
|
G | A | 4 | a0001c0001t0001g0070a0002c0002t0003g0204a0002c0002t0003g0212others(1): Show | 4 | NA18941.hp2 NA18954.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+516C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493915 | ||||||
| chr2:164494050
|
C | T | 32 | a0001c0001t0007g0082a0001c0001t0007g0091a0001c0001t0007g0101others(29): Show | 32 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1476+381G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164494050 | ||||||
| chr2:164494174
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1476+257G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164494174 | ||||||
| chr2:164494401
|
T | C | 7 | a0001c0001t0007g0113a0001c0001t0008g0149a0001c0001t0008g0150others(4): Show | 7 | HG01169.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476+30A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164494401 | ||||||
| chr2:164494678
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1383-154T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494678 | ||||||
| chr2:164494698
|
C | T | 142 | a0001c0001t0001g0094a0001c0001t0001g0102a0001c0001t0001g0107others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1383-174G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494698 | ||||||
| chr2:164494720
|
C | T | 1 | a0007c0008t0013g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1383-196G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494720 | ||||||
| chr2:164494953
|
AT | A | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-430delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494953 | ||||||
| chr2:164495028
|
G | A | 1 | a0001c0001t0011g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1383-504C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495028 | ||||||
| chr2:164495230
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135 | 3 | HG02257.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1383-706G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495230 | ||||||
| chr2:164495386
|
G | A | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-862C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495386 | ||||||
| chr2:164495401
|
TA | T | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-878delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495401 | ||||||
| chr2:164495445
|
G | T | 9 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0086others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1383-921C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495445 | ||||||
| chr2:164495591
|
C | T | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-1067G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495591 | ||||||
| chr2:164495655
|
C | T | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-1131G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495655 | ||||||
| chr2:164495895
|
G | A | 131 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 133 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1382+1113C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495895 | ||||||
| chr2:164496017
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1382+991G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496017 | ||||||
| chr2:164496030
|
T | A | 1 | a0001c0001t0004g0009 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1382+978A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496030 | ||||||
| chr2:164496035
|
T | A | 275 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1382+973A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496035 | ||||||
| chr2:164496066
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1382+942G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496066 | ||||||
| chr2:164496157
|
T | C | 62 | a0001c0001t0001g0138a0001c0001t0004g0004a0001c0001t0004g0012others(59): Show | 62 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1382+851A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496157 | ||||||
| chr2:164496198
|
T | C | 4 | a0001c0001t0009g0111a0001c0001t0009g0119a0001c0001t0009g0120others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+810A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496198 | ||||||
| chr2:164496621
|
CAT | C | 61 | a0001c0001t0004g0004a0001c0001t0004g0012a0001c0001t0004g0017others(58): Show | 61 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1382+385_1382+386d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496621 | ||||||
| chr2:164496648
|
C | T | 136 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 138 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1382+360G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496648 | ||||||
| chr2:164496779
|
C | T | 284 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1382+229G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496779 | ||||||
| chr2:164496813
|
A | G | 33 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0007g0082others(30): Show | 33 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1382+195T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496813 | ||||||
| chr2:164497202
|
C | T | 170 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1294+9G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 11/13 | chr2 | 164497202 | ||||||
| chr2:164497608
|
T | G | 6 | a0001c0001t0001g0056a0001c0001t0004g0112a0001c0001t0004g0127others(3): Show | 6 | HG01516.hp1 HG01517.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-118A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164497608 | ||||||
| chr2:164497999
|
T | C | 19 | a0001c0001t0007g0082a0001c0001t0007g0134a0001c0003t0007g0042others(16): Show | 19 | HG00609.hp1 HG00639.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1105-509A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164497999 | ||||||
| chr2:164498473
|
C | A | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1105-983G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498473 | ||||||
| chr2:164498499
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0114a0001c0001t0006g0145others(1): Show | 4 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105-1009T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498499 | ||||||
| chr2:164498597
|
A | C | 1 | a0001c0001t0008g0149 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1105-1107T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498597 | ||||||
| chr2:164498659
|
C | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(11): Show | 14 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1105-1169G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498659 | ||||||
| chr2:164498694
|
T | C | 1 | a0001c0001t0004g0127 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1105-1204A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498694 | ||||||
| chr2:164498955
|
G | C | 1 | a0001c0001t0001g0016 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1105-1465C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498955 | ||||||
| chr2:164499035
|
C | G | 1 | a0001c0001t0004g0041 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1105-1545G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499035 | ||||||
| chr2:164499236
|
T | G | 2 | a0001c0001t0004g0096a0008c0007t0003g0220 | 2 | HG02723.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1105-1746A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499236 | ||||||
| chr2:164499361
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1105-1871G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499361 | ||||||
| chr2:164499434
|
T | C | 68 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0069others(65): Show | 68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1105-1944A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499434 | ||||||
| chr2:164499609
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1105-2119G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499609 | ||||||
| chr2:164499833
|
A | G | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1105-2343T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499833 | ||||||
| chr2:164499842
|
C | A | 4 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0115others(1): Show | 4 | HG02109.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105-2352G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499842 | ||||||
| chr2:164499956
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1104+2299C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499956 | ||||||
| chr2:164500293
|
C | T | 1 | a0001c0001t0006g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1104+1962G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500293 | ||||||
| chr2:164500394
|
A | G | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1104+1861T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500394 | ||||||
| chr2:164500450
|
A | G | 14 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0107others(11): Show | 14 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1104+1805T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500450 | ||||||
| chr2:164500525
|
C | A | 2 | a0001c0001t0006g0141a0001c0001t0006g0151 | 2 | NA18974.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1104+1730G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500525 | ||||||
| chr2:164500626
|
A | G | 29 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0114others(26): Show | 30 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1104+1629T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500626 | ||||||
| chr2:164500837
|
C | A | 4 | a0002c0002t0002g0215a0002c0002t0002g0246a0002c0002t0002g0270others(1): Show | 4 | NA18951.hp2 NA18975.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104+1418G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500837 | ||||||
| chr2:164500843
|
A | G | 7 | a0001c0001t0004g0097a0001c0001t0004g0098a0001c0001t0004g0099others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1104+1412T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500843 | ||||||
| chr2:164501053
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0032 | 2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1104+1202A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164501053 | ||||||
| chr2:164501126
|
T | A | 4 | a0002c0002t0002g0215a0002c0002t0002g0246a0002c0002t0002g0270others(1): Show | 4 | NA18951.hp2 NA18975.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104+1129A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164501126 | ||||||
| chr2:164501184
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1104+1071A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164501184 | ||||||
| chr2:164502127
|
G | C | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1104+128C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164502127 | ||||||
| chr2:164502145
|
T | A | 30 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0094others(27): Show | 31 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1104+110A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164502145 | ||||||
| chr2:164502162
|
A | G | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1104+93T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164502162 | ||||||
| chr2:164502516
|
A | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1024-181T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502516 | ||||||
| chr2:164502532
|
T | C | 29 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0094others(26): Show | 30 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1024-197A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502532 | ||||||
| chr2:164502651
|
T | TA | 69 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0069others(66): Show | 69 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1024-317dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502651 | ||||||
| chr2:164502749
|
T | A | 1 | a0002c0002t0002g0221 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1024-414A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502749 | ||||||
| chr2:164503051
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1024-716A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503051 | ||||||
| chr2:164503169
|
T | TA | 32 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0061others(29): Show | 32 | HG00735.hp1 HG01123.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1024-835dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503169 | ||||||
| chr2:164503169
|
T | TAA | 63 | a0001c0001t0001g0033a0001c0001t0001g0069a0001c0001t0004g0004others(60): Show | 63 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1024-836_1024-835d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503169 | ||||||
| chr2:164503169
|
TA | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0055others(34): Show | 38 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1024-835delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503169 | ||||||
| chr2:164503183
|
A | AG | 4 | a0001c0001t0006g0154a0001c0001t0006g0158a0001c0001t0006g0159others(1): Show | 4 | HG02257.hp1 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-849_1024-848i others(3): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503183 | ||||||
| chr2:164503183
|
A | G | 20 | a0001c0001t0006g0001a0001c0001t0007g0082a0001c0001t0010g0143others(17): Show | 21 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-848T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503183 | ||||||
| chr2:164503184
|
A | G | 2 | a0002c0002t0002g0244a0002c0002t0002g0272 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1024-849T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503184 | ||||||
| chr2:164503375
|
C | T | 5 | a0002c0002t0003g0166a0002c0002t0003g0169a0002c0002t0003g0188others(2): Show | 5 | HG00423.hp1 NA18970.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-1040G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503375 | ||||||
| chr2:164503442
|
C | CA | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00423.hp2 HG00738.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1024-1108dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
C | CAA | 10 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0039others(7): Show | 10 | HG00423.hp1 HG01070.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1024-1109_1024-110 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CA | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1024-1108delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAA | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0102a0001c0001t0004g0004others(3): Show | 6 | HG01433.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1109_1024-110 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAAA | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0128others(35): Show | 38 | HG00544.hp1 HG00673.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.1024-1110_1024-110 others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAAAA | C | 59 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0105others(56): Show | 59 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1024-1111_1024-110 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1024-1118_1024-110 others(15): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAAAAAAA others(7): Show |
C | 28 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0114others(25): Show | 29 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1024-1121_1024-110 others(18): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1024-1122_1024-110 others(19): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAAAAAAA others(10): Show |
C | 27 | a0001c0001t0004g0009a0001c0001t0004g0022a0001c0001t0008g0155others(24): Show | 28 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.1024-1124_1024-110 others(21): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503442
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1024-1130_1024-110 others(27): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | ||||||
| chr2:164503765
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1024-1430T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503765 | ||||||
| chr2:164504314
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1024-1979C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504314 | ||||||
| chr2:164504326
|
G | A | 2 | a0001c0001t0008g0149a0001c0001t0008g0150 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1024-1991C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504326 | ||||||
| chr2:164504371
|
T | C | 2 | a0002c0002t0002g0228a0002c0002t0003g0206 | 2 | HG02083.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1024-2036A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504371 | ||||||
| chr2:164504669
|
C | T | 1 | a0007c0008t0013g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1024-2334G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504669 | ||||||
| chr2:164505113
|
A | G | 2 | a0002c0002t0003g0200a0002c0002t0003g0203 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1024-2778T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505113 | ||||||
| chr2:164505318
|
AGT | A | 13 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0118others(10): Show | 13 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024-2985_1024-298 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505318 | ||||||
| chr2:164505435
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1023+3020G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505435 | ||||||
| chr2:164505891
|
G | A | 1 | a0002c0002t0003g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1023+2564C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505891 | ||||||
| chr2:164506331
|
G | T | 28 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0094others(25): Show | 29 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1023+2124C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506331 | ||||||
| chr2:164506471
|
T | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(10): Show | 13 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023+1984A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506471 | ||||||
| chr2:164506643
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1023+1812T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506643 | ||||||
| chr2:164506706
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1023+1749A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506706 | ||||||
| chr2:164506840
|
C | T | 6 | a0002c0002t0002g0289a0002c0002t0002g0292a0002c0002t0003g0002others(3): Show | 7 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1023+1615G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506840 | ||||||
| chr2:164506853
|
T | G | 1 | a0007c0008t0013g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1023+1602A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506853 | ||||||
| chr2:164506895
|
T | C | 1 | a0002c0002t0003g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1023+1560A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506895 | ||||||
| chr2:164506932
|
CACAG | C | 5 | a0001c0001t0001g0072a0001c0001t0001g0118a0001c0001t0009g0111others(2): Show | 5 | HG01106.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1023+1519_1023+152 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506932 | ||||||
| chr2:164507403
|
C | G | 29 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0094others(26): Show | 30 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1023+1052G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507403 | ||||||
| chr2:164507498
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1023+957T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507498 | ||||||
| chr2:164507661
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1023+794C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507661 | ||||||
| chr2:164507663
|
G | A | 2 | a0001c0005t0001g0026a0001c0005t0007g0047 | 2 | HG00639.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1023+792C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507663 | ||||||
| chr2:164507758
|
G | GATAATTG others(2): Show |
145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(142): Show | 146 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.1023+696_1023+697i others(11): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507758 | ||||||
| chr2:164508068
|
C | T | 1 | a0002c0002t0003g0229 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1023+387G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508068 | ||||||
| chr2:164508106
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1023+349G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508106 | ||||||
| chr2:164508128
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1023+327G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508128 | ||||||
| chr2:164508352
|
A | G | 1 | a0002c0002t0003g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1023+103T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508352 | ||||||
| chr2:164508370
|
A | C | 4 | a0001c0001t0004g0029a0001c0001t0004g0088a0001c0001t0004g0137others(1): Show | 4 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+85T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508370 | ||||||
| chr2:164508377
|
G | A | 26 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0114others(23): Show | 26 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1023+78C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508377 | ||||||
| chr2:164508587
|
T | C | 2 | a0001c0001t0004g0063a0001c0001t0004g0066 | 2 | NA18963.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.928-37A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 7/13 | chr2 | 164508587 | ||||||
| chr2:164508958
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0133 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-106C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164508958 | ||||||
| chr2:164509007
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0114a0001c0001t0006g0145others(1): Show | 4 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-155G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509007 | ||||||
| chr2:164509106
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.817-254C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509106 | ||||||
| chr2:164509176
|
G | A | 1 | a0001c0001t0004g0012 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.817-324C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509176 | ||||||
| chr2:164509399
|
C | T | 2 | a0002c0002t0002g0256a0002c0002t0002g0274 | 2 | HG00140.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.817-547G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509399 | ||||||
| chr2:164509419
|
A | G | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(11): Show | 14 | HG00408.hp1 HG00621.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.817-567T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509419 | ||||||
| chr2:164509792
|
G | GA | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.817-941dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509792 | ||||||
| chr2:164509792
|
G | GAA | 10 | a0001c0001t0001g0008a0001c0001t0006g0148a0001c0001t0007g0103others(7): Show | 10 | HG00733.hp2 HG01243.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-942_817-941dup others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509792 | ||||||
| chr2:164509804
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.817-952T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509804 | ||||||
| chr2:164509897
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0006g0145a0001c0001t0006g0157 | 3 | HG02258.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.817-1045C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509897 | ||||||
| chr2:164510082
|
A | C | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.817-1230T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510082 | ||||||
| chr2:164510309
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-1457A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510309 | ||||||
| chr2:164510413
|
G | A | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.817-1561C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510413 | ||||||
| chr2:164510460
|
C | T | 64 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0069others(61): Show | 64 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.817-1608G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510460 | ||||||
| chr2:164510634
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | NA18972.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.817-1782G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510634 | ||||||
| chr2:164510775
|
A | G | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.817-1923T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510775 | ||||||
| chr2:164510896
|
G | A | 1 | a0001c0012t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.817-2044C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510896 | ||||||
| chr2:164511040
|
CTACCCAT others(11): Show |
C | 5 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-2206_817-2189d others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511040 | ||||||
| chr2:164511305
|
T | G | 1 | a0004c0006t0001g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.817-2453A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511305 | ||||||
| chr2:164511331
|
C | T | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.817-2479G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511331 | ||||||
| chr2:164511836
|
T | C | 24 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(21): Show | 24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.817-2984A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511836 | ||||||
| chr2:164512060
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.817-3208C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512060 | ||||||
| chr2:164512070
|
T | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0032others(7): Show | 10 | HG00621.hp1 NA18941.hp1 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-3218A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512070 | ||||||
| chr2:164512078
|
C | A | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.817-3226G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512078 | ||||||
| chr2:164512111
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-3259T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512111 | ||||||
| chr2:164512467
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0107 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-3615C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512467 | ||||||
| chr2:164512539
|
A | G | 12 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.817-3687T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512539 | ||||||
| chr2:164512878
|
C | T | 1 | a0005c0010t0012g0011 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.817-4026G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512878 | ||||||
| chr2:164513117
|
T | C | 1 | a0002c0002t0002g0281 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.817-4265A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513117 | ||||||
| chr2:164513300
|
GC | G | 12 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.817-4449delG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513300 | ||||||
