Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80055 |
| ensemblid | ENSG00000197121.15 |
| hgncid | 25712 |
| symbol | PGAP1 |
| name | post-GPI attachment to proteins inositol deacylase 1 |
| refseq_nuc | NM_024989.4 |
| refseq_prot | NP_079265.2 |
| ensembl_nuc | ENST00000354764.9 |
| ensembl_prot | ENSP00000346809.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 196833004 |
| end | 196926707 |
| strand | - |
| ver | v1.2 |
| region | chr2:196833004-196926707 |
| region5000 | chr2:196828004-196931707 |
| regionname0 | PGAP1_chr2_196833004_196926707 |
| regionname5000 | PGAP1_chr2_196828004_196931707 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 922 | 185 | 76 | 34 | 39 | 6 | 28 | 35 | PGAP1_chr2_196828004_196931707 | PGAP1 | MFLHS others(917): Show |
chr2 | 196828004 | 196931707 |
| a0002 | 0/0 | 922 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | MFLHS others(917): Show |
chr2 | 196828004 | 196931707 |
| a0003 | 0/0 | 922 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | MFLHS others(917): Show |
chr2 | 196828004 | 196931707 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2766 | 174 | 66 | 34 | 39 | 6 | 27 | PGAP1_chr2_196828004_196931707 | PGAP1 | ATGTT others(2761): Show |
chr2 | 196828004 | 196931707 | ||
| a0001c0002 | 0/0 | 2766 | 5 | 5 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | ATGTT others(2761): Show |
chr2 | 196828004 | 196931707 | ||
| a0001c0003 | 0/0 | 2766 | 5 | 5 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | ATGTT others(2761): Show |
chr2 | 196828004 | 196931707 | ||
| a0001c0006 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | ATGTT others(2761): Show |
chr2 | 196828004 | 196931707 | ||
| a0002c0004 | 0/0 | 2766 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | ATGTT others(2761): Show |
chr2 | 196828004 | 196931707 | ||
| a0003c0005 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | ATGTT others(2761): Show |
chr2 | 196828004 | 196931707 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11090 | 56 | 16 | 12 | 18 | 3 | 7 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0002 | 0/0 | 11093 | 41 | 15 | 7 | 13 | 0 | 6 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11088): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0003 | 0/0 | 11089 | 20 | 6 | 3 | 2 | 2 | 7 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0004 | 1/0 | 11090 | 3 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0005 | 0/0 | 11089 | 6 | 6 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0006 | 0/0 | 11090 | 5 | 0 | 4 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0008 | 0/0 | 11089 | 3 | 3 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0009 | 0/0 | 11089 | 3 | 2 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0010 | 0/0 | 11090 | 3 | 0 | 1 | 2 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0011 | 0/0 | 11093 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11088): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0012 | 0/0 | 11089 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0013 | 0/0 | 11089 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0014 | 0/0 | 11090 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0015 | 0/0 | 11090 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0016 | 0/0 | 11088 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11083): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0018 | 0/1 | 11093 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11088): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0019 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0020 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0021 | 0/0 | 11090 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0022 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0023 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0024 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0025 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0026 | 0/0 | 11089 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0027 | 0/0 | 11089 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0028 | 0/0 | 11089 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0029 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0030 | 0/0 | 11090 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0031 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0032 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0034 | 0/0 | 11090 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0035 | 0/0 | 11090 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0036 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0037 | 0/0 | 11090 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0038 | 0/0 | 11090 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0039 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0001t0040 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0002t0004 | 0/0 | 11090 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0002t0033 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0001c0003t0007 | 0/0 | 11089 | 4 | 4 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0003t0017 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11084): Show |
chr2 | 196828004 | 196931707 |
| a0001c0006t0002 | 0/0 | 11093 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11088): Show |
chr2 | 196828004 | 196931707 |
| a0002c0004t0004 | 0/0 | 11090 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11085): Show |
chr2 | 196828004 | 196931707 |
| a0003c0005t0002 | 0/0 | 11093 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | AGTGT others(11088): Show |
chr2 | 196828004 | 196931707 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0004g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0009g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0011g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0011g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0013g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0014g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0014g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0016g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0016g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0018g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0019g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0020g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0021g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0022g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0023g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0024g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0025g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0026g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0027g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0028g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0029g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0030g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0031g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0032g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0034g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0035g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0036g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0037g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0038g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0039g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0001t0040g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0002t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0002t0033g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0003t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0003t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0003t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0003t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0003t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0001c0006t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0002c0004t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0002c0004t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| a0003c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0100 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0102 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0103 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01167 | hp1 | a0001 | c0001 | t0016 | g0020 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01168 | hp1 | a0001 | c0001 | t0011 | g0171 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01169 | hp1 | a0001 | c0001 | t0011 | g0145 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01169 | hp2 | a0001 | c0001 | t0016 | g0019 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0101 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01358 | hp1 | a0001 | c0001 | t0029 | g0092 | AMR | CLM | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | CLM | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01496 | hp2 | a0001 | c0001 | t0031 | g0104 | AMR | CLM | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0111 | EUR | IBS | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01884 | hp1 | a0001 | c0001 | t0023 | g0009 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02135 | hp1 | a0001 | c0001 | t0020 | g0015 | EAS | KHV | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02293 | hp2 | a0001 | c0001 | t0010 | g0054 | AMR | PEL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02451 | hp1 | a0001 | c0001 | t0039 | g0039 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0035 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02630 | hp2 | a0001 | c0003 | t0007 | g0178 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02647 | hp2 | a0001 | c0001 | t0025 | g0097 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02683 | hp1 | a0001 | c0001 | t0037 | g0037 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0011 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02723 | hp2 | a0001 | c0001 | t0036 | g0075 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02735 | hp2 | a0001 | c0001 | t0027 | g0117 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0091 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02895 | hp1 | a0002 | c0004 | t0004 | g0051 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02897 | hp1 | a0001 | c0001 | t0024 | g0105 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02897 | hp2 | a0002 | c0004 | t0004 | g0040 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02922 | hp2 | a0001 | c0003 | t0007 | g0177 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0031 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02965 | hp2 | a0001 | c0001 | t0040 | g0180 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02970 | hp2 | a0001 | c0002 | t0033 | g0033 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0003 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0046 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03098 | hp2 | a0001 | c0003 | t0017 | g0179 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0003 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ESN | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03225 | hp2 | a0001 | c0003 | t0007 | g0175 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03453 | hp1 | a0001 | c0003 | t0007 | g0176 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03486 | hp1 | a0001 | c0001 | t0022 | g0174 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03579 | hp1 | a0001 | c0001 | t0032 | g0049 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0099 | SAS | STU | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03704 | hp1 | a0001 | c0006 | t0002 | g0159 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03831 | hp2 | a0001 | c0001 | t0035 | g0072 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03942 | hp1 | a0001 | c0001 | t0034 | g0080 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03942 | hp2 | a0001 | c0001 | t0026 | g0114 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | STU | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG04228 | hp1 | a0001 | c0001 | t0030 | g0062 | SAS | STU | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | STU | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | YRI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0004 | AFR | YRI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | YRI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18979 | hp1 | a0001 | c0001 | t0021 | g0057 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18984 | hp1 | a0001 | c0001 | t0019 | g0016 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18992 | hp2 | a0001 | c0001 | t0038 | g0025 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19003 | hp1 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | LWK | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | LWK | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19068 | hp2 | a0003 | c0005 | t0002 | g0148 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19079 | hp2 | a0001 | c0001 | t0010 | g0077 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA20752 | hp1 | a0001 | c0001 | t0028 | g0113 | EUR | TSI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0122 | EUR | TSI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0041 | AFR | MSL | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | USA | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0098 | AFR | USA | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0134 | REF | REF | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0121 | REF | REF | PGAP1_chr2_196828004_196931707 | PGAP1 | chr2 | 196828004 | 196931707 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196843946 | G | C | 1 | a0003 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.2467C>G | p.Leu823Val | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 25/27 | 2558/11090 | 2467/2769 | 823/922 | chr2 | 196843946 | |||
| chr2:196902610 | T | C | 1 | a0002 | 2 | HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.782A>G | p.His261Arg | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/27 | 873/11090 | 782/2769 | 261/922 | chr2 | 196902610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196842747 | A | G | 1 | a0001c0003 | 5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.2604T>C | p.Asn868Asn | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 26/27 | 2695/11090 | 2604/2769 | 868/922 | chr2 | 196842747 | |||
| chr2:196893189 | G | A | 1 | a0001c0006 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.984C>T | p.His328His | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 8/27 | 1075/11090 | 984/2769 | 328/922 | chr2 | 196893189 | |||
| chr2:196912997 | A | C | 1 | a0001c0002 | 5 | HG02572.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.534T>G | p.Leu178Leu | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/27 | 625/11090 | 534/2769 | 178/922 | chr2 | 196912997 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196833048 | T | C | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8186A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 8186 | chr2 | 196833048 | ||||||
| chr2:196833248 | C | T | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03831.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7986G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7986 | chr2 | 196833248 | ||||||
| chr2:196833625 | A | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
176 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*7609T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7609 | chr2 | 196833625 | ||||||
| chr2:196833649 | G | A | 2 | a0001c0001t0023 a0001c0001t0040 |
2 | HG01884.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7585C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7585 | chr2 | 196833649 | ||||||
| chr2:196833658 | A | G | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*7576T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7576 | chr2 | 196833658 | ||||||
| chr2:196833701 | A | G | 1 | a0001c0003t0017 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7533T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7533 | chr2 | 196833701 | ||||||
| chr2:196833725 | T | C | 1 | a0001c0001t0035 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7509A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7509 | chr2 | 196833725 | ||||||
| chr2:196833803 | G | A | 1 | a0001c0002t0033 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7431C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7431 | chr2 | 196833803 | ||||||
| chr2:196833899 | G | A | 1 | a0001c0001t0027 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7335C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7335 | chr2 | 196833899 | ||||||
| chr2:196833912 | G | A | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
176 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*7322C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7322 | chr2 | 196833912 | ||||||
| chr2:196833996 | T | A | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7238A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7238 | chr2 | 196833996 | ||||||
| chr2:196834064 | A | C | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7170T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7170 | chr2 | 196834064 | ||||||
| chr2:196834142 | A | C | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7092T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7092 | chr2 | 196834142 | ||||||
| chr2:196834158 | G | A | 1 | a0001c0001t0028 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7076C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7076 | chr2 | 196834158 | ||||||
| chr2:196834176 | T | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(20): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*7058A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 7058 | chr2 | 196834176 | ||||||
| chr2:196834244 | T | A | 1 | a0001c0001t0036 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6990A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6990 | chr2 | 196834244 | ||||||
| chr2:196834305 | T | A | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*6929A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6929 | chr2 | 196834305 | ||||||
| chr2:196834398 | G | C | 1 | a0001c0001t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6836C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6836 | chr2 | 196834398 | ||||||
| chr2:196834454 | A | G | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6780T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6780 | chr2 | 196834454 | ||||||
| chr2:196834577 | A | G | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6657T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6657 | chr2 | 196834577 | ||||||
| chr2:196834582 | A | G | 1 | a0001c0001t0027 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6652T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6652 | chr2 | 196834582 | ||||||
| chr2:196834606 | A | G | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*6628T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6628 | chr2 | 196834606 | ||||||
