Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29899 |
| ensemblid | ENSG00000121957.15 |
| hgncid | 29501 |
| symbol | GPSM2 |
| name | G protein signaling modulator 2 |
| refseq_nuc | NM_013296.5 |
| refseq_prot | NP_037428.3 |
| ensembl_nuc | ENST00000264126.9 |
| ensembl_prot | ENSP00000264126.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 108876985 |
| end | 108934545 |
| strand | + |
| ver | v1.2 |
| region | chr1:108876985-108934545 |
| region5000 | chr1:108871985-108939545 |
| regionname0 | GPSM2_chr1_108876985_108934545 |
| regionname5000 | GPSM2_chr1_108871985_108939545 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 684 | 154 | 25 | 31 | 73 | 6 | 17 | 53 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(679): Show |
chr1 | 108871985 | 108939545 |
| a0002 | 0/0 | 683 | 60 | 33 | 11 | 9 | 4 | 3 | 9 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(678): Show |
chr1 | 108871985 | 108939545 |
| a0003 | 0/0 | 683 | 19 | 14 | 1 | 0 | 2 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(678): Show |
chr1 | 108871985 | 108939545 |
| a0004 | 0/0 | 683 | 19 | 7 | 0 | 4 | 0 | 8 | 4 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(678): Show |
chr1 | 108871985 | 108939545 |
| a0005 | 0/0 | 684 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(679): Show |
chr1 | 108871985 | 108939545 |
| a0006 | 0/0 | 684 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(679): Show |
chr1 | 108871985 | 108939545 |
| a0007 | 0/0 | 683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(678): Show |
chr1 | 108871985 | 108939545 |
| a0008 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | MEENL others(679): Show |
chr1 | 108871985 | 108939545 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2052 | 153 | 25 | 31 | 73 | 6 | 16 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2047): Show |
chr1 | 108871985 | 108939545 | ||
| a0001c0014 | 0/0 | 2052 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2047): Show |
chr1 | 108871985 | 108939545 | ||
| a0002c0002 | 0/0 | 2049 | 41 | 16 | 9 | 9 | 4 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0002c0005 | 0/0 | 2049 | 10 | 9 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0002c0006 | 0/0 | 2049 | 5 | 5 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0002c0008 | 0/0 | 2049 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0002c0010 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0003c0003 | 0/0 | 2049 | 19 | 14 | 1 | 0 | 2 | 2 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0004c0004 | 0/0 | 2049 | 18 | 6 | 0 | 4 | 0 | 8 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0004c0013 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0005c0007 | 0/0 | 2052 | 4 | 4 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2047): Show |
chr1 | 108871985 | 108939545 | ||
| a0006c0009 | 0/0 | 2052 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2047): Show |
chr1 | 108871985 | 108939545 | ||
| a0007c0011 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2044): Show |
chr1 | 108871985 | 108939545 | ||
| a0008c0012 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | ATGGA others(2047): Show |
chr1 | 108871985 | 108939545 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7152 | 75 | 16 | 18 | 29 | 3 | 8 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0002 | 0/0 | 7152 | 48 | 1 | 6 | 32 | 3 | 6 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0007 | 0/0 | 7152 | 6 | 6 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0012 | 0/0 | 7156 | 4 | 0 | 0 | 4 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7151): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0015 | 0/0 | 7152 | 3 | 0 | 3 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0016 | 0/0 | 7152 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0023 | 0/0 | 7152 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0024 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0028 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0029 | 0/0 | 7152 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0033 | 0/1 | 7152 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0034 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0035 | 0/0 | 7153 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7148): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0036 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0037 | 0/0 | 7152 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0038 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0039 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0040 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0044 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0001t0050 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0001c0014t0001 | 0/0 | 7152 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0002 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0005 | 0/0 | 7148 | 9 | 5 | 4 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7143): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0006 | 0/0 | 7003 | 7 | 0 | 1 | 4 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(6998): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0009 | 0/0 | 7003 | 5 | 3 | 0 | 0 | 2 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(6998): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0011 | 0/0 | 7150 | 4 | 0 | 2 | 0 | 0 | 2 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0017 | 0/0 | 7150 | 3 | 0 | 0 | 2 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0018 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0019 | 0/0 | 7003 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(6998): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0020 | 0/0 | 7149 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0025 | 0/0 | 7003 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(6998): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0026 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0027 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0041 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0002c0002t0043 | 0/0 | 7004 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(6999): Show |
chr1 | 108871985 | 108939545 |
| a0002c0005t0008 | 0/0 | 7149 | 6 | 5 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0002c0005t0014 | 0/0 | 7145 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7140): Show |
chr1 | 108871985 | 108939545 |
| a0002c0005t0049 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0002c0006t0010 | 0/0 | 7004 | 5 | 5 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(6999): Show |
chr1 | 108871985 | 108939545 |
| a0002c0008t0018 | 0/0 | 7150 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0002c0008t0042 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0002c0010t0030 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0003c0003t0003 | 0/0 | 7149 | 13 | 12 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0003c0003t0021 | 0/0 | 7149 | 3 | 0 | 0 | 0 | 2 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0003c0003t0045 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0003c0003t0046 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0003c0003t0047 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7144): Show |
chr1 | 108871985 | 108939545 |
| a0004c0004t0004 | 0/0 | 7154 | 10 | 2 | 0 | 3 | 0 | 5 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7149): Show |
chr1 | 108871985 | 108939545 |
| a0004c0004t0013 | 0/0 | 7154 | 4 | 0 | 0 | 1 | 0 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7149): Show |
chr1 | 108871985 | 108939545 |
| a0004c0004t0022 | 0/0 | 7150 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0004c0004t0031 | 0/0 | 7152 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0004c0004t0032 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7145): Show |
chr1 | 108871985 | 108939545 |
| a0004c0013t0048 | 0/0 | 7016 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7011): Show |
chr1 | 108871985 | 108939545 |
| a0005c0007t0001 | 0/0 | 7152 | 4 | 4 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0006c0009t0001 | 0/0 | 7152 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| a0007c0011t0006 | 0/0 | 7003 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(6998): Show |
chr1 | 108871985 | 108939545 |
| a0008c0012t0016 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | GCAGA others(7147): Show |
chr1 | 108871985 | 108939545 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0024 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0007g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0015g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0015g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0015g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0016g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0016g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0023g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0023g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0024g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0028g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0029g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0033g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0034g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0035g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0036g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0037g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0038g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0039g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0040g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0044g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0001t0050g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0001c0014t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0005g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0005g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0009g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0011g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0011g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0011g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0011g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0017g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0017g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0018g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0019g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0019g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0019g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0020g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0025g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0026g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0027g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0041g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0002t0043g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0008g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0014g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0005t0049g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0006t0010g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0006t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0006t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0006t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0008t0018g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0008t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0008t0042g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0002c0010t0030g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0021g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0021g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0021g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0045g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0046g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0003c0003t0047g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0013g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0022g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0022g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0031g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0004t0032g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0004c0013t0048g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0005c0007t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0005c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0005c0007t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0005c0007t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0006c0009t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0006c0009t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0007c0011t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| a0008c0012t0016g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00140 | hp1 | a0003 | c0003 | t0021 | g0209 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00280 | hp2 | a0003 | c0003 | t0021 | g0210 | EUR | FIN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00408 | hp2 | a0001 | c0001 | t0012 | g0164 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG00741 | hp2 | a0001 | c0001 | t0028 | g0167 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01071 | hp1 | a0006 | c0009 | t0001 | g0154 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01071 | hp2 | a0001 | c0001 | t0035 | g0001 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01081 | hp1 | a0001 | c0001 | t0040 | g0001 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01099 | hp1 | a0002 | c0002 | t0019 | g0045 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01099 | hp2 | a0002 | c0002 | t0011 | g0054 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01109 | hp1 | a0002 | c0008 | t0018 | g0028 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01109 | hp2 | a0001 | c0001 | t0015 | g0093 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01167 | hp2 | a0002 | c0002 | t0005 | g0019 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01169 | hp1 | a0002 | c0002 | t0005 | g0019 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01175 | hp1 | a0002 | c0002 | t0011 | g0058 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01243 | hp1 | a0001 | c0001 | t0036 | g0155 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01243 | hp2 | a0003 | c0003 | t0003 | g0212 | AMR | PUR | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01346 | hp2 | a0002 | c0002 | t0025 | g0005 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01433 | hp2 | a0002 | c0005 | t0008 | g0069 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01515 | hp2 | a0002 | c0002 | t0006 | g0038 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01516 | hp1 | a0002 | c0002 | t0009 | g0048 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0119 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01517 | hp1 | a0002 | c0002 | t0006 | g0033 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01517 | hp2 | a0002 | c0002 | t0009 | g0046 | EUR | IBS | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01884 | hp1 | a0002 | c0002 | t0041 | g0057 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01884 | hp2 | a0002 | c0006 | t0010 | g0007 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01891 | hp2 | a0003 | c0003 | t0003 | g0214 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01952 | hp1 | a0002 | c0002 | t0005 | g0021 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0009 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01981 | hp1 | a0001 | c0001 | t0015 | g0092 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02027 | hp1 | a0001 | c0001 | t0024 | g0097 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02040 | hp2 | a0001 | c0001 | t0044 | g0078 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02055 | hp1 | a0002 | c0010 | t0030 | g0193 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02132 | hp1 | a0001 | c0001 | t0039 | g0179 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02145 | hp1 | a0002 | c0005 | t0014 | g0072 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02257 | hp2 | a0003 | c0003 | t0003 | g0225 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02258 | hp1 | a0002 | c0002 | t0005 | g0191 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02258 | hp2 | a0002 | c0005 | t0049 | g0067 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02300 | hp2 | a0002 | c0002 | t0006 | g0005 | AMR | PEL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02451 | hp1 | a0003 | c0003 | t0045 | g0216 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02572 | hp1 | a0003 | c0003 | t0003 | g0226 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02572 | hp2 | a0002 | c0002 | t0020 | g0049 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02615 | hp2 | a0004 | c0004 | t0032 | g0042 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02622 | hp2 | a0005 | c0007 | t0001 | g0142 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02630 | hp2 | a0002 | c0005 | t0008 | g0008 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0219 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02647 | hp2 | a0002 | c0006 | t0010 | g0053 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02698 | hp2 | a0002 | c0002 | t0011 | g0055 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02717 | hp2 | a0002 | c0008 | t0042 | g0027 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02723 | hp1 | a0001 | c0001 | t0023 | g0059 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02723 | hp2 | a0002 | c0005 | t0008 | g0065 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02735 | hp1 | a0002 | c0002 | t0011 | g0056 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02738 | hp2 | a0003 | c0003 | t0021 | g0211 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02809 | hp1 | a0003 | c0003 | t0003 | g0215 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02809 | hp2 | a0005 | c0007 | t0001 | g0204 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02818 | hp1 | a0002 | c0006 | t0010 | g0031 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02818 | hp2 | a0002 | c0002 | t0005 | g0190 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02886 | hp1 | a0004 | c0004 | t0004 | g0189 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02886 | hp2 | a0002 | c0002 | t0020 | g0006 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02895 | hp1 | a0002 | c0002 | t0009 | g0051 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02895 | hp2 | a0003 | c0003 | t0003 | g0221 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02897 | hp1 | a0002 | c0002 | t0009 | g0050 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02897 | hp2 | a0002 | c0005 | t0008 | g0068 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02922 | hp1 | a0005 | c0007 | t0001 | g0205 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02922 | hp2 | a0002 | c0005 | t0008 | g0008 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02965 | hp1 | a0002 | c0002 | t0019 | g0044 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02965 | hp2 | a0005 | c0007 | t0001 | g0207 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02970 | hp1 | a0004 | c0004 | t0004 | g0188 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02970 | hp2 | a0002 | c0002 | t0020 | g0006 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02976 | hp2 | a0002 | c0006 | t0010 | g0007 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03041 | hp1 | a0004 | c0004 | t0031 | g0052 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03041 | hp2 | a0002 | c0002 | t0005 | g0020 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0222 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03098 | hp2 | a0004 | c0013 | t0048 | g0066 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03130 | hp2 | a0003 | c0003 | t0003 | g0227 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03139 | hp2 | a0002 | c0002 | t0043 | g0029 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03195 | hp1 | a0002 | c0008 | t0018 | g0202 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | ESN | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03209 | hp1 | a0002 | c0002 | t0005 | g0020 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03209 | hp2 | a0001 | c0001 | t0023 | g0060 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03239 | hp1 | a0001 | c0014 | t0001 | g0135 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03239 | hp2 | a0001 | c0001 | t0029 | g0139 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03453 | hp2 | a0002 | c0006 | t0010 | g0030 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03486 | hp2 | a0003 | c0003 | t0003 | g0224 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03490 | hp2 | a0004 | c0004 | t0013 | g0002 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03491 | hp2 | a0004 | c0004 | t0004 | g0187 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03492 | hp1 | a0004 | c0004 | t0004 | g0185 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03492 | hp2 | a0004 | c0004 | t0013 | g0002 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03540 | hp1 | a0002 | c0002 | t0019 | g0047 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03540 | hp2 | a0002 | c0002 | t0018 | g0026 | AFR | GWD | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03579 | hp1 | a0004 | c0004 | t0022 | g0073 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03579 | hp2 | a0002 | c0005 | t0008 | g0064 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03654 | hp1 | a0004 | c0004 | t0004 | g0183 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03704 | hp1 | a0004 | c0004 | t0013 | g0002 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG04115 | hp1 | a0003 | c0003 | t0047 | g0213 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG04115 | hp2 | a0004 | c0004 | t0004 | g0186 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG04228 | hp1 | a0002 | c0002 | t0017 | g0036 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG04228 | hp2 | a0001 | c0001 | t0037 | g0075 | SAS | STU | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18522 | hp2 | a0003 | c0003 | t0003 | g0223 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0218 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18906 | hp2 | a0002 | c0005 | t0014 | g0071 | AFR | YRI | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18944 | hp1 | a0004 | c0004 | t0004 | g0182 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18945 | hp2 | a0001 | c0001 | t0050 | g0105 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18948 | hp1 | a0007 | c0011 | t0006 | g0035 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18959 | hp1 | a0001 | c0001 | t0016 | g0198 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18959 | hp2 | a0001 | c0001 | t0012 | g0017 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18965 | hp1 | a0002 | c0002 | t0006 | g0061 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18968 | hp2 | a0002 | c0002 | t0006 | g0062 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18969 | hp2 | a0004 | c0004 | t0004 | g0184 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18970 | hp2 | a0002 | c0002 | t0017 | g0032 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18972 | hp1 | a0001 | c0001 | t0016 | g0163 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18983 | hp2 | a0002 | c0002 | t0026 | g0040 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18990 | hp1 | a0004 | c0004 | t0004 | g0018 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA18990 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19000 | hp2 | a0008 | c0012 | t0016 | g0157 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19001 | hp1 | a0002 | c0002 | t0006 | g0041 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19003 | hp2 | a0001 | c0001 | t0034 | g0162 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19005 | hp2 | a0001 | c0001 | t0012 | g0169 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19030 | hp1 | a0003 | c0003 | t0046 | g0217 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0143 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19043 | hp2 | a0004 | c0004 | t0022 | g0074 | AFR | LWK | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19066 | hp2 | a0004 | c0004 | t0013 | g0018 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19075 | hp1 | a0002 | c0002 | t0027 | g0037 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19080 | hp2 | a0001 | c0001 | t0038 | g0102 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19084 | hp2 | a0002 | c0002 | t0017 | g0039 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19085 | hp1 | a0002 | c0002 | t0006 | g0063 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA20129 | hp2 | a0002 | c0002 | t0005 | g0192 | AFR | ASW | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| NA20905 | hp2 | a0004 | c0004 | t0004 | g0181 | SAS | GIH | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG01123 | hp2 | a0002 | c0002 | t0005 | g0021 | AMR | CLM | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02109 | hp2 | a0002 | c0005 | t0014 | g0070 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02486 | hp2 | a0002 | c0002 | t0009 | g0043 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02559 | hp1 | a0006 | c0009 | t0001 | g0001 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG02559 | hp2 | a0003 | c0003 | t0003 | g0220 | AFR | ACB | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0033 | g0124 | REF | REF | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0024 | REF | REF | GPSM2_chr1_108871985_108939545 | GPSM2 | chr1 | 108871985 | 108939545 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:108897593 | G | A | 2 | a0003 a0005 |