| chr2:164513444
|
T | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(22): Show | 25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.817-4592A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513444 | ||||||
| chr2:164513551
|
A | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(43): Show | 48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.817-4699T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513551 | ||||||
| chr2:164513776
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-4924T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513776 | ||||||
| chr2:164513833
|
A | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(22): Show | 25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.817-4981T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513833 | ||||||
| chr2:164513948
|
GGACATAG others(4): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.817-5107_817-5097d others(13): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513948 | ||||||
| chr2:164514148
|
T | A | 24 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(21): Show | 24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.817-5296A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514148 | ||||||
| chr2:164514176
|
A | T | 1 | a0002c0002t0002g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.817-5324T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514176 | ||||||
| chr2:164514255
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0069 | 2 | HG02027.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.817-5403A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514255 | ||||||
| chr2:164514374
|
T | A | 1 | a0002c0002t0003g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.817-5522A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514374 | ||||||
| chr2:164514916
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-6064G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514916 | ||||||
| chr2:164514923
|
C | T | 24 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(21): Show | 24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.817-6071G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514923 | ||||||
| chr2:164514925
|
T | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.817-6073A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514925 | ||||||
| chr2:164515230
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.817-6378G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515230 | ||||||
| chr2:164515255
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.817-6403G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515255 | ||||||
| chr2:164515287
|
T | C | 1 | a0006c0011t0007g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.817-6435A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515287 | ||||||
| chr2:164515511
|
G | A | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+6469C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515511 | ||||||
| chr2:164515518
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.816+6462G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515518 | ||||||
| chr2:164515748
|
T | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0093a0001c0001t0001g0110others(1): Show | 4 | HG01261.hp2 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+6232A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515748 | ||||||
| chr2:164515803
|
G | GA | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.816+6176dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515803 | ||||||
| chr2:164515803
|
G | GAA | 23 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0105others(20): Show | 24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.816+6175_816+6176d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515803 | ||||||
| chr2:164515879
|
A | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0060others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+6101T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515879 | ||||||
| chr2:164516007
|
A | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0060others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+5973T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516007 | ||||||
| chr2:164516026
|
T | A | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.816+5954A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516026 | ||||||
| chr2:164516076
|
G | T | 12 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.816+5904C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516076 | ||||||
| chr2:164516435
|
C | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+5545G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516435 | ||||||
| chr2:164516795
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0006g0141a0001c0001t0006g0151 | 3 | NA18954.hp1 NA18974.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.816+5185C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516795 | ||||||
| chr2:164516883
|
G | C | 2 | a0002c0002t0005g0167a0002c0002t0005g0181 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.816+5097C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516883 | ||||||
| chr2:164516900
|
T | C | 4 | a0001c0001t0006g0154a0001c0001t0006g0158a0001c0001t0006g0159others(1): Show | 4 | HG02257.hp1 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+5080A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516900 | ||||||
| chr2:164516948
|
C | A | 7 | a0001c0001t0004g0097a0001c0001t0004g0098a0001c0001t0004g0099others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+5032G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516948 | ||||||
| chr2:164517041
|
C | T | 1 | a0002c0002t0003g0250 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.816+4939G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517041 | ||||||
| chr2:164517091
|
G | T | 65 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(62): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.816+4889C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517091 | ||||||
| chr2:164517253
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0032 | 2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.816+4727C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517253 | ||||||
| chr2:164517442
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.816+4538T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517442 | ||||||
| chr2:164517450
|
A | C | 89 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(86): Show | 89 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.816+4530T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517450 | ||||||
| chr2:164517529
|
A | G | 1 | a0002c0002t0002g0195 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.816+4451T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517529 | ||||||
| chr2:164518152
|
G | C | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.816+3828C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164518152 | ||||||
| chr2:164518186
|
T | G | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+3794A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164518186 | ||||||
| chr2:164518734
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.816+3246T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164518734 | ||||||
| chr2:164519019
|
T | C | 2 | a0001c0001t0001g0068a0002c0002t0002g0221 | 2 | NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.816+2961A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519019 | ||||||
| chr2:164519270
|
T | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(22): Show | 25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.816+2710A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519270 | ||||||
| chr2:164519841
|
A | G | 1 | a0001c0001t0006g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.816+2139T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519841 | ||||||
| chr2:164519869
|
C | A | 1 | a0007c0008t0013g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816+2111G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519869 | ||||||
| chr2:164520101
|
C | T | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+1879G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520101 | ||||||
| chr2:164520298
|
G | A | 24 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(21): Show | 24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.816+1682C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520298 | ||||||
| chr2:164520304
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.816+1676A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520304 | ||||||
| chr2:164520358
|
A | C | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.816+1622T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520358 | ||||||
| chr2:164520536
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.816+1444G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520536 | ||||||
| chr2:164520593
|
T | C | 22 | a0001c0001t0004g0009a0001c0001t0004g0022a0001c0001t0008g0155others(19): Show | 23 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.816+1387A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520593 | ||||||
| chr2:164520650
|
A | G | 1 | a0002c0002t0003g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.816+1330T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520650 | ||||||
| chr2:164520771
|
C | A | 1 | a0007c0008t0013g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816+1209G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520771 | ||||||
| chr2:164521030
|
A | C | 1 | a0001c0001t0004g0041 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.816+950T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521030 | ||||||
| chr2:164521049
|
T | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+931A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521049 | ||||||
| chr2:164521101
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816+879T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521101 | ||||||
| chr2:164521396
|
T | G | 3 | a0001c0001t0004g0004a0002c0002t0002g0177a0002c0002t0002g0183 | 3 | HG00673.hp2 HG01433.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.816+584A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521396 | ||||||
| chr2:164521412
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.816+568A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521412 | ||||||
| chr2:164521623
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.816+357C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521623 | ||||||
| chr2:164521670
|
A | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.816+310T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521670 | ||||||
| chr2:164521820
|
T | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0084others(5): Show | 8 | HG01891.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+160A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521820 | ||||||
| chr2:164521917
|
C | A | 25 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(22): Show | 25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.816+63G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521917 | ||||||
| chr2:164522324
|
T | A | 1 | a0002c0002t0002g0161 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.679-207A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522324 | ||||||
| chr2:164522444
|
G | A | 1 | a0002c0002t0003g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.679-327C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522444 | ||||||
| chr2:164522454
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.679-337A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522454 | ||||||
| chr2:164522635
|
G | A | 2 | a0001c0003t0001g0074a0001c0003t0007g0042 | 2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.679-518C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522635 | ||||||
| chr2:164522659
|
G | A | 13 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0118others(10): Show | 13 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.679-542C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522659 | ||||||
| chr2:164522840
|
C | T | 9 | a0001c0001t0001g0121a0002c0002t0003g0234a0002c0002t0003g0235others(6): Show | 9 | HG00738.hp1 HG01106.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.679-723G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522840 | ||||||
| chr2:164523054
|
G | C | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.679-937C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523054 | ||||||
| chr2:164523068
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.679-951C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523068 | ||||||
| chr2:164523107
|
G | C | 1 | a0002c0002t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.679-990C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523107 | ||||||
| chr2:164523188
|
G | A | 2 | a0002c0002t0002g0258a0002c0002t0002g0276 | 2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.679-1071C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523188 | ||||||
| chr2:164523211
|
C | G | 6 | a0001c0001t0001g0094a0001c0001t0001g0129a0001c0001t0001g0135others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.679-1094G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523211 | ||||||
| chr2:164523251
|
A | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(22): Show | 25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.679-1134T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523251 | ||||||
| chr2:164523412
|
C | T | 1 | a0002c0002t0003g0206 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.679-1295G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523412 | ||||||
| chr2:164523417
|
A | T | 2 | a0001c0001t0004g0017a0002c0002t0002g0199 | 2 | NA18955.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.679-1300T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523417 | ||||||
| chr2:164523908
|
G | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.678+1096C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523908 | ||||||
| chr2:164524066
|
A | G | 1 | a0002c0002t0003g0266 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.678+938T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524066 | ||||||
| chr2:164524323
|
A | G | 3 | a0001c0001t0007g0101a0001c0001t0007g0103a0002c0002t0005g0201 | 3 | HG02572.hp2 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.678+681T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524323 | ||||||
| chr2:164524342
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0004g0064others(1): Show | 4 | HG02080.hp2 HG02165.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+662T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524342 | ||||||
| chr2:164524396
|
T | C | 24 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(21): Show | 24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.678+608A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524396 | ||||||
| chr2:164524517
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.678+487A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524517 | ||||||
| chr2:164524844
|
T | C | 2 | a0001c0001t0001g0007a0002c0002t0002g0192 | 2 | HG01255.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.678+160A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524844 | ||||||
| chr2:164524959
|
T | C | 11 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0118others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.678+45A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524959 | ||||||
| chr2:164525105
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.604-27G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525105 | ||||||
| chr2:164525107
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.604-29G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525107 | ||||||
| chr2:164525375
|
A | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.604-297T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525375 | ||||||
| chr2:164525411
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0015 | 2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.604-333C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525411 | ||||||
| chr2:164525438
|
C | A | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.604-360G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525438 | ||||||
| chr2:164525790
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0060others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.604-712G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525790 | ||||||
| chr2:164526032
|
T | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.604-954A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526032 | ||||||
| chr2:164526062
|
A | C | 12 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0118others(9): Show | 12 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.603+952T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526062 | ||||||
| chr2:164526237
|
A | G | 2 | a0001c0001t0004g0083a0002c0002t0003g0205 | 2 | HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.603+777T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526237 | ||||||
| chr2:164526274
|
C | T | 9 | a0001c0001t0001g0121a0002c0002t0003g0234a0002c0002t0003g0235others(6): Show | 9 | HG00738.hp1 HG01106.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.603+740G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526274 | ||||||
| chr2:164526294
|
T | C | 3 | a0002c0002t0003g0168a0002c0002t0003g0172a0002c0002t0003g0230 | 3 | HG02738.hp1 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.603+720A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526294 | ||||||
| chr2:164526528
|
C | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(10): Show | 13 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.603+486G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526528 | ||||||
| chr2:164526574
|
C | A | 13 | a0001c0001t0001g0094a0001c0001t0001g0129a0001c0001t0001g0135others(10): Show | 13 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.603+440G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526574 | ||||||
| chr2:164526613
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.603+401A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526613 | ||||||
| chr2:164526667
|
G | C | 1 | a0002c0002t0005g0265 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.603+347C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526667 | ||||||
| chr2:164527151
|
C | T | 3 | a0001c0001t0010g0140a0002c0002t0002g0184a0002c0002t0002g0223 | 3 | HG01123.hp1 HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.482-16G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527151 | ||||||
| chr2:164527174
|
CAAATATA others(1): Show |
C | 3 | a0001c0001t0004g0009a0002c0002t0002g0256a0002c0002t0003g0210 | 3 | HG00140.hp1 HG00140.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.482-47_482-40delAT others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527174 | ||||||
| chr2:164527175
|
AAATATAT others(4): Show |
A | 1 | a0002c0002t0003g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.482-51_482-41delAT others(9): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527175 | ||||||
| chr2:164527176
|
A | AAT | 9 | a0001c0001t0001g0013a0001c0001t0001g0036a0001c0001t0001g0054others(6): Show | 9 | HG01175.hp1 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-43_482-42dupAT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
A | AATAT | 4 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0008g0150others(1): Show | 4 | HG00733.hp1 HG01099.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-45_482-42dupAT others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
A | AATATAT | 6 | a0001c0001t0001g0050a0001c0001t0001g0070a0001c0001t0008g0149others(3): Show | 6 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-47_482-42dupAT others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0024 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.482-53_482-42dupAT others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.482-41T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AAT | A | 29 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0052others(26): Show | 29 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.482-43_482-42delAT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATAT | A | 36 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0033others(33): Show | 36 | HG00408.hp2 HG00738.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.482-45_482-42delAT others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATAT | A | 36 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0068others(33): Show | 37 | HG00609.hp2 HG00673.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.482-47_482-42delAT others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(1): Show |
A | 30 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(27): Show | 30 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.482-49_482-42delAT others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(3): Show |
A | 26 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0040others(23): Show | 26 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.482-51_482-42delAT others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(5): Show |
A | 31 | a0001c0001t0001g0057a0001c0001t0001g0084a0001c0001t0001g0086others(28): Show | 32 | HG00544.hp1 HG01069.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.482-53_482-42delAT others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(7): Show |
A | 20 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0092others(17): Show | 20 | HG01123.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.482-55_482-42delAT others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(9): Show |
A | 25 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0055others(22): Show | 25 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.482-57_482-42delAT others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(11): Show |
A | 8 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(5): Show | 8 | HG00099.hp1 HG00609.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-59_482-42delAT others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(13): Show |
A | 1 | a0001c0003t0001g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482-61_482-42delAT others(18): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(15): Show |
A | 1 | a0002c0002t0002g0258 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.482-63_482-42delAT others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(19): Show |
A | 1 | a0001c0001t0004g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.482-67_482-42delAT others(24): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527176
|
AATATATA others(23): Show |
A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-71_482-42delAT others(28): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | ||||||
| chr2:164527218
|
T | C | 1 | a0001c0001t0009g0111 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.482-83A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527218 | ||||||
| chr2:164527220
|
T | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0053others(33): Show | 36 | HG00639.hp2 HG00738.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.482-85A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527220 | ||||||
| chr2:164527259
|
G | A | 1 | a0001c0001t0004g0080 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.482-124C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527259 | ||||||
| chr2:164527522
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-387T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527522 | ||||||
| chr2:164528027
|
C | T | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-892G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528027 | ||||||
| chr2:164528177
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.482-1042C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528177 | ||||||
| chr2:164528304
|
C | T | 1 | a0001c0001t0006g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.482-1169G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528304 | ||||||
| chr2:164528548
|
T | G | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.482-1413A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528548 | ||||||
| chr2:164528600
|
T | C | 3 | a0003c0004t0008g0142a0003c0004t0008g0156a0009c0009t0005g0288 | 3 | HG01099.hp1 HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.482-1465A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528600 | ||||||
| chr2:164528740
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.482-1605G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528740 | ||||||
| chr2:164528742
|
A | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-1607T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528742 | ||||||
| chr2:164528747
|
G | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0130a0001c0001t0009g0111others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-1612C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528747 | ||||||
| chr2:164528932
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-1797C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528932 | ||||||
| chr2:164529241
|
T | C | 4 | a0001c0001t0001g0057a0001c0001t0006g0001a0002c0002t0003g0160others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-2106A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529241 | ||||||
| chr2:164529337
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2202G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529337 | ||||||
| chr2:164529350
|
T | G | 1 | a0006c0011t0007g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-2215A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529350 | ||||||
| chr2:164529375
|
C | T | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-2240G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529375 | ||||||
| chr2:164529398
|
A | G | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-2263T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529398 | ||||||
| chr2:164529438
|
C | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0092a0001c0001t0001g0095others(5): Show | 8 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-2303G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529438 | ||||||
| chr2:164529528
|
G | A | 1 | a0002c0002t0003g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482-2393C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529528 | ||||||
| chr2:164529571
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.482-2436G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529571 | ||||||
| chr2:164529747
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.482-2612A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529747 | ||||||
| chr2:164529800
|
G | C | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.482-2665C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529800 | ||||||
| chr2:164529803
|
T | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02109.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.482-2668A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529803 | ||||||
| chr2:164529998
|
T | C | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.482-2863A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529998 | ||||||
