Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55041 |
| ensemblid | ENSG00000115762.17 |
| hgncid | 19236 |
| symbol | PLEKHB2 |
| name | pleckstrin homology domain containing B2 |
| refseq_nuc | NM_001100623.2 |
| refseq_prot | NP_001094093.1 |
| ensembl_nuc | ENST00000693505.1 |
| ensembl_prot | ENSP00000510611.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 131105336 |
| end | 131149845 |
| strand | + |
| ver | v1.2 |
| region | chr2:131105336-131149845 |
| region5000 | chr2:131100336-131154845 |
| regionname0 | PLEKHB2_chr2_131105336_131149845 |
| regionname5000 | PLEKHB2_chr2_131100336_131154845 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 666 | 263 | 94 | 54 | 70 | 12 | 31 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | ATGGC others(661): Show |
chr2 | 131100336 | 131154845 | ||
| a0001c0002 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | ATGGC others(661): Show |
chr2 | 131100336 | 131154845 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3812 | 146 | 32 | 39 | 43 | 7 | 24 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0002 | 0/1 | 3814 | 66 | 23 | 11 | 22 | 5 | 4 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0003 | 0/0 | 3813 | 9 | 9 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3808): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0004 | 0/0 | 3814 | 6 | 6 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0005 | 0/0 | 3813 | 6 | 4 | 2 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3808): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0006 | 0/0 | 3811 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3806): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0007 | 0/0 | 3812 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0008 | 0/0 | 3812 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0009 | 0/0 | 3813 | 3 | 1 | 0 | 2 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3808): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0010 | 0/0 | 3812 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0011 | 0/0 | 3812 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0012 | 0/0 | 3812 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0013 | 0/0 | 3814 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0014 | 0/0 | 3812 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0015 | 0/0 | 3812 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0016 | 0/0 | 3812 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0017 | 0/0 | 3812 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0018 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0019 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0020 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3808): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0021 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3808): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0022 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0023 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| a0001c0001t0024 | 0/0 | 3812 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3807): Show |
chr2 | 131100336 | 131154845 |
| a0001c0002t0002 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | AGTTG others(3809): Show |
chr2 | 131100336 | 131154845 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0001 | 0/0 | 9 | 1 | 0 | 6 | 0 | 2 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0006g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0015g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0016g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0017g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0018g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0020g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0021g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0022g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0023g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0001t0024g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | GBR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | FIN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00438 | hp1 | a0001 | c0001 | t0014 | g0073 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0074 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00733 | hp1 | a0001 | c0001 | t0012 | g0160 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | IBS | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01891 | hp1 | a0001 | c0001 | t0023 | g0006 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02015 | hp1 | a0001 | c0001 | t0021 | g0199 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CDX | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CDX | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02602 | hp1 | a0001 | c0001 | t0024 | g0064 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0176 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0168 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0125 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0169 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0221 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0222 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0025 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0035 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03491 | hp2 | a0001 | c0001 | t0015 | g0047 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ESN | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04115 | hp2 | a0001 | c0001 | t0022 | g0223 | SAS | STU | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18981 | hp2 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19030 | hp1 | a0001 | c0001 | t0020 | g0226 | AFR | LWK | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | LWK | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | LWK | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19083 | hp1 | a0001 | c0001 | t0013 | g0080 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20129 | hp1 | a0001 | c0001 | t0019 | g0124 | AFR | ASW | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ASW | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0197 | EUR | TSI | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02109 | hp1 | a0001 | c0001 | t0018 | g0040 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02486 | hp2 | a0001 | c0001 | t0017 | g0159 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | USA | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | USA | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | USA | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0185 | REF | REF | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0149 | REF | REF | PLEKHB2_chr2_131100336_131154845 | PLEKHB2 | chr2 | 131100336 | 131154845 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:131125823 | T | C | 1 | a0001c0002 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.108T>C | p.Asp36Asp | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 3/8 | 179/3812 | 108/669 | 36/222 | chr2 | 131125823 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:131105382 | T | C | 2 | a0001c0001t0006 a0001c0001t0011 |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-25T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/8 | 15560 | chr2 | 131105382 | ||||||
| chr2:131146963 | C | G | 1 | a0001c0001t0024 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 190 | chr2 | 131146963 | ||||||
| chr2:131146996 | C | A | 1 | a0001c0001t0010 | 2 | HG02622.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*223C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 223 | chr2 | 131146996 | ||||||
| chr2:131147121 | A | G | 2 | a0001c0001t0006 a0001c0001t0011 |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*348A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 348 | chr2 | 131147121 | ||||||
| chr2:131147370 | A | C | 1 | a0001c0001t0023 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*597A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 597 | chr2 | 131147370 | ||||||
| chr2:131147388 | AGCT | A | 2 | a0001c0001t0006 a0001c0001t0011 |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*628_*630delGCT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 628 | INFO_REALIGN_3_PRIME | chr2 | 131147388 | |||||
| chr2:131147436 | C | T | 1 | a0001c0001t0022 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 663 | chr2 | 131147436 | ||||||
| chr2:131147497 | C | A | 1 | a0001c0001t0012 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*724C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 724 | chr2 | 131147497 | ||||||
| chr2:131147527 | G | A | 1 | a0001c0001t0008 | 3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*754G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 754 | chr2 | 131147527 | ||||||
| chr2:131147566 | A | G | 2 | a0001c0001t0006 a0001c0001t0011 |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*793A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 793 | chr2 | 131147566 | ||||||
| chr2:131147723 | A | G | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(10): Show |
98 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*950A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 950 | chr2 | 131147723 | ||||||
| chr2:131147755 | G | GC | 2 | a0001c0001t0006 a0001c0001t0011 |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*984dupC | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 985 | INFO_REALIGN_3_PRIME | chr2 | 131147755 | |||||
| chr2:131147797 | C | CA | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(3): Show |
24 | HG00558.hp2 HG01243.hp1 HG01257.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1040dupA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 1041 | INFO_REALIGN_3_PRIME | chr2 | 131147797 | |||||
| chr2:131147797 | C | CAA | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(6): Show |
78 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1039_*1040dupAA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 1041 | INFO_REALIGN_3_PRIME | chr2 | 131147797 | |||||
| chr2:131147885 | G | C | 1 | a0001c0001t0020 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1112G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 1112 | chr2 | 131147885 | ||||||
| chr2:131148122 | C | T | 1 | a0001c0001t0007 | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1349C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 1349 | chr2 | 131148122 | ||||||
| chr2:131148458 | C | T | 1 | a0001c0001t0004 | 6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1685C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 1685 | chr2 | 131148458 | ||||||
| chr2:131148593 | C | T | 1 | a0001c0001t0017 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1820C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 1820 | chr2 | 131148593 | ||||||
| chr2:131148677 | C | G | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0019 others(4): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1904C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 1904 | chr2 | 131148677 | ||||||
| chr2:131148780 | T | C | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2007T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 2007 | chr2 | 131148780 | ||||||