23 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(20): Show |
missense_variant | MODERATE | c.380G>A | p.Arg127Gln | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 4/15 | 872/7152 | 380/2055 | 127/684 | chr1 | 108897593 | |||
| chr1:108901810 | G | A | 1 | a0007 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.818G>A | p.Arg273Gln | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/15 | 1310/7152 | 818/2055 | 273/684 | chr1 | 108901810 | |||
| chr1:108904128 | G | A | 1 | a0006 | 2 | HG01071.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.1066G>A | p.Gly356Arg | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/15 | 1558/7152 | 1066/2055 | 356/684 | chr1 | 108904128 | |||
| chr1:108914392 | A | G | 1 | a0008 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.1247A>G | p.Lys416Arg | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/15 | 1739/7152 | 1247/2055 | 416/684 | chr1 | 108914392 | |||
| chr1:108918719 | C | T | 1 | a0004 | 19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
missense_variant | MODERATE | c.1370C>T | p.Thr457Met | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/15 | 1862/7152 | 1370/2055 | 457/684 | chr1 | 108918719 | |||
| chr1:108922543 | ACTT | A | 4 | a0002 a0003 a0004 others(1): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
disruptive_inframe_deletion | MODERATE | c.1572_1574delTTC | p.Ser525del | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/15 | 2064/7152 | 1572/2055 | 524/684 | INFO_REALIGN_3_PRIME | chr1 | 108922543 | ||
| chr1:108924138 | C | T | 1 | a0004 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1739C>T | p.Ser580Leu | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/15 | 2231/7152 | 1739/2055 | 580/684 | chr1 | 108924138 | |||
| chr1:108929705 | C | T | 1 | a0002 | 3 | HG01109.hp1 HG02717.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.1820C>T | p.Ser607Phe | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2312/7152 | 1820/2055 | 607/684 | chr1 | 108929705 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:108896894 | G | A | 1 | a0002c0010 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.87G>A | p.Leu29Leu | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/15 | 579/7152 | 87/2055 | 29/684 | chr1 | 108896894 | |||
| chr1:108896993 | C | T | 1 | a0001c0014 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.186C>T | p.Ser62Ser | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/15 | 678/7152 | 186/2055 | 62/684 | chr1 | 108896993 | |||
| chr1:108898950 | A | G | 2 | a0002c0005 a0004c0013 |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
synonymous_variant | LOW | c.753A>G | p.Ala251Ala | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/15 | 1245/7152 | 753/2055 | 251/684 | chr1 | 108898950 | |||
| chr1:108901820 | A | G | 1 | a0002c0006 | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
synonymous_variant | LOW | c.828A>G | p.Lys276Lys | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/15 | 1320/7152 | 828/2055 | 276/684 | chr1 | 108901820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:108876991 | G | C | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-486G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | 8532 | chr1 | 108876991 | ||||||
| chr1:108877008 | C | G | 1 | a0001c0001t0050 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-469C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | 8515 | chr1 | 108877008 | ||||||
| chr1:108877048 | C | T | 4 | a0002c0005t0008 a0002c0005t0014 a0002c0005t0049 others(1): Show |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-429C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | chr1 | 108877048 | |||||||
| chr1:108877219 | C | T | 5 | a0003c0003t0003 a0003c0003t0021 a0003c0003t0045 others(2): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-258C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/15 | 8304 | chr1 | 108877219 | ||||||
| chr1:108885293 | G | A | 1 | a0001c0001t0024 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-230G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/15 | 230 | chr1 | 108885293 | ||||||
| chr1:108885409 | C | T | 1 | a0001c0001t0044 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/15 | 114 | chr1 | 108885409 | ||||||
| chr1:108930151 | G | A | 28 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(25): Show |
119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*211G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 211 | chr1 | 108930151 | ||||||
| chr1:108930191 | T | C | 13 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(10): Show |
64 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*251T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 251 | chr1 | 108930191 | ||||||
| chr1:108930291 | C | T | 1 | a0002c0005t0049 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 351 | chr1 | 108930291 | ||||||
| chr1:108930299 | T | G | 6 | a0002c0002t0006 a0002c0002t0017 a0002c0002t0025 others(3): Show |
14 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*359T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 359 | chr1 | 108930299 | ||||||
| chr1:108930395 | C | T | 20 | a0002c0002t0005 a0002c0002t0009 a0002c0002t0011 others(17): Show |
61 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*455C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 455 | chr1 | 108930395 | ||||||
| chr1:108930407 | G | T | 1 | a0003c0003t0046 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 467 | chr1 | 108930407 | ||||||
| chr1:108930432 | G | T | 1 | a0002c0006t0010 | 5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 492 | chr1 | 108930432 | ||||||
| chr1:108930496 | TCCTGTAA others(124): Show |
T | 1 | a0004c0013t0048 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*573_*703del | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 573 | INFO_REALIGN_3_PRIME | chr1 | 108930496 | |||||
| chr1:108930614 | C | A | 1 | a0001c0001t0002 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 674 | chr1 | 108930614 | ||||||
| chr1:108930654 | C | T | 1 | a0004c0004t0031 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 714 | chr1 | 108930654 | ||||||
| chr1:108930664 | G | A | 1 | a0001c0001t0034 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*724G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 724 | chr1 | 108930664 | ||||||
| chr1:108930696 | C | G | 1 | a0004c0013t0048 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 756 | chr1 | 108930696 | ||||||
| chr1:108930808 | G | A | 1 | a0001c0001t0028 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 868 | chr1 | 108930808 | ||||||
| chr1:108930890 | CAA | C | 30 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0009 others(27): Show |
94 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*963_*964delAA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 963 | INFO_REALIGN_3_PRIME | chr1 | 108930890 | |||||
| chr1:108930905 | C | T | 32 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0009 others(29): Show |
98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*965C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 965 | chr1 | 108930905 | ||||||
| chr1:108930983 | T | C | 6 | a0002c0002t0006 a0002c0002t0025 a0004c0004t0004 others(3): Show |
24 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1043T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1043 | chr1 | 108930983 | ||||||
| chr1:108930991 | G | A | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1051G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1051 | chr1 | 108930991 | ||||||
| chr1:108931019 | TC | T | 1 | a0002c0002t0005 | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1081delC | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1081 | INFO_REALIGN_3_PRIME | chr1 | 108931019 | |||||
| chr1:108931104 | A | C | 1 | a0002c0010t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1164 | chr1 | 108931104 | ||||||
| chr1:108931184 | G | A | 1 | a0001c0001t0015 | 3 | HG01109.hp2 HG01952.hp2 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1244G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1244 | chr1 | 108931184 | ||||||
| chr1:108931204 | G | A | 32 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0009 others(29): Show |
98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1264G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1264 | chr1 | 108931204 | ||||||
| chr1:108931211 | TAAAC | T | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1277_*1280delAACA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1277 | INFO_REALIGN_3_PRIME | chr1 | 108931211 | |||||
| chr1:108931316 | T | C | 1 | a0003c0003t0045 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1376 | chr1 | 108931316 | ||||||
| chr1:108931399 | AG | A | 1 | a0002c0005t0014 | 3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1460delG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1460 | chr1 | 108931399 | ||||||
| chr1:108931400 | G | A | 1 | a0004c0004t0004 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1460 | chr1 | 108931400 | ||||||
| chr1:108931599 | C | T | 32 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0009 others(29): Show |
98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1659C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1659 | chr1 | 108931599 | ||||||
| chr1:108931628 | T | TA | 3 | a0001c0001t0035 a0002c0002t0027 a0002c0005t0014 |
5 | HG01071.hp2 HG02109.hp2 HG02145.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1703dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1704 | INFO_REALIGN_3_PRIME | chr1 | 108931628 | |||||
| chr1:108931628 | T | TAA | 26 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0009 others(23): Show |
74 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1702_*1703dupAA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1704 | INFO_REALIGN_3_PRIME | chr1 | 108931628 | |||||
| chr1:108931628 | T | TAAA | 3 | a0002c0006t0010 a0004c0004t0004 a0004c0004t0013 |
19 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1701_*1703dupAAA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1704 | INFO_REALIGN_3_PRIME | chr1 | 108931628 | |||||
| chr1:108931679 | T | C | 2 | a0002c0002t0009 a0002c0002t0019 |
8 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1739T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1739 | chr1 | 108931679 | ||||||
| chr1:108931725 | G | GGTAA | 1 | a0001c0001t0012 | 4 | HG00408.hp2 NA18959.hp2 NA18990.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1788_*1791dupAAGT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 1792 | INFO_REALIGN_3_PRIME | chr1 | 108931725 | |||||
| chr1:108931959 | T | C | 1 | a0001c0001t0007 | 6 | HG02055.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2019T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2019 | chr1 | 108931959 | ||||||