| chr2:164530085
|
G | A | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-2950C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530085 | ||||||
| chr2:164530184
|
G | A | 8 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0128others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-3049C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530184 | ||||||
| chr2:164530273
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.482-3138A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530273 | ||||||
| chr2:164530292
|
G | A | 2 | a0001c0001t0006g0145a0001c0001t0006g0157 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.482-3157C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530292 | ||||||
| chr2:164530361
|
C | T | 1 | a0001c0001t0004g0022 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.482-3226G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530361 | ||||||
| chr2:164530436
|
G | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0085a0001c0001t0006g0144 | 3 | NA18940.hp1 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.482-3301C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530436 | ||||||
| chr2:164530552
|
A | C | 1 | a0001c0001t0006g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.482-3417T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530552 | ||||||
| chr2:164530606
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482-3471C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530606 | ||||||
| chr2:164530807
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.482-3672C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530807 | ||||||
| chr2:164530886
|
T | G | 1 | a0002c0002t0003g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.482-3751A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530886 | ||||||
| chr2:164531003
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.482-3868C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531003 | ||||||
| chr2:164531117
|
C | A | 1 | a0001c0003t0001g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482-3982G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531117 | ||||||
| chr2:164531370
|
T | C | 101 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(98): Show | 101 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.482-4235A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531370 | ||||||
| chr2:164531467
|
T | G | 49 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(46): Show | 51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.482-4332A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531467 | ||||||
| chr2:164531478
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.482-4343G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531478 | ||||||
| chr2:164531596
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.482-4461G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531596 | ||||||
| chr2:164531859
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.482-4724G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531859 | ||||||
| chr2:164531903
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.482-4768T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531903 | ||||||
| chr2:164531963
|
C | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0092a0001c0001t0001g0095others(5): Show | 8 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-4828G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531963 | ||||||
| chr2:164532108
|
G | C | 1 | a0002c0002t0003g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.482-4973C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532108 | ||||||
| chr2:164532148
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.482-5013A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532148 | ||||||
| chr2:164532196
|
T | C | 1 | a0001c0001t0004g0012 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.482-5061A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532196 | ||||||
| chr2:164532226
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482-5091T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532226 | ||||||
| chr2:164532390
|
A | G | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.482-5255T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532390 | ||||||
| chr2:164532577
|
T | C | 2 | a0001c0001t0008g0149a0001c0001t0008g0150 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.482-5442A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532577 | ||||||
| chr2:164532585
|
G | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-5450C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532585 | ||||||
| chr2:164532914
|
G | A | 24 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0007g0082others(21): Show | 24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-5779C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532914 | ||||||
| chr2:164533053
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-5918T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533053 | ||||||
| chr2:164533124
|
C | T | 1 | a0002c0002t0002g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.482-5989G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533124 | ||||||
| chr2:164533224
|
C | CT | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0086others(25): Show | 28 | HG00438.hp1 HG00642.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.482-6090dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | ||||||
| chr2:164533224
|
CT | C | 98 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0018others(95): Show | 98 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.482-6090delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | ||||||
| chr2:164533224
|
CTT | C | 10 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0133others(7): Show | 10 | HG01255.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-6091_482-6090d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | ||||||
| chr2:164533224
|
CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-6099_482-6090d others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | ||||||
| chr2:164533279
|
G | A | 2 | a0001c0003t0001g0074a0001c0003t0007g0042 | 2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.482-6144C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533279 | ||||||
| chr2:164533408
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.482-6273T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533408 | ||||||
| chr2:164533474
|
C | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0130a0001c0001t0009g0111others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-6339G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533474 | ||||||
| chr2:164533734
|
T | C | 1 | a0006c0011t0007g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-6599A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533734 | ||||||
| chr2:164533818
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-6683G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533818 | ||||||
| chr2:164533931
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.482-6796C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533931 | ||||||
| chr2:164534024
|
C | T | 1 | a0001c0001t0010g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.482-6889G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534024 | ||||||
| chr2:164534055
|
T | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-6920A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534055 | ||||||
| chr2:164534108
|
A | G | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.482-6973T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534108 | ||||||
| chr2:164534276
|
A | G | 1 | a0002c0002t0003g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482-7141T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534276 | ||||||
| chr2:164534417
|
T | G | 1 | a0001c0001t0007g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.482-7282A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534417 | ||||||
| chr2:164534480
|
A | G | 1 | a0002c0002t0002g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.482-7345T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534480 | ||||||
| chr2:164534541
|
G | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-7406C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534541 | ||||||
| chr2:164534710
|
C | A | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-7575G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534710 | ||||||
| chr2:164535262
|
T | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-8127A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535262 | ||||||
| chr2:164535512
|
C | T | 3 | a0001c0001t0007g0082a0002c0002t0002g0233a0002c0002t0002g0243 | 3 | HG00735.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.482-8377G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535512 | ||||||
| chr2:164535520
|
G | A | 1 | a0001c0001t0007g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.482-8385C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535520 | ||||||
| chr2:164535821
|
G | A | 1 | a0001c0001t0004g0037 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.482-8686C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535821 | ||||||
| chr2:164535826
|
T | C | 2 | a0001c0001t0001g0007a0002c0002t0002g0192 | 2 | HG01255.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.482-8691A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535826 | ||||||
| chr2:164535877
|
G | A | 1 | a0001c0001t0006g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.482-8742C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535877 | ||||||
| chr2:164536135
|
A | G | 68 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.482-9000T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536135 | ||||||
| chr2:164536415
|
GTTTA | G | 12 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.482-9284_482-9281d others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536415 | ||||||
| chr2:164536442
|
A | G | 1 | a0001c0001t0008g0155 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.482-9307T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536442 | ||||||
| chr2:164536559
|
G | A | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-9424C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536559 | ||||||
| chr2:164536644
|
A | G | 1 | a0001c0001t0010g0147 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.482-9509T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536644 | ||||||
| chr2:164536645
|
A | G | 1 | a0001c0001t0004g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.482-9510T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536645 | ||||||
| chr2:164536742
|
A | G | 96 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(93): Show | 96 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.482-9607T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536742 | ||||||
| chr2:164536788
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.482-9653A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536788 | ||||||
| chr2:164536847
|
G | T | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.482-9712C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536847 | ||||||
| chr2:164537168
|
T | A | 3 | a0001c0001t0001g0019a0001c0001t0006g0141a0001c0001t0006g0151 | 3 | NA18954.hp1 NA18974.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.482-10033A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537168 | ||||||
| chr2:164537272
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.482-10137C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537272 | ||||||
| chr2:164537536
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.481+10124C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537536 | ||||||
| chr2:164537693
|
G | A | 1 | a0001c0001t0006g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.481+9967C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537693 | ||||||
| chr2:164537760
|
A | G | 10 | a0001c0001t0001g0121a0002c0002t0002g0248a0002c0002t0003g0234others(7): Show | 10 | HG00738.hp1 HG01106.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+9900T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537760 | ||||||
| chr2:164537773
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.481+9887C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537773 | ||||||
| chr2:164537981
|
A | C | 1 | a0002c0002t0003g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.481+9679T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537981 | ||||||
| chr2:164538001
|
T | TA | 9 | a0002c0002t0005g0222a0002c0002t0005g0245a0002c0002t0005g0259others(6): Show | 9 | HG00642.hp2 HG01257.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+9658dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538001 | ||||||
| chr2:164538070
|
T | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(44): Show | 49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.481+9590A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538070 | ||||||
| chr2:164538176
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.481+9484T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538176 | ||||||
| chr2:164538670
|
A | C | 2 | a0001c0001t0006g0159a0001c0001t0007g0134 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.481+8990T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538670 | ||||||
| chr2:164538857
|
T | C | 4 | a0001c0001t0004g0029a0001c0001t0004g0088a0001c0001t0004g0137others(1): Show | 4 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+8803A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538857 | ||||||
| chr2:164538874
|
A | G | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.481+8786T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538874 | ||||||
| chr2:164538927
|
C | T | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.481+8733G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538927 | ||||||
| chr2:164538996
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.481+8664C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538996 | ||||||
| chr2:164539447
|
C | G | 3 | a0002c0002t0002g0209a0002c0002t0002g0242a0002c0002t0003g0210 | 3 | NA18979.hp2 NA19065.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.481+8213G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539447 | ||||||
| chr2:164539475
|
G | GA | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.481+8184dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539475 | ||||||
| chr2:164539503
|
T | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0114a0001c0001t0006g0145others(1): Show | 4 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+8157A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539503 | ||||||
| chr2:164539753
|
A | C | 2 | a0002c0002t0002g0228a0002c0002t0003g0206 | 2 | HG02083.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.481+7907T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539753 | ||||||
| chr2:164539902
|
T | C | 1 | a0001c0005t0007g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.481+7758A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539902 | ||||||
| chr2:164540440
|
C | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0125others(1): Show | 4 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+7220G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164540440 | ||||||
| chr2:164540682
|
T | C | 1 | a0002c0002t0003g0204 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.481+6978A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164540682 | ||||||
| chr2:164540719
|
A | G | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.481+6941T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164540719 | ||||||
| chr2:164541132
|
G | A | 1 | a0001c0001t0006g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481+6528C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541132 | ||||||
| chr2:164541233
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.481+6427G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541233 | ||||||
| chr2:164541428
|
C | T | 1 | a0007c0008t0013g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.481+6232G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541428 | ||||||
| chr2:164541579
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.481+6081G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541579 | ||||||
| chr2:164541749
|
G | T | 67 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.481+5911C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541749 | ||||||
| chr2:164541795
|
C | T | 5 | a0002c0002t0002g0244a0002c0002t0002g0272a0002c0002t0003g0168others(2): Show | 5 | HG02738.hp1 HG03017.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+5865G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541795 | ||||||
| chr2:164541873
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.481+5787C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541873 | ||||||
| chr2:164541890
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.481+5770A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541890 | ||||||
| chr2:164542665
|
G | C | 3 | a0002c0002t0003g0168a0002c0002t0003g0172a0002c0002t0003g0230 | 3 | HG02738.hp1 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.481+4995C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164542665 | ||||||
| chr2:164542822
|
A | G | 1 | a0002c0002t0003g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.481+4838T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164542822 | ||||||
| chr2:164542831
|
G | A | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+4829C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164542831 | ||||||
| chr2:164543117
|
A | G | 1 | a0002c0002t0003g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.481+4543T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543117 | ||||||
| chr2:164543126
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.481+4534G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543126 | ||||||
| chr2:164543142
|
T | TA | 12 | a0001c0001t0001g0056a0001c0001t0001g0118a0001c0001t0001g0128others(9): Show | 12 | HG01516.hp1 HG01517.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.481+4517dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543142 | ||||||
| chr2:164543143
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.481+4517T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543143 | ||||||
| chr2:164543186
|
A | T | 1 | a0001c0001t0006g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.481+4474T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543186 | ||||||
| chr2:164543232
|
C | T | 2 | a0001c0001t0001g0114a0002c0002t0003g0229 | 2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.481+4428G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543232 | ||||||
| chr2:164543721
|
T | C | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+3939A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543721 | ||||||
| chr2:164543928
|
G | A | 1 | a0002c0002t0003g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.481+3732C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543928 | ||||||
| chr2:164544180
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.481+3480G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544180 | ||||||
| chr2:164544241
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.481+3419C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544241 | ||||||
| chr2:164544414
|
T | G | 1 | a0002c0002t0003g0229 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.481+3246A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544414 | ||||||
| chr2:164544619
|
C | A | 3 | a0002c0002t0002g0182a0002c0002t0002g0211a0002c0002t0002g0213 | 3 | NA18974.hp1 NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.481+3041G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544619 | ||||||
| chr2:164544691
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0053 | 2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.481+2969T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544691 | ||||||
| chr2:164544746
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.481+2914T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544746 | ||||||
| chr2:164544977
|
A | G | 45 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(42): Show | 47 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.481+2683T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544977 | ||||||
| chr2:164545136
|
A | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.481+2524T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545136 | ||||||
| chr2:164545217
|
A | G | 1 | a0001c0001t0006g0153 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.481+2443T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545217 | ||||||
| chr2:164545240
|
G | A | 2 | a0002c0002t0002g0244a0002c0002t0002g0272 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.481+2420C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545240 | ||||||
| chr2:164545291
|
T | C | 110 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(107): Show | 110 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.481+2369A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545291 | ||||||
| chr2:164545714
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.481+1946T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545714 | ||||||
| chr2:164545944
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.481+1716T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545944 | ||||||
| chr2:164546028
|
A | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(44): Show | 49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.481+1632T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164546028 | ||||||
| chr2:164546783
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.481+877G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164546783 | ||||||
| chr2:164547118
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481+542C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164547118 | ||||||
| chr2:164547433
|
T | C | 2 | a0002c0002t0002g0289a0002c0002t0002g0292 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.481+227A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164547433 | ||||||
| chr2:164548076
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.325-260G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548076 | ||||||
| chr2:164548284
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.325-468G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548284 | ||||||
| chr2:164548396
|
G | T | 2 | a0001c0001t0001g0016a0001c0001t0004g0049 | 2 | NA18985.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.325-580C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548396 | ||||||
| chr2:164548492
|
T | G | 2 | a0002c0002t0002g0269a0002c0002t0002g0284 | 2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.325-676A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548492 | ||||||
| chr2:164548520
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-704C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548520 | ||||||
| chr2:164548581
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-765C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548581 | ||||||
| chr2:164548733
|
T | G | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325-917A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548733 | ||||||
| chr2:164548946
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.325-1130G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548946 | ||||||
| chr2:164549026
|
C | A | 3 | a0002c0002t0002g0217a0002c0002t0002g0283a0002c0002t0005g0278 | 3 | HG01975.hp1 HG02273.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.325-1210G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549026 | ||||||
| chr2:164549051
|
A | AT | 48 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(45): Show | 50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.325-1236dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549051 | ||||||
| chr2:164549424
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.325-1608C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549424 | ||||||
| chr2:164549558
|
T | C | 2 | a0002c0002t0002g0269a0002c0002t0002g0284 | 2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.325-1742A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549558 | ||||||
| chr2:164549563
|
A | C | 1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.325-1747T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549563 | ||||||
| chr2:164549566
|
T | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02109.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.325-1750A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549566 | ||||||
| chr2:164549674
|
C | T | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-1858G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549674 | ||||||
| chr2:164549770
|
A | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-1954T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549770 | ||||||
| chr2:164549863
|
A | AAAAAT | 4 | a0001c0001t0001g0058a0001c0001t0001g0125a0002c0002t0002g0195others(1): Show | 4 | HG01123.hp2 HG02630.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-2052_325-2048d others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
A | AAAAATAA others(3): Show |
5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0061others(2): Show | 5 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-2057_325-2048d others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
A | AAAAATAA others(8): Show |
1 | a0001c0001t0001g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-2062_325-2048d others(17): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
A | AAAAATAA others(13): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0084a0001c0001t0001g0109 | 3 | HG03041.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.325-2067_325-2048d others(22): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
A | AAAAATAA others(18): Show |
1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-2072_325-2048d others(27): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
AAAAAT | A | 66 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(63): Show | 67 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.325-2052_325-2048d others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
AAAAATAA others(3): Show |
A | 61 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0021others(58): Show | 62 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.325-2057_325-2048d others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
AAAAATAA others(8): Show |
A | 81 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(78): Show | 81 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.325-2062_325-2048d others(17): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
AAAAATAA others(13): Show |
A | 28 | a0001c0001t0001g0071a0001c0001t0001g0094a0001c0001t0001g0102others(25): Show | 28 | HG00673.hp1 HG00735.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-2067_325-2048d others(22): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
AAAAATAA others(18): Show |