| chr2:131149033 | G | A | 1 | a0001c0001t0015 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2260G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 2260 | chr2 | 131149033 | ||||||
| chr2:131149317 | C | G | 2 | a0001c0001t0006 a0001c0001t0011 |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2544C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 2544 | chr2 | 131149317 | ||||||
| chr2:131149318 | A | G | 1 | a0001c0001t0005 | 6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2545A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 2545 | chr2 | 131149318 | ||||||
| chr2:131149726 | A | G | 1 | a0001c0001t0019 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2953A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 2953 | chr2 | 131149726 | ||||||
| chr2:131149752 | C | G | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2979C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 8/8 | 2979 | chr2 | 131149752 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:131105409 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-9+11C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131105409 | |||||||
| chr2:131105509 | C | T | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+111C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131105509 | |||||||
| chr2:131105581 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-9+183C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131105581 | |||||||
| chr2:131106118 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+720G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131106118 | |||||||
| chr2:131106148 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+750G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131106148 | |||||||
| chr2:131106387 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-9+989G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131106387 | |||||||
| chr2:131106660 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-9+1262G>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131106660 | |||||||
| chr2:131107237 | A | G | 1 | a0001c0001t0022g0223 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-9+1839A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107237 | |||||||
| chr2:131107288 | C | T | 2 | a0001c0001t0007g0221 a0001c0001t0007g0222 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+1890C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107288 | |||||||
| chr2:131107464 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01168.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-9+2066G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107464 | |||||||
| chr2:131107491 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(48): Show |
67 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-9+2093A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107491 | |||||||
| chr2:131107594 | T | C | 4 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0221 others(1): Show |
4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2196T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107594 | |||||||
| chr2:131107697 | C | T | 10 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(7): Show |
12 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+2299C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107697 | |||||||
| chr2:131107732 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9+2334G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107732 | |||||||
| chr2:131107738 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG01175.hp1 HG01261.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2340C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107738 | |||||||
| chr2:131107837 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-9+2439T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107837 | |||||||
| chr2:131107912 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-9+2514C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131107912 | |||||||
| chr2:131108123 | A | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01175.hp1 HG01261.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+2725A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108123 | |||||||
| chr2:131108195 | G | C | 1 | a0001c0001t0002g0220 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-9+2797G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108195 | |||||||
| chr2:131108206 | A | G | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+2808A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108206 | |||||||
| chr2:131108412 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-9+3014G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108412 | |||||||
| chr2:131108477 | T | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(191): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-9+3079T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108477 | |||||||
| chr2:131108488 | T | G | 1 | a0001c0001t0003g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-9+3090T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108488 | |||||||
| chr2:131108584 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3186T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108584 | |||||||
| chr2:131108609 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+3211A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108609 | |||||||
| chr2:131108812 | G | C | 1 | a0001c0001t0004g0008 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-9+3414G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108812 | |||||||
| chr2:131108888 | A | G | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+3490A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108888 | |||||||
| chr2:131108894 | C | T | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3496C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108894 | |||||||
| chr2:131108935 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-9+3537A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131108935 | |||||||
| chr2:131109323 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3925G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109323 | |||||||
| chr2:131109461 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-9+4063G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109461 | |||||||
| chr2:131109527 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-9+4129T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109527 | |||||||
| chr2:131109631 | A | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+4233A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109631 | |||||||
| chr2:131109644 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9+4246C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109644 | |||||||
| chr2:131109677 | C | T | 59 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(56): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-9+4279C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109677 | |||||||
| chr2:131109749 | AT | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01175.hp1 HG01261.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+4352delT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109749 | |||||||
| chr2:131109836 | T | C | 81 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(78): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-9+4438T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109836 | |||||||
| chr2:131109979 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-9+4581G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109979 | |||||||
| chr2:131109986 | T | G | 100 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(97): Show |
121 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-9+4588T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131109986 | |||||||
| chr2:131110004 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9+4606A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110004 | |||||||
| chr2:131110039 | T | C | 100 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(97): Show |
121 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-9+4641T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110039 | |||||||
| chr2:131110071 | C | T | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+4673C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110071 | |||||||
| chr2:131110089 | T | C | 1 | a0001c0001t0015g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-9+4691T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110089 | |||||||
| chr2:131110114 | C | CA | 7 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(4): Show |
8 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+4728dupA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131110114 | ||||||
| chr2:131110137 | T | A | 1 | a0001c0001t0002g0018 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9+4739T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110137 | |||||||
| chr2:131110317 | G | GT | 28 | a0001c0001t0001g0046 a0001c0001t0001g0111 a0001c0001t0001g0112 others(25): Show |
30 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+4936dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131110317 | ||||||
| chr2:131110322 | T | G | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+4924T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110322 | |||||||
| chr2:131110412 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+5014G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110412 | |||||||
| chr2:131110433 | C | G | 1 | a0001c0001t0008g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-9+5035C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110433 | |||||||
| chr2:131110534 | T | C | 104 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(101): Show |
125 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-9+5136T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110534 | |||||||
| chr2:131110570 | C | A | 33 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0019 others(30): Show |
47 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9+5172C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110570 | |||||||
| chr2:131110828 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+5430C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110828 | |||||||
| chr2:131110887 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+5489G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110887 | |||||||
| chr2:131110888 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+5490C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131110888 | |||||||
| chr2:131111098 | G | A | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+5700G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131111098 | |||||||
| chr2:131111160 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9+5762A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131111160 | |||||||
| chr2:131111302 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+5904A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131111302 | |||||||