| chr1:108932093 | T | C | 5 | a0002c0002t0011 a0002c0002t0017 a0002c0002t0026 others(2): Show |
10 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2153T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2153 | chr1 | 108932093 | ||||||
| chr1:108932110 | T | TA | 12 | a0002c0002t0011 a0002c0002t0017 a0002c0002t0018 others(9): Show |
19 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2176dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2177 | INFO_REALIGN_3_PRIME | chr1 | 108932110 | |||||
| chr1:108932113 | A | AAAAT | 2 | a0004c0004t0004 a0004c0004t0013 |
14 | HG02886.hp1 HG02970.hp1 HG03490.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2178dupAATA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2179 | INFO_REALIGN_3_PRIME | chr1 | 108932113 | |||||
| chr1:108932122 | A | T | 1 | a0002c0010t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2182A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2182 | chr1 | 108932122 | ||||||
| chr1:108932545 | T | G | 1 | a0004c0013t0048 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2605T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2605 | chr1 | 108932545 | ||||||
| chr1:108932548 | A | T | 1 | a0001c0001t0040 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2608A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2608 | chr1 | 108932548 | ||||||
| chr1:108932805 | T | C | 2 | a0004c0004t0022 a0004c0004t0032 |
3 | HG02615.hp2 HG03579.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2865T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2865 | chr1 | 108932805 | ||||||
| chr1:108932814 | T | C | 2 | a0001c0001t0028 a0001c0001t0029 |
2 | HG00741.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2874T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2874 | chr1 | 108932814 | ||||||
| chr1:108932826 | T | C | 1 | a0001c0001t0036 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2886T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 2886 | chr1 | 108932826 | ||||||
| chr1:108933081 | GCTTAAGC others(139): Show |
G | 7 | a0002c0002t0006 a0002c0002t0009 a0002c0002t0019 others(4): Show |
23 | HG01099.hp1 HG01346.hp2 HG01515.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3425_*3570del | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3425 | INFO_REALIGN_3_PRIME | chr1 | 108933081 | |||||
| chr1:108933209 | C | CTGCATTT others(139): Show |
1 | a0002c0002t0005 | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3414_*3415insTTGC others(142): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3415 | INFO_REALIGN_3_PRIME | chr1 | 108933209 | |||||
| chr1:108933287 | G | A | 1 | a0002c0010t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3347 | chr1 | 108933287 | ||||||
| chr1:108933392 | C | G | 1 | a0001c0001t0039 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3452C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3452 | chr1 | 108933392 | ||||||
| chr1:108933453 | T | C | 1 | a0003c0003t0047 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3513T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3513 | chr1 | 108933453 | ||||||
| chr1:108933651 | T | C | 1 | a0002c0002t0005 | 9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3711T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3711 | chr1 | 108933651 | ||||||
| chr1:108933676 | G | C | 1 | a0004c0004t0031 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3736G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3736 | chr1 | 108933676 | ||||||
| chr1:108933733 | T | C | 3 | a0004c0004t0004 a0004c0004t0013 a0004c0013t0048 |
15 | HG02886.hp1 HG02970.hp1 HG03098.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3793T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3793 | chr1 | 108933733 | ||||||
| chr1:108933741 | A | G | 32 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0009 others(29): Show |
98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*3801A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3801 | chr1 | 108933741 | ||||||
| chr1:108933828 | T | C | 2 | a0001c0001t0016 a0008c0012t0016 |
3 | NA18959.hp1 NA18972.hp1 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3888T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 3888 | chr1 | 108933828 | ||||||
| chr1:108934069 | C | T | 1 | a0001c0001t0038 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4129C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4129 | chr1 | 108934069 | ||||||
| chr1:108934158 | C | T | 30 | a0002c0002t0005 a0002c0002t0006 a0002c0002t0009 others(27): Show |
96 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4218C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4218 | chr1 | 108934158 | ||||||
| chr1:108934223 | C | T | 1 | a0002c0010t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4283C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4283 | chr1 | 108934223 | ||||||
| chr1:108934316 | T | C | 12 | a0002c0002t0011 a0002c0002t0017 a0002c0002t0018 others(9): Show |
19 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4376T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4376 | chr1 | 108934316 | ||||||
| chr1:108934495 | C | T | 1 | a0001c0001t0037 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4555C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4555 | chr1 | 108934495 | ||||||
| chr1:108934529 | G | A | 3 | a0004c0004t0004 a0004c0004t0013 a0004c0013t0048 |
15 | HG02886.hp1 HG02970.hp1 HG03098.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4589G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 15/15 | 4589 | chr1 | 108934529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:108877253 | C | T | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-249+25C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877253 | |||||||
| chr1:108877330 | G | C | 1 | a0001c0001t0002g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-249+102G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877330 | |||||||
| chr1:108877466 | G | A | 1 | a0004c0004t0013g0002 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-249+238G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877466 | |||||||
| chr1:108877514 | CT | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(223): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-249+299delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 108877514 | ||||||
| chr1:108877527 | T | C | 5 | a0002c0002t0018g0026 a0002c0002t0043g0029 a0002c0008t0018g0028 others(2): Show |
5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-249+299T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877527 | |||||||
| chr1:108877967 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-249+739C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877967 | |||||||
| chr1:108877978 | A | T | 8 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
9 | HG00438.hp2 HG00544.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-249+750A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108877978 | |||||||
| chr1:108878035 | G | T | 1 | a0001c0001t0001g0022 | 2 | HG02523.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-249+807G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108878035 | |||||||
| chr1:108878455 | A | C | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-249+1227A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108878455 | |||||||
| chr1:108879069 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-249+1841A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879069 | |||||||
| chr1:108879279 | C | T | 1 | a0002c0002t0005g0021 | 2 | HG01123.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.-249+2051C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879279 | |||||||
| chr1:108879283 | G | A | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-249+2055G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879283 | |||||||
| chr1:108879308 | G | A | 93 | a0001c0001t0023g0059 a0001c0001t0023g0060 a0002c0002t0002g0034 others(90): Show |
101 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(98): Show |
intron_variant | MODIFIER | c.-249+2080G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879308 | |||||||
| chr1:108879452 | T | G | 1 | a0001c0001t0037g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-249+2224T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879452 | |||||||
| chr1:108879600 | C | T | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-249+2372C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879600 | |||||||
| chr1:108879823 | A | G | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-249+2595A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879823 | |||||||
| chr1:108879991 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-249+2763T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108879991 | |||||||
| chr1:108880208 | A | G | 1 | a0001c0001t0039g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-249+2980A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880208 | |||||||
| chr1:108880314 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-249+3086G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880314 | |||||||
| chr1:108880430 | A | C | 10 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(7): Show |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-249+3202A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880430 | |||||||
| chr1:108880455 | G | T | 1 | a0001c0001t0002g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-249+3227G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880455 | |||||||
| chr1:108880579 | C | CA | 60 | a0001c0001t0001g0011 a0001c0001t0001g0085 a0001c0001t0001g0086 others(57): Show |
65 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-249+3365dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 108880579 | ||||||
| chr1:108880579 | C | CAAA | 6 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(3): Show |
7 | HG02258.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-249+3363_-249+336 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 108880579 | ||||||
| chr1:108880746 | G | T | 1 | a0003c0003t0003g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-249+3518G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880746 | |||||||
| chr1:108880944 | A | T | 3 | a0002c0002t0006g0061 a0002c0002t0006g0062 a0002c0002t0006g0063 |
3 | NA18965.hp1 NA18968.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-249+3716A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108880944 | |||||||
| chr1:108881343 | A | G | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-248-3932A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881343 | |||||||
| chr1:108881354 | A | G | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-248-3921A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881354 | |||||||
| chr1:108881460 | A | G | 1 | a0003c0003t0003g0226 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-248-3815A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881460 | |||||||
| chr1:108881858 | A | T | 2 | a0001c0001t0023g0059 a0001c0001t0023g0060 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-248-3417A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108881858 | |||||||
| chr1:108882279 | A | G | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-248-2996A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882279 | |||||||
| chr1:108882280 | T | A | 15 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0200 others(12): Show |
18 | HG00438.hp2 HG00544.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-248-2995T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882280 | |||||||
| chr1:108882325 | A | G | 1 | a0002c0005t0008g0068 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-248-2950A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882325 | |||||||
| chr1:108882344 | A | G | 29 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(26): Show |
34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.-248-2931A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882344 | |||||||