A | 8 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0129others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-2072_325-2048d others(27): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549863
|
AAAAATAA others(23): Show |
A | 12 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0130others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-2077_325-2048d others(32): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | ||||||
| chr2:164549867
|
A | C | 1 | a0001c0001t0004g0051 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.325-2051T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549867 | ||||||
| chr2:164549961
|
C | T | 1 | a0001c0001t0006g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.325-2145G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549961 | ||||||
| chr2:164550009
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(44): Show | 49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.325-2193A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550009 | ||||||
| chr2:164550046
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.325-2230C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550046 | ||||||
| chr2:164550056
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-2240A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550056 | ||||||
| chr2:164550087
|
C | T | 1 | a0002c0002t0003g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.325-2271G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550087 | ||||||
| chr2:164550121
|
C | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-2305G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550121 | ||||||
| chr2:164550299
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-2483A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550299 | ||||||
| chr2:164550428
|
C | A | 1 | a0002c0002t0003g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325-2612G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550428 | ||||||
| chr2:164550491
|
A | G | 1 | a0001c0001t0006g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.325-2675T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550491 | ||||||
| chr2:164550661
|
G | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-2845C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550661 | ||||||
| chr2:164551012
|
T | C | 1 | a0002c0002t0003g0266 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.325-3196A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551012 | ||||||
| chr2:164551451
|
C | T | 3 | a0001c0001t0001g0056a0002c0002t0005g0167a0002c0002t0005g0181 | 3 | HG01516.hp1 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.325-3635G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551451 | ||||||
| chr2:164551747
|
A | C | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-3931T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551747 | ||||||
| chr2:164551761
|
G | A | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-3945C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551761 | ||||||
| chr2:164551824
|
T | A | 1 | a0002c0002t0005g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.325-4008A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551824 | ||||||
| chr2:164551986
|
C | A | 1 | a0002c0002t0003g0279 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.325-4170G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551986 | ||||||
| chr2:164552083
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-4267T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164552083 | ||||||
| chr2:164552154
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-4338T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164552154 | ||||||
| chr2:164552190
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-4374C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164552190 | ||||||
| chr2:164553206
|
A | T | 178 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.325-5390T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553206 | ||||||
| chr2:164553207
|
A | T | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-5391T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553207 | ||||||
| chr2:164553397
|
T | A | 1 | a0001c0001t0001g0033 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.325-5581A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553397 | ||||||
| chr2:164553592
|
T | C | 8 | a0001c0001t0001g0059a0001c0001t0001g0092a0001c0001t0001g0095others(5): Show | 8 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-5776A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553592 | ||||||
| chr2:164553765
|
G | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-5949C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553765 | ||||||
| chr2:164553795
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-5979A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553795 | ||||||
| chr2:164553877
|
C | T | 26 | a0001c0001t0001g0055a0001c0001t0001g0123a0001c0001t0004g0096others(23): Show | 26 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-6061G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553877 | ||||||
| chr2:164553895
|
G | A | 2 | a0002c0002t0002g0221a0002c0002t0002g0262 | 2 | NA18972.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.325-6079C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553895 | ||||||
| chr2:164554618
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-6802G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554618 | ||||||
| chr2:164554619
|
C | T | 46 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(43): Show | 48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.325-6803G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554619 | ||||||
| chr2:164554692
|
T | C | 68 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.325-6876A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554692 | ||||||
| chr2:164554912
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0004g0041 | 3 | HG01070.hp1 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.325-7096A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554912 | ||||||
| chr2:164555051
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.325-7235G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555051 | ||||||
| chr2:164555149
|
G | A | 2 | a0002c0002t0005g0167a0002c0002t0005g0181 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.325-7333C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555149 | ||||||
| chr2:164555268
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.325-7452G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555268 | ||||||
| chr2:164555269
|
G | A | 2 | a0001c0003t0001g0074a0001c0003t0007g0042 | 2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.325-7453C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555269 | ||||||
| chr2:164555284
|
G | A | 191 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.325-7468C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555284 | ||||||
| chr2:164555549
|
T | C | 1 | a0002c0002t0003g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.325-7733A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555549 | ||||||
| chr2:164555895
|
A | G | 2 | a0001c0001t0004g0078a0002c0002t0003g0286 | 2 | HG01346.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.325-8079T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555895 | ||||||
| chr2:164555930
|
TTAATAGA others(12): Show |
T | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-8133_325-8115d others(21): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555930 | ||||||
| chr2:164555965
|
G | A | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-8149C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555965 | ||||||
| chr2:164556128
|
A | G | 1 | a0002c0002t0003g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-8312T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556128 | ||||||
| chr2:164556189
|
T | A | 1 | a0001c0001t0004g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.325-8373A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556189 | ||||||
| chr2:164556230
|
A | T | 1 | a0001c0001t0006g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.325-8414T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556230 | ||||||
| chr2:164556874
|
A | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(68): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.325-9058T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556874 | ||||||
| chr2:164556938
|
AT | A | 29 | a0001c0001t0004g0009a0001c0001t0004g0022a0001c0001t0008g0155others(26): Show | 30 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.325-9123delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556938 | ||||||
| chr2:164557084
|
T | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-9268A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557084 | ||||||
| chr2:164557262
|
T | G | 3 | a0002c0002t0002g0182a0002c0002t0002g0211a0002c0002t0002g0213 | 3 | NA18974.hp1 NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.325-9446A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557262 | ||||||
| chr2:164557408
|
T | C | 1 | a0001c0001t0007g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.325-9592A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557408 | ||||||
| chr2:164557642
|
G | A | 1 | a0002c0002t0002g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.325-9826C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557642 | ||||||
| chr2:164557758
|
A | G | 1 | a0001c0001t0004g0108 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.325-9942T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557758 | ||||||
| chr2:164557764
|
C | T | 1 | a0002c0002t0002g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.325-9948G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557764 | ||||||
| chr2:164558063
|
G | A | 1 | a0002c0002t0005g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325-10247C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558063 | ||||||
| chr2:164558097
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.325-10281C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558097 | ||||||
| chr2:164558224
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0128 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.325-10408C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558224 | ||||||
| chr2:164558231
|
C | T | 70 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(67): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.325-10415G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558231 | ||||||
| chr2:164558312
|
T | C | 1 | a0001c0001t0004g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.325-10496A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558312 | ||||||
| chr2:164558742
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.325-10926A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558742 | ||||||
| chr2:164558944
|
C | A | 1 | a0002c0002t0003g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325-11128G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558944 | ||||||
| chr2:164559020
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.325-11204G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559020 | ||||||
| chr2:164559026
|
G | A | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.325-11210C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559026 | ||||||
| chr2:164559237
|
T | C | 1 | a0002c0002t0003g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-11421A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559237 | ||||||
| chr2:164559683
|
G | A | 1 | a0002c0002t0003g0237 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.325-11867C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559683 | ||||||
| chr2:164559768
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-11952G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559768 | ||||||
| chr2:164559901
|
T | A | 1 | a0001c0001t0001g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.325-12085A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559901 | ||||||
| chr2:164560016
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-12200T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560016 | ||||||
| chr2:164560080
|
A | G | 1 | a0001c0001t0010g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.325-12264T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560080 | ||||||
| chr2:164560103
|
T | C | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.325-12287A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560103 | ||||||
| chr2:164560162
|
G | A | 1 | a0002c0002t0002g0217 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.325-12346C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560162 | ||||||
| chr2:164560630
|
G | C | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-12814C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560630 | ||||||
| chr2:164560653
|
T | C | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-12837A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560653 | ||||||
| chr2:164560724
|
A | C | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.325-12908T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560724 | ||||||
| chr2:164560733
|
G | C | 1 | a0008c0007t0003g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-12917C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560733 | ||||||
| chr2:164560738
|
C | G | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.325-12922G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560738 | ||||||
| chr2:164560894
|
A | T | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.325-13078T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560894 | ||||||
| chr2:164560902
|
C | T | 1 | a0002c0002t0002g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.325-13086G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560902 | ||||||
| chr2:164560937
|
G | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-13121C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560937 | ||||||
| chr2:164560985
|
A | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG01099.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.325-13169T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560985 | ||||||
| chr2:164560990
|
A | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-13174T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560990 | ||||||
| chr2:164561629
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0004g0049a0001c0001t0004g0083 | 3 | HG02056.hp2 NA18985.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.325-13813C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561629 | ||||||
| chr2:164561703
|
C | A | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-13887G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561703 | ||||||
| chr2:164561708
|
C | T | 1 | a0001c0001t0010g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.325-13892G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561708 | ||||||
| chr2:164561818
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.325-14002A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561818 | ||||||
| chr2:164561950
|
A | T | 1 | a0002c0002t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.325-14134T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561950 | ||||||
| chr2:164562181
|
G | C | 2 | a0001c0001t0008g0149a0001c0001t0008g0150 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.325-14365C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562181 | ||||||
| chr2:164562245
|
T | C | 1 | a0001c0001t0004g0012 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.325-14429A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562245 | ||||||
| chr2:164562262
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-14446G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562262 | ||||||
| chr2:164562283
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-14467G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562283 | ||||||
| chr2:164562293
|
G | T | 1 | a0006c0011t0007g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-14477C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562293 | ||||||
| chr2:164562385
|
T | A | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-14569A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562385 | ||||||
| chr2:164562499
|
T | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.325-14683A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562499 | ||||||
| chr2:164562501
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.325-14685A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562501 | ||||||
| chr2:164562553
|
A | G | 1 | a0002c0002t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.325-14737T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562553 | ||||||
| chr2:164562750
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-14934A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562750 | ||||||
| chr2:164562837
|
T | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-15021A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562837 | ||||||
| chr2:164562859
|
T | A | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.325-15043A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562859 | ||||||
| chr2:164562965
|
A | G | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-15149T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562965 | ||||||
| chr2:164563180
|
T | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-15364A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563180 | ||||||
| chr2:164563195
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.325-15379A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563195 | ||||||
| chr2:164563233
|
T | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-15417A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563233 | ||||||
| chr2:164563891
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-16075A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563891 | ||||||
| chr2:164564027
|
T | G | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-16211A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564027 | ||||||
| chr2:164564165
|
G | A | 1 | a0002c0002t0002g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.325-16349C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564165 | ||||||
| chr2:164564264
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.325-16448A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564264 | ||||||
| chr2:164564293
|
T | C | 1 | a0002c0002t0002g0192 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.325-16477A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564293 | ||||||
| chr2:164564372
|
A | G | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-16556T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564372 | ||||||
| chr2:164564539
|
G | A | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-16723C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564539 | ||||||
| chr2:164564604
|
A | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-16788T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564604 | ||||||
| chr2:164565047
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325-17231T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565047 | ||||||
| chr2:164565120
|
G | C | 1 | a0001c0012t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.325-17304C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565120 | ||||||
| chr2:164565235
|
C | T | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-17419G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565235 | ||||||
| chr2:164565278
|
T | TCA | 46 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0058others(43): Show | 46 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.325-17464_325-1746 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565278 | ||||||
| chr2:164565278
|
T | TCACA | 19 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0057others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.325-17466_325-1746 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565278 | ||||||
| chr2:164565278
|
T | TCACACA | 33 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0055others(30): Show | 33 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.325-17468_325-1746 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565278 | ||||||
| chr2:164565292
|
A | ACACG | 34 | a0001c0001t0001g0038a0001c0001t0004g0009a0001c0001t0004g0022others(31): Show | 35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-17477_325-1747 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565292 | ||||||
| chr2:164565644
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0006g0001 | 3 | HG01069.hp1 HG01071.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.325-17828C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565644 | ||||||
| chr2:164565710
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0004g0049 | 2 | NA18985.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.325-17894G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565710 | ||||||
| chr2:164565711
|
G | C | 83 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(80): Show | 83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.325-17895C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565711 | ||||||
| chr2:164565948
|
C | A | 1 | a0002c0002t0003g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.325-18132G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565948 | ||||||
| chr2:164566083
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-18267G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566083 | ||||||
| chr2:164566352
|
A | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.325-18536T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566352 | ||||||
| chr2:164566367
|
G | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0058others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-18551C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566367 | ||||||
| chr2:164566495
|
A | G | 9 | a0001c0001t0004g0031a0001c0001t0004g0080a0002c0002t0002g0161others(6): Show | 9 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-18679T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566495 | ||||||
| chr2:164566619
|
G | C | 1 | a0002c0002t0003g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.325-18803C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566619 | ||||||
| chr2:164566679
|
C | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-18863G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566679 | ||||||
| chr2:164566774
|
A | C | 1 | a0001c0001t0006g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-18958T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566774 | ||||||
| chr2:164567111
|
T | C | 1 | a0002c0002t0003g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.325-19295A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567111 | ||||||
| chr2:164567343
|
C | T | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-19527G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567343 | ||||||
| chr2:164567602
|
A | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-19786T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567602 | ||||||
| chr2:164567670
|
C | T | 3 | a0002c0002t0003g0178a0002c0002t0003g0185a0002c0002t0003g0214 | 3 | NA18998.hp1 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.325-19854G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567670 | ||||||
| chr2:164567699
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.325-19883G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567699 | ||||||
| chr2:164568065
|
G | A | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.325-20249C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568065 | ||||||
| chr2:164568202
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-20386C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568202 | ||||||
| chr2:164568288
|
GA | G | 7 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0130others(4): Show | 7 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-20473delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568288 | ||||||
| chr2:164568327
|
A | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(45): Show | 49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.325-20511T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568327 | ||||||
| chr2:164568407
|
G | A | 1 | a0001c0001t0006g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.325-20591C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568407 | ||||||
| chr2:164568484
|
T | C | 83 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(80): Show | 83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.325-20668A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568484 | ||||||
| chr2:164568808
|
T | A | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-20992A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568808 | ||||||
| chr2:164568809
|
A | C | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-20993T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568809 | ||||||
| chr2:164568810
|
A | T | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-20994T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568810 | ||||||
| chr2:164568811
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0106others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-20995A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568811 | ||||||
| chr2:164569233
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.325-21417T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569233 | ||||||
| chr2:164569537
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.325-21721A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569537 | ||||||
| chr2:164569562
|
C | T | 1 | a0002c0002t0002g0209 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.325-21746G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569562 | ||||||
| chr2:164569876
|
C | G | 129 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.325-22060G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569876 | ||||||
| chr2:164570145
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-22329G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570145 | ||||||
| chr2:164570180
|
G | A | 2 | a0002c0002t0003g0240a0002c0002t0003g0260 | 2 | HG00642.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.325-22364C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570180 | ||||||
| chr2:164570272
|
A | G | 14 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-22456T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570272 | ||||||
| chr2:164570275
|
T | TA | 61 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0057others(58): Show | 62 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.325-22460dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | ||||||
| chr2:164570275
|
T | TAA | 6 | a0001c0001t0001g0015a0001c0001t0004g0031a0001c0001t0004g0080others(3): Show | 6 | HG00408.hp2 HG00438.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-22461_325-2246 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | ||||||
| chr2:164570275
|
TA | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0106others(7): Show | 10 | HG00738.hp2 HG01255.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-22460delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | ||||||