| chr2:131111358 | GTCT | G | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+5962_-9+5964del others(3): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131111358 | ||||||
| chr2:131111360 | C | CT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0227 others(9): Show |
12 | HG01261.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+5980dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131111360 | ||||||
| chr2:131111380 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+5982G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131111380 | |||||||
| chr2:131111493 | G | GT | 9 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0120 others(6): Show |
10 | HG00639.hp2 HG01243.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+6109dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131111493 | ||||||
| chr2:131111611 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-9+6213C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131111611 | |||||||
| chr2:131111864 | T | G | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+6466T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131111864 | |||||||
| chr2:131111884 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-9+6486A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131111884 | |||||||
| chr2:131112091 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-9+6693C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131112091 | |||||||
| chr2:131112174 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(191): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-9+6776G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131112174 | |||||||
| chr2:131112335 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-9+6937A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131112335 | |||||||
| chr2:131112535 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-9+7137A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131112535 | |||||||
| chr2:131112648 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9+7250A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131112648 | |||||||
| chr2:131112650 | T | C | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+7252T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131112650 | |||||||
| chr2:131112761 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-9+7363C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131112761 | |||||||
| chr2:131113087 | AT | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(83): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-9+7704delT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131113087 | ||||||
| chr2:131113104 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+7706A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113104 | |||||||
| chr2:131113120 | C | T | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+7722C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113120 | |||||||
| chr2:131113244 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0009g0044 |
3 | HG02258.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-7690G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113244 | |||||||
| chr2:131113355 | G | A | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-8-7579G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113355 | |||||||
| chr2:131113421 | A | C | 1 | a0001c0001t0019g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-7513A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113421 | |||||||
| chr2:131113451 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-8-7483T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113451 | |||||||
| chr2:131113582 | C | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0138 |
4 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-7352C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113582 | |||||||
| chr2:131113598 | CTG | C | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-8-7335_-8-7334del others(2): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113598 | |||||||
| chr2:131113620 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-8-7314T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113620 | |||||||
| chr2:131113654 | A | G | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-7280A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113654 | |||||||
| chr2:131113716 | A | C | 2 | a0001c0001t0002g0018 a0001c0001t0002g0213 |
3 | HG03098.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-7218A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113716 | |||||||
| chr2:131113741 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-8-7193C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113741 | |||||||
| chr2:131113769 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-7165C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113769 | |||||||
| chr2:131113961 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-8-6973A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131113961 | |||||||
| chr2:131114135 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01109.hp1 HG02258.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-6799C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131114135 | |||||||
| chr2:131114212 | G | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-6722G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131114212 | |||||||
| chr2:131114240 | C | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-6694C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131114240 | |||||||
| chr2:131114314 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-6620C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131114314 | |||||||
| chr2:131114346 | C | G | 1 | a0001c0001t0011g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-8-6588C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131114346 | |||||||
| chr2:131114573 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-6361A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131114573 | |||||||
| chr2:131115287 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-8-5647A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115287 | |||||||
| chr2:131115341 | C | CT | 40 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(37): Show |
45 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-5562dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115341 | C | CTT | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0097 others(10): Show |
13 | HG00408.hp2 HG00558.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-5563_-8-5562dup others(2): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115341 | CT | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0103 others(2): Show |
5 | HG00323.hp1 HG01515.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5562delT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115341 | CTT | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
9 | HG01884.hp2 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-5563_-8-5562del others(2): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115341 | CTTTT | C | 6 | a0001c0001t0005g0017 a0001c0001t0005g0174 a0001c0001t0006g0007 others(3): Show |
8 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-5565_-8-5562del others(4): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115341 | CTTTTTTT others(1): Show |
C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(61): Show |
82 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8-5569_-8-5562del others(8): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115341 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-5572_-8-5562del others(11): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115341 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0046 a0001c0001t0007g0028 a0001c0001t0007g0221 others(1): Show |
4 | HG01109.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-5573_-8-5562del others(12): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131115341 | ||||||
| chr2:131115377 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-8-5557T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115377 | |||||||
| chr2:131115441 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-8-5493C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115441 | |||||||
| chr2:131115479 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-8-5455G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115479 | |||||||
| chr2:131115502 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-8-5432C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115502 | |||||||
| chr2:131115535 | A | G | 59 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(56): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-8-5399A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115535 | |||||||
| chr2:131115621 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-8-5313G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115621 | |||||||
| chr2:131115649 | T | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-5285T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131115649 | |||||||
| chr2:131116124 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0109 a0001c0001t0001g0120 |
3 | HG00642.hp1 HG01358.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-8-4810G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116124 | |||||||
| chr2:131116174 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4760C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116174 | |||||||
| chr2:131116316 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-8-4618A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116316 | |||||||
| chr2:131116347 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-4587C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116347 | |||||||
| chr2:131116539 | C | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-4395C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116539 | |||||||
| chr2:131116787 | T | C | 19 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(16): Show |
22 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8-4147T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116787 | |||||||
| chr2:131116853 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-8-4081C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116853 | |||||||
| chr2:131116917 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0085 a0001c0001t0001g0118 others(1): Show |
4 | HG00408.hp2 HG00438.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-4017G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116917 | |||||||
| chr2:131116996 | C | G | 3 | a0001c0001t0004g0134 a0001c0001t0004g0135 a0001c0001t0004g0136 |
3 | HG02055.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-8-3938C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131116996 | |||||||
| chr2:131117094 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3840T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117094 | |||||||
| chr2:131117114 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3820C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117114 | |||||||
| chr2:131117170 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-3764G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117170 | |||||||