| chr2:196834727 | T | C | 1 | a0001c0001t0038 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6507A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6507 | chr2 | 196834727 | ||||||
| chr2:196834952 | C | T | 1 | a0001c0001t0010 | 3 | HG02293.hp2 NA19003.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6282G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6282 | chr2 | 196834952 | ||||||
| chr2:196835087 | G | A | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*6147C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 6147 | chr2 | 196835087 | ||||||
| chr2:196835346 | C | T | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*5888G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 5888 | chr2 | 196835346 | ||||||
| chr2:196835502 | C | T | 6 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0023 others(3): Show |
9 | HG01496.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5732G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 5732 | chr2 | 196835502 | ||||||
| chr2:196835616 | C | T | 1 | a0001c0001t0032 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5618G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 5618 | chr2 | 196835616 | ||||||
| chr2:196835804 | T | C | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5430A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 5430 | chr2 | 196835804 | ||||||
| chr2:196835860 | G | A | 1 | a0001c0001t0024 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5374C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 5374 | chr2 | 196835860 | ||||||
| chr2:196836075 | T | C | 1 | a0001c0001t0039 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5159A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 5159 | chr2 | 196836075 | ||||||
| chr2:196836251 | A | G | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*4983T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 4983 | chr2 | 196836251 | ||||||
| chr2:196836298 | A | G | 1 | a0001c0001t0031 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4936T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 4936 | chr2 | 196836298 | ||||||
| chr2:196836692 | CA | C | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(19): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4541delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 4541 | chr2 | 196836692 | ||||||
| chr2:196836855 | A | G | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4379T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 4379 | chr2 | 196836855 | ||||||
| chr2:196836923 | C | T | 1 | a0001c0001t0006 | 5 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4311G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 4311 | chr2 | 196836923 | ||||||
| chr2:196836980 | A | G | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*4254T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 4254 | chr2 | 196836980 | ||||||
| chr2:196837360 | G | A | 2 | a0001c0003t0007 a0001c0003t0017 |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3874C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3874 | chr2 | 196837360 | ||||||
| chr2:196837407 | C | T | 1 | a0001c0001t0040 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3827G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3827 | chr2 | 196837407 | ||||||
| chr2:196837503 | T | C | 1 | a0001c0001t0013 | 2 | HG02976.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3731A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3731 | chr2 | 196837503 | ||||||
| chr2:196837576 | T | C | 1 | a0001c0001t0008 | 3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3658A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3658 | chr2 | 196837576 | ||||||
| chr2:196837698 | T | G | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3536A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3536 | chr2 | 196837698 | ||||||
| chr2:196837955 | A | G | 1 | a0001c0001t0021 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3279T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3279 | chr2 | 196837955 | ||||||
| chr2:196838076 | C | T | 1 | a0001c0001t0011 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3158G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3158 | chr2 | 196838076 | ||||||
| chr2:196838089 | C | A | 1 | a0001c0001t0020 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3145G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3145 | chr2 | 196838089 | ||||||
| chr2:196838100 | T | C | 1 | a0001c0001t0015 | 2 | HG02280.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3134A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 3134 | chr2 | 196838100 | ||||||
| chr2:196838352 | C | T | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2882G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 2882 | chr2 | 196838352 | ||||||
| chr2:196838782 | C | T | 1 | a0001c0001t0008 | 3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2452G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 2452 | chr2 | 196838782 | ||||||
| chr2:196839023 | A | G | 1 | a0001c0001t0026 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2211T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 2211 | chr2 | 196839023 | ||||||
| chr2:196839044 | A | AAAAC | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2186_*2189dupGTTT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 2189 | chr2 | 196839044 | ||||||
| chr2:196839330 | T | C | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0006t0002 others(1): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1904A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1904 | chr2 | 196839330 | ||||||
| chr2:196839383 | C | T | 1 | a0001c0001t0022 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1851G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1851 | chr2 | 196839383 | ||||||
| chr2:196839682 | T | C | 2 | a0001c0003t0007 a0001c0003t0017 |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1552A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1552 | chr2 | 196839682 | ||||||
| chr2:196839712 | ACT | A | 1 | a0001c0001t0016 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1520_*1521delAG | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1520 | chr2 | 196839712 | ||||||
| chr2:196839785 | T | A | 2 | a0001c0003t0007 a0001c0003t0017 |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1449A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1449 | chr2 | 196839785 | ||||||
| chr2:196839948 | C | A | 2 | a0001c0003t0007 a0001c0003t0017 |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1286G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1286 | chr2 | 196839948 | ||||||
| chr2:196840032 | C | T | 1 | a0001c0001t0030 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1202G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1202 | chr2 | 196840032 | ||||||
| chr2:196840033 | G | A | 2 | a0001c0001t0013 a0001c0001t0025 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1201C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1201 | chr2 | 196840033 | ||||||
| chr2:196840089 | A | T | 2 | a0001c0003t0007 a0001c0003t0017 |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1145T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 1145 | chr2 | 196840089 | ||||||
| chr2:196840250 | A | T | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0025 |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*984T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 984 | chr2 | 196840250 | ||||||
| chr2:196840377 | C | T | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*857G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 857 | chr2 | 196840377 | ||||||
| chr2:196840499 | T | G | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(6): Show |
36 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*735A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 735 | chr2 | 196840499 | ||||||
| chr2:196840632 | C | G | 1 | a0001c0001t0014 | 2 | HG02818.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*602G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 602 | chr2 | 196840632 | ||||||
| chr2:196840643 | A | G | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*591T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 591 | chr2 | 196840643 | ||||||
| chr2:196840817 | T | C | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG02135.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*417A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 417 | chr2 | 196840817 | ||||||
| chr2:196840889 | C | T | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(20): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*345G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 345 | chr2 | 196840889 | ||||||
| chr2:196840934 | C | T | 1 | a0001c0001t0021 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 300 | chr2 | 196840934 | ||||||
| chr2:196841029 | C | G | 8 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0019 others(5): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*205G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 205 | chr2 | 196841029 | ||||||
| chr2:196841031 | A | G | 2 | a0001c0003t0007 a0001c0003t0017 |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*203T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 203 | chr2 | 196841031 | ||||||
| chr2:196841084 | A | G | 1 | a0001c0001t0005 | 6 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*150T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 27/27 | 150 | chr2 | 196841084 | ||||||
| chr2:196926691 | T | C | 1 | a0001c0001t0040 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/27 | 75 | chr2 | 196926691 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196841414 | C | G | 1 | a0001c0001t0035g0072 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2631-42G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 26/26 | chr2 | 196841414 | |||||||
| chr2:196841582 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2631-210T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 26/26 | chr2 | 196841582 | |||||||
| chr2:196841611 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 |
4 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2631-239C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 26/26 | chr2 | 196841611 | |||||||
| chr2:196841809 | G | A | 6 | a0001c0001t0002g0137 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2631-437C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 26/26 | chr2 | 196841809 | |||||||
| chr2:196841853 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2631-481G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 26/26 | chr2 | 196841853 | |||||||
| chr2:196842057 | A | C | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2630+664T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 26/26 | chr2 | 196842057 | |||||||
| chr2:196843020 | A | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2526-195T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 25/26 | chr2 | 196843020 | |||||||
| chr2:196843184 | G | T | 2 | a0001c0001t0009g0004 a0001c0001t0009g0098 |
3 | HG01496.hp1 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2526-359C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 25/26 | chr2 | 196843184 | |||||||
| chr2:196843526 | T | C | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2525+362A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 25/26 | chr2 | 196843526 | |||||||
| chr2:196843727 | C | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2525+161G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 25/26 | chr2 | 196843727 | |||||||
| chr2:196844157 | A | G | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.2338-82T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 24/26 | chr2 | 196844157 | |||||||
| chr2:196844449 | TA | T | 42 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(39): Show |
44 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.2337+74delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 24/26 | chr2 | 196844449 | |||||||
| chr2:196844648 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2287-74T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196844648 | |||||||
| chr2:196844750 | T | A | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2287-176A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196844750 | |||||||
| chr2:196844818 | T | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2287-244A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196844818 | |||||||
| chr2:196845044 | A | G | 51 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(48): Show |
53 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.2287-470T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845044 | |||||||
| chr2:196845045 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2287-471T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845045 | |||||||
| chr2:196845340 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2286+542T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845340 | |||||||
| chr2:196845352 | AT | A | 15 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0139 others(12): Show |
15 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2286+529delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845352 | |||||||
| chr2:196845406 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2286+476A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845406 | |||||||
| chr2:196845588 | T | TA | 13 | a0001c0001t0003g0005 a0001c0001t0003g0108 a0001c0001t0003g0115 others(10): Show |
14 | HG00741.hp1 HG01358.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.2286+293dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845588 | |||||||
| chr2:196845781 | C | G | 1 | a0001c0001t0002g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2286+101G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845781 | |||||||
| chr2:196845815 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2286+67G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845815 | |||||||
| chr2:196845818 | A | G | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.2286+64T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 23/26 | chr2 | 196845818 | |||||||
| chr2:196846169 | G | A | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2151-152C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 22/26 | chr2 | 196846169 | |||||||
| chr2:196846171 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2151-154C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 22/26 | chr2 | 196846171 | |||||||
| chr2:196846369 | C | T | 2 | a0001c0001t0015g0041 a0001c0001t0015g0076 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2151-352G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 22/26 | chr2 | 196846369 | |||||||
| chr2:196846515 | G | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2150+488C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 22/26 | chr2 | 196846515 | |||||||
| chr2:196846566 | T | C | 1 | a0001c0001t0006g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2150+437A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 22/26 | chr2 | 196846566 | |||||||
| chr2:196846664 | T | C | 30 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(27): Show |
32 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.2150+339A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 22/26 | chr2 | 196846664 | |||||||
| chr2:196847379 | G | A | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1953-179C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847379 | |||||||
| chr2:196847382 | C | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1953-182G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847382 | |||||||
| chr2:196847458 | C | CT | 44 | a0001c0001t0001g0058 a0001c0001t0002g0007 a0001c0001t0002g0008 others(41): Show |
46 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1953-259dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847458 | |||||||
| chr2:196847483 | C | T | 1 | a0001c0001t0032g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1953-283G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847483 | |||||||
| chr2:196847503 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1953-303T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847503 | |||||||
| chr2:196847569 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1953-369C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847569 | |||||||
| chr2:196847639 | C | T | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1952+308G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847639 | |||||||
| chr2:196847813 | GA | G | 6 | a0001c0001t0039g0039 a0001c0003t0007g0175 a0001c0003t0007g0176 others(3): Show |
6 | HG02451.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1952+133delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847813 | |||||||
| chr2:196847842 | G | A | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1952+105C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847842 | |||||||
| chr2:196847850 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1952+97G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847850 | |||||||
| chr2:196847937 | T | G | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1952+10A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 21/26 | chr2 | 196847937 | |||||||
| chr2:196848040 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0043 others(6): Show |
10 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1862-3C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196848040 | |||||||
| chr2:196848141 | T | C | 53 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(50): Show |
55 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.1862-104A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196848141 | |||||||
| chr2:196848706 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0029g0092 |
3 | HG00639.hp2 HG01069.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1862-669A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196848706 | |||||||
| chr2:196848904 | C | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1862-867G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196848904 | |||||||
| chr2:196849067 | G | A | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-1030C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849067 | |||||||
| chr2:196849240 | T | A | 1 | a0001c0001t0009g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1862-1203A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849240 | |||||||
| chr2:196849261 | A | AT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0089 others(3): Show |
6 | HG01069.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1862-1225dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849261 | |||||||
| chr2:196849261 | AT | A | 10 | a0001c0001t0003g0108 a0001c0001t0008g0012 a0001c0001t0008g0014 others(7): Show |
10 | HG02280.hp1 HG02451.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1862-1225delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849261 | |||||||
| chr2:196849261 | ATTTTT | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1862-1229_1862-122 others(9): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849261 | |||||||