| chr2:164570275
|
TAA | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0129a0001c0001t0001g0135others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.325-22461_325-2246 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | ||||||
| chr2:164570368
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.325-22552A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570368 | ||||||
| chr2:164570546
|
C | T | 1 | a0006c0011t0007g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-22730G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570546 | ||||||
| chr2:164570753
|
A | G | 14 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-22937T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570753 | ||||||
| chr2:164570838
|
A | G | 1 | a0002c0002t0003g0253 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.325-23022T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570838 | ||||||
| chr2:164570878
|
C | T | 5 | a0001c0001t0001g0086a0001c0001t0001g0114a0001c0001t0006g0145others(2): Show | 5 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-23062G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570878 | ||||||
| chr2:164571266
|
CA | C | 14 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-23451delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571266 | ||||||
| chr2:164571315
|
G | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.325-23499C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571315 | ||||||
| chr2:164571546
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.325-23730G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571546 | ||||||
| chr2:164571639
|
T | G | 2 | a0001c0001t0006g0159a0001c0001t0007g0134 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.325-23823A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571639 | ||||||
| chr2:164571844
|
G | A | 1 | a0002c0002t0003g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-24028C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571844 | ||||||
| chr2:164571844
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.325-24028C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571844 | ||||||
| chr2:164571951
|
C | T | 1 | a0002c0002t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.325-24135G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571951 | ||||||
| chr2:164571960
|
G | A | 14 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-24144C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571960 | ||||||
| chr2:164571961
|
C | A | 3 | a0002c0002t0002g0232a0002c0002t0002g0281a0002c0002t0005g0238 | 3 | HG00639.hp2 HG00738.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.325-24145G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571961 | ||||||
| chr2:164572462
|
G | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0067a0002c0002t0003g0194 | 3 | HG00544.hp2 NA18977.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.325-24646C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572462 | ||||||
| chr2:164572557
|
T | C | 3 | a0002c0002t0003g0002a0002c0002t0003g0163a0002c0002t0003g0237 | 4 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-24741A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572557 | ||||||
| chr2:164572629
|
G | C | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-24813C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572629 | ||||||
| chr2:164572725
|
G | A | 47 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.325-24909C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572725 | ||||||
| chr2:164572725
|
G | T | 4 | a0002c0002t0002g0221a0002c0002t0002g0262a0002c0002t0002g0291others(1): Show | 4 | HG02056.hp1 NA18972.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-24909C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572725 | ||||||
| chr2:164572788
|
T | A | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.325-24972A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572788 | ||||||
| chr2:164572799
|
G | A | 1 | a0002c0002t0003g0250 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.325-24983C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572799 | ||||||
| chr2:164572917
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-25101G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572917 | ||||||
| chr2:164573027
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 31 | HG01175.hp2 HG01255.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-25211A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573027 | ||||||
| chr2:164573203
|
G | C | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-25387C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573203 | ||||||
| chr2:164573338
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-25522G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573338 | ||||||
| chr2:164573393
|
C | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0053 | 3 | NA19006.hp2 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.325-25577G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573393 | ||||||
| chr2:164573632
|
G | GT | 46 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 46 | HG00735.hp1 HG01175.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.325-25817dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573632 | ||||||
| chr2:164573711
|
C | T | 1 | a0002c0002t0003g0266 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.325-25895G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573711 | ||||||
| chr2:164573894
|
C | T | 7 | a0001c0001t0004g0097a0001c0001t0004g0098a0001c0001t0004g0099others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-26078G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573894 | ||||||
| chr2:164573913
|
T | TATGGGTA others(21): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0044 | 2 | NA19005.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.325-26125_325-2609 others(32): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573913 | ||||||
| chr2:164574211
|
T | C | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-26395A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574211 | ||||||
| chr2:164574241
|
CT | C | 20 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0129others(17): Show | 20 | HG00735.hp1 HG01515.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.325-26426delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574241 | ||||||
| chr2:164574335
|
G | A | 2 | a0001c0001t0006g0159a0001c0001t0007g0134 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.325-26519C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574335 | ||||||
| chr2:164574432
|
G | C | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-26616C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574432 | ||||||
| chr2:164574469
|
G | A | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-26653C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574469 | ||||||
| chr2:164574473
|
T | C | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-26657A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574473 | ||||||
| chr2:164574546
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.325-26730A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574546 | ||||||
| chr2:164574632
|
C | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-26816G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574632 | ||||||
| chr2:164574652
|
A | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 31 | HG01175.hp2 HG01255.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-26836T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574652 | ||||||
| chr2:164574659
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.325-26843C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574659 | ||||||
| chr2:164574661
|
T | C | 34 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0060others(31): Show | 35 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-26845A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574661 | ||||||
| chr2:164574797
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-26981C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574797 | ||||||
| chr2:164574896
|
C | T | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-27080G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574896 | ||||||
| chr2:164575179
|
C | A | 1 | a0002c0002t0003g0204 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.325-27363G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575179 | ||||||
| chr2:164575573
|
T | C | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-27757A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575573 | ||||||
| chr2:164575681
|
G | C | 5 | a0001c0001t0001g0118a0001c0001t0001g0130a0001c0001t0009g0111others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-27865C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575681 | ||||||
| chr2:164575975
|
G | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 33 | HG00735.hp1 HG01255.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.325-28159C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575975 | ||||||
| chr2:164576073
|
A | T | 1 | a0002c0002t0002g0182 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.325-28257T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576073 | ||||||
| chr2:164576356
|
ATTTAAC | A | 3 | a0001c0001t0006g0158a0001c0001t0008g0149a0001c0001t0008g0150 | 3 | HG02723.hp1 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.325-28546_325-2854 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576356 | ||||||
| chr2:164576409
|
T | TA | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-28594dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576409 | ||||||
| chr2:164576422
|
G | C | 1 | a0001c0001t0004g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325-28606C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576422 | ||||||
| chr2:164576647
|
T | C | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-28831A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576647 | ||||||
| chr2:164576708
|
G | A | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-28892C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576708 | ||||||
| chr2:164576733
|
T | C | 34 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0060others(31): Show | 35 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-28917A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576733 | ||||||
| chr2:164576825
|
GA | G | 57 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.325-29010delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576825 | ||||||
| chr2:164576920
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.325-29104T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576920 | ||||||
| chr2:164576969
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0053 | 2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.325-29153T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576969 | ||||||
| chr2:164577055
|
T | C | 1 | a0002c0002t0002g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.325-29239A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577055 | ||||||
| chr2:164577087
|
T | C | 46 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 46 | HG00735.hp1 HG01175.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.325-29271A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577087 | ||||||
| chr2:164577106
|
G | T | 34 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0060others(31): Show | 35 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-29290C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577106 | ||||||
| chr2:164577178
|
T | C | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-29362A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577178 | ||||||
| chr2:164577317
|
C | T | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-29501G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577317 | ||||||
| chr2:164577381
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.325-29565C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577381 | ||||||
| chr2:164577386
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-29570C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577386 | ||||||
| chr2:164577508
|
A | C | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-29692T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577508 | ||||||
| chr2:164577529
|
C | T | 2 | a0001c0003t0001g0074a0001c0003t0007g0042 | 2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.325-29713G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577529 | ||||||
| chr2:164577537
|
C | A | 3 | a0002c0002t0003g0178a0002c0002t0003g0185a0002c0002t0003g0214 | 3 | NA18998.hp1 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.325-29721G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577537 | ||||||
| chr2:164577569
|
C | T | 1 | a0002c0002t0003g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.325-29753G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577569 | ||||||
| chr2:164577676
|
C | T | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-29860G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577676 | ||||||
| chr2:164577678
|
C | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0076 | 2 | HG02523.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.325-29862G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577678 | ||||||
| chr2:164577856
|
C | G | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-30040G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577856 | ||||||
| chr2:164577889
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-30073C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577889 | ||||||
| chr2:164578295
|
G | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-30479C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578295 | ||||||
| chr2:164578363
|
A | G | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-30547T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578363 | ||||||
| chr2:164578386
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-30570A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578386 | ||||||
| chr2:164578522
|
G | GCA | 16 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0001g0102others(13): Show | 16 | HG01106.hp1 HG01175.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.325-30708_325-3070 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | ||||||
| chr2:164578522
|
G | GCACA | 27 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0069others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.325-30710_325-3070 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | ||||||
| chr2:164578522
|
G | GCACACA | 74 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0040others(71): Show | 75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.325-30712_325-3070 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | ||||||
| chr2:164578522
|
G | GCACACAC others(1): Show |
10 | a0001c0001t0004g0041a0002c0002t0002g0182a0002c0002t0002g0186others(7): Show | 10 | HG01070.hp1 HG01934.hp2 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-30714_325-3070 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | ||||||
| chr2:164578522
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.325-30716_325-3070 others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | ||||||
| chr2:164578522
|
GCA | G | 15 | a0001c0001t0001g0095a0001c0001t0001g0122a0001c0001t0001g0129others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-30708_325-3070 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | ||||||
| chr2:164578524
|
A | G | 3 | a0001c0001t0001g0089a0001c0001t0011g0087a0001c0001t0011g0090 | 3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.325-30708T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578524 | ||||||
| chr2:164578526
|
A | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-30710T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578526 | ||||||
| chr2:164578528
|
A | G | 4 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-30712T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578528 | ||||||
| chr2:164578542
|
A | G | 9 | a0001c0001t0001g0072a0002c0002t0002g0248a0002c0002t0003g0234others(6): Show | 9 | HG00738.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-30726T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578542 | ||||||
| chr2:164578599
|
T | G | 3 | a0002c0002t0003g0235a0002c0002t0003g0253a0002c0002t0003g0287 | 3 | HG01934.hp1 NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.325-30783A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578599 | ||||||
| chr2:164578767
|
C | A | 1 | a0002c0002t0002g0211 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.325-30951G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578767 | ||||||
| chr2:164579032
|
T | TAA | 14 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(11): Show | 14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-31217_325-3121 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579032 | ||||||
| chr2:164579033
|
T | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 34 | HG00735.hp1 HG01255.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.325-31217A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579033 | ||||||
| chr2:164579050
|
T | C | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-31234A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579050 | ||||||
| chr2:164579056
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0032 | 2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.325-31240T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579056 | ||||||
| chr2:164579169
|
G | C | 1 | a0001c0001t0007g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.325-31353C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579169 | ||||||
| chr2:164579500
|
T | TGCGC | 4 | a0001c0001t0001g0089a0001c0001t0007g0103a0001c0001t0011g0087others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-31685_325-3168 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579500 | ||||||
| chr2:164579500
|
T | TGCGCGCA others(1): Show |
10 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-31685_325-3168 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579500 | ||||||
| chr2:164579501
|
G | GCA | 22 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0071others(19): Show | 22 | HG00438.hp2 HG00673.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.325-31687_325-3168 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579501
|
G | GCACA | 5 | a0001c0001t0001g0033a0001c0001t0006g0146a0002c0002t0003g0160others(2): Show | 5 | HG01099.hp1 HG02630.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-31689_325-3168 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579501
|
GCA | G | 27 | a0001c0001t0001g0055a0001c0001t0001g0070a0001c0001t0001g0102others(24): Show | 27 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.325-31687_325-3168 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579501
|
GCACA | G | 10 | a0001c0003t0001g0074a0002c0002t0003g0203a0002c0002t0005g0222others(7): Show | 10 | HG00642.hp2 HG01257.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-31689_325-3168 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579501
|
GCACACAC others(3): Show |
G | 1 | a0002c0002t0002g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.325-31695_325-3168 others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579501
|
GCACACAC others(5): Show |
G | 2 | a0001c0001t0001g0005a0002c0002t0003g0206 | 2 | HG02083.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.325-31697_325-3168 others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579501
|
GCACACAC others(7): Show |
G | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.325-31699_325-3168 others(18): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579501
|
GCACACAC others(9): Show |
G | 1 | a0002c0002t0002g0255 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.325-31701_325-3168 others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | ||||||
| chr2:164579503
|
A | G | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-31687T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579503 | ||||||
| chr2:164579505
|
A | G | 4 | a0001c0001t0001g0089a0001c0001t0007g0103a0001c0001t0011g0087others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-31689T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579505 | ||||||
| chr2:164579545
|
A | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.325-31729T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579545 | ||||||
| chr2:164579627
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-31811G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579627 | ||||||
| chr2:164579688
|
AT | A | 16 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(13): Show | 16 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.325-31873delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579688 | ||||||
| chr2:164579797
|
C | T | 14 | a0001c0001t0004g0017a0001c0001t0010g0147a0002c0002t0002g0174others(11): Show | 14 | HG00544.hp1 HG02056.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-31981G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579797 | ||||||
| chr2:164579919
|
C | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-32103G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579919 | ||||||
| chr2:164580069
|
A | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.325-32253T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580069 | ||||||
| chr2:164580085
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.325-32269A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580085 | ||||||
| chr2:164580096
|
AT | A | 100 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(97): Show | 100 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.325-32281delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580096 | ||||||
| chr2:164580096
|
ATT | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.325-32282_325-3228 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580096 | ||||||
| chr2:164580096
|
ATTTT | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-32284_325-3228 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580096 | ||||||
| chr2:164580238
|
G | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0133a0001c0001t0004g0029others(3): Show | 6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-32422C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580238 | ||||||
| chr2:164580268
|
T | C | 1 | a0001c0001t0004g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-32452A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580268 | ||||||
| chr2:164580281
|
C | T | 2 | a0002c0002t0003g0261a0008c0007t0003g0220 | 2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-32465G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580281 | ||||||
| chr2:164580324
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-32508G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580324 | ||||||
| chr2:164580430
|
C | T | 2 | a0002c0002t0002g0256a0002c0002t0002g0274 | 2 | HG00140.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.325-32614G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580430 | ||||||
| chr2:164580539
|
T | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.325-32723A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580539 | ||||||
| chr2:164580580
|
T | C | 13 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0118others(10): Show | 13 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.325-32764A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580580 | ||||||
| chr2:164580586
|
C | T | 3 | a0001c0001t0001g0056a0002c0002t0005g0167a0002c0002t0005g0181 | 3 | HG01516.hp1 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.325-32770G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580586 | ||||||
| chr2:164580628
|
C | T | 6 | a0002c0002t0002g0289a0002c0002t0002g0292a0002c0002t0003g0002others(3): Show | 7 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-32812G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580628 | ||||||
| chr2:164580629
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.325-32813C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580629 | ||||||
| chr2:164580709
|
GA | G | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-32894delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580709 | ||||||
| chr2:164580709
|
GAA | G | 18 | a0001c0001t0001g0089a0001c0001t0001g0105a0001c0001t0001g0129others(15): Show | 18 | HG00735.hp1 HG01993.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-32895_325-3289 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580709 | ||||||
| chr2:164580726
|
G | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0135others(12): Show | 15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-32910C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580726 | ||||||
| chr2:164580770
|
A | G | 9 | a0001c0001t0004g0031a0001c0001t0004g0080a0002c0002t0002g0161others(6): Show | 9 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-32954T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580770 | ||||||
| chr2:164580910
|
T | C | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.325-33094A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580910 | ||||||
| chr2:164581034
|
C | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0025others(51): Show | 55 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.325-33218G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581034 | ||||||
| chr2:164581067
|
T | C | 1 | a0001c0001t0009g0111 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.325-33251A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581067 | ||||||
| chr2:164581082
|
A | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.325-33266T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581082 | ||||||
| chr2:164581212
|
A | G | 201 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.325-33396T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581212 | ||||||
| chr2:164581226
|
C | G | 108 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0033others(105): Show | 109 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.325-33410G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581226 | ||||||
| chr2:164581380
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325-33564C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581380 | ||||||
| chr2:164581702
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-33886A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581702 | ||||||
| chr2:164581720
|
G | A | 119 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0016others(116): Show | 119 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.325-33904C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581720 | ||||||
| chr2:164581749
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0069 | 2 | HG02027.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.325-33933C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581749 | ||||||
| chr2:164581871
|
T | A | 4 | a0001c0001t0001g0104a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02976.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-34055A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581871 | ||||||
| chr2:164581886