| chr2:131117221 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-8-3713C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117221 | |||||||
| chr2:131117299 | C | T | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8-3635C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117299 | |||||||
| chr2:131117375 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01261.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-8-3559G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117375 | |||||||
| chr2:131117630 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-8-3304A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117630 | |||||||
| chr2:131117702 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-8-3232C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117702 | |||||||
| chr2:131117716 | C | T | 1 | a0001c0001t0007g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-3218C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117716 | |||||||
| chr2:131117740 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-3194T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117740 | |||||||
| chr2:131117746 | ACC | A | 16 | a0001c0001t0002g0006 a0001c0001t0002g0204 a0001c0001t0002g0205 others(13): Show |
17 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-3185_-8-3184del others(2): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131117746 | ||||||
| chr2:131117906 | A | T | 1 | a0001c0001t0003g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-3028A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131117906 | |||||||
| chr2:131118049 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2885G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118049 | |||||||
| chr2:131118082 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-2852T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118082 | |||||||
| chr2:131118189 | T | TG | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG02717.hp1 HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-8-2744dupG | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118189 | ||||||
| chr2:131118242 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-8-2692T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118242 | |||||||
| chr2:131118457 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(191): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-2477A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118457 | |||||||
| chr2:131118523 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-8-2411C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118523 | |||||||
| chr2:131118591 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-8-2343C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118591 | |||||||
| chr2:131118829 | C | T | 31 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0019 others(28): Show |
45 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8-2105C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118829 | |||||||
| chr2:131118862 | C | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2072C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118862 | |||||||
| chr2:131118867 | C | CA | 15 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0145 others(12): Show |
15 | HG00558.hp1 HG01109.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8-2036dupA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118867 | CA | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(40): Show |
48 | HG00408.hp1 HG00642.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-8-2036delA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118867 | CAA | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(48): Show |
57 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-8-2037_-8-2036del others(2): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118867 | CAAAAA | C | 19 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0180 others(16): Show |
25 | HG00544.hp1 HG00741.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-2040_-8-2036del others(5): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118867 | CAAAAAA | C | 40 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(37): Show |
52 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.-8-2041_-8-2036del others(6): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118867 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0005g0017 a0001c0001t0005g0174 a0001c0001t0005g0176 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2045_-8-2036del others(10): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118867 | CAAAAAAA others(7): Show |
C | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-2049_-8-2036del others(14): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118867 | CAAAAAAA others(10): Show |
C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG01175.hp1 HG01261.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-2052_-8-2036del others(17): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131118867 | ||||||
| chr2:131118983 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-8-1951G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131118983 | |||||||
| chr2:131119097 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-8-1837A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119097 | |||||||
| chr2:131119187 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1747T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119187 | |||||||
| chr2:131119299 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8-1635C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119299 | |||||||
| chr2:131119444 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-1490G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119444 | |||||||
| chr2:131119749 | C | T | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-1185C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119749 | |||||||
| chr2:131119900 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0001g0141 others(9): Show |
14 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-1034A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119900 | |||||||
| chr2:131119911 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-8-1023T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119911 | |||||||
| chr2:131119973 | T | C | 1 | a0001c0001t0002g0018 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-8-961T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131119973 | |||||||
| chr2:131120073 | G | A | 77 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(74): Show |
97 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-8-861G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131120073 | |||||||
| chr2:131120081 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-853G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131120081 | |||||||
| chr2:131120104 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-8-830G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131120104 | |||||||
| chr2:131120107 | T | TAC | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-826_-8-825insCA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 131120107 | ||||||
| chr2:131120217 | G | A | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-717G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131120217 | |||||||
| chr2:131120677 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-257T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131120677 | |||||||
| chr2:131120784 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-8-150G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131120784 | |||||||
| chr2:131120922 | T | C | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-12T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 1/7 | chr2 | 131120922 | |||||||
| chr2:131121002 | C | T | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+24C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121002 | |||||||
| chr2:131121016 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA19011.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.37+38G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121016 | |||||||
| chr2:131121064 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.37+86G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121064 | |||||||
| chr2:131121257 | T | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+279T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121257 | |||||||
| chr2:131121358 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.37+380C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121358 | |||||||
| chr2:131121409 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0206 a0001c0001t0002g0207 others(4): Show |
8 | HG01243.hp2 HG01891.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.37+431C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121409 | |||||||
| chr2:131121423 | T | G | 1 | a0001c0001t0003g0038 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37+445T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121423 | |||||||
| chr2:131121495 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+517A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121495 | |||||||
| chr2:131121525 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.37+547G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121525 | |||||||
| chr2:131121556 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.37+578A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121556 | |||||||
| chr2:131121831 | A | G | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37+853A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131121831 | |||||||
| chr2:131121903 | T | TTTTA | 22 | a0001c0001t0002g0006 a0001c0001t0002g0179 a0001c0001t0002g0187 others(19): Show |
23 | HG01243.hp2 HG01891.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+945_37+948dupAT others(2): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131121903 | ||||||
| chr2:131122031 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+1053T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122031 | |||||||
| chr2:131122079 | G | A | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.37+1101G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122079 | |||||||
| chr2:131122141 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+1163C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122141 | |||||||
| chr2:131122146 | C | T | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.37+1168C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122146 | |||||||
| chr2:131122181 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.37+1203C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122181 | |||||||
| chr2:131122204 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.37+1226C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122204 | |||||||
| chr2:131122231 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.37+1253A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122231 | |||||||
| chr2:131122564 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01433.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.37+1586G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122564 | |||||||