| chr2:196849357 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1862-1320C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849357 | |||||||
| chr2:196849440 | AT | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0023g0009 others(2): Show |
5 | HG01884.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1862-1404delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849440 | |||||||
| chr2:196849521 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1862-1484C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849521 | |||||||
| chr2:196849548 | A | C | 1 | a0001c0001t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1862-1511T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849548 | |||||||
| chr2:196849627 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1862-1590G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849627 | |||||||
| chr2:196849938 | C | A | 1 | a0001c0001t0010g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1862-1901G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196849938 | |||||||
| chr2:196850089 | G | T | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1862-2052C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196850089 | |||||||
| chr2:196850195 | G | A | 1 | a0001c0001t0012g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1862-2158C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196850195 | |||||||
| chr2:196850354 | G | A | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.1862-2317C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196850354 | |||||||
| chr2:196850565 | C | T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-2528G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196850565 | |||||||
| chr2:196850981 | A | C | 1 | a0001c0001t0012g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1862-2944T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196850981 | |||||||
| chr2:196851146 | GT | G | 87 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(84): Show |
93 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(90): Show |
intron_variant | MODIFIER | c.1862-3110delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851146 | |||||||
| chr2:196851153 | T | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-3116A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851153 | |||||||
| chr2:196851154 | G | T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-3117C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851154 | |||||||
| chr2:196851162 | T | A | 1 | a0001c0001t0003g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1862-3125A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851162 | |||||||
| chr2:196851163 | A | T | 2 | a0001c0001t0009g0004 a0001c0001t0009g0098 |
3 | HG01496.hp1 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1862-3126T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851163 | |||||||
| chr2:196851193 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1862-3156G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851193 | |||||||
| chr2:196851357 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1862-3320G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851357 | |||||||
| chr2:196851363 | C | T | 1 | a0001c0003t0017g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1862-3326G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851363 | |||||||
| chr2:196851529 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1862-3492G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851529 | |||||||
| chr2:196851577 | T | C | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1862-3540A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851577 | |||||||
| chr2:196851708 | G | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1862-3671C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851708 | |||||||
| chr2:196851917 | C | G | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.1862-3880G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196851917 | |||||||
| chr2:196852058 | T | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1862-4021A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852058 | |||||||
| chr2:196852074 | G | A | 1 | a0001c0001t0035g0072 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1862-4037C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852074 | |||||||
| chr2:196852083 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1862-4046T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852083 | |||||||
| chr2:196852097 | A | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(24): Show |
29 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1862-4060T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852097 | |||||||
| chr2:196852104 | T | A | 1 | a0001c0001t0003g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1862-4067A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852104 | |||||||
| chr2:196852269 | C | T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-4232G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852269 | |||||||
| chr2:196852514 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1862-4477T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852514 | |||||||
| chr2:196852541 | G | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1862-4504C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852541 | |||||||
| chr2:196852682 | C | A | 1 | a0001c0001t0031g0104 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1862-4645G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852682 | |||||||
| chr2:196852842 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1862-4805A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196852842 | |||||||
| chr2:196853278 | G | C | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1862-5241C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853278 | |||||||
| chr2:196853473 | T | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-5436A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853473 | |||||||
| chr2:196853559 | G | A | 11 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0070 others(8): Show |
11 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1862-5522C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853559 | |||||||
| chr2:196853796 | T | C | 2 | a0001c0001t0015g0041 a0001c0001t0015g0076 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1862-5759A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853796 | |||||||
| chr2:196853867 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1862-5830C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853867 | |||||||
| chr2:196853910 | A | AT | 14 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(11): Show |
16 | HG01496.hp1 HG02027.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1862-5874dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853910 | |||||||
| chr2:196853910 | A | ATT | 6 | a0001c0001t0020g0015 a0001c0001t0030g0062 a0001c0003t0007g0175 others(3): Show |
6 | HG02135.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1862-5875_1862-587 others(6): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853910 | |||||||
| chr2:196853910 | AT | A | 50 | a0001c0001t0001g0065 a0001c0001t0001g0089 a0001c0001t0002g0007 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1862-5874delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196853910 | |||||||
| chr2:196854018 | G | A | 1 | a0001c0006t0002g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1862-5981C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854018 | |||||||
| chr2:196854193 | C | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1862-6156G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854193 | |||||||
| chr2:196854199 | G | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1862-6162C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854199 | |||||||
| chr2:196854321 | T | C | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1862-6284A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854321 | |||||||
| chr2:196854376 | A | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0153 a0001c0001t0002g0154 |
3 | HG00733.hp1 HG02717.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1862-6339T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854376 | |||||||
| chr2:196854460 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1862-6423A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854460 | |||||||
| chr2:196854471 | T | A | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1862-6434A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854471 | |||||||
| chr2:196854557 | T | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1862-6520A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854557 | |||||||
| chr2:196854739 | A | G | 43 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(40): Show |
47 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(44): Show |
intron_variant | MODIFIER | c.1862-6702T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854739 | |||||||
| chr2:196854795 | G | A | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1862-6758C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196854795 | |||||||
| chr2:196855160 | C | T | 1 | a0001c0001t0004g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1862-7123G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855160 | |||||||
| chr2:196855253 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1862-7216C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855253 | |||||||
| chr2:196855266 | C | T | 1 | a0001c0003t0017g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1862-7229G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855266 | |||||||
| chr2:196855325 | C | CA | 49 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(46): Show |
53 | HG00741.hp1 HG01070.hp2 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.1862-7289dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855325 | |||||||
| chr2:196855325 | C | CAA | 39 | a0001c0001t0002g0007 a0001c0001t0002g0132 a0001c0001t0002g0133 others(36): Show |
40 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1862-7290_1862-728 others(6): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855325 | |||||||
| chr2:196855325 | C | CAAA | 10 | a0001c0001t0002g0008 a0001c0001t0002g0135 a0001c0001t0002g0153 others(7): Show |
11 | HG00642.hp1 HG00733.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1862-7291_1862-728 others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855325 | |||||||
| chr2:196855631 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1862-7594C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855631 | |||||||
| chr2:196855694 | T | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-7657A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855694 | |||||||
| chr2:196855960 | G | A | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1862-7923C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855960 | |||||||
| chr2:196855967 | T | G | 1 | a0001c0001t0003g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1862-7930A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196855967 | |||||||
| chr2:196856010 | T | G | 28 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(25): Show |
30 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1862-7973A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856010 | |||||||
| chr2:196856075 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1862-8038T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856075 | |||||||
| chr2:196856082 | C | T | 1 | a0001c0001t0003g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1862-8045G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856082 | |||||||
| chr2:196856251 | A | G | 1 | a0001c0001t0025g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1862-8214T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856251 | |||||||
| chr2:196856408 | T | A | 1 | a0001c0001t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1862-8371A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856408 | |||||||
| chr2:196856462 | T | C | 2 | a0002c0004t0004g0040 a0002c0004t0004g0051 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1862-8425A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856462 | |||||||
| chr2:196856472 | T | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1862-8435A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856472 | |||||||
| chr2:196856575 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1861+8412A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856575 | |||||||
| chr2:196856995 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1861+7992A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196856995 | |||||||
| chr2:196857184 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1861+7803G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857184 | |||||||
| chr2:196857240 | T | C | 1 | a0001c0001t0003g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1861+7747A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857240 | |||||||
| chr2:196857667 | A | T | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1861+7320T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857667 | |||||||
| chr2:196857824 | C | T | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1861+7163G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857824 | |||||||
| chr2:196857835 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+7152A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857835 | |||||||
| chr2:196857871 | ATTGTAAT others(4): Show |
A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+7105_1861+711 others(15): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857871 | |||||||
| chr2:196857921 | C | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1861+7066G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857921 | |||||||
| chr2:196857934 | T | C | 28 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(25): Show |
30 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1861+7053A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857934 | |||||||
| chr2:196857955 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1861+7032T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857955 | |||||||
| chr2:196857967 | G | A | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.1861+7020C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196857967 | |||||||
| chr2:196858033 | CA | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1861+6953delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858033 | |||||||
| chr2:196858104 | A | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1861+6883T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858104 | |||||||
| chr2:196858195 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1861+6792T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858195 | |||||||
| chr2:196858245 | CA | C | 55 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(52): Show |
57 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.1861+6741delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858245 | |||||||
| chr2:196858350 | T | C | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1861+6637A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858350 | |||||||
| chr2:196858365 | A | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1861+6622T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858365 | |||||||
| chr2:196858397 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1861+6590C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858397 | |||||||
| chr2:196858401 | C | CAAAAAAA others(5): Show |
5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+6574_1861+658 others(16): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858401 | |||||||
| chr2:196858503 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+6484G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858503 | |||||||
| chr2:196858647 | C | A | 1 | a0001c0001t0003g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1861+6340G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858647 | |||||||
| chr2:196858732 | C | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+6255G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858732 | |||||||
| chr2:196858773 | T | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1861+6214A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196858773 | |||||||
| chr2:196859407 | T | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+5580A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196859407 | |||||||
| chr2:196859471 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1861+5516T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196859471 | |||||||
| chr2:196859526 | T | A | 1 | a0001c0001t0002g0165 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1861+5461A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196859526 | |||||||
| chr2:196859622 | T | C | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1861+5365A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196859622 | |||||||
| chr2:196860145 | GT | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+4841delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196860145 | |||||||
| chr2:196860156 | A | G | 1 | a0001c0001t0009g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1861+4831T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196860156 | |||||||
| chr2:196860313 | T | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1861+4674A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196860313 | |||||||
| chr2:196860324 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+4663C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196860324 | |||||||
| chr2:196860437 | G | C | 4 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1861+4550C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196860437 | |||||||
| chr2:196860690 | C | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(24): Show |
29 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1861+4297G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196860690 | |||||||
| chr2:196860884 | G | C | 1 | a0001c0001t0023g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1861+4103C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196860884 | |||||||
| chr2:196861218 | C | T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1861+3769G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861218 | |||||||
| chr2:196861307 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1861+3680T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861307 | |||||||
| chr2:196861321 | A | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1861+3666T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861321 | |||||||
| chr2:196861358 | G | A | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1861+3629C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861358 | |||||||
| chr2:196861369 | C | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+3618G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861369 | |||||||
| chr2:196861755 | A | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+3232T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861755 | |||||||