|
G | A | 6 | a0001c0001t0001g0118a0001c0001t0001g0130a0001c0001t0004g0117others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-34070C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581886 | ||||||
| chr2:164581963
|
T | C | 64 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 64 | HG00140.hp1 HG00609.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.325-34147A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581963 | ||||||
| chr2:164582140
|
G | A | 1 | a0001c0001t0004g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.325-34324C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582140 | ||||||
| chr2:164582150
|
C | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(25): Show | 28 | HG00140.hp1 HG01175.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.325-34334G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582150 | ||||||
| chr2:164582193
|
A | G | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-34377T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582193 | ||||||
| chr2:164582420
|
TA | T | 8 | a0001c0001t0001g0086a0001c0001t0001g0102a0001c0001t0004g0097others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.325-34605delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582420 | ||||||
| chr2:164582421
|
A | T | 1 | a0001c0001t0004g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.325-34605T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582421 | ||||||
| chr2:164582422
|
TTA | T | 42 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(39): Show | 43 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.325-34608_325-3460 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582422 | ||||||
| chr2:164582423
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.325-34607A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582423 | ||||||
| chr2:164582423
|
TA | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(32): Show | 35 | HG00609.hp1 HG01175.hp2 HG02027.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-34608delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582423 | ||||||
| chr2:164582424
|
A | T | 11 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0102others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-34608T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582424 | ||||||
| chr2:164582424
|
AT | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-34609delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582424 | ||||||
| chr2:164582425
|
T | A | 2 | a0001c0001t0001g0055a0001c0001t0004g0029 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.325-34609A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582425 | ||||||
| chr2:164582426
|
T | A | 31 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0032others(28): Show | 31 | HG00609.hp1 HG01175.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-34610A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582426 | ||||||
| chr2:164582427
|
T | A | 39 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0089others(36): Show | 40 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.325-34611A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582427 | ||||||
| chr2:164582428
|
T | A | 1 | a0002c0002t0002g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.325-34612A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582428 | ||||||
| chr2:164582430
|
T | A | 8 | a0001c0001t0001g0104a0001c0001t0001g0116a0001c0001t0001g0132others(5): Show | 8 | HG02109.hp2 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-34614A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582430 | ||||||
| chr2:164582431
|
T | A | 32 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0105others(29): Show | 33 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-34615A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582431 | ||||||
| chr2:164582435
|
T | A | 1 | a0001c0001t0006g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.325-34619A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582435 | ||||||
| chr2:164582490
|
C | T | 1 | a0002c0002t0003g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.325-34674G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582490 | ||||||
| chr2:164582618
|
G | A | 9 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0105others(6): Show | 9 | HG00735.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-34802C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582618 | ||||||
| chr2:164582715
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0004g0051a0001c0001t0006g0146 | 3 | HG00099.hp2 HG00621.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.325-34899C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582715 | ||||||
| chr2:164582768
|
G | C | 1 | a0002c0002t0002g0192 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.325-34952C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582768 | ||||||
| chr2:164583153
|
T | C | 291 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(288): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.325-35337A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164583153 | ||||||
| chr2:164583168
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 14 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-35352G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164583168 | ||||||
| chr2:164583469
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0128 | 2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.325-35653A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164583469 | ||||||
| chr2:164583864
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0058others(9): Show | 12 | HG00735.hp1 HG01255.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+35823A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164583864 | ||||||
| chr2:164584049
|
G | A | 1 | a0002c0002t0002g0207 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.324+35638C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584049 | ||||||
| chr2:164584132
|
A | C | 1 | a0001c0001t0004g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324+35555T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584132 | ||||||
| chr2:164584147
|
A | AT | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0036others(13): Show | 16 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.324+35539dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | ||||||
| chr2:164584147
|
AT | A | 145 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(142): Show | 147 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.324+35539delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | ||||||
| chr2:164584147
|
ATT | A | 12 | a0001c0001t0001g0138a0001c0001t0004g0049a0001c0001t0004g0112others(9): Show | 12 | HG01517.hp1 HG02080.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+35538_324+3553 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | ||||||
| chr2:164584147
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0021a0001c0001t0001g0053 | 2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.324+35528_324+3553 others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | ||||||
| chr2:164584240
|
G | A | 6 | a0002c0002t0002g0161a0002c0002t0002g0196a0002c0002t0002g0197others(3): Show | 6 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+35447C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584240 | ||||||
| chr2:164584433
|
G | A | 3 | a0001c0001t0004g0112a0001c0001t0004g0127a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.324+35254C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584433 | ||||||
| chr2:164584585
|
T | TA | 8 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0034others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+35101dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584585 | ||||||
| chr2:164584949
|
G | A | 2 | a0001c0001t0004g0079a0004c0006t0001g0003 | 2 | HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.324+34738C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584949 | ||||||
| chr2:164584986
|
GGCTAGAG others(1): Show |
G | 46 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0058others(43): Show | 47 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.324+34693_324+3470 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584986 | ||||||
| chr2:164585085
|
C | CT | 8 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0076others(5): Show | 8 | HG00621.hp1 HG01255.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+34601dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
C | CTTTTT | 7 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0102others(4): Show | 7 | HG02922.hp1 HG03540.hp2 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+34597_324+3460 others(9): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
C | CTTTTTT | 6 | a0001c0001t0001g0075a0001c0001t0004g0097a0001c0001t0004g0098others(3): Show | 6 | HG02055.hp2 HG02071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+34596_324+3460 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0036 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.324+34591_324+3460 others(15): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CT | C | 37 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(34): Show | 37 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.324+34601delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTT | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0054others(13): Show | 17 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.324+34600_324+3460 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTT | C | 8 | a0001c0001t0001g0095a0001c0001t0006g0145a0001c0001t0006g0148others(5): Show | 8 | HG00733.hp2 HG01099.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+34599_324+3460 others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTT | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(6): Show | 9 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+34598_324+3460 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(1): Show |
C | 27 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0069others(24): Show | 27 | HG01123.hp1 HG01169.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+34594_324+3460 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(2): Show |
C | 83 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0033others(80): Show | 84 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.324+34593_324+3460 others(13): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0001g0086a0001c0001t0001g0122a0001c0001t0001g0128others(7): Show | 10 | HG01975.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+34592_324+3460 others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0001g0104a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG02622.hp1 HG02895.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+34591_324+3460 others(15): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0002g0195 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.324+34590_324+3460 others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(6): Show |
C | 1 | a0004c0006t0001g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.324+34589_324+3460 others(17): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(9): Show |
C | 12 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0123others(9): Show | 12 | HG01175.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+34586_324+3460 others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(10): Show |
C | 15 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+34585_324+3460 others(21): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324+34581_324+3460 others(25): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585085
|
CTTTTTTT others(15): Show |
C | 1 | a0002c0002t0003g0261 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+34580_324+3460 others(26): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | ||||||
| chr2:164585168
|
G | A | 1 | a0001c0001t0006g0153 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.324+34519C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585168 | ||||||
| chr2:164585198
|
T | C | 120 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(117): Show | 121 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.324+34489A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585198 | ||||||
| chr2:164585341
|
A | C | 1 | a0002c0002t0002g0199 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324+34346T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585341 | ||||||
| chr2:164585624
|
T | C | 1 | a0001c0012t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.324+34063A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585624 | ||||||
| chr2:164585802
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+33885A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585802 | ||||||
| chr2:164585852
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.324+33835T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585852 | ||||||
| chr2:164586215
|
T | C | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.324+33472A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586215 | ||||||
| chr2:164586292
|
T | C | 1 | a0001c0001t0010g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.324+33395A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586292 | ||||||
| chr2:164586296
|
T | C | 1 | a0002c0002t0003g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.324+33391A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586296 | ||||||
| chr2:164586493
|
T | C | 1 | a0002c0002t0002g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.324+33194A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586493 | ||||||
| chr2:164586617
|
T | C | 210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.324+33070A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586617 | ||||||
| chr2:164587255
|
T | C | 1 | a0009c0009t0005g0288 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.324+32432A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587255 | ||||||
| chr2:164587336
|
T | A | 1 | a0002c0002t0003g0279 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.324+32351A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587336 | ||||||
| chr2:164587351
|
C | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(24): Show | 27 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.324+32336G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587351 | ||||||
| chr2:164587372
|
C | T | 1 | a0002c0002t0002g0231 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.324+32315G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587372 | ||||||
| chr2:164587380
|
T | A | 1 | a0002c0002t0003g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.324+32307A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587380 | ||||||
| chr2:164587404
|
G | T | 3 | a0001c0001t0001g0132a0001c0001t0004g0096a0006c0011t0007g0131 | 3 | HG02723.hp2 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+32283C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587404 | ||||||
| chr2:164587474
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(12): Show | 15 | HG00609.hp1 HG02027.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+32213C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587474 | ||||||
| chr2:164587562
|
T | C | 7 | a0002c0002t0002g0289a0002c0002t0002g0292a0002c0002t0003g0163others(4): Show | 7 | HG00642.hp1 HG01256.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+32125A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587562 | ||||||
| chr2:164587714
|
C | T | 1 | a0002c0002t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.324+31973G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587714 | ||||||
| chr2:164587742
|
C | T | 7 | a0002c0002t0002g0218a0002c0002t0002g0226a0002c0002t0002g0232others(4): Show | 7 | HG00639.hp2 HG00738.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+31945G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587742 | ||||||
| chr2:164587853
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0075 | 2 | HG02071.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.324+31834T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587853 | ||||||
| chr2:164588142
|
C | A | 1 | a0002c0002t0002g0192 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.324+31545G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588142 | ||||||
| chr2:164588164
|
T | C | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+31523A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588164 | ||||||
| chr2:164588546
|
AT | A | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(32): Show | 35 | HG00609.hp1 HG02027.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+31140delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588546 | ||||||
| chr2:164588555
|
A | T | 1 | a0001c0001t0004g0066 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.324+31132T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588555 | ||||||
| chr2:164588556
|
C | A | 1 | a0001c0001t0004g0066 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.324+31131G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588556 | ||||||
| chr2:164588841
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+30846G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588841 | ||||||
| chr2:164588888
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+30799C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588888 | ||||||
| chr2:164588958
|
G | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 100 | HG00609.hp1 HG00642.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.324+30729C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588958 | ||||||
| chr2:164589110
|
T | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(11): Show | 14 | HG00609.hp1 HG02027.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.324+30577A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589110 | ||||||
| chr2:164589117
|
A | G | 1 | a0002c0002t0002g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.324+30570T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589117 | ||||||
| chr2:164589125
|
C | G | 1 | a0002c0002t0003g0250 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.324+30562G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589125 | ||||||
| chr2:164589285
|
C | T | 1 | a0002c0002t0003g0261 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+30402G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589285 | ||||||
| chr2:164589364
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.324+30323T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589364 | ||||||
| chr2:164589549
|
G | C | 6 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0135others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+30138C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589549 | ||||||
| chr2:164589637
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+30050C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589637 | ||||||
| chr2:164589877
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+29810G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589877 | ||||||
| chr2:164589901
|
G | A | 1 | a0002c0002t0003g0261 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+29786C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589901 | ||||||
| chr2:164590000
|
T | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0133a0001c0001t0004g0137others(3): Show | 6 | HG02559.hp2 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+29687A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590000 | ||||||
| chr2:164590036
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0038 | 3 | HG01070.hp2 HG01099.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.324+29651G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590036 | ||||||
| chr2:164590052
|
C | T | 12 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0123others(9): Show | 12 | HG01175.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+29635G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590052 | ||||||
| chr2:164590223
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.324+29464A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590223 | ||||||
| chr2:164590236
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+29451A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590236 | ||||||
| chr2:164590314
|
A | C | 1 | a0006c0011t0007g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+29373T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590314 | ||||||
| chr2:164590801
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02976.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.324+28886T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590801 | ||||||
| chr2:164590835
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+28852G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590835 | ||||||
| chr2:164591283
|
A | G | 1 | a0001c0001t0006g0153 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.324+28404T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591283 | ||||||
| chr2:164591344
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+28343A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591344 | ||||||
| chr2:164591447
|
G | A | 1 | a0002c0002t0005g0265 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.324+28240C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591447 | ||||||
| chr2:164591553
|
C | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0058others(2): Show | 5 | HG01255.hp2 HG03239.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+28134G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591553 | ||||||
| chr2:164591794
|
C | A | 28 | a0001c0001t0004g0004a0002c0002t0002g0161a0002c0002t0002g0177others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.324+27893G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591794 | ||||||
| chr2:164591892
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0058others(9): Show | 12 | HG00735.hp1 HG01255.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+27795A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591892 | ||||||
| chr2:164592079
|
G | A | 15 | a0001c0001t0001g0102a0001c0001t0001g0122a0001c0001t0001g0128others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+27608C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592079 | ||||||
| chr2:164592123
|
G | GT | 17 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0075others(14): Show | 17 | HG01123.hp1 HG01934.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.324+27563dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592123 | ||||||
| chr2:164592129
|
T | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0102a0001c0001t0001g0122others(10): Show | 13 | HG00423.hp2 HG02055.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+27558A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592129 | ||||||
| chr2:164592236
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0004g0029a0002c0002t0003g0160 | 3 | HG02630.hp2 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+27451C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592236 | ||||||
| chr2:164592355
|
C | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0056others(49): Show | 53 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.324+27332G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592355 | ||||||
| chr2:164592544
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.324+27143C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592544 | ||||||
| chr2:164592566
|
A | G | 1 | a0002c0002t0002g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.324+27121T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592566 | ||||||
| chr2:164592619
|
T | C | 3 | a0001c0001t0001g0057a0001c0001t0004g0029a0002c0002t0003g0160 | 3 | HG02630.hp2 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+27068A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592619 | ||||||
| chr2:164592663
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02976.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.324+27024T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592663 | ||||||
| chr2:164593110
|
T | C | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 114 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.324+26577A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593110 | ||||||
| chr2:164593130
|
C | T | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+26557G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593130 | ||||||
| chr2:164593139
|
A | G | 68 | a0001c0001t0001g0072a0001c0001t0004g0004a0001c0001t0004g0031others(65): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.324+26548T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593139 | ||||||
| chr2:164593241
|
A | G | 53 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0056others(50): Show | 54 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.324+26446T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593241 | ||||||
| chr2:164593403
|
T | C | 6 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+26284A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593403 | ||||||
| chr2:164593446
|
C | T | 1 | a0001c0001t0006g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.324+26241G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593446 | ||||||
| chr2:164593453
|
C | CA | 4 | a0002c0002t0002g0224a0002c0002t0003g0178a0002c0002t0003g0185others(1): Show | 4 | NA18991.hp1 NA18998.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+26233dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593453 | ||||||
| chr2:164593614
|
T | C | 11 | a0001c0001t0001g0102a0001c0001t0001g0122a0001c0001t0001g0128others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+26073A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593614 | ||||||
| chr2:164593735
|
G | T | 1 | a0002c0002t0003g0261 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+25952C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593735 | ||||||
| chr2:164594146
|
A | C | 1 | a0001c0001t0004g0031 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.324+25541T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594146 | ||||||
| chr2:164594236
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0004g0029 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+25451G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594236 | ||||||
| chr2:164594295
|
A | G | 2 | a0003c0004t0008g0142a0003c0004t0008g0156 | 2 | HG01099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.324+25392T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594295 | ||||||
| chr2:164594322
|
C | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0004g0088others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+25365G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594322 | ||||||
| chr2:164594490
|
G | A | 1 | a0002c0002t0002g0274 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.324+25197C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594490 | ||||||
| chr2:164594522
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324+25165G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594522 | ||||||
| chr2:164594582
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324+25105T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594582 | ||||||
| chr2:164594843