| chr2:131122587 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.37+1609T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122587 | |||||||
| chr2:131122923 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG01175.hp1 HG01261.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+1945G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122923 | |||||||
| chr2:131122980 | T | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+2002T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122980 | |||||||
| chr2:131122993 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.37+2015T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131122993 | |||||||
| chr2:131123002 | C | T | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+2024C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123002 | |||||||
| chr2:131123065 | C | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+2087C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123065 | |||||||
| chr2:131123130 | C | T | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.37+2152C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123130 | |||||||
| chr2:131123394 | G | C | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-2359G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123394 | |||||||
| chr2:131123675 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.38-2078C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123675 | |||||||
| chr2:131123766 | A | AC | 29 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0032 others(26): Show |
30 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.38-1979dupC | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123766 | ||||||
| chr2:131123766 | ACCCCCCC others(10): Show |
A | 4 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0221 others(1): Show |
4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-1983_38-1967del others(17): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123766 | ||||||
| chr2:131123768 | C | T | 3 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0011g0025 |
4 | HG02818.hp2 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-1985C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123768 | |||||||
| chr2:131123769 | C | A | 13 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(10): Show |
15 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.38-1984C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123769 | |||||||
| chr2:131123770 | CCCCCA | C | 21 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0002g0020 others(18): Show |
23 | HG00099.hp2 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-1978_38-1974del others(5): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123770 | ||||||
| chr2:131123771 | CCCCA | C | 17 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0018 others(14): Show |
20 | HG01928.hp2 HG01943.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-1978_38-1975del others(4): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123771 | ||||||
| chr2:131123772 | CCCA | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0129 a0001c0001t0002g0001 others(12): Show |
17 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.38-1978_38-1976del others(3): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123772 | ||||||
| chr2:131123774 | CA | C | 17 | a0001c0001t0001g0132 a0001c0001t0002g0192 a0001c0001t0003g0009 others(14): Show |
19 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.38-1978delA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123774 | |||||||
| chr2:131123775 | A | AC | 13 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(10): Show |
13 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.38-1967dupC | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123775 | ||||||
| chr2:131123775 | A | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(37): Show |
41 | HG00639.hp1 HG00673.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.38-1978A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123775 | |||||||
| chr2:131123775 | AC | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(19): Show |
24 | HG00323.hp1 HG00639.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.38-1967delC | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123775 | ||||||
| chr2:131123776 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.38-1977C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123776 | |||||||
| chr2:131123782 | C | T | 1 | a0001c0001t0008g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.38-1971C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123782 | |||||||
| chr2:131123787 | G | C | 1 | a0001c0001t0008g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.38-1966G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123787 | |||||||
| chr2:131123794 | G | A | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | NA18968.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.38-1959G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123794 | |||||||
| chr2:131123797 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-1956C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123797 | |||||||
| chr2:131123798 | T | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.38-1955T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123798 | |||||||
| chr2:131123800 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0109 a0001c0001t0001g0120 |
3 | HG00642.hp1 HG01358.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.38-1953G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131123800 | |||||||
| chr2:131123846 | C | CT | 8 | a0001c0001t0001g0063 a0001c0001t0001g0137 a0001c0001t0002g0200 others(5): Show |
9 | HG00738.hp2 HG01243.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.38-1893dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131123846 | ||||||
| chr2:131124172 | T | TAGTC | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-1579_38-1576dup others(4): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131124172 | ||||||
| chr2:131124247 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02602.hp1 HG02895.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-1506G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131124247 | |||||||
| chr2:131124279 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01109.hp1 HG02258.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-1474G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131124279 | |||||||
| chr2:131124431 | C | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.38-1322C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131124431 | |||||||
| chr2:131124624 | C | T | 6 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-1129C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131124624 | |||||||
| chr2:131124803 | G | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-950G>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131124803 | |||||||
| chr2:131124814 | G | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-939G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131124814 | |||||||
| chr2:131124928 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0088 |
2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.38-825G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131124928 | |||||||
| chr2:131125387 | G | C | 1 | a0001c0001t0014g0073 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.38-366G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131125387 | |||||||
| chr2:131125492 | G | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01175.hp1 HG01261.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-261G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131125492 | |||||||
| chr2:131125558 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-195G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131125558 | |||||||
| chr2:131125694 | C | T | 6 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-59C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | chr2 | 131125694 | |||||||
| chr2:131125714 | T | TA | 9 | a0001c0001t0001g0071 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
10 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.38-26dupA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131125714 | ||||||
| chr2:131125714 | TA | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0004g0008 others(1): Show |
5 | HG02976.hp1 HG03195.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.38-26delA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 131125714 | ||||||
| chr2:131125927 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0098 |
2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.190+22A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 3/7 | chr2 | 131125927 | |||||||
| chr2:131126061 | T | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.190+156T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 3/7 | chr2 | 131126061 | |||||||
| chr2:131126385 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-299A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 3/7 | chr2 | 131126385 | |||||||
| chr2:131126505 | C | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0213 |
3 | HG03098.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.191-179C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 3/7 | chr2 | 131126505 | |||||||
| chr2:131126870 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.293+84G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131126870 | |||||||
| chr2:131126978 | C | T | 1 | a0001c0001t0008g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.293+192C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131126978 | |||||||
| chr2:131127207 | T | G | 1 | a0001c0001t0002g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.293+421T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131127207 | |||||||
| chr2:131127297 | G | A | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.293+511G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131127297 | |||||||
| chr2:131127350 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.293+564G>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131127350 | |||||||
| chr2:131127454 | C | T | 6 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+668C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131127454 | |||||||
| chr2:131127529 | A | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG02717.hp1 HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.293+743A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131127529 | |||||||
| chr2:131127597 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+811A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131127597 | |||||||
| chr2:131127803 | C | G | 8 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0208 others(5): Show |
8 | HG02559.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.293+1017C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131127803 | |||||||
| chr2:131128064 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+1278C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128064 | |||||||