| chr2:196861811 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+3176A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861811 | |||||||
| chr2:196861866 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+3121G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861866 | |||||||
| chr2:196861876 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1861+3111A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196861876 | |||||||
| chr2:196862033 | A | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+2954T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862033 | |||||||
| chr2:196862038 | A | G | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1861+2949T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862038 | |||||||
| chr2:196862052 | T | G | 1 | a0001c0002t0004g0031 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1861+2935A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862052 | |||||||
| chr2:196862108 | C | A | 1 | a0001c0001t0002g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1861+2879G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862108 | |||||||
| chr2:196862301 | C | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1861+2686G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862301 | |||||||
| chr2:196862319 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1861+2668A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862319 | |||||||
| chr2:196862428 | G | A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(24): Show |
28 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.1861+2559C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862428 | |||||||
| chr2:196862432 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1861+2555G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862432 | |||||||
| chr2:196862433 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1861+2554C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862433 | |||||||
| chr2:196862727 | G | A | 2 | a0001c0001t0003g0119 a0001c0001t0003g0127 |
2 | HG02027.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1861+2260C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862727 | |||||||
| chr2:196862930 | A | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+2057T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862930 | |||||||
| chr2:196862980 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1861+2007T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196862980 | |||||||
| chr2:196863049 | A | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+1938T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863049 | |||||||
| chr2:196863049 | A | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1861+1938T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863049 | |||||||
| chr2:196863206 | C | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1861+1781G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863206 | |||||||
| chr2:196863427 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1861+1560C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863427 | |||||||
| chr2:196863557 | G | A | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1861+1430C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863557 | |||||||
| chr2:196863608 | T | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+1379A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863608 | |||||||
| chr2:196863722 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1861+1265G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863722 | |||||||
| chr2:196863818 | A | C | 1 | a0001c0001t0002g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1861+1169T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863818 | |||||||
| chr2:196863976 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1861+1011A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196863976 | |||||||
| chr2:196864013 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+974A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864013 | |||||||
| chr2:196864038 | C | G | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1861+949G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864038 | |||||||
| chr2:196864093 | CT | C | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1861+893delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864093 | |||||||
| chr2:196864390 | C | CA | 72 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(69): Show |
77 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.1861+596dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864390 | |||||||
| chr2:196864390 | C | CAA | 11 | a0001c0001t0002g0141 a0001c0001t0002g0150 a0001c0001t0002g0160 others(8): Show |
11 | HG01070.hp2 HG01358.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1861+595_1861+596d others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864390 | |||||||
| chr2:196864593 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1861+394G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864593 | |||||||
| chr2:196864651 | T | C | 1 | a0001c0001t0039g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1861+336A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864651 | |||||||
| chr2:196864653 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1861+334G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864653 | |||||||
| chr2:196864874 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1861+113C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 20/26 | chr2 | 196864874 | |||||||
| chr2:196865339 | A | T | 2 | a0001c0001t0006g0102 a0001c0001t0006g0103 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1768-259T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196865339 | |||||||
| chr2:196865532 | T | G | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1768-452A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196865532 | |||||||
| chr2:196865761 | G | GCCT | 53 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(50): Show |
55 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.1768-682_1768-681i others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196865761 | |||||||
| chr2:196865772 | T | C | 2 | a0001c0001t0014g0046 a0001c0001t0014g0091 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1768-692A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196865772 | |||||||
| chr2:196865794 | T | C | 8 | a0001c0001t0002g0138 a0001c0001t0002g0143 a0001c0001t0002g0144 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-714A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196865794 | |||||||
| chr2:196865974 | G | C | 1 | a0001c0002t0033g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1768-894C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196865974 | |||||||
| chr2:196866038 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1768-958G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866038 | |||||||
| chr2:196866205 | T | C | 3 | a0001c0001t0002g0152 a0001c0001t0002g0161 a0001c0006t0002g0159 |
3 | HG03239.hp1 HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1768-1125A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866205 | |||||||
| chr2:196866446 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1768-1366G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866446 | |||||||
| chr2:196866489 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1768-1409G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866489 | |||||||
| chr2:196866627 | T | C | 3 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 |
3 | HG02922.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1768-1547A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866627 | |||||||
| chr2:196866872 | C | A | 2 | a0001c0001t0010g0063 a0001c0001t0010g0077 |
2 | NA19003.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1768-1792G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866872 | |||||||
| chr2:196866928 | CAAT | C | 12 | a0001c0001t0002g0007 a0001c0001t0002g0132 a0001c0001t0002g0133 others(9): Show |
13 | HG01167.hp2 HG01192.hp1 HG04184.hp1 others(10): Show |
intron_variant | MODIFIER | c.1768-1851_1768-184 others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866928 | |||||||
| chr2:196866962 | G | A | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1768-1882C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196866962 | |||||||
| chr2:196867051 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1768-1971G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867051 | |||||||
| chr2:196867113 | C | G | 29 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(26): Show |
31 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.1768-2033G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867113 | |||||||
| chr2:196867115 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1768-2035A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867115 | |||||||
| chr2:196867140 | C | A | 1 | a0001c0001t0006g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1768-2060G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867140 | |||||||
| chr2:196867219 | A | T | 2 | a0001c0001t0015g0041 a0001c0001t0015g0076 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1768-2139T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867219 | |||||||
| chr2:196867234 | A | C | 1 | a0001c0001t0001g0017 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1768-2154T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867234 | |||||||
| chr2:196867262 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 |
4 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1768-2182A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867262 | |||||||
| chr2:196867441 | C | A | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1768-2361G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867441 | |||||||
| chr2:196867459 | A | T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1768-2379T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867459 | |||||||
| chr2:196867556 | A | G | 3 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 |
3 | HG02922.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1768-2476T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867556 | |||||||
| chr2:196867589 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1768-2509G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867589 | |||||||
| chr2:196867624 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1768-2544A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867624 | |||||||
| chr2:196867787 | A | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1768-2707T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196867787 | |||||||
| chr2:196868029 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1767+2912C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868029 | |||||||
| chr2:196868225 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1767+2716A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868225 | |||||||
| chr2:196868426 | TA | T | 99 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0089 others(96): Show |
105 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(102): Show |
intron_variant | MODIFIER | c.1767+2514delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868426 | |||||||
| chr2:196868459 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1767+2482A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868459 | |||||||
| chr2:196868472 | A | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1767+2469T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868472 | |||||||
| chr2:196868518 | T | C | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1767+2423A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868518 | |||||||
| chr2:196868538 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1767+2403A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868538 | |||||||
| chr2:196868669 | A | G | 1 | a0001c0003t0007g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1767+2272T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868669 | |||||||
| chr2:196868759 | A | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1767+2182T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868759 | |||||||
| chr2:196868996 | T | C | 1 | a0001c0001t0040g0180 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1767+1945A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196868996 | |||||||
| chr2:196869056 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1767+1885G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196869056 | |||||||
| chr2:196869224 | T | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1767+1717A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196869224 | |||||||
| chr2:196869254 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1767+1687A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196869254 | |||||||
| chr2:196869332 | T | C | 1 | a0001c0006t0002g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1767+1609A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196869332 | |||||||
| chr2:196869344 | A | AT | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1767+1596dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196869344 | |||||||
| chr2:196869570 | G | A | 4 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG02622.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1767+1371C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196869570 | |||||||
| chr2:196869705 | T | C | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1767+1236A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196869705 | |||||||
| chr2:196870002 | C | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1767+939G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196870002 | |||||||
| chr2:196870017 | G | A | 1 | a0001c0001t0003g0119 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1767+924C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196870017 | |||||||
| chr2:196870463 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1767+478T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196870463 | |||||||
| chr2:196870550 | C | A | 1 | a0001c0001t0037g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1767+391G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 19/26 | chr2 | 196870550 | |||||||
| chr2:196871092 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1729-113A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196871092 | |||||||
| chr2:196871187 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1729-208G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196871187 | |||||||
| chr2:196871358 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0043 others(6): Show |
10 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1729-379G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196871358 | |||||||
| chr2:196871404 | T | C | 3 | a0001c0001t0002g0157 a0001c0001t0011g0145 a0001c0001t0011g0171 |
3 | HG00642.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1729-425A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196871404 | |||||||
| chr2:196871454 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG00639.hp2 HG01069.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1729-475C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196871454 | |||||||
| chr2:196872024 | AAAT | A | 8 | a0001c0001t0002g0138 a0001c0001t0002g0143 a0001c0001t0002g0144 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1728+414_1728+416d others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196872024 | |||||||
| chr2:196872035 | G | A | 1 | a0001c0001t0020g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1728+406C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196872035 | |||||||
| chr2:196872066 | C | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1728+375G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196872066 | |||||||
| chr2:196872113 | C | T | 1 | a0001c0001t0004g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1728+328G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 18/26 | chr2 | 196872113 | |||||||
| chr2:196872577 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1620-28A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 17/26 | chr2 | 196872577 | |||||||
| chr2:196872697 | T | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1620-148A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 17/26 | chr2 | 196872697 | |||||||
| chr2:196872863 | T | G | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1619+97A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 17/26 | chr2 | 196872863 | |||||||
| chr2:196873098 | C | T | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1553-72G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 16/26 | chr2 | 196873098 | |||||||
| chr2:196873109 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1553-83A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 16/26 | chr2 | 196873109 | |||||||
| chr2:196873168 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1553-142A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 16/26 | chr2 | 196873168 | |||||||
| chr2:196873276 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1553-250A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 16/26 | chr2 | 196873276 | |||||||
| chr2:196873394 | C | CCTTT | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1552+133_1552+134i others(6): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 16/26 | chr2 | 196873394 | |||||||
| chr2:196873918 | A | ATTTGT | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1427-161_1427-160i others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196873918 | |||||||
| chr2:196873919 | A | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1427-161T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196873919 | |||||||
| chr2:196874244 | G | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1427-486C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196874244 | |||||||
| chr2:196874359 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1427-601T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196874359 | |||||||
| chr2:196874685 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1427-927T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196874685 | |||||||
| chr2:196874770 | T | C | 3 | a0001c0001t0006g0099 a0001c0001t0006g0102 a0001c0001t0006g0103 |
3 | HG01070.hp1 HG01071.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1426+976A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196874770 | |||||||
| chr2:196874778 | C | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426+968G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196874778 | |||||||
| chr2:196875048 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1426+698G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196875048 | |||||||
| chr2:196875054 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1426+692T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196875054 | |||||||
| chr2:196875065 | C | T | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1426+681G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196875065 | |||||||