| chr1:108882521 | A | G | 10 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(7): Show |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-248-2754A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882521 | |||||||
| chr1:108882548 | T | C | 1 | a0002c0002t0018g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-248-2727T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882548 | |||||||
| chr1:108882573 | T | C | 2 | a0002c0006t0010g0030 a0002c0006t0010g0031 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-248-2702T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882573 | |||||||
| chr1:108882696 | C | T | 10 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(7): Show |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-248-2579C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882696 | |||||||
| chr1:108882738 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-248-2537A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882738 | |||||||
| chr1:108882978 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-248-2297G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108882978 | |||||||
| chr1:108883137 | T | A | 1 | a0004c0004t0004g0181 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-248-2138T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108883137 | |||||||
| chr1:108883331 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-248-1944T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108883331 | |||||||
| chr1:108883666 | G | A | 72 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(69): Show |
78 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.-248-1609G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108883666 | |||||||
| chr1:108884004 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-248-1271C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884004 | |||||||
| chr1:108884035 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-248-1240C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884035 | |||||||
| chr1:108884049 | T | A | 5 | a0002c0002t0018g0026 a0002c0002t0043g0029 a0002c0008t0018g0028 others(2): Show |
5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-248-1226T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884049 | |||||||
| chr1:108884226 | G | A | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-248-1049G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884226 | |||||||
| chr1:108884421 | A | T | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-248-854A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884421 | |||||||
| chr1:108884612 | A | G | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.-248-663A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884612 | |||||||
| chr1:108884639 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-248-636G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884639 | |||||||
| chr1:108884688 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-248-587T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884688 | |||||||
| chr1:108884836 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-248-439A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108884836 | |||||||
| chr1:108885096 | C | A | 1 | a0004c0004t0032g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-248-179C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108885096 | |||||||
| chr1:108885096 | C | G | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-248-179C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108885096 | |||||||
| chr1:108885119 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-248-156C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 1/14 | chr1 | 108885119 | |||||||
| chr1:108885627 | G | A | 88 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(85): Show |
95 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(92): Show |
intron_variant | MODIFIER | c.56+49G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108885627 | |||||||
| chr1:108885722 | G | GT | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.56+145dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108885722 | ||||||
| chr1:108885953 | T | G | 1 | a0002c0002t0017g0032 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.56+375T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108885953 | |||||||
| chr1:108886037 | A | T | 2 | a0002c0006t0010g0007 a0002c0006t0010g0053 |
3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.56+459A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886037 | |||||||
| chr1:108886134 | A | G | 3 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 |
3 | HG01169.hp2 HG01516.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.56+556A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886134 | |||||||
| chr1:108886485 | G | A | 6 | a0004c0004t0004g0018 a0004c0004t0004g0182 a0004c0004t0004g0183 others(3): Show |
8 | HG03490.hp2 HG03492.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+907G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886485 | |||||||
| chr1:108886486 | G | GGAGAAAT | 3 | a0001c0001t0001g0012 a0001c0001t0001g0085 a0001c0001t0001g0125 |
4 | HG01175.hp2 HG01978.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+908_56+909insGA others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886486 | |||||||
| chr1:108886652 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56+1074G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886652 | |||||||
| chr1:108886721 | C | T | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+1143C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886721 | |||||||
| chr1:108886863 | A | AGT | 3 | a0002c0005t0014g0070 a0004c0004t0022g0073 a0004c0004t0022g0074 |
3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.56+1300_56+1301dup others(2): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108886863 | ||||||
| chr1:108886950 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.56+1372G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108886950 | |||||||
| chr1:108887011 | C | T | 1 | a0004c0004t0031g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.56+1433C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887011 | |||||||
| chr1:108887043 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.56+1465C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887043 | |||||||
| chr1:108887157 | G | A | 1 | a0004c0004t0032g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.56+1579G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887157 | |||||||
| chr1:108887214 | C | A | 1 | a0002c0008t0042g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.56+1636C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887214 | |||||||
| chr1:108887355 | G | A | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+1777G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887355 | |||||||
| chr1:108887438 | C | T | 3 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 |
3 | HG01169.hp2 HG01516.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.56+1860C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887438 | |||||||
| chr1:108887760 | C | G | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.56+2182C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887760 | |||||||
| chr1:108887793 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.56+2215A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887793 | |||||||
| chr1:108887963 | C | G | 90 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(87): Show |
98 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.56+2385C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887963 | |||||||
| chr1:108887987 | G | A | 3 | a0002c0008t0018g0028 a0002c0008t0018g0202 a0002c0008t0042g0027 |
3 | HG01109.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.56+2409G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108887987 | |||||||
| chr1:108888029 | G | A | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+2451G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888029 | |||||||
| chr1:108888032 | G | A | 14 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(11): Show |
15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.56+2454G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888032 | |||||||
| chr1:108888224 | A | C | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.56+2646A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888224 | |||||||
| chr1:108888351 | CT | C | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+2780delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108888351 | ||||||
| chr1:108888488 | C | A | 5 | a0003c0003t0003g0212 a0003c0003t0021g0209 a0003c0003t0021g0210 others(2): Show |
5 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+2910C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888488 | |||||||
| chr1:108888492 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(226): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.56+2914T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888492 | |||||||
| chr1:108888948 | A | T | 1 | a0004c0004t0013g0002 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.56+3370A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108888948 | |||||||
| chr1:108889225 | G | A | 9 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(6): Show |
10 | HG01433.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.56+3647G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889225 | |||||||
| chr1:108889466 | C | T | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.56+3888C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889466 | |||||||
| chr1:108889586 | G | A | 1 | a0001c0001t0007g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.56+4008G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889586 | |||||||
| chr1:108889789 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.56+4211C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108889789 | |||||||
| chr1:108890021 | A | G | 5 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+4443A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890021 | |||||||
| chr1:108890033 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.56+4455T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890033 | |||||||
| chr1:108890394 | G | A | 1 | a0003c0003t0003g0214 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.56+4816G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890394 | |||||||
| chr1:108890592 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0129 |
2 | NA18947.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.56+5014G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890592 | |||||||
| chr1:108890748 | A | G | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.56+5170A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890748 | |||||||
| chr1:108890880 | TA | T | 16 | a0001c0001t0002g0083 a0001c0001t0002g0117 a0003c0003t0003g0214 others(13): Show |
16 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.56+5311delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108890880 | ||||||
| chr1:108890913 | T | C | 1 | a0002c0002t0009g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.56+5335T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890913 | |||||||
| chr1:108890993 | G | T | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+5415G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108890993 | |||||||
| chr1:108891154 | C | T | 10 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(7): Show |
11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+5576C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891154 | |||||||
| chr1:108891367 | C | G | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-5497C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891367 | |||||||
| chr1:108891486 | G | T | 1 | a0004c0004t0032g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.57-5378G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891486 | |||||||
| chr1:108891664 | A | AT | 45 | a0001c0001t0001g0125 a0001c0001t0001g0168 a0001c0001t0001g0176 others(42): Show |
48 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.57-5180dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | ||||||