| chr2:131128274 | C | A | 54 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(51): Show |
70 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.293+1488C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128274 | |||||||
| chr2:131128401 | C | G | 1 | a0001c0001t0010g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.293+1615C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128401 | |||||||
| chr2:131128656 | C | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+1870C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128656 | |||||||
| chr2:131128695 | A | G | 19 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(16): Show |
22 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.293+1909A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128695 | |||||||
| chr2:131128708 | G | C | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+1922G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128708 | |||||||
| chr2:131128819 | C | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-1902C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128819 | |||||||
| chr2:131128891 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-1830T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131128891 | |||||||
| chr2:131129142 | T | A | 1 | a0001c0001t0002g0018 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.294-1579T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129142 | |||||||
| chr2:131129186 | G | A | 33 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0019 others(30): Show |
47 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.294-1535G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129186 | |||||||
| chr2:131129324 | C | CA | 11 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0101 others(8): Show |
11 | HG01175.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.294-1369dupA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CA | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(63): Show |
76 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.294-1369delA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CAAA | C | 7 | a0001c0001t0001g0045 a0001c0001t0001g0131 a0001c0001t0001g0173 others(4): Show |
8 | HG01175.hp1 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.294-1371_294-1369d others(5): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CAAAA | C | 35 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0046 others(32): Show |
37 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.294-1372_294-1369d others(6): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CAAAAA | C | 46 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0001 others(43): Show |
62 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.294-1373_294-1369d others(7): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CAAAAAA | C | 7 | a0001c0001t0002g0201 a0001c0001t0005g0017 a0001c0001t0005g0174 others(4): Show |
8 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.294-1374_294-1369d others(8): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CAAAAAAA | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-1375_294-1369d others(9): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0191 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.294-1378_294-1369d others(12): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129324 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0008g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.294-1383_294-1369d others(17): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129324 | ||||||
| chr2:131129353 | G | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0066 |
3 | HG00099.hp1 HG01192.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.294-1368G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129353 | |||||||
| chr2:131129510 | A | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(75): Show |
98 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.294-1211A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129510 | |||||||
| chr2:131129535 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.294-1186G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129535 | |||||||
| chr2:131129544 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.294-1177G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129544 | |||||||
| chr2:131129645 | C | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-1076C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129645 | |||||||
| chr2:131129689 | A | T | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.294-1032A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129689 | |||||||
| chr2:131129729 | C | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0009g0044 |
3 | HG02258.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.294-992C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129729 | |||||||
| chr2:131129733 | A | ACCTCAGG others(104): Show |
76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(73): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.294-976_294-975ins others(111): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 131129733 | ||||||
| chr2:131129762 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-959C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129762 | |||||||
| chr2:131129991 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0009g0044 |
3 | HG02258.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.294-730G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131129991 | |||||||
| chr2:131130078 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
7 | HG02602.hp1 HG02895.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.294-643C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131130078 | |||||||
| chr2:131130411 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0002g0198 |
5 | HG00280.hp1 HG00639.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.294-310A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131130411 | |||||||
| chr2:131130519 | T | G | 6 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.294-202T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131130519 | |||||||
| chr2:131130536 | A | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
7 | HG02602.hp1 HG02895.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.294-185A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131130536 | |||||||
| chr2:131130546 | T | C | 6 | a0001c0001t0002g0179 a0001c0001t0002g0187 a0001c0001t0002g0188 others(3): Show |
6 | HG02080.hp2 NA18957.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.294-175T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131130546 | |||||||
| chr2:131130587 | C | G | 2 | a0001c0001t0002g0018 a0001c0001t0002g0213 |
3 | HG03098.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.294-134C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 4/7 | chr2 | 131130587 | |||||||
| chr2:131130851 | C | G | 78 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(75): Show |
98 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.333+91C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131130851 | |||||||
| chr2:131130898 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
7 | HG02602.hp1 HG02895.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+138A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131130898 | |||||||
| chr2:131131028 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.333+268A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131028 | |||||||
| chr2:131131122 | A | G | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.333+362A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131122 | |||||||
| chr2:131131242 | C | G | 59 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(56): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.333+482C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131242 | |||||||
| chr2:131131376 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+616C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131376 | |||||||
| chr2:131131405 | A | G | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+645A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131405 | |||||||
| chr2:131131568 | T | C | 78 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(75): Show |
98 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.333+808T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131568 | |||||||
| chr2:131131575 | T | C | 1 | a0001c0001t0019g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.333+815T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131575 | |||||||
| chr2:131131606 | C | T | 59 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(56): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.333+846C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131606 | |||||||
| chr2:131131650 | G | C | 1 | a0001c0001t0002g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.333+890G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131650 | |||||||
| chr2:131131667 | G | C | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.333+907G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131667 | |||||||
| chr2:131131757 | C | CT | 14 | a0001c0001t0002g0200 a0001c0001t0003g0009 a0001c0001t0003g0033 others(11): Show |
16 | HG00738.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.333+997_333+998ins others(1): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131757 | |||||||
| chr2:131131758 | C | CT | 26 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(23): Show |
28 | HG01071.hp1 HG01109.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.333+1015dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 131131758 | ||||||
| chr2:131131758 | C | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(68): Show |
90 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.333+998C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131758 | |||||||
| chr2:131131758 | CT | C | 18 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0059 others(15): Show |
18 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.333+1015delT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 131131758 | ||||||
| chr2:131131797 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.333+1037T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131797 | |||||||
| chr2:131131841 | A | AT | 7 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0002g0021 others(4): Show |
8 | HG00099.hp2 HG00642.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-1049dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 131131841 | ||||||
| chr2:131131872 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.334-1030C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131872 | |||||||
| chr2:131131880 | C | T | 8 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0208 others(5): Show |
8 | HG02559.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-1022C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131880 | |||||||
| chr2:131131892 | G | A | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.334-1010G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131131892 | |||||||