|
A | G | 53 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0056others(50): Show | 54 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.324+24844T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594843 | ||||||
| chr2:164594962
|
T | C | 12 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0123others(9): Show | 12 | HG01175.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+24725A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594962 | ||||||
| chr2:164595043
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.324+24644A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595043 | ||||||
| chr2:164595094
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324+24593A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595094 | ||||||
| chr2:164595226
|
C | T | 15 | a0001c0001t0001g0102a0001c0001t0001g0122a0001c0001t0001g0128others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+24461G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595226 | ||||||
| chr2:164595252
|
G | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(16): Show | 19 | HG00609.hp1 HG02027.hp2 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.324+24435C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595252 | ||||||
| chr2:164595280
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324+24407T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595280 | ||||||
| chr2:164595379
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+24308G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595379 | ||||||
| chr2:164595515
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.324+24172T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595515 | ||||||
| chr2:164595520
|
G | A | 1 | a0002c0002t0003g0229 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.324+24167C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595520 | ||||||
| chr2:164595750
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324+23937G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595750 | ||||||
| chr2:164595856
|
A | T | 31 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(28): Show | 32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.324+23831T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595856 | ||||||
| chr2:164595905
|
G | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0014others(42): Show | 46 | HG00140.hp1 HG00408.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.324+23782C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595905 | ||||||
| chr2:164595952
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.324+23735A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595952 | ||||||
| chr2:164595991
|
G | A | 47 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059others(44): Show | 48 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.324+23696C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595991 | ||||||
| chr2:164595994
|
T | G | 8 | a0001c0001t0004g0096a0001c0001t0004g0097a0001c0001t0004g0098others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+23693A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595994 | ||||||
| chr2:164596004
|
G | A | 2 | a0001c0001t0001g0132a0006c0011t0007g0131 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+23683C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596004 | ||||||
| chr2:164596099
|
G | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0058a0002c0002t0002g0192 | 3 | HG01255.hp2 HG04204.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.324+23588C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596099 | ||||||
| chr2:164596104
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0004g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.324+23583G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596104 | ||||||
| chr2:164596232
|
C | T | 211 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+23455G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596232 | ||||||
| chr2:164596348
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+23339C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596348 | ||||||
| chr2:164596398
|
T | C | 5 | a0001c0001t0001g0086a0001c0001t0001g0104a0001c0001t0001g0122others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+23289A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596398 | ||||||
| chr2:164596476
|
G | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(32): Show | 35 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+23211C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596476 | ||||||
| chr2:164596738
|
T | C | 1 | a0002c0002t0002g0224 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.324+22949A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596738 | ||||||
| chr2:164596870
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+22817A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596870 | ||||||
| chr2:164596895
|
C | A | 102 | a0001c0001t0001g0072a0001c0001t0004g0031a0001c0001t0010g0140others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.324+22792G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596895 | ||||||
| chr2:164596909
|
TA | T | 6 | a0001c0001t0001g0086a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+22777delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596909 | ||||||
| chr2:164596970
|
T | C | 2 | a0002c0002t0002g0268a0002c0002t0002g0280 | 2 | HG02080.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.324+22717A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596970 | ||||||
| chr2:164597337
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+22350T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597337 | ||||||
| chr2:164597352
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.324+22335A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597352 | ||||||
| chr2:164597450
|
A | G | 1 | a0001c0001t0004g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.324+22237T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597450 | ||||||
| chr2:164597487
|
C | A | 13 | a0002c0002t0002g0171a0002c0002t0003g0168a0002c0002t0003g0172others(10): Show | 13 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+22200G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597487 | ||||||
| chr2:164597555
|
T | C | 1 | a0001c0001t0007g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.324+22132A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597555 | ||||||
| chr2:164597580
|
G | A | 1 | a0005c0010t0012g0011 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.324+22107C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597580 | ||||||
| chr2:164597590
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(3): Show | 6 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+22097T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597590 | ||||||
| chr2:164597602
|
G | T | 34 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+22085C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597602 | ||||||
| chr2:164597777
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.324+21910T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597777 | ||||||
| chr2:164598192
|
G | A | 10 | a0001c0001t0001g0102a0001c0001t0004g0096a0001c0001t0004g0097others(7): Show | 10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+21495C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598192 | ||||||
| chr2:164598283
|
T | G | 35 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(32): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.324+21404A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598283 | ||||||
| chr2:164598467
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+21220A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598467 | ||||||
| chr2:164598525
|
T | C | 102 | a0001c0001t0001g0072a0001c0001t0004g0031a0001c0001t0010g0140others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.324+21162A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598525 | ||||||
| chr2:164598939
|
TAA | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+20746_324+2074 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598939 | ||||||
| chr2:164598943
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324+20744C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598943 | ||||||
| chr2:164599308
|
CG | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+20378delC | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599308 | ||||||
| chr2:164599472
|
C | T | 2 | a0001c0001t0008g0149a0001c0001t0008g0150 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.324+20215G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599472 | ||||||
| chr2:164599683
|
T | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(16): Show | 19 | HG00140.hp1 HG01261.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.324+20004A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599683 | ||||||
| chr2:164599718
|
T | C | 2 | a0002c0002t0002g0189a0002c0002t0002g0274 | 2 | HG01123.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.324+19969A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599718 | ||||||
| chr2:164600462
|
A | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+19225T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600462 | ||||||
| chr2:164600552
|
C | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0067others(1): Show | 4 | HG00544.hp2 HG00621.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+19135G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600552 | ||||||
| chr2:164600585
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0004g0080 | 3 | NA19006.hp1 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.324+19102C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600585 | ||||||
| chr2:164600756
|
T | A | 200 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.324+18931A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600756 | ||||||
| chr2:164601041
|
C | G | 1 | a0001c0001t0006g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.324+18646G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601041 | ||||||
| chr2:164601077
|
T | C | 1 | a0002c0002t0003g0234 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.324+18610A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601077 | ||||||
| chr2:164601127
|
C | A | 9 | a0001c0001t0001g0102a0001c0001t0004g0096a0001c0001t0004g0097others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+18560G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601127 | ||||||
| chr2:164601142
|
A | G | 2 | a0002c0002t0005g0167a0002c0002t0005g0181 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.324+18545T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601142 | ||||||
| chr2:164601612
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.324+18075A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601612 | ||||||
| chr2:164601823
|
C | T | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+17864G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601823 | ||||||
| chr2:164601843
|
T | C | 1 | a0002c0002t0005g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.324+17844A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601843 | ||||||
| chr2:164601937
|
A | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+17750T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601937 | ||||||
| chr2:164602012
|
G | A | 1 | a0002c0002t0002g0217 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.324+17675C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602012 | ||||||
| chr2:164602133
|
T | A | 1 | a0002c0002t0005g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.324+17554A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602133 | ||||||
| chr2:164602133
|
T | TA | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(9): Show | 12 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+17553dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602133 | ||||||
| chr2:164602134
|
A | T | 1 | a0001c0001t0004g0112 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.324+17553T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602134 | ||||||
| chr2:164602176
|
A | G | 1 | a0001c0001t0007g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.324+17511T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602176 | ||||||
| chr2:164602194
|
A | G | 1 | a0001c0001t0004g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+17493T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602194 | ||||||
| chr2:164602198
|
A | T | 13 | a0002c0002t0002g0171a0002c0002t0003g0168a0002c0002t0003g0172others(10): Show | 13 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+17489T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602198 | ||||||
| chr2:164602380
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+17307T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602380 | ||||||
| chr2:164602431
|
G | A | 8 | a0001c0001t0004g0096a0001c0001t0004g0097a0001c0001t0004g0098others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+17256C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602431 | ||||||
| chr2:164602638
|
G | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+17049C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602638 | ||||||
| chr2:164602986
|
T | C | 34 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+16701A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602986 | ||||||
| chr2:164603239
|
GGAAAA | G | 34 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+16443_324+1644 others(9): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603239 | ||||||
| chr2:164603568
|
G | T | 1 | a0001c0001t0007g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.324+16119C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603568 | ||||||
| chr2:164603629
|
A | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+16058T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603629 | ||||||
| chr2:164603662
|
C | CAA | 9 | a0001c0001t0001g0005a0001c0001t0001g0093a0001c0001t0001g0109others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+16023_324+1602 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603662 | ||||||
| chr2:164603671
|
A | AT | 10 | a0001c0001t0001g0102a0001c0001t0004g0096a0001c0001t0004g0097others(7): Show | 10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+16015_324+1601 others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603671 | ||||||
| chr2:164603671
|
A | T | 3 | a0001c0001t0001g0057a0001c0001t0004g0063a0002c0002t0003g0160 | 3 | HG02630.hp2 HG03453.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.324+16016T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603671 | ||||||
| chr2:164603671
|
AAT | A | 16 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0107others(13): Show | 16 | HG00735.hp1 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.324+16014_324+1601 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603671 | ||||||
| chr2:164603672
|
AT | A | 83 | a0001c0001t0001g0008a0001c0001t0001g0059a0001c0001t0001g0060others(80): Show | 85 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.324+16014delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603672 | ||||||
| chr2:164603673
|
T | A | 98 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.324+16014A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603673 | ||||||
| chr2:164603675
|
T | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.324+16012A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603675 | ||||||
| chr2:164603677
|
T | A | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.324+16010A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603677 | ||||||
| chr2:164603692
|
C | T | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+15995G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603692 | ||||||
| chr2:164603889
|
T | C | 10 | a0001c0001t0001g0102a0001c0001t0004g0096a0001c0001t0004g0097others(7): Show | 10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+15798A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603889 | ||||||
| chr2:164604203
|
C | T | 13 | a0001c0001t0001g0094a0001c0001t0001g0107a0001c0001t0001g0115others(10): Show | 13 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+15484G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604203 | ||||||
| chr2:164604270
|
T | C | 2 | a0001c0001t0001g0132a0006c0011t0007g0131 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+15417A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604270 | ||||||
| chr2:164604294
|
G | T | 33 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.324+15393C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604294 | ||||||
| chr2:164604355
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0004g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.324+15332G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604355 | ||||||
| chr2:164604419
|
C | T | 7 | a0001c0001t0001g0084a0001c0001t0001g0133a0001c0001t0004g0137others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+15268G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604419 | ||||||
| chr2:164604453
|
T | C | 1 | a0001c0001t0006g0153 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.324+15234A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604453 | ||||||
| chr2:164604570
|
G | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+15117C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604570 | ||||||
| chr2:164604606
|
A | G | 222 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(219): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.324+15081T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604606 | ||||||
| chr2:164604858
|
C | T | 2 | a0001c0001t0001g0057a0002c0002t0003g0160 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+14829G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604858 | ||||||
| chr2:164604869
|
A | C | 1 | a0002c0002t0002g0186 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.324+14818T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604869 | ||||||
| chr2:164605011
|
G | A | 1 | a0002c0002t0003g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.324+14676C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605011 | ||||||
| chr2:164605129
|
G | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(2): Show | 5 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+14558C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605129 | ||||||
| chr2:164605145
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+14542A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605145 | ||||||
| chr2:164605228
|
AC | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+14458delG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605228 | ||||||
| chr2:164605335
|
G | A | 13 | a0001c0001t0001g0094a0001c0001t0001g0107a0001c0001t0001g0115others(10): Show | 13 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+14352C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605335 | ||||||
| chr2:164605465
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+14222G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605465 | ||||||
| chr2:164605563
|
A | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0093a0001c0001t0001g0109others(20): Show | 23 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.324+14124T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605563 | ||||||
| chr2:164605721
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00140.hp1 HG01261.hp1 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.324+13966C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605721 | ||||||
| chr2:164605785
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0068 | 3 | NA18972.hp1 NA19056.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.324+13902T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605785 | ||||||
| chr2:164605901
|
C | A | 108 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0092others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.324+13786G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605901 | ||||||
| chr2:164606033
|
T | C | 108 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0092others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.324+13654A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606033 | ||||||
| chr2:164606417
|
A | G | 1 | a0001c0001t0004g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+13270T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606417 | ||||||
| chr2:164606510
|
A | G | 2 | a0002c0002t0003g0237a0002c0002t0003g0273 | 2 | HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.324+13177T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606510 | ||||||
| chr2:164606736
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0004g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.324+12951A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606736 | ||||||
| chr2:164607219
|
G | A | 10 | a0001c0001t0001g0102a0001c0001t0004g0096a0001c0001t0004g0097others(7): Show | 10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+12468C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164607219 | ||||||
| chr2:164607443
|
C | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(209): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.324+12244G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164607443 | ||||||
| chr2:164608238
|
G | A | 1 | a0002c0002t0002g0182 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.324+11449C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608238 | ||||||
| chr2:164608246
|
C | A | 33 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0084others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.324+11441G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608246 | ||||||
| chr2:164608330
|
C | A | 1 | a0002c0002t0003g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.324+11357G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608330 | ||||||
| chr2:164608338
|
C | T | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.324+11349G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608338 | ||||||
| chr2:164608447
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+11240T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608447 | ||||||
| chr2:164608590
|
AG | A | 39 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(36): Show | 40 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.324+11096delC | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608590 | ||||||
| chr2:164608591
|
G | A | 169 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.324+11096C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608591 | ||||||
| chr2:164608592
|
A | G | 4 | a0002c0002t0002g0231a0002c0002t0002g0248a0002c0002t0002g0251others(1): Show | 4 | HG01069.hp2 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+11095T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608592 | ||||||
| chr2:164608644
|
A | T | 1 | a0002c0002t0003g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.324+11043T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608644 | ||||||
| chr2:164608918
|
G | T | 1 | a0001c0003t0007g0042 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.324+10769C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608918 | ||||||
| chr2:164609084
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.324+10603A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609084 | ||||||
| chr2:164609316
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.324+10371G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609316 | ||||||
| chr2:164609429
|
G | A | 1 | a0002c0002t0003g0235 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.324+10258C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609429 | ||||||
| chr2:164609547
|
A | G | 1 | a0002c0002t0003g0261 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+10140T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609547 | ||||||
| chr2:164609588
|
T | C | 1 | a0002c0002t0003g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.324+10099A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609588 | ||||||
| chr2:164609633
|
G | A | 1 | a0001c0003t0007g0042 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.324+10054C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609633 | ||||||
| chr2:164609667
|
G | A | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+10020C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609667 | ||||||
| chr2:164609931
|
T | G | 1 | a0001c0001t0004g0022 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.324+9756A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609931 | ||||||
| chr2:164609939
|
T | G | 151 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(148): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.324+9748A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609939 | ||||||
| chr2:164609999
|
T | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0095 | 3 | HG01891.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324+9688A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609999 | ||||||
| chr2:164610059
|
G | A | 13 | a0001c0001t0001g0094a0001c0001t0001g0107a0001c0001t0001g0115others(10): Show | 13 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+9628C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610059 | ||||||
| chr2:164610132
|
T | C | 1 | a0001c0001t0001g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.324+9555A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610132 | ||||||
| chr2:164610278
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.324+9409G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610278 | ||||||
| chr2:164610327
|
C | T | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+9360G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610327 | ||||||
| chr2:164610344
|
G | A | 199 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(196): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.324+9343C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610344 | ||||||
| chr2:164610384
|
A | T | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.324+9303T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610384 | ||||||
| chr2:164610392
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+9295A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610392 | ||||||
| chr2:164610558
|
A | C | 32 | a0002c0002t0002g0189a0002c0002t0002g0218a0002c0002t0002g0226others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.324+9129T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610558 | ||||||
| chr2:164610562
|
T | C | 27 | a0001c0001t0001g0072a0001c0001t0004g0031a0002c0002t0002g0174others(24): Show | 27 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+9125A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610562 | ||||||
| chr2:164610663
|
A | G | 2 | a0002c0002t0002g0268a0002c0002t0002g0280 | 2 | HG02080.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.324+9024T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610663 | ||||||
| chr2:164610765
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0093a0001c0001t0001g0109others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+8922T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610765 | ||||||
| chr2:164610822
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+8865A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610822 | ||||||