| chr2:196875268 | C | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1426+478G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196875268 | |||||||
| chr2:196875478 | G | A | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1426+268C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196875478 | |||||||
| chr2:196875547 | A | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1426+199T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196875547 | |||||||
| chr2:196875572 | T | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426+174A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 14/26 | chr2 | 196875572 | |||||||
| chr2:196875879 | C | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351-58G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196875879 | |||||||
| chr2:196876070 | C | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351-249G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876070 | |||||||
| chr2:196876091 | A | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1351-270T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876091 | |||||||
| chr2:196876191 | T | C | 2 | a0002c0004t0004g0040 a0002c0004t0004g0051 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1351-370A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876191 | |||||||
| chr2:196876258 | G | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1351-437C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876258 | |||||||
| chr2:196876501 | T | G | 1 | a0001c0001t0002g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1351-680A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876501 | |||||||
| chr2:196876510 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1351-689C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876510 | |||||||
| chr2:196876541 | G | T | 5 | a0001c0001t0005g0006 a0001c0001t0005g0125 a0001c0001t0005g0129 others(2): Show |
6 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1351-720C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876541 | |||||||
| chr2:196876598 | CAT | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351-779_1351-778d others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876598 | |||||||
| chr2:196876801 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1351-980G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196876801 | |||||||
| chr2:196877077 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1351-1256A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196877077 | |||||||
| chr2:196877206 | G | A | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351-1385C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196877206 | |||||||
| chr2:196877433 | A | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1351-1612T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196877433 | |||||||
| chr2:196877706 | C | T | 1 | a0001c0003t0017g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1351-1885G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196877706 | |||||||
| chr2:196877952 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1350+2124A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196877952 | |||||||
| chr2:196878068 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1350+2008C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878068 | |||||||
| chr2:196878155 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350+1921G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878155 | |||||||
| chr2:196878171 | C | T | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1350+1905G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878171 | |||||||
| chr2:196878189 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350+1887G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878189 | |||||||
| chr2:196878240 | C | G | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1350+1836G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878240 | |||||||
| chr2:196878422 | G | T | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1350+1654C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878422 | |||||||
| chr2:196878547 | A | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350+1529T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878547 | |||||||
| chr2:196878716 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350+1360G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878716 | |||||||
| chr2:196878906 | G | A | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1350+1170C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878906 | |||||||
| chr2:196878931 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1350+1145G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196878931 | |||||||
| chr2:196879077 | T | G | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1350+999A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196879077 | |||||||
| chr2:196879135 | A | T | 1 | a0001c0001t0001g0029 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1350+941T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196879135 | |||||||
| chr2:196879182 | T | A | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1350+894A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196879182 | |||||||
| chr2:196879543 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1350+533G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196879543 | |||||||
| chr2:196879721 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350+355A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196879721 | |||||||
| chr2:196879988 | C | CTG | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1350+86_1350+87dup others(2): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196879988 | |||||||
| chr2:196880031 | T | C | 5 | a0001c0001t0006g0099 a0001c0001t0006g0100 a0001c0001t0006g0101 others(2): Show |
5 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350+45A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 13/26 | chr2 | 196880031 | |||||||
| chr2:196880160 | T | TA | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
splice_region_variant&intron_variant | LOW | c.1273-8dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196880160 | |||||||
| chr2:196880208 | AAAGAAAA others(23): Show |
A | 7 | a0001c0001t0002g0136 a0001c0001t0002g0146 a0001c0001t0002g0158 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273-85_1273-56del others(30): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196880208 | |||||||
| chr2:196880214 | A | G | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1273-61T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196880214 | |||||||
| chr2:196880397 | T | C | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1273-244A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196880397 | |||||||
| chr2:196880470 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1273-317A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196880470 | |||||||
| chr2:196880733 | A | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1273-580T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196880733 | |||||||
| chr2:196881045 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1273-892C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881045 | |||||||
| chr2:196881114 | T | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1273-961A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881114 | |||||||
| chr2:196881123 | T | C | 30 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(27): Show |
32 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1273-970A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881123 | |||||||
| chr2:196881136 | C | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1273-983G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881136 | |||||||
| chr2:196881144 | A | G | 2 | a0002c0004t0004g0040 a0002c0004t0004g0051 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1273-991T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881144 | |||||||
| chr2:196881270 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1273-1117A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881270 | |||||||
| chr2:196881662 | T | C | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1273-1509A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881662 | |||||||
| chr2:196881714 | T | C | 47 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(44): Show |
51 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.1273-1561A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881714 | |||||||
| chr2:196881801 | C | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-1648G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881801 | |||||||
| chr2:196881990 | C | T | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1273-1837G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196881990 | |||||||
| chr2:196882124 | G | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1273-1971C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196882124 | |||||||
| chr2:196882129 | C | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-1976G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196882129 | |||||||
| chr2:196882350 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | NA18984.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1273-2197A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196882350 | |||||||
| chr2:196882550 | TG | T | 2 | a0001c0001t0006g0102 a0001c0001t0006g0103 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1273-2398delC | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196882550 | |||||||
| chr2:196883173 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1272+2251C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196883173 | |||||||
| chr2:196883192 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1272+2232A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196883192 | |||||||
| chr2:196883236 | C | T | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1272+2188G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196883236 | |||||||
| chr2:196883564 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0078 others(1): Show |
4 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+1860C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196883564 | |||||||
| chr2:196883569 | C | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1272+1855G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196883569 | |||||||
| chr2:196883738 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1272+1686T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196883738 | |||||||
| chr2:196883902 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1272+1522T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196883902 | |||||||
| chr2:196884041 | A | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1272+1383T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884041 | |||||||
| chr2:196884100 | T | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1272+1324A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884100 | |||||||
| chr2:196884156 | T | A | 1 | a0001c0001t0003g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1272+1268A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884156 | |||||||
| chr2:196884323 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1272+1101G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884323 | |||||||
| chr2:196884429 | A | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(24): Show |
29 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1272+995T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884429 | |||||||
| chr2:196884466 | G | A | 1 | a0001c0001t0019g0016 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1272+958C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884466 | |||||||
| chr2:196884475 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0074 |
2 | NA18971.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1272+949T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884475 | |||||||
| chr2:196884565 | G | C | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1272+859C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196884565 | |||||||
| chr2:196885003 | C | T | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1272+421G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196885003 | |||||||
| chr2:196885296 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1272+128T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196885296 | |||||||
| chr2:196885318 | G | A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(24): Show |
29 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1272+106C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 12/26 | chr2 | 196885318 | |||||||
| chr2:196885612 | G | C | 1 | a0001c0001t0030g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1221-137C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 11/26 | chr2 | 196885612 | |||||||
| chr2:196886013 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-133G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886013 | |||||||
| chr2:196886157 | C | CT | 34 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0149 others(31): Show |
38 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1174-278dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886157 | |||||||
| chr2:196886157 | C | CTTT | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-280_1174-278d others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886157 | |||||||
| chr2:196886157 | CT | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0096 a0001c0001t0002g0142 others(4): Show |
7 | HG01167.hp1 HG02818.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174-278delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886157 | |||||||
| chr2:196886308 | C | A | 3 | a0001c0001t0003g0106 a0001c0001t0003g0107 a0001c0001t0003g0124 |
3 | HG02258.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1174-428G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886308 | |||||||
| chr2:196886386 | C | T | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1174-506G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886386 | |||||||
| chr2:196886472 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1174-592C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886472 | |||||||
| chr2:196886505 | A | G | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1174-625T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886505 | |||||||
| chr2:196886705 | C | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1174-825G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886705 | |||||||
| chr2:196886996 | T | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1174-1116A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196886996 | |||||||
| chr2:196887167 | A | G | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1174-1287T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196887167 | |||||||
| chr2:196887210 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1174-1330G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196887210 | |||||||
| chr2:196887315 | C | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1174-1435G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196887315 | |||||||
| chr2:196887338 | C | G | 1 | a0001c0001t0039g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1174-1458G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196887338 | |||||||
| chr2:196887622 | T | C | 2 | a0001c0001t0014g0046 a0001c0001t0014g0091 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1174-1742A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196887622 | |||||||
| chr2:196887967 | G | A | 2 | a0001c0001t0009g0004 a0001c0001t0009g0098 |
3 | HG01496.hp1 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-2087C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196887967 | |||||||
| chr2:196888061 | T | C | 29 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(26): Show |
31 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.1174-2181A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196888061 | |||||||
| chr2:196888205 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1174-2325T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196888205 | |||||||
| chr2:196888265 | G | GT | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-2386dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196888265 | |||||||
| chr2:196888298 | AGACT | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-2422_1174-241 others(8): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196888298 | |||||||
| chr2:196888417 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1173+2411G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196888417 | |||||||
| chr2:196888421 | C | A | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1173+2407G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196888421 | |||||||
| chr2:196888965 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1173+1863C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196888965 | |||||||
| chr2:196889154 | G | A | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1173+1674C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889154 | |||||||
| chr2:196889394 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1173+1434A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889394 | |||||||
| chr2:196889518 | C | CA | 6 | a0001c0001t0002g0151 a0001c0003t0007g0175 a0001c0003t0007g0176 others(3): Show |
6 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+1309dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889518 | |||||||
| chr2:196889622 | C | T | 2 | a0001c0001t0003g0106 a0001c0001t0003g0107 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1173+1206G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889622 | |||||||
| chr2:196889662 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1173+1166G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889662 | |||||||
| chr2:196889692 | TA | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(170): Show |
181 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(178): Show |
intron_variant | MODIFIER | c.1173+1135delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889692 | |||||||
| chr2:196889775 | C | T | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1173+1053G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889775 | |||||||
| chr2:196889858 | C | CA | 8 | a0001c0001t0001g0018 a0001c0001t0002g0152 a0001c0001t0002g0161 others(5): Show |
8 | HG02145.hp1 HG02717.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+969dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889858 | |||||||
| chr2:196889858 | CA | C | 6 | a0001c0001t0002g0147 a0001c0001t0014g0046 a0001c0001t0014g0091 others(3): Show |
6 | HG02630.hp2 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+969delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196889858 | |||||||
| chr2:196890028 | G | A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(24): Show |
29 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1173+800C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196890028 | |||||||
| chr2:196890229 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1173+599G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196890229 | |||||||