| chr2:131132037 | T | C | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-865T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131132037 | |||||||
| chr2:131132076 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG01175.hp1 HG01261.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-826C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131132076 | |||||||
| chr2:131132222 | A | G | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-680A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131132222 | |||||||
| chr2:131132553 | C | T | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-349C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131132553 | |||||||
| chr2:131132665 | G | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-237G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131132665 | |||||||
| chr2:131132768 | C | A | 2 | a0001c0001t0001g0154 a0001c0001t0009g0144 |
2 | NA18953.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.334-134C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 5/7 | chr2 | 131132768 | |||||||
| chr2:131133248 | C | T | 19 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(16): Show |
22 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.423+257C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131133248 | |||||||
| chr2:131133901 | G | GT | 17 | a0001c0001t0001g0062 a0001c0001t0001g0111 a0001c0001t0001g0143 others(14): Show |
18 | HG00733.hp1 HG01175.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.423+926dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131133901 | ||||||
| chr2:131133901 | GT | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0128 others(4): Show |
8 | HG01884.hp2 HG02630.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.423+926delT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131133901 | ||||||
| chr2:131133901 | GTTT | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+924_423+926del others(3): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131133901 | ||||||
| chr2:131134051 | C | T | 1 | a0001c0001t0011g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.423+1060C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134051 | |||||||
| chr2:131134127 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.423+1136C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134127 | |||||||
| chr2:131134142 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.423+1151G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134142 | |||||||
| chr2:131134217 | G | A | 5 | a0001c0001t0005g0017 a0001c0001t0005g0174 a0001c0001t0005g0175 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+1226G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134217 | |||||||
| chr2:131134396 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.423+1405A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134396 | |||||||
| chr2:131134413 | A | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+1422A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134413 | |||||||
| chr2:131134475 | T | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+1484T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134475 | |||||||
| chr2:131134488 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.423+1497T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134488 | |||||||
| chr2:131134587 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+1596C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134587 | |||||||
| chr2:131134959 | A | G | 6 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+1968A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131134959 | |||||||
| chr2:131135078 | C | A | 6 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+2087C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135078 | |||||||
| chr2:131135135 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.423+2144G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135135 | |||||||
| chr2:131135212 | C | A | 3 | a0001c0001t0003g0033 a0001c0001t0003g0039 a0001c0001t0018g0040 |
3 | HG02109.hp1 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.423+2221C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135212 | |||||||
| chr2:131135259 | G | A | 5 | a0001c0001t0004g0008 a0001c0001t0004g0133 a0001c0001t0004g0134 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+2268G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135259 | |||||||
| chr2:131135273 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.423+2282G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135273 | |||||||
| chr2:131135420 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0009g0044 |
3 | HG02258.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.423+2429C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135420 | |||||||
| chr2:131135431 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.423+2440A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135431 | |||||||
| chr2:131135469 | G | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+2478G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135469 | |||||||
| chr2:131135599 | A | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG01175.hp1 HG01261.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+2608A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135599 | |||||||
| chr2:131135775 | A | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(74): Show |
97 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.423+2784A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135775 | |||||||
| chr2:131135776 | T | A | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+2785T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135776 | |||||||
| chr2:131135944 | G | A | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+2953G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135944 | |||||||
| chr2:131135976 | A | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+2985A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131135976 | |||||||
| chr2:131136139 | TGCCTGCC others(1053): Show |
T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
7 | HG02602.hp1 HG02895.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+3153_424-2964d others(2): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131136139 | ||||||
| chr2:131136376 | T | A | 6 | a0001c0001t0001g0022 a0001c0001t0004g0008 a0001c0001t0004g0133 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+3385T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131136376 | |||||||
| chr2:131136382 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.423+3391T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131136382 | |||||||
| chr2:131136385 | T | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(83): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.423+3394T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131136385 | |||||||
| chr2:131136947 | TC | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-3219delC | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131136947 | |||||||
| chr2:131136969 | G | A | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424-3198G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131136969 | |||||||
| chr2:131137007 | C | T | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424-3160C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131137007 | |||||||
| chr2:131137032 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.424-3135C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131137032 | |||||||
| chr2:131137095 | T | C | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.424-3072T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131137095 | |||||||
| chr2:131137137 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.424-3030C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131137137 | |||||||
| chr2:131137183 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424-2984G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131137183 | |||||||
| chr2:131137657 | T | C | 78 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(75): Show |
98 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.424-2510T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131137657 | |||||||
| chr2:131137751 | T | TATTCTTT others(17): Show |
1 | a0001c0001t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424-2415_424-2392d others(26): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131137751 | ||||||
| chr2:131137800 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.424-2367A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131137800 | |||||||
| chr2:131138015 | A | AT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0045 others(10): Show |
14 | HG01928.hp2 HG02027.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.424-2131dupT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131138015 | ||||||
| chr2:131138015 | AT | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0099 others(9): Show |
13 | HG01243.hp1 HG01256.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.424-2131delT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131138015 | ||||||
| chr2:131138189 | A | C | 1 | a0001c0001t0002g0197 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.424-1978A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131138189 | |||||||
| chr2:131138668 | C | T | 2 | a0001c0001t0006g0023 a0001c0001t0011g0025 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424-1499C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131138668 | |||||||
| chr2:131138698 | T | C | 11 | a0001c0001t0001g0060 a0001c0001t0001g0086 a0001c0001t0003g0038 others(8): Show |
12 | HG01099.hp2 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.424-1469T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131138698 | |||||||
| chr2:131138705 | C | A | 59 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(56): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.424-1462C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131138705 | |||||||
| chr2:131138903 | T | C | 90 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(87): Show |
111 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.424-1264T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131138903 | |||||||
| chr2:131138943 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.424-1224C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131138943 | |||||||
| chr2:131138981 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0109 a0001c0001t0001g0120 |
3 | HG00642.hp1 HG01358.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.424-1186C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131138981 | |||||||
| chr2:131139176 | C | T | 18 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(15): Show |
21 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.424-991C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131139176 | |||||||
| chr2:131139243 | G | C | 1 | a0001c0001t0002g0220 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.424-924G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131139243 | |||||||