| chr1:108891664 | A | ATT | 18 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(15): Show |
22 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.57-5181_57-5180dup others(2): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | ||||||
| chr1:108891664 | A | ATTTT | 14 | a0003c0003t0003g0214 a0003c0003t0003g0215 a0003c0003t0003g0218 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-5183_57-5180dup others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | ||||||
| chr1:108891664 | A | ATTTTT | 17 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(14): Show |
17 | HG01099.hp1 HG01243.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.57-5184_57-5180dup others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108891664 | ||||||
| chr1:108891750 | C | A | 12 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(9): Show |
14 | HG02886.hp1 HG02970.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-5114C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891750 | |||||||
| chr1:108891754 | C | G | 5 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.57-5110C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108891754 | |||||||
| chr1:108892090 | C | T | 14 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(11): Show |
15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.57-4774C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892090 | |||||||
| chr1:108892204 | T | C | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-4660T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892204 | |||||||
| chr1:108892323 | G | A | 1 | a0003c0003t0003g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.57-4541G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892323 | |||||||
| chr1:108892404 | A | G | 1 | a0001c0001t0028g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.57-4460A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892404 | |||||||
| chr1:108892474 | G | GA | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.57-4386dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108892474 | ||||||
| chr1:108892512 | T | C | 10 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(7): Show |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.57-4352T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892512 | |||||||
| chr1:108892867 | C | T | 3 | a0001c0001t0002g0116 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.57-3997C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108892867 | |||||||
| chr1:108893226 | T | C | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-3638T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893226 | |||||||
| chr1:108893315 | C | T | 1 | a0004c0004t0031g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57-3549C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893315 | |||||||
| chr1:108893506 | A | G | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-3358A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893506 | |||||||
| chr1:108893510 | G | C | 1 | a0002c0002t0011g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.57-3354G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893510 | |||||||
| chr1:108893764 | T | C | 1 | a0003c0003t0003g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.57-3100T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893764 | |||||||
| chr1:108893769 | T | C | 29 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(26): Show |
34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.57-3095T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893769 | |||||||
| chr1:108893829 | C | T | 1 | a0001c0001t0012g0164 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.57-3035C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108893829 | |||||||
| chr1:108894039 | A | G | 1 | a0002c0006t0010g0007 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.57-2825A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894039 | |||||||
| chr1:108894212 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57-2652A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894212 | |||||||
| chr1:108894651 | T | C | 10 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(7): Show |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.57-2213T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894651 | |||||||
| chr1:108894753 | TA | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0200 a0001c0001t0002g0113 others(3): Show |
6 | HG01099.hp2 HG03195.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.57-2099delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 108894753 | ||||||
| chr1:108894771 | C | T | 2 | a0003c0003t0003g0224 a0003c0003t0003g0225 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.57-2093C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108894771 | |||||||
| chr1:108895428 | C | CA | 93 | a0001c0001t0001g0176 a0001c0001t0023g0059 a0001c0001t0023g0060 others(90): Show |
101 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(98): Show |
intron_variant | MODIFIER | c.57-1436_57-1435ins others(1): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895428 | |||||||
| chr1:108895458 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.57-1406G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895458 | |||||||
| chr1:108895496 | G | A | 3 | a0004c0004t0004g0185 a0004c0004t0004g0186 a0004c0004t0004g0187 |
3 | HG03491.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.57-1368G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895496 | |||||||
| chr1:108895610 | T | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0130 |
2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.57-1254T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108895610 | |||||||
| chr1:108896155 | C | T | 1 | a0002c0005t0049g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.57-709C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896155 | |||||||
| chr1:108896202 | T | G | 1 | a0003c0003t0003g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.57-662T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896202 | |||||||
| chr1:108896390 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.57-474C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896390 | |||||||
| chr1:108896450 | T | A | 2 | a0002c0006t0010g0030 a0002c0006t0010g0031 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.57-414T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896450 | |||||||
| chr1:108896740 | C | T | 2 | a0002c0006t0010g0007 a0002c0006t0010g0053 |
3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.57-124C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896740 | |||||||
| chr1:108896778 | C | T | 14 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(11): Show |
15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.57-86C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896778 | |||||||
| chr1:108896779 | G | A | 1 | a0004c0004t0004g0182 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.57-85G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 2/14 | chr1 | 108896779 | |||||||
| chr1:108897090 | T | C | 10 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(7): Show |
11 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.278+5T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897090 | |||||||
| chr1:108897156 | A | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
6 | HG00099.hp2 HG01496.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.278+71A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897156 | |||||||
| chr1:108897250 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.278+165A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897250 | |||||||
| chr1:108897267 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.278+182G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897267 | |||||||
| chr1:108897408 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.279-84T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 3/14 | chr1 | 108897408 | |||||||
| chr1:108898118 | A | G | 13 | a0002c0010t0030g0193 a0004c0004t0004g0018 a0004c0004t0004g0181 others(10): Show |
15 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.557+17A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 5/14 | chr1 | 108898118 | |||||||
| chr1:108898246 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.557+145T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 5/14 | chr1 | 108898246 | |||||||
| chr1:108898359 | T | A | 1 | a0002c0002t0002g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.557+258T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 5/14 | chr1 | 108898359 | |||||||
| chr1:108898835 | T | G | 3 | a0001c0001t0002g0116 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.682-44T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 6/14 | chr1 | 108898835 | |||||||
| chr1:108899398 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0112 |
2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.797+404C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899398 | |||||||
| chr1:108899528 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.797+534T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899528 | |||||||
| chr1:108899656 | A | G | 2 | a0001c0001t0023g0059 a0001c0001t0023g0060 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.797+662A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899656 | |||||||
| chr1:108899731 | T | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0168 |
2 | HG02040.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.797+737T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108899731 | |||||||
| chr1:108900032 | A | G | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.797+1038A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900032 | |||||||
| chr1:108900137 | A | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0121 a0001c0001t0002g0130 |
3 | HG00738.hp1 HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.797+1143A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900137 | |||||||
| chr1:108900187 | A | G | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.797+1193A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900187 | |||||||
| chr1:108900233 | A | AT | 18 | a0001c0001t0001g0085 a0001c0001t0001g0199 a0001c0001t0002g0088 others(15): Show |
20 | HG02055.hp1 HG02738.hp1 HG02886.hp1 others(17): Show |
intron_variant | MODIFIER | c.797+1261dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 108900233 | ||||||
| chr1:108900233 | AT | A | 9 | a0001c0001t0001g0134 a0001c0014t0001g0135 a0002c0002t0006g0061 others(6): Show |
9 | HG01099.hp1 HG01167.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.797+1261delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 108900233 | ||||||
| chr1:108900256 | A | T | 2 | a0002c0006t0010g0007 a0002c0006t0010g0053 |
3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.797+1262A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900256 | |||||||
| chr1:108900333 | C | T | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.797+1339C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900333 | |||||||
| chr1:108900481 | C | T | 2 | a0001c0001t0023g0059 a0001c0001t0023g0060 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.798-1309C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900481 | |||||||
| chr1:108900490 | C | T | 5 | a0002c0002t0009g0046 a0002c0002t0009g0048 a0002c0002t0019g0044 others(2): Show |
5 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.798-1300C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900490 | |||||||
| chr1:108900695 | T | C | 2 | a0001c0001t0001g0176 a0007c0011t0006g0035 |
2 | NA18948.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.798-1095T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900695 | |||||||
| chr1:108900906 | TG | T | 14 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(11): Show |
15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.798-883delG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108900906 | |||||||
| chr1:108901090 | C | T | 1 | a0004c0004t0032g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.798-700C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901090 | |||||||