| chr2:196890497 | T | G | 30 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(27): Show |
32 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1173+331A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196890497 | |||||||
| chr2:196890524 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1173+304T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196890524 | |||||||
| chr2:196890571 | C | T | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1173+257G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196890571 | |||||||
| chr2:196890633 | A | G | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1173+195T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196890633 | |||||||
| chr2:196890668 | T | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1173+160A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 10/26 | chr2 | 196890668 | |||||||
| chr2:196891172 | C | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1090-261G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891172 | |||||||
| chr2:196891192 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1090-281A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891192 | |||||||
| chr2:196891210 | C | T | 1 | a0001c0001t0019g0016 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1090-299G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891210 | |||||||
| chr2:196891314 | A | G | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1090-403T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891314 | |||||||
| chr2:196891366 | A | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1090-455T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891366 | |||||||
| chr2:196891429 | G | A | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.1090-518C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891429 | |||||||
| chr2:196891440 | T | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(170): Show |
181 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(178): Show |
intron_variant | MODIFIER | c.1090-529A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891440 | |||||||
| chr2:196891534 | A | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-623T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891534 | |||||||
| chr2:196891845 | A | G | 14 | a0001c0001t0003g0005 a0001c0001t0003g0108 a0001c0001t0003g0111 others(11): Show |
15 | HG00741.hp1 HG01358.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1089+501T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 9/26 | chr2 | 196891845 | |||||||
| chr2:196892565 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1034-164G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 8/26 | chr2 | 196892565 | |||||||
| chr2:196892838 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1033+302A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 8/26 | chr2 | 196892838 | |||||||
| chr2:196892954 | T | C | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1033+186A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 8/26 | chr2 | 196892954 | |||||||
| chr2:196893354 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.928-109T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196893354 | |||||||
| chr2:196893423 | G | A | 1 | a0001c0001t0020g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.928-178C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196893423 | |||||||
| chr2:196893457 | G | C | 1 | a0001c0001t0001g0030 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.928-212C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196893457 | |||||||
| chr2:196893650 | C | T | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.928-405G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196893650 | |||||||
| chr2:196893988 | T | G | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-743A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196893988 | |||||||
| chr2:196894250 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.928-1005A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196894250 | |||||||
| chr2:196894255 | C | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.928-1010G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196894255 | |||||||
| chr2:196894469 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-1224G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196894469 | |||||||
| chr2:196894488 | A | G | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.928-1243T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196894488 | |||||||
| chr2:196894734 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.928-1489C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196894734 | |||||||
| chr2:196895097 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.928-1852T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196895097 | |||||||
| chr2:196896434 | T | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.927+697A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196896434 | |||||||
| chr2:196896584 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+547C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196896584 | |||||||
| chr2:196896786 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.927+345C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196896786 | |||||||
| chr2:196896828 | T | TA | 35 | a0001c0001t0001g0047 a0001c0001t0001g0065 a0001c0001t0001g0066 others(32): Show |
39 | HG00741.hp1 HG01070.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.927+302dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196896828 | |||||||
| chr2:196896828 | T | TAA | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+301_927+302dup others(2): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196896828 | |||||||
| chr2:196896828 | T | TAAAAAAA | 29 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(26): Show |
31 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.927+296_927+302dup others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196896828 | |||||||
| chr2:196896828 | T | TAAAAAAA others(1): Show |
11 | a0001c0001t0002g0133 a0001c0001t0002g0139 a0001c0001t0002g0152 others(8): Show |
11 | HG00733.hp1 HG01891.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+295_927+302dup others(8): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196896828 | |||||||
| chr2:196897100 | T | C | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.927+31A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 7/26 | chr2 | 196897100 | |||||||
| chr2:196897221 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.861-24T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196897221 | |||||||
| chr2:196897289 | T | C | 53 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(50): Show |
55 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.861-92A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196897289 | |||||||
| chr2:196897469 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.861-272T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196897469 | |||||||
| chr2:196897586 | A | T | 1 | a0001c0001t0001g0030 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.861-389T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196897586 | |||||||
| chr2:196897588 | C | T | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.861-391G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196897588 | |||||||
| chr2:196897972 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.860+345G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196897972 | |||||||
| chr2:196898022 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.860+295C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196898022 | |||||||
| chr2:196898225 | A | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.860+92T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196898225 | |||||||
| chr2:196898305 | G | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.860+12C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 6/26 | chr2 | 196898305 | |||||||
| chr2:196898406 | C | T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.808-37G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196898406 | |||||||
| chr2:196898526 | C | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.808-157G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196898526 | |||||||
| chr2:196898661 | T | A | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.808-292A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196898661 | |||||||
| chr2:196898919 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.808-550T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196898919 | |||||||
| chr2:196898926 | G | GA | 32 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(29): Show |
34 | HG00741.hp1 HG01070.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.808-558dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196898926 | |||||||
| chr2:196899144 | T | A | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-775A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899144 | |||||||
| chr2:196899210 | C | A | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.808-841G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899210 | |||||||
| chr2:196899254 | C | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.808-885G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899254 | |||||||
| chr2:196899417 | T | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.808-1048A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899417 | |||||||
| chr2:196899472 | A | T | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-1103T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899472 | |||||||
| chr2:196899804 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.808-1435G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899804 | |||||||
| chr2:196899804 | CG | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.808-1436delC | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899804 | |||||||
| chr2:196899843 | G | A | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-1474C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899843 | |||||||
| chr2:196899872 | A | T | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.808-1503T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899872 | |||||||
| chr2:196899890 | T | C | 1 | a0001c0001t0012g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.808-1521A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899890 | |||||||
| chr2:196899911 | G | T | 2 | a0001c0003t0007g0178 a0001c0003t0017g0179 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.808-1542C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196899911 | |||||||
| chr2:196900082 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.808-1713C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900082 | |||||||
| chr2:196900207 | C | T | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.808-1838G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900207 | |||||||
| chr2:196900306 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.808-1937A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900306 | |||||||
| chr2:196900325 | T | C | 91 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(88): Show |
97 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.808-1956A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900325 | |||||||
| chr2:196900454 | A | T | 1 | a0001c0003t0007g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.808-2085T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900454 | |||||||
| chr2:196900607 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 |
4 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+1978G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900607 | |||||||
| chr2:196900627 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0079 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.807+1958C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900627 | |||||||
| chr2:196900789 | T | C | 1 | a0001c0001t0036g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.807+1796A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900789 | |||||||
| chr2:196900820 | G | A | 42 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(39): Show |
44 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.807+1765C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900820 | |||||||
| chr2:196900869 | G | C | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+1716C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196900869 | |||||||
| chr2:196901522 | T | C | 1 | a0001c0001t0034g0080 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.807+1063A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196901522 | |||||||
| chr2:196901648 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.807+937G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196901648 | |||||||
| chr2:196901701 | A | G | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.807+884T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196901701 | |||||||
| chr2:196901961 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.807+624G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196901961 | |||||||
| chr2:196902160 | T | A | 1 | a0001c0001t0002g0149 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.807+425A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196902160 | |||||||
| chr2:196902173 | C | A | 12 | a0001c0001t0002g0007 a0001c0001t0002g0132 a0001c0001t0002g0133 others(9): Show |
13 | HG01167.hp2 HG01192.hp1 HG04184.hp1 others(10): Show |
intron_variant | MODIFIER | c.807+412G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196902173 | |||||||
| chr2:196902396 | T | TATTCATT others(1): Show |
84 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(81): Show |
90 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.807+181_807+188dup others(8): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196902396 | |||||||
| chr2:196902396 | T | TATTCATT others(5): Show |
3 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 |
3 | HG02922.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.807+177_807+188dup others(12): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196902396 | |||||||
| chr2:196902396 | T | TATTCATT others(9): Show |
1 | a0001c0003t0017g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.807+173_807+188dup others(16): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196902396 | |||||||
| chr2:196902396 | T | TATTCATT others(13): Show |
1 | a0001c0003t0007g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.807+188_807+189ins others(20): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196902396 | |||||||
| chr2:196902402 | T | TTCATTCA others(1): Show |
2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.807+182_807+183ins others(8): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 5/26 | chr2 | 196902402 | |||||||
| chr2:196903131 | A | G | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.650-389T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196903131 | |||||||
| chr2:196903214 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-472G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196903214 | |||||||
| chr2:196903253 | A | T | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.650-511T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196903253 | |||||||
| chr2:196903363 | C | G | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.650-621G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196903363 | |||||||
| chr2:196903560 | CA | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(167): Show |
178 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(175): Show |
intron_variant | MODIFIER | c.650-819delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196903560 | |||||||
| chr2:196903575 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.650-833T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196903575 | |||||||
| chr2:196903897 | C | A | 1 | a0001c0001t0002g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.650-1155G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196903897 | |||||||
| chr2:196904356 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.650-1614C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904356 | |||||||
| chr2:196904465 | C | A | 1 | a0001c0001t0003g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.650-1723G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904465 | |||||||
| chr2:196904504 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-1762C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904504 | |||||||
| chr2:196904562 | A | G | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.650-1820T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904562 | |||||||
| chr2:196904570 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.650-1828A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904570 | |||||||
| chr2:196904704 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.650-1962C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904704 | |||||||
| chr2:196904710 | G | C | 6 | a0001c0001t0006g0099 a0001c0001t0006g0100 a0001c0001t0006g0101 others(3): Show |
6 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.650-1968C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904710 | |||||||
| chr2:196904732 | A | T | 2 | a0001c0001t0001g0042 a0001c0001t0002g0155 |
2 | HG03492.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.650-1990T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196904732 | |||||||
| chr2:196905155 | T | C | 1 | a0001c0001t0002g0150 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.650-2413A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905155 | |||||||
| chr2:196905161 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.650-2419A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905161 | |||||||
| chr2:196905173 | G | A | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(47): Show |
52 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.650-2431C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905173 | |||||||
| chr2:196905216 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-2474G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905216 | |||||||
| chr2:196905231 | C | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.650-2489G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905231 | |||||||
| chr2:196905320 | G | C | 5 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0002g0141 others(2): Show |
5 | HG02622.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-2578C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905320 | |||||||
| chr2:196905421 | T | C | 2 | a0001c0001t0015g0041 a0001c0001t0015g0076 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.650-2679A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905421 | |||||||
| chr2:196905436 | C | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.650-2694G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905436 | |||||||
| chr2:196905437 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-2695C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905437 | |||||||