| chr2:164610875
|
A | T | 2 | a0001c0001t0001g0057a0002c0002t0003g0160 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+8812T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610875 | ||||||
| chr2:164610886
|
A | C | 31 | a0001c0001t0001g0084a0001c0001t0001g0114a0001c0001t0001g0133others(28): Show | 32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.324+8801T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610886 | ||||||
| chr2:164610911
|
C | CA | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(166): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.324+8775dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610911 | ||||||
| chr2:164610911
|
C | CAA | 9 | a0001c0001t0001g0102a0002c0002t0002g0161a0002c0002t0002g0196others(6): Show | 9 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+8774_324+8775d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610911 | ||||||
| chr2:164611025
|
T | A | 31 | a0001c0001t0001g0084a0001c0001t0001g0114a0001c0001t0001g0133others(28): Show | 32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.324+8662A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611025 | ||||||
| chr2:164611270
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.324+8417C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611270 | ||||||
| chr2:164611305
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0004g0049a0001c0001t0004g0066 | 3 | NA18963.hp2 NA18985.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.324+8382C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611305 | ||||||
| chr2:164611317
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.324+8370A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611317 | ||||||
| chr2:164611449
|
T | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0044 | 2 | NA19005.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.324+8238A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611449 | ||||||
| chr2:164611605
|
G | A | 2 | a0001c0001t0001g0024a0002c0002t0002g0227 | 2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.324+8082C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611605 | ||||||
| chr2:164611676
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(7): Show | 10 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+8011T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611676 | ||||||
| chr2:164611850
|
G | T | 12 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0116others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+7837C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611850 | ||||||
| chr2:164611852
|
A | C | 213 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(210): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.324+7835T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611852 | ||||||
| chr2:164611869
|
A | G | 213 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(210): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.324+7818T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611869 | ||||||
| chr2:164611879
|
T | G | 2 | a0001c0001t0001g0132a0006c0011t0007g0131 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+7808A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611879 | ||||||
| chr2:164611925
|
G | A | 212 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(209): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.324+7762C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611925 | ||||||
| chr2:164611940
|
G | A | 7 | a0002c0002t0002g0180a0002c0002t0002g0182a0002c0002t0002g0187others(4): Show | 7 | NA18941.hp2 NA18974.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+7747C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611940 | ||||||
| chr2:164612001
|
G | C | 1 | a0002c0002t0002g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.324+7686C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612001 | ||||||
| chr2:164612030
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0058 | 2 | HG04204.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.324+7657A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612030 | ||||||
| chr2:164612106
|
T | G | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+7581A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612106 | ||||||
| chr2:164612149
|
T | A | 1 | a0002c0002t0002g0199 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324+7538A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612149 | ||||||
| chr2:164612155
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126 | 3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+7532G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612155 | ||||||
| chr2:164612212
|
T | G | 1 | a0001c0001t0006g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.324+7475A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612212 | ||||||
| chr2:164612240
|
T | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+7447A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612240 | ||||||
| chr2:164612433
|
T | G | 4 | a0002c0002t0002g0171a0002c0002t0003g0168a0002c0002t0003g0172others(1): Show | 4 | HG01261.hp1 HG02738.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+7254A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612433 | ||||||
| chr2:164612515
|
T | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+7172A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612515 | ||||||
| chr2:164612547
|
T | C | 12 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0116others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+7140A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612547 | ||||||
| chr2:164612714
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0006g0145a0001c0001t0006g0157 | 3 | HG02895.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.324+6973A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612714 | ||||||
| chr2:164612791
|
C | G | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+6896G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612791 | ||||||
| chr2:164612807
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(7): Show | 10 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+6880C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612807 | ||||||
| chr2:164612936
|
T | G | 1 | a0002c0002t0002g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.324+6751A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612936 | ||||||
| chr2:164613007
|
C | G | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0084others(25): Show | 29 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+6680G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613007 | ||||||
| chr2:164613033
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+6654C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613033 | ||||||
| chr2:164613042
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.324+6645C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613042 | ||||||
| chr2:164613056
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+6631C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613056 | ||||||
| chr2:164613433
|
T | G | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+6254A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613433 | ||||||
| chr2:164613469
|
A | G | 1 | a0002c0002t0002g0276 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.324+6218T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613469 | ||||||
| chr2:164613527
|
C | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0124others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+6160G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613527 | ||||||
| chr2:164613703
|
A | G | 4 | a0002c0002t0003g0249a0002c0002t0003g0286a0002c0002t0005g0167others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5984T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613703 | ||||||
| chr2:164613776
|
T | A | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0126others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+5911A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613776 | ||||||
| chr2:164613991
|
C | T | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.324+5696G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613991 | ||||||
| chr2:164614002
|
C | T | 3 | a0002c0002t0002g0174a0002c0002t0002g0191a0002c0002t0002g0236 | 3 | NA18944.hp2 NA19007.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.324+5685G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614002 | ||||||
| chr2:164614146
|
G | A | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+5541C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614146 | ||||||
| chr2:164614157
|
C | T | 2 | a0001c0005t0001g0026a0001c0005t0007g0047 | 2 | HG00639.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.324+5530G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614157 | ||||||
| chr2:164614161
|
C | CA | 3 | a0002c0002t0003g0286a0002c0002t0005g0167a0002c0002t0005g0181 | 3 | HG01516.hp1 HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.324+5525dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614161 | ||||||
| chr2:164614162
|
A | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0067others(1): Show | 4 | HG00544.hp2 HG00621.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5525T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614162 | ||||||
| chr2:164614225
|
T | C | 3 | a0001c0001t0008g0155a0003c0004t0008g0142a0003c0004t0008g0156 | 3 | HG00733.hp2 HG01099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.324+5462A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614225 | ||||||
| chr2:164614399
|
T | C | 1 | a0001c0001t0004g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+5288A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614399 | ||||||
| chr2:164614460
|
A | G | 12 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0116others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+5227T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614460 | ||||||
| chr2:164614494
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.324+5193G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614494 | ||||||
| chr2:164614588
|
GGGT | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0067others(1): Show | 4 | HG00544.hp2 HG00621.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5096_324+5098d others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614588 | ||||||
| chr2:164614638
|
T | A | 1 | a0002c0002t0002g0213 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.324+5049A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614638 | ||||||
| chr2:164614886
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+4801C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614886 | ||||||
| chr2:164615014
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324+4673T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615014 | ||||||
| chr2:164615069
|
C | T | 1 | a0002c0002t0003g0229 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.324+4618G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615069 | ||||||
| chr2:164615088
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.324+4599G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615088 | ||||||
| chr2:164615097
|
C | T | 2 | a0001c0001t0008g0149a0001c0001t0008g0150 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.324+4590G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615097 | ||||||
| chr2:164615328
|
T | C | 3 | a0001c0001t0001g0072a0001c0005t0001g0026a0001c0005t0007g0047 | 3 | HG00639.hp1 HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.324+4359A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615328 | ||||||
| chr2:164615371
|
A | G | 9 | a0002c0002t0002g0248a0002c0002t0003g0234a0002c0002t0003g0235others(6): Show | 9 | HG00738.hp1 HG01255.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+4316T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615371 | ||||||
| chr2:164615509
|
A | T | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0102others(20): Show | 23 | HG01261.hp1 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.324+4178T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615509 | ||||||
| chr2:164615832
|
A | T | 8 | a0001c0001t0001g0102a0001c0001t0004g0096a0001c0001t0004g0097others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+3855T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615832 | ||||||
| chr2:164615838
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.324+3849T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615838 | ||||||
| chr2:164615858
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.324+3829A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615858 | ||||||
| chr2:164615895
|
C | T | 209 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(206): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.324+3792G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615895 | ||||||
| chr2:164615967
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324+3720T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615967 | ||||||
| chr2:164616244
|
A | G | 291 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(288): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.324+3443T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616244 | ||||||
| chr2:164616287
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.324+3400C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616287 | ||||||
| chr2:164616425
|
C | CA | 29 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0058others(26): Show | 29 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+3261dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616425 | ||||||
| chr2:164616425
|
CA | C | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(112): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.324+3261delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616425 | ||||||
| chr2:164616425
|
CAAAAAAA others(5): Show |
C | 3 | a0002c0002t0003g0204a0002c0002t0003g0219a0008c0007t0003g0220 | 3 | NA18940.hp2 NA18954.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.324+3250_324+3261d others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616425 | ||||||
| chr2:164616470
|
C | T | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+3217G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616470 | ||||||
| chr2:164616720
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.324+2967A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616720 | ||||||
| chr2:164616837
|
G | T | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2850C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616837 | ||||||
| chr2:164616840
|
A | C | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2847T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616840 | ||||||
| chr2:164616844
|
T | C | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2843A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616844 | ||||||
| chr2:164616845
|
C | T | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2842G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616845 | ||||||
| chr2:164616847
|
C | A | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2840G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616847 | ||||||
| chr2:164616850
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324+2837T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616850 | ||||||
| chr2:164616861
|
A | T | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2826T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616861 | ||||||
| chr2:164616871
|
A | T | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2816T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616871 | ||||||
| chr2:164616872
|
T | G | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2815A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616872 | ||||||
| chr2:164616881
|
G | T | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2806C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616881 | ||||||
| chr2:164616906
|
C | G | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2781G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616906 | ||||||
| chr2:164616916
|
G | T | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2771C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616916 | ||||||
| chr2:164616930
|
A | C | 1 | a0002c0002t0003g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2757T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616930 | ||||||
| chr2:164617002
|
A | G | 203 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(200): Show | 205 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.324+2685T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617002 | ||||||
| chr2:164617272
|
C | T | 12 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+2415G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617272 | ||||||
| chr2:164617273
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.324+2414C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617273 | ||||||
| chr2:164617372
|
C | A | 1 | a0001c0001t0004g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.324+2315G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617372 | ||||||
| chr2:164617523
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.324+2164G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617523 | ||||||
| chr2:164617903
|
T | C | 206 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0059others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.324+1784A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617903 | ||||||
| chr2:164617925
|
A | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0085 | 2 | NA18940.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.324+1762T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617925 | ||||||
| chr2:164617951
|
C | CT | 66 | a0001c0001t0001g0094a0001c0001t0001g0105a0001c0001t0001g0106others(63): Show | 67 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.324+1735dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617951 | ||||||
| chr2:164617959
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.324+1728A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | ||||||
| chr2:164617959
|
T | TTG | 50 | a0001c0001t0001g0130a0001c0001t0007g0113a0001c0001t0010g0140others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+1727_324+1728i others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | ||||||
| chr2:164617959
|
T | TTGG | 7 | a0002c0002t0002g0189a0002c0002t0002g0225a0002c0002t0002g0274others(4): Show | 7 | HG01123.hp2 HG02071.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+1727_324+1728i others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | ||||||
| chr2:164617959
|
TG | T | 53 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(50): Show | 53 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.324+1727delC | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | ||||||
| chr2:164617959
|
TGG | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(52): Show | 56 | HG00140.hp1 HG00733.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.324+1726_324+1727d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | ||||||
| chr2:164617960
|
G | T | 17 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0001g0118others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.324+1727C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617960 | ||||||
| chr2:164617961
|
G | T | 17 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0085others(14): Show | 17 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.324+1726C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617961 | ||||||
| chr2:164617962
|
G | T | 42 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0084others(39): Show | 43 | HG00733.hp2 HG00735.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.324+1725C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617962 | ||||||
| chr2:164617963
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+1724C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617963 | ||||||
| chr2:164617967
|
G | C | 1 | a0002c0002t0002g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.324+1720C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617967 | ||||||
| chr2:164617973
|
T | G | 1 | a0001c0001t0004g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.324+1714A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617973 | ||||||
| chr2:164617999
|
C | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(4): Show | 7 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+1688G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617999 | ||||||
| chr2:164618011
|
G | A | 194 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0084others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.324+1676C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618011 | ||||||
| chr2:164618053
|
G | A | 186 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0053others(183): Show | 188 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(185): Show |
intron_variant | MODIFIER | c.324+1634C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618053 | ||||||
| chr2:164618084
|
C | T | 1 | a0002c0002t0002g0192 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.324+1603G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618084 | ||||||
| chr2:164618266
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0095 | 3 | HG01891.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324+1421T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618266 | ||||||
| chr2:164618275
|
CT | C | 23 | a0001c0001t0001g0114a0001c0001t0006g0001a0001c0001t0006g0141others(20): Show | 24 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.324+1411delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618275 | ||||||
| chr2:164618353
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+1334G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618353 | ||||||
| chr2:164618388
|
G | GT | 3 | a0001c0001t0001g0006a0001c0001t0001g0056a0002c0002t0003g0169 | 3 | HG04204.hp1 NA19001.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.324+1298dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618388 | ||||||
| chr2:164618453
|
T | C | 2 | a0001c0001t0001g0132a0006c0011t0007g0131 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+1234A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618453 | ||||||
| chr2:164618751
|
C | T | 1 | a0002c0002t0003g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.324+936G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618751 | ||||||
| chr2:164619507
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.324+180C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164619507 | ||||||
| chr2:164619616
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+71C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164619616 | ||||||
| chr2:164620038
|
G | GTC | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG02258.hp2 HG02630.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-221_192-220dup others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620038 | ||||||
| chr2:164620038
|
GTCTC | G | 177 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0115others(174): Show | 179 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.192-223_192-220del others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620038 | ||||||
| chr2:164620038
|
GTCTCTCT others(1): Show |
G | 21 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0104others(18): Show | 21 | HG00735.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.192-227_192-220del others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620038 | ||||||
| chr2:164620054
|
CTCT | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-238_192-236del others(3): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620054 | ||||||
| chr2:164620059
|
T | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-240A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620059 | ||||||
| chr2:164620067
|
C | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-248G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620067 | ||||||
| chr2:164620073
|
A | AC | 29 | a0001c0001t0006g0144a0001c0001t0006g0145a0001c0001t0006g0146others(26): Show | 29 | HG00544.hp1 HG00673.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.192-255dupG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620073 | ||||||
| chr2:164620073
|
A | ACC | 11 | a0001c0001t0006g0141a0001c0001t0010g0140a0001c0001t0010g0143others(8): Show | 11 | HG00438.hp1 HG01099.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-256_192-255dup others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620073 | ||||||
| chr2:164620076
|
C | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-257G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620076 | ||||||
| chr2:164620076
|
C | T | 8 | a0001c0001t0001g0102a0001c0001t0004g0096a0001c0001t0004g0097others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.192-257G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620076 | ||||||
| chr2:164620076
|
CCT | C | 30 | a0001c0001t0001g0092a0001c0001t0001g0124a0001c0001t0001g0125others(27): Show | 30 | HG00099.hp1 HG00639.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.192-259_192-258del others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620076 | ||||||
| chr2:164620077
|
CT | C | 73 | a0001c0001t0001g0102a0001c0001t0001g0109a0001c0001t0001g0110others(70): Show | 74 | HG00140.hp2 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.192-259delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620077 | ||||||
| chr2:164620078
|
T | C | 96 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(93): Show | 97 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.192-259A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620078 | ||||||
| chr2:164620078
|
T | TC | 30 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(27): Show | 30 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.192-260dupG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620078 | ||||||
| chr2:164620083
|
C | G | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192-264G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620083 | ||||||
| chr2:164620092
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0004g0088others(3): Show | 6 | HG00735.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-273G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620092 | ||||||
| chr2:164620518
|
G | GA | 207 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0093others(204): Show | 209 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.191+600dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620518 | ||||||
| chr2:164620652
|
C | G | 1 | a0001c0001t0004g0004 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.191+467G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620652 | ||||||
| chr2:164620741
|
T | C | 6 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+378A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620741 | ||||||
| chr2:164620826
|
A | G | 21 | a0001c0001t0006g0001a0001c0001t0006g0141a0001c0001t0006g0144others(18): Show | 22 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.191+293T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620826 |