| chr1:108901110 | A | T | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.798-680A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901110 | |||||||
| chr1:108901236 | C | T | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.798-554C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901236 | |||||||
| chr1:108901241 | G | A | 7 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(4): Show |
8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.798-549G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901241 | |||||||
| chr1:108901407 | C | T | 1 | a0004c0004t0022g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.798-383C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901407 | |||||||
| chr1:108901676 | A | G | 15 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.798-114A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901676 | |||||||
| chr1:108901748 | A | T | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.798-42A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 7/14 | chr1 | 108901748 | |||||||
| chr1:108902176 | A | G | 2 | a0002c0006t0010g0007 a0002c0006t0010g0053 |
3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.953+231A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108902176 | |||||||
| chr1:108902239 | G | T | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.953+294G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108902239 | |||||||
| chr1:108902379 | C | CA | 26 | a0001c0001t0001g0136 a0001c0001t0001g0174 a0001c0001t0001g0199 others(23): Show |
31 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.953+452dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 108902379 | ||||||
| chr1:108902379 | CA | C | 6 | a0001c0001t0001g0156 a0001c0001t0002g0082 a0002c0002t0009g0048 others(3): Show |
6 | HG01516.hp1 HG02735.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.953+452delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 108902379 | ||||||
| chr1:108902744 | C | T | 1 | a0003c0003t0003g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.954-382C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108902744 | |||||||
| chr1:108903011 | A | C | 1 | a0002c0002t0026g0040 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.954-115A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108903011 | |||||||
| chr1:108903084 | T | G | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.954-42T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108903084 | |||||||
| chr1:108903107 | G | T | 1 | a0001c0001t0007g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.954-19G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 8/14 | chr1 | 108903107 | |||||||
| chr1:108903286 | G | A | 3 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0113 |
3 | NA19009.hp2 NA19079.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1062+52G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903286 | |||||||
| chr1:108903286 | G | C | 5 | a0002c0002t0009g0046 a0002c0002t0009g0048 a0002c0002t0019g0044 others(2): Show |
5 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062+52G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903286 | |||||||
| chr1:108903331 | A | G | 7 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(4): Show |
8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1062+97A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903331 | |||||||
| chr1:108903393 | A | G | 1 | a0001c0001t0002g0003 | 3 | NA18947.hp1 NA19068.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1062+159A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903393 | |||||||
| chr1:108903423 | C | G | 89 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(86): Show |
97 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(94): Show |
intron_variant | MODIFIER | c.1062+189C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903423 | |||||||
| chr1:108903518 | G | A | 12 | a0003c0003t0003g0214 a0003c0003t0003g0215 a0003c0003t0003g0218 others(9): Show |
12 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+284G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903518 | |||||||
| chr1:108903835 | T | C | 1 | a0001c0001t0015g0092 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1063-290T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903835 | |||||||
| chr1:108903853 | G | A | 1 | a0002c0005t0008g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1063-272G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 9/14 | chr1 | 108903853 | |||||||
| chr1:108904502 | C | G | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192+248C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108904502 | |||||||
| chr1:108904979 | TA | T | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1192+733delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108904979 | ||||||
| chr1:108905001 | T | C | 1 | a0003c0003t0003g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1192+747T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905001 | |||||||
| chr1:108905022 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1192+768A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905022 | |||||||
| chr1:108905078 | GT | G | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192+825delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905078 | |||||||
| chr1:108905317 | T | C | 1 | a0003c0003t0003g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1192+1063T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905317 | |||||||
| chr1:108905377 | C | G | 1 | a0001c0001t0016g0198 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1192+1123C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905377 | |||||||
| chr1:108905442 | A | G | 14 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(11): Show |
15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.1192+1188A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905442 | |||||||
| chr1:108905452 | G | A | 2 | a0002c0006t0010g0030 a0002c0006t0010g0031 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1192+1198G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905452 | |||||||
| chr1:108905575 | C | T | 4 | a0002c0002t0018g0026 a0002c0008t0018g0028 a0002c0008t0018g0202 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+1321C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905575 | |||||||
| chr1:108905876 | T | C | 7 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(4): Show |
8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+1622T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905876 | |||||||
| chr1:108905913 | G | T | 1 | a0002c0010t0030g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1192+1659G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108905913 | |||||||
| chr1:108906165 | G | GGAAA | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+1911_1192+191 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906165 | |||||||
| chr1:108906199 | A | T | 7 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(4): Show |
8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+1945A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906199 | |||||||
| chr1:108906279 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1192+2025T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906279 | |||||||
| chr1:108906556 | CT | C | 94 | a0001c0001t0001g0123 a0001c0001t0001g0137 a0001c0001t0001g0159 others(91): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.1192+2320delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108906556 | ||||||
| chr1:108906574 | T | C | 1 | a0003c0003t0003g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1192+2320T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906574 | |||||||
| chr1:108906684 | C | T | 7 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(4): Show |
8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+2430C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108906684 | |||||||
| chr1:108907002 | CAGTT | C | 5 | a0003c0003t0003g0220 a0003c0003t0003g0221 a0003c0003t0003g0223 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192+2753_1192+275 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108907002 | ||||||
| chr1:108907028 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1192+2774G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907028 | |||||||
| chr1:108907133 | A | G | 74 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0005g0019 others(71): Show |
80 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.1192+2879A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907133 | |||||||
| chr1:108907301 | G | A | 1 | a0004c0004t0004g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1192+3047G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907301 | |||||||
| chr1:108907372 | TC | T | 3 | a0004c0004t0004g0181 a0004c0004t0004g0186 a0004c0004t0004g0187 |
3 | HG03491.hp2 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1192+3120delC | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108907372 | ||||||
| chr1:108907395 | G | A | 10 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(7): Show |
11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192+3141G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907395 | |||||||
| chr1:108907443 | C | G | 92 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0005g0019 others(89): Show |
100 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(97): Show |
intron_variant | MODIFIER | c.1192+3189C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907443 | |||||||
| chr1:108907527 | T | A | 74 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0005g0019 others(71): Show |
80 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.1192+3273T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907527 | |||||||
| chr1:108907862 | C | T | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+3608C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108907862 | |||||||
| chr1:108908094 | G | A | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192+3840G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908094 | |||||||
| chr1:108908185 | C | T | 10 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(7): Show |
11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192+3931C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908185 | |||||||
| chr1:108908264 | G | C | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192+4010G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908264 | |||||||
| chr1:108908357 | C | G | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+4103C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908357 | |||||||
| chr1:108908409 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1192+4155C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908409 | |||||||
| chr1:108908466 | G | A | 1 | a0002c0002t0019g0045 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1192+4212G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908466 | |||||||
| chr1:108908496 | A | G | 2 | a0001c0001t0023g0059 a0001c0001t0023g0060 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1192+4242A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908496 | |||||||
| chr1:108908629 | C | G | 35 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1192+4375C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908629 | |||||||
| chr1:108908680 | T | C | 87 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0005g0019 others(84): Show |
94 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1192+4426T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908680 | |||||||
| chr1:108908687 | A | G | 1 | a0004c0004t0031g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1192+4433A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908687 | |||||||
| chr1:108908722 | A | AACACACA others(37): Show |
1 | a0003c0003t0003g0226 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1192+4473_1192+447 others(48): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908722 | ||||||
| chr1:108908728 | A | AACACACA others(5): Show |
19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(9): Show |