| chr2:131139314 | GTATA | G | 5 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-850_424-847del others(4): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 131139314 | ||||||
| chr2:131139321 | A | G | 5 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-846A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131139321 | |||||||
| chr2:131139353 | G | C | 4 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0195 others(1): Show |
4 | HG00738.hp2 HG01928.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-814G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131139353 | |||||||
| chr2:131139442 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424-725A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131139442 | |||||||
| chr2:131140152 | C | A | 1 | a0001c0001t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.424-15C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131140152 | |||||||
| chr2:131140159 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02602.hp2 | splice_region_variant&intron_variant | LOW | c.424-8C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 6/7 | chr2 | 131140159 | |||||||
| chr2:131140500 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+225A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131140500 | |||||||
| chr2:131140501 | G | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+226G>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131140501 | |||||||
| chr2:131140614 | G | C | 1 | a0001c0001t0021g0199 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.532+339G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131140614 | |||||||
| chr2:131140827 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0138 |
4 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+552A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131140827 | |||||||
| chr2:131141238 | A | G | 59 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(56): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.532+963A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131141238 | |||||||
| chr2:131141291 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.532+1016T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131141291 | |||||||
| chr2:131141337 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.532+1062C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131141337 | |||||||
| chr2:131141362 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.532+1087G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131141362 | |||||||
| chr2:131141391 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+1116G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131141391 | |||||||
| chr2:131141548 | C | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+1273C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131141548 | |||||||
| chr2:131141639 | C | CA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0095 a0001c0001t0001g0098 others(11): Show |
15 | HG00733.hp1 HG01175.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.532+1385dupA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 131141639 | ||||||
| chr2:131141639 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.532+1364C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131141639 | |||||||
| chr2:131141639 | CA | C | 29 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(26): Show |
31 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.532+1385delA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 131141639 | ||||||
| chr2:131142326 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+2051A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131142326 | |||||||
| chr2:131142576 | CT | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+2313delT | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 131142576 | ||||||
| chr2:131142580 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+2305T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131142580 | |||||||
| chr2:131142812 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+2537T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131142812 | |||||||
| chr2:131142845 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.532+2570C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131142845 | |||||||
| chr2:131142916 | C | G | 1 | a0001c0001t0005g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.532+2641C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131142916 | |||||||
| chr2:131142993 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG02602.hp1 HG02895.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+2718G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131142993 | |||||||
| chr2:131143313 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0009g0044 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.532+3038A>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143313 | |||||||
| chr2:131143317 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.532+3042G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143317 | |||||||
| chr2:131143435 | C | T | 1 | a0001c0001t0015g0047 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.532+3160C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143435 | |||||||
| chr2:131143541 | T | G | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.533-3096T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143541 | |||||||
| chr2:131143567 | T | C | 8 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0037 others(5): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.533-3070T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143567 | |||||||
| chr2:131143661 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-2976T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143661 | |||||||
| chr2:131143701 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01261.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.533-2936T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143701 | |||||||
| chr2:131143706 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.533-2931A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143706 | |||||||
| chr2:131143931 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0090 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.533-2706T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131143931 | |||||||
| chr2:131144310 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0119 |
2 | HG00408.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.533-2327C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131144310 | |||||||
| chr2:131144415 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.533-2222C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131144415 | |||||||
| chr2:131144621 | C | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-2016C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131144621 | |||||||
| chr2:131144681 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.533-1956C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131144681 | |||||||
| chr2:131144713 | A | T | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.533-1924A>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131144713 | |||||||
| chr2:131145142 | C | A | 1 | a0001c0001t0002g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.533-1495C>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145142 | |||||||
| chr2:131145335 | TTTC | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-1299_533-1297d others(5): Show |
PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 131145335 | ||||||
| chr2:131145338 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.533-1299C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145338 | |||||||
| chr2:131145339 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.533-1298T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145339 | |||||||
| chr2:131145369 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.533-1268T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145369 | |||||||
| chr2:131145543 | C | G | 1 | a0001c0001t0003g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.533-1094C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145543 | |||||||
| chr2:131145571 | G | C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.533-1066G>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145571 | |||||||
| chr2:131145605 | C | T | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-1032C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145605 | |||||||
| chr2:131145667 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(55): Show |
75 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.533-970A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145667 | |||||||
| chr2:131145734 | T | C | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01175.hp1 HG01261.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-903T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145734 | |||||||
| chr2:131145740 | T | A | 5 | a0001c0001t0005g0017 a0001c0001t0005g0174 a0001c0001t0005g0175 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.533-897T>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145740 | |||||||
| chr2:131145785 | T | G | 1 | a0001c0001t0020g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.533-852T>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145785 | |||||||
| chr2:131145978 | C | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-659C>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131145978 | |||||||
| chr2:131146032 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-605A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131146032 | |||||||
| chr2:131146050 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(222): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.533-587T>C | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131146050 | |||||||
| chr2:131146059 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(1): Show |
5 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-578A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131146059 | |||||||
| chr2:131146180 | C | CA | 5 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0001g0154 others(2): Show |
5 | HG00408.hp2 HG02622.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-443dupA | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 131146180 | ||||||
| chr2:131146238 | G | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
10 | HG01884.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-399G>A | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131146238 | |||||||
| chr2:131146343 | C | T | 6 | a0001c0001t0003g0178 a0001c0001t0005g0017 a0001c0001t0005g0174 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.533-294C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131146343 | |||||||
| chr2:131146491 | A | G | 3 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 |
3 | HG02055.hp1 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.533-146A>G | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131146491 | |||||||
| chr2:131146549 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.533-88C>T | PLEKHB2 | ENSG00000115762.17 | transcript | ENST00000693505.1 | protein_coding | 7/7 | chr2 | 131146549 |