| chr2:196905501 | CTGTTA | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-2764_650-2760d others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905501 | |||||||
| chr2:196905595 | G | A | 1 | a0001c0003t0007g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.650-2853C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905595 | |||||||
| chr2:196905623 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.650-2881G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905623 | |||||||
| chr2:196905665 | A | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.650-2923T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905665 | |||||||
| chr2:196905672 | C | T | 22 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(19): Show |
23 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.650-2930G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905672 | |||||||
| chr2:196905691 | A | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-2949T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905691 | |||||||
| chr2:196905820 | G | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01891.hp2 HG04184.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.650-3078C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905820 | |||||||
| chr2:196905894 | G | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.650-3152C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905894 | |||||||
| chr2:196905909 | G | A | 1 | a0001c0003t0007g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.650-3167C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905909 | |||||||
| chr2:196905920 | C | T | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-3178G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905920 | |||||||
| chr2:196905928 | C | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-3186G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905928 | |||||||
| chr2:196905929 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-3187T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905929 | |||||||
| chr2:196905940 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-3198T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905940 | |||||||
| chr2:196905961 | A | G | 3 | a0001c0001t0002g0138 a0001c0001t0002g0143 a0001c0001t0002g0144 |
3 | HG01069.hp1 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.650-3219T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196905961 | |||||||
| chr2:196906039 | A | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0089 others(6): Show |
9 | HG00639.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.650-3297T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906039 | |||||||
| chr2:196906070 | C | T | 2 | a0001c0003t0007g0178 a0001c0003t0017g0179 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.650-3328G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906070 | |||||||
| chr2:196906071 | A | G | 6 | a0001c0001t0040g0180 a0001c0003t0007g0175 a0001c0003t0007g0176 others(3): Show |
6 | HG02630.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.650-3329T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906071 | |||||||
| chr2:196906161 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG00639.hp2 HG01069.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-3419G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906161 | |||||||
| chr2:196906302 | C | T | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.650-3560G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906302 | |||||||
| chr2:196906355 | C | G | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG00733.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.650-3613G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906355 | |||||||
| chr2:196906370 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.650-3628T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906370 | |||||||
| chr2:196906437 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.650-3695C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906437 | |||||||
| chr2:196906534 | C | A | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.650-3792G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906534 | |||||||
| chr2:196906541 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0021 others(50): Show |
54 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.650-3799A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906541 | |||||||
| chr2:196906583 | A | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.650-3841T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906583 | |||||||
| chr2:196906607 | T | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.650-3865A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906607 | |||||||
| chr2:196906614 | A | G | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.650-3872T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906614 | |||||||
| chr2:196906716 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.650-3974C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906716 | |||||||
| chr2:196906881 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0002g0152 |
2 | HG03239.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.650-4139G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906881 | |||||||
| chr2:196906927 | A | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.650-4185T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196906927 | |||||||
| chr2:196907246 | G | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.650-4504C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196907246 | |||||||
| chr2:196907304 | C | G | 1 | a0001c0001t0019g0016 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.650-4562G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196907304 | |||||||
| chr2:196907351 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.650-4609T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196907351 | |||||||
| chr2:196907748 | T | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.650-5006A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196907748 | |||||||
| chr2:196907960 | C | G | 72 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(69): Show |
76 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.649+4922G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196907960 | |||||||
| chr2:196908043 | C | G | 27 | a0001c0001t0003g0005 a0001c0001t0003g0106 a0001c0001t0003g0107 others(24): Show |
29 | HG00741.hp1 HG01070.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.649+4839G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908043 | |||||||
| chr2:196908195 | G | C | 1 | a0001c0001t0012g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.649+4687C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908195 | |||||||
| chr2:196908203 | A | C | 1 | a0001c0001t0012g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.649+4679T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908203 | |||||||
| chr2:196908203 | A | T | 53 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(50): Show |
55 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.649+4679T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908203 | |||||||
| chr2:196908285 | A | C | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.649+4597T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908285 | |||||||
| chr2:196908307 | GC | G | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.649+4574delG | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908307 | |||||||
| chr2:196908310 | G | A | 2 | a0001c0001t0009g0004 a0001c0001t0009g0098 |
3 | HG01496.hp1 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.649+4572C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908310 | |||||||
| chr2:196908488 | C | A | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.649+4394G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908488 | |||||||
| chr2:196908626 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.649+4256C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908626 | |||||||
| chr2:196908674 | C | T | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.649+4208G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908674 | |||||||
| chr2:196908702 | C | A | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.649+4180G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908702 | |||||||
| chr2:196908747 | A | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0073 |
3 | HG01358.hp2 NA18981.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.649+4135T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196908747 | |||||||
| chr2:196909222 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+3660C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909222 | |||||||
| chr2:196909336 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0037g0037 |
3 | HG02683.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.649+3546C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909336 | |||||||
| chr2:196909369 | T | C | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.649+3513A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909369 | |||||||
| chr2:196909381 | T | A | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.649+3501A>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909381 | |||||||
| chr2:196909382 | G | A | 90 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(87): Show |
96 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.649+3500C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909382 | |||||||
| chr2:196909405 | C | T | 2 | a0001c0001t0016g0019 a0001c0001t0016g0020 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.649+3477G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909405 | |||||||
| chr2:196909506 | G | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+3376C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909506 | |||||||
| chr2:196909568 | G | A | 1 | a0001c0001t0008g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.649+3314C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909568 | |||||||
| chr2:196909616 | G | A | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.649+3266C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909616 | |||||||
| chr2:196909679 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+3203G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909679 | |||||||
| chr2:196909890 | A | C | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.649+2992T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909890 | |||||||
| chr2:196909906 | A | G | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.649+2976T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909906 | |||||||
| chr2:196909957 | A | C | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.649+2925T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909957 | |||||||
| chr2:196909987 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0044 |
2 | NA18995.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.649+2895G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196909987 | |||||||
| chr2:196910207 | C | T | 1 | a0001c0001t0040g0180 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.649+2675G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910207 | |||||||
| chr2:196910260 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.649+2622A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910260 | |||||||
| chr2:196910264 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.649+2618A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910264 | |||||||
| chr2:196910297 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.649+2585C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910297 | |||||||
| chr2:196910300 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.649+2582C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910300 | |||||||
| chr2:196910303 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.649+2579A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910303 | |||||||
| chr2:196910336 | C | G | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(45): Show |
50 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.649+2546G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910336 | |||||||
| chr2:196910455 | C | A | 1 | a0001c0001t0027g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.649+2427G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910455 | |||||||
| chr2:196910484 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(84): Show |
89 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.649+2398G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910484 | |||||||
| chr2:196910677 | C | A | 1 | a0001c0001t0003g0110 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.649+2205G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910677 | |||||||
| chr2:196910742 | C | G | 2 | a0001c0001t0013g0003 a0001c0001t0025g0097 |
3 | HG02647.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.649+2140G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910742 | |||||||
| chr2:196910792 | G | A | 3 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0022g0174 |
3 | HG02717.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.649+2090C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910792 | |||||||
| chr2:196910842 | A | C | 2 | a0001c0002t0004g0031 a0001c0002t0004g0034 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.649+2040T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910842 | |||||||
| chr2:196910862 | T | C | 2 | a0001c0002t0004g0031 a0001c0002t0004g0034 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.649+2020A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910862 | |||||||
| chr2:196910975 | C | T | 46 | a0001c0001t0001g0043 a0001c0001t0002g0007 a0001c0001t0002g0008 others(43): Show |
48 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.649+1907G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196910975 | |||||||
| chr2:196911029 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.649+1853T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911029 | |||||||
| chr2:196911169 | A | C | 45 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(42): Show |
47 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.649+1713T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911169 | |||||||
| chr2:196911169 | A | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+1713T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911169 | |||||||
| chr2:196911174 | C | T | 2 | a0001c0002t0004g0031 a0001c0002t0004g0034 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.649+1708G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911174 | |||||||
| chr2:196911271 | C | G | 1 | a0001c0001t0020g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.649+1611G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911271 | |||||||
| chr2:196911307 | G | A | 31 | a0001c0001t0002g0008 a0001c0001t0002g0135 a0001c0001t0002g0136 others(28): Show |
32 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.649+1575C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911307 | |||||||
| chr2:196911449 | A | T | 1 | a0001c0003t0007g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.649+1433T>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911449 | |||||||
| chr2:196911574 | T | C | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+1308A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911574 | |||||||
| chr2:196911606 | TA | T | 19 | a0001c0001t0001g0073 a0001c0001t0003g0005 a0001c0001t0003g0108 others(16): Show |
21 | HG00741.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.649+1275delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911606 | TAA | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0086 a0001c0001t0001g0087 others(9): Show |
12 | HG01070.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.649+1274_649+1275d others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911606 | TAAA | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(62): Show |
67 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.649+1273_649+1275d others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911606 | TAAAA | T | 45 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0042 others(42): Show |
47 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.649+1272_649+1275d others(6): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911606 | TAAAAA | T | 16 | a0001c0001t0002g0135 a0001c0001t0002g0138 a0001c0001t0002g0139 others(13): Show |
16 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.649+1271_649+1275d others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911606 | TAAAAAA | T | 6 | a0001c0001t0001g0038 a0001c0001t0002g0163 a0001c0001t0005g0130 others(3): Show |
7 | HG01167.hp2 HG02647.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.649+1270_649+1275d others(8): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911606 | TAAAAAAA others(3): Show |
T | 3 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 |
3 | HG02922.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.649+1266_649+1275d others(12): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911606 | TAAAAAAA others(4): Show |
T | 2 | a0001c0003t0007g0178 a0001c0003t0017g0179 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.649+1265_649+1275d others(13): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911606 | |||||||
| chr2:196911612 | A | G | 3 | a0001c0001t0002g0137 a0001c0001t0002g0141 a0001c0001t0002g0142 |
3 | HG01884.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.649+1270T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911612 | |||||||
| chr2:196911613 | A | G | 3 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0002g0170 |
3 | HG02622.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.649+1269T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911613 | |||||||
| chr2:196911855 | T | G | 1 | a0001c0001t0036g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.649+1027A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911855 | |||||||
| chr2:196911935 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+947A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911935 | |||||||
| chr2:196911974 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+908A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196911974 | |||||||
| chr2:196912057 | A | G | 2 | a0001c0001t0003g0112 a0001c0001t0028g0113 |
2 | HG04204.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.649+825T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912057 | |||||||
| chr2:196912226 | T | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.649+656A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912226 | |||||||
| chr2:196912282 | C | G | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.649+600G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912282 | |||||||
| chr2:196912580 | T | TA | 22 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0030 others(19): Show |
23 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.649+301dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912580 | |||||||
| chr2:196912580 | T | TAAA | 5 | a0001c0001t0008g0012 a0001c0001t0008g0014 a0001c0003t0007g0175 others(2): Show |
5 | HG02922.hp2 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.649+299_649+301dup others(3): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912580 | |||||||
| chr2:196912580 | TA | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0003g0111 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.649+301delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912580 | |||||||
| chr2:196912580 | TAAAAAAA | T | 40 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(37): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.649+295_649+301del others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912580 | |||||||
| chr2:196912593 | A | C | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.649+289T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912593 | |||||||
| chr2:196912865 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(147): Show |
156 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.649+17G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 4/26 | chr2 | 196912865 | |||||||
| chr2:196913074 | G | A | 1 | a0001c0001t0034g0080 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-21C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913074 | |||||||
| chr2:196913184 | A | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-131T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913184 | |||||||
| chr2:196913266 | A | G | 1 | a0001c0001t0003g0110 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.478-213T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913266 | |||||||
| chr2:196913324 | G | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(145): Show |
154 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(151): Show |
intron_variant | MODIFIER | c.478-271C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913324 | |||||||
| chr2:196913449 | C | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.478-396G>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913449 | |||||||
| chr2:196913456 | A | G | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.478-403T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913456 | |||||||
| chr2:196913487 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.478-434A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913487 | |||||||
| chr2:196913543 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.478-490C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913543 | |||||||
| chr2:196913895 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-842G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196913895 | |||||||
| chr2:196914370 | C | T | 5 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0002g0141 others(2): Show |
5 | HG02622.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1317G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914370 | |||||||
| chr2:196914398 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.478-1345T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914398 | |||||||
| chr2:196914615 | G | A | 1 | a0001c0001t0024g0105 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.478-1562C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914615 | |||||||
| chr2:196914618 | TCAAACAA others(7): Show |
T | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.478-1579_478-1566d others(16): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914618 | |||||||
| chr2:196914619 | C | CAAACA | 2 | a0001c0001t0003g0128 a0001c0001t0008g0014 |
2 | HG02698.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.478-1571_478-1567d others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914619 | |||||||
| chr2:196914619 | CAAACA | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0026 others(16): Show |
21 | HG00639.hp2 HG01069.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.478-1571_478-1567d others(7): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914619 | |||||||
| chr2:196914619 | CAAACAAA others(3): Show |
C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0022 others(119): Show |
127 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(124): Show |
intron_variant | MODIFIER | c.478-1576_478-1567d others(12): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914619 | |||||||
| chr2:196914619 | CAAACAAA others(8): Show |
C | 9 | a0001c0001t0012g0011 a0001c0001t0019g0016 a0001c0001t0020g0015 others(6): Show |
9 | HG02135.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.478-1581_478-1567d others(17): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914619 | |||||||
| chr2:196914709 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(83): Show |
88 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.478-1656G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914709 | |||||||
| chr2:196914813 | C | CT | 8 | a0001c0001t0002g0138 a0001c0001t0002g0166 a0001c0001t0003g0108 others(5): Show |
10 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.477+1604dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914813 | |||||||
| chr2:196914866 | C | T | 44 | a0001c0001t0001g0081 a0001c0001t0002g0007 a0001c0001t0002g0008 others(41): Show |
46 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.477+1552G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914866 | |||||||
| chr2:196914901 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.477+1517T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914901 | |||||||
| chr2:196914964 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.477+1454C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196914964 | |||||||
| chr2:196915089 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.477+1329A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196915089 | |||||||
| chr2:196915275 | T | C | 4 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+1143A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196915275 | |||||||
| chr2:196915924 | T | TC | 49 | a0001c0001t0001g0081 a0001c0001t0002g0007 a0001c0001t0002g0008 others(46): Show |
51 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.477+493dupG | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196915924 | |||||||
| chr2:196916338 | G | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.477+80C>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196916338 | |||||||
| chr2:196916377 | G | A | 2 | a0001c0001t0008g0013 a0001c0001t0008g0014 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.477+41C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 3/26 | chr2 | 196916377 | |||||||
| chr2:196917046 | C | T | 1 | a0001c0003t0007g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.302-453G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196917046 | |||||||
| chr2:196917563 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-970G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196917563 | |||||||
| chr2:196917629 | C | CATG | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-1039_302-1037d others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196917629 | |||||||
| chr2:196917719 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-1126A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196917719 | |||||||
| chr2:196917851 | A | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-1258T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196917851 | |||||||
| chr2:196918193 | A | C | 1 | a0001c0001t0001g0029 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.302-1600T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196918193 | |||||||
| chr2:196918243 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.302-1650C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196918243 | |||||||
| chr2:196918667 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01891.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.301+1330C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196918667 | |||||||
| chr2:196918843 | A | G | 1 | a0001c0001t0008g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301+1154T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196918843 | |||||||
| chr2:196919042 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+955C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196919042 | |||||||
| chr2:196919105 | C | T | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.301+892G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196919105 | |||||||
| chr2:196919389 | T | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.301+608A>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 2/26 | chr2 | 196919389 | |||||||
| chr2:196920450 | G | C | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.148-300C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196920450 | |||||||
| chr2:196920735 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.148-585G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196920735 | |||||||
| chr2:196921053 | G | A | 3 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.148-903C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921053 | |||||||
| chr2:196921188 | TA | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(73): Show |
78 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.148-1039delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921188 | |||||||
| chr2:196921188 | TAA | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-1040_148-1039d others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921188 | |||||||
| chr2:196921201 | A | AC | 4 | a0001c0001t0001g0028 a0001c0001t0002g0135 a0001c0001t0003g0106 others(1): Show |
4 | HG02258.hp1 HG03239.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-1052_148-1051i others(3): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921201 | |||||||
| chr2:196921215 | AAAC | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-1068_148-1066d others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921215 | |||||||
| chr2:196921304 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.148-1154C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921304 | |||||||
| chr2:196921684 | C | CA | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-1535dupT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921684 | |||||||
| chr2:196921821 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.148-1671T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921821 | |||||||
| chr2:196921858 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.148-1708T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921858 | |||||||
| chr2:196921949 | A | G | 7 | a0001c0001t0019g0016 a0001c0001t0020g0015 a0001c0003t0007g0175 others(4): Show |
7 | HG02135.hp1 HG02630.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-1799T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921949 | |||||||
| chr2:196921989 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-1839C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196921989 | |||||||
| chr2:196922464 | TA | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02615.hp2 HG03688.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-2315delT | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922464 | |||||||
| chr2:196922563 | CACACACA others(7): Show |
C | 4 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(1): Show |
4 | HG02922.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-2427_148-2414d others(16): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922563 | |||||||
| chr2:196922565 | CACACACA others(5): Show |
C | 1 | a0001c0003t0007g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148-2427_148-2416d others(14): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922565 | |||||||
| chr2:196922577 | G | C | 1 | a0001c0001t0003g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.148-2427C>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | G | GAC | 51 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(48): Show |
53 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.148-2429_148-2428d others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | G | GACAC | 8 | a0001c0001t0001g0024 a0001c0001t0001g0058 a0001c0001t0001g0073 others(5): Show |
8 | HG00642.hp2 HG01070.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-2431_148-2428d others(6): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | G | GACACAC | 2 | a0001c0001t0001g0064 a0001c0001t0024g0105 |
2 | HG02897.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.148-2433_148-2428d others(8): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | G | GACACACA others(1): Show |
3 | a0001c0001t0016g0019 a0001c0001t0016g0020 a0001c0001t0023g0009 |
3 | HG01167.hp1 HG01169.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.148-2435_148-2428d others(10): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | GAC | G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0003g0005 others(15): Show |
19 | HG00741.hp1 HG01358.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.148-2429_148-2428d others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | GACAC | G | 7 | a0001c0001t0002g0141 a0001c0001t0002g0170 a0001c0001t0003g0107 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-2431_148-2428d others(6): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | GACACAC | G | 41 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.148-2433_148-2428d others(8): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922577 | GACACACA others(3): Show |
G | 3 | a0001c0001t0008g0014 a0001c0001t0019g0016 a0001c0001t0020g0015 |
3 | HG02135.hp1 HG03486.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.148-2437_148-2428d others(12): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922577 | |||||||
| chr2:196922579 | C | G | 1 | a0001c0001t0003g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.148-2429G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922579 | |||||||
| chr2:196922581 | C | CAG | 2 | a0001c0001t0001g0059 a0001c0001t0001g0081 |
2 | HG00733.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.148-2432_148-2431i others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922581 | |||||||
| chr2:196922591 | C | G | 1 | a0001c0003t0007g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148-2441G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922591 | |||||||
| chr2:196922593 | C | G | 4 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(1): Show |
4 | HG02922.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-2443G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922593 | |||||||
| chr2:196922672 | C | CT | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0021 others(9): Show |
12 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.148-2523dupA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922672 | |||||||
| chr2:196922672 | CT | C | 22 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(19): Show |
25 | HG01168.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.148-2523delA | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922672 | |||||||
| chr2:196922672 | CTTT | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-2525_148-2523d others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922672 | |||||||
| chr2:196922774 | G | A | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-2624C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922774 | |||||||
| chr2:196922851 | T | C | 1 | a0001c0001t0040g0180 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.148-2701A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922851 | |||||||
| chr2:196922886 | C | T | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-2736G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922886 | |||||||
| chr2:196922965 | C | T | 4 | a0001c0001t0009g0004 a0001c0001t0009g0098 a0001c0001t0013g0003 others(1): Show |
6 | HG01496.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-2815G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196922965 | |||||||
| chr2:196923211 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.148-3061A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923211 | |||||||
| chr2:196923245 | C | T | 1 | a0001c0001t0008g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-3095G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923245 | |||||||
| chr2:196923332 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(79): Show |
84 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.147+3138G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923332 | |||||||
| chr2:196923520 | C | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+2950G>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923520 | |||||||
| chr2:196923628 | A | G | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.147+2842T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923628 | |||||||
| chr2:196923699 | C | T | 2 | a0001c0001t0012g0010 a0001c0001t0012g0011 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.147+2771G>A | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923699 | |||||||
| chr2:196923715 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(148): Show |
157 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.147+2755T>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923715 | |||||||
| chr2:196923837 | G | A | 2 | a0001c0001t0019g0016 a0001c0001t0020g0015 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.147+2633C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196923837 | |||||||
| chr2:196924907 | A | G | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+1563T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196924907 | |||||||
| chr2:196924918 | A | G | 55 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(52): Show |
57 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.147+1552T>C | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196924918 | |||||||
| chr2:196925109 | ATCT | A | 43 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0132 others(40): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.147+1358_147+1360d others(5): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196925109 | |||||||
| chr2:196925233 | G | A | 1 | a0001c0003t0017g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.147+1237C>T | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196925233 | |||||||
| chr2:196925439 | T | C | 3 | a0001c0001t0002g0008 a0001c0001t0002g0172 a0001c0001t0002g0173 |
4 | NA18971.hp1 NA18992.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+1031A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196925439 | |||||||
| chr2:196925516 | T | C | 1 | a0001c0001t0022g0174 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147+954A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196925516 | |||||||
| chr2:196925897 | T | C | 5 | a0001c0003t0007g0175 a0001c0003t0007g0176 a0001c0003t0007g0177 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+573A>G | PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196925897 | |||||||
| chr2:196926255 | TAACA | T | 2 | a0001c0001t0023g0009 a0001c0001t0040g0180 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+211_147+214del others(4): Show |
PGAP1 | ENSG00000197121.15 | transcript | ENST00000354764.9 | protein_coding | 1/26 | chr2 | 196926255 |