8 | a0002c0002t0006g0005 a0002c0002t0006g0033 a0002c0002t0006g0038 others(5): Show |
8 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(11): Show |
5 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0061 others(2): Show |
5 | NA18965.hp1 NA18968.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(13): Show |
2 | a0002c0002t0006g0041 a0007c0011t0006g0035 |
2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(17): Show |
1 | a0002c0006t0010g0007 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(28): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(19): Show |
3 | a0002c0002t0011g0058 a0002c0006t0010g0053 a0003c0003t0003g0219 |
3 | HG01175.hp1 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(30): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(21): Show |
4 | a0002c0006t0010g0030 a0002c0006t0010g0031 a0004c0004t0032g0042 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(32): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(23): Show |
14 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(11): Show |
14 | HG01099.hp1 HG01099.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(34): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(25): Show |
10 | a0002c0002t0020g0006 a0002c0002t0020g0049 a0002c0005t0008g0008 others(7): Show |
12 | HG01109.hp1 HG01433.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(36): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(27): Show |
6 | a0002c0002t0043g0029 a0002c0005t0014g0071 a0002c0005t0014g0072 others(3): Show |
6 | HG00280.hp2 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(38): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(29): Show |
7 | a0002c0002t0018g0026 a0002c0005t0008g0065 a0002c0005t0008g0068 others(4): Show |
7 | HG00140.hp1 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(40): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(31): Show |
1 | a0002c0008t0042g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1192+4484_1192+448 others(42): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(35): Show |
2 | a0003c0003t0003g0218 a0003c0003t0003g0227 |
2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(46): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(37): Show |
2 | a0003c0003t0003g0215 a0003c0003t0046g0217 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(48): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(39): Show |
2 | a0003c0003t0003g0220 a0003c0003t0003g0225 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(50): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(41): Show |
2 | a0003c0003t0003g0214 a0003c0003t0003g0221 |
2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1192+4484_1192+448 others(52): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(43): Show |
1 | a0003c0003t0003g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1192+4484_1192+448 others(54): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | AACACACA others(49): Show |
1 | a0003c0003t0003g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1192+4484_1192+448 others(60): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108908728 | ||||||
| chr1:108908728 | A | ACACACAC others(10): Show |
1 | a0002c0002t0017g0039 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1192+4474_1192+447 others(21): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908728 | |||||||
| chr1:108908728 | A | C | 1 | a0003c0003t0003g0226 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1192+4474A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908728 | |||||||
| chr1:108908897 | G | A | 13 | a0002c0010t0030g0193 a0004c0004t0004g0018 a0004c0004t0004g0181 others(10): Show |
15 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.1192+4643G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908897 | |||||||
| chr1:108908908 | G | A | 7 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(4): Show |
8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+4654G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908908 | |||||||
| chr1:108908963 | C | G | 14 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(11): Show |
15 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.1192+4709C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908963 | |||||||
| chr1:108908980 | A | T | 12 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(9): Show |
13 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192+4726A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908980 | |||||||
| chr1:108908988 | A | G | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+4734A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108908988 | |||||||
| chr1:108909054 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(226): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1192+4800A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909054 | |||||||
| chr1:108909079 | C | T | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1192+4825C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909079 | |||||||
| chr1:108909098 | T | C | 88 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0005g0019 others(85): Show |
95 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(92): Show |
intron_variant | MODIFIER | c.1192+4844T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909098 | |||||||
| chr1:108909146 | G | A | 5 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192+4892G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909146 | |||||||
| chr1:108909185 | TTTG | T | 13 | a0002c0010t0030g0193 a0004c0004t0004g0018 a0004c0004t0004g0181 others(10): Show |
15 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.1192+4936_1192+493 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909185 | ||||||
| chr1:108909299 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0177 |
3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1193-5039T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909299 | |||||||
| chr1:108909406 | G | A | 1 | a0004c0004t0031g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1193-4932G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909406 | |||||||
| chr1:108909567 | T | A | 1 | a0001c0001t0029g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1193-4771T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909567 | |||||||
| chr1:108909597 | A | G | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-4741A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909597 | |||||||
| chr1:108909644 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0177 |
3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1193-4694C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909644 | |||||||
| chr1:108909902 | C | CA | 31 | a0001c0001t0001g0077 a0001c0001t0001g0125 a0001c0001t0001g0127 others(28): Show |
32 | HG00544.hp1 HG01109.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1193-4411dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | ||||||
| chr1:108909902 | CA | C | 10 | a0002c0002t0009g0043 a0002c0002t0009g0050 a0002c0002t0009g0051 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1193-4411delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | ||||||
| chr1:108909902 | CAAAAAAA | C | 4 | a0002c0002t0005g0020 a0002c0002t0005g0190 a0002c0002t0005g0191 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-4417_1193-441 others(11): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | ||||||
| chr1:108909902 | CAAAAAAA others(5): Show |
C | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-4422_1193-441 others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108909902 | ||||||
| chr1:108909921 | A | G | 5 | a0002c0002t0018g0026 a0002c0002t0043g0029 a0002c0008t0018g0028 others(2): Show |
5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-4417A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909921 | |||||||
| chr1:108909922 | A | G | 5 | a0002c0002t0018g0026 a0002c0002t0043g0029 a0002c0008t0018g0028 others(2): Show |
5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-4416A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909922 | |||||||
| chr1:108909940 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1193-4398A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909940 | |||||||
| chr1:108909974 | A | G | 1 | a0001c0001t0036g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1193-4364A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909974 | |||||||
| chr1:108909981 | C | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0101 a0001c0001t0001g0103 others(3): Show |
7 | HG01496.hp1 HG01978.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-4357C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108909981 | |||||||
| chr1:108910081 | T | C | 1 | a0003c0003t0003g0219 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1193-4257T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910081 | |||||||
| chr1:108910082 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0177 |
3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1193-4256T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910082 | |||||||
| chr1:108910123 | T | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0177 a0002c0005t0008g0008 others(9): Show |
14 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-4215T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910123 | |||||||
| chr1:108910383 | C | CA | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
24 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1193-3950dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108910383 | ||||||
| chr1:108910507 | T | C | 29 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(26): Show |
34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1193-3831T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910507 | |||||||
| chr1:108910591 | G | A | 3 | a0002c0002t0009g0043 a0002c0002t0009g0050 a0002c0002t0009g0051 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1193-3747G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910591 | |||||||
| chr1:108910815 | A | C | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1193-3523A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108910815 | |||||||
| chr1:108910862 | C | CA | 40 | a0001c0001t0001g0110 a0001c0001t0001g0123 a0001c0001t0001g0137 others(37): Show |
42 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1193-3462dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108910862 | ||||||
| chr1:108911103 | CTAATA | C | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1193-3231_1193-322 others(9): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911103 | ||||||
| chr1:108911158 | A | G | 1 | a0006c0009t0001g0154 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1193-3180A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911158 | |||||||
| chr1:108911168 | A | G | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-3170A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911168 | |||||||
| chr1:108911214 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1193-3124G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911214 | |||||||
| chr1:108911265 | C | T | 1 | a0001c0001t0016g0163 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1193-3073C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911265 | |||||||
| chr1:108911357 | G | A | 16 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0006g0005 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-2981G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911357 | |||||||
| chr1:108911663 | T | C | 87 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0005g0019 others(84): Show |
94 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1193-2675T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911663 | |||||||
| chr1:108911664 | G | A | 2 | a0003c0003t0003g0224 a0003c0003t0003g0225 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1193-2674G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911664 | |||||||
| chr1:108911734 | G | A | 29 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(26): Show |
34 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1193-2604G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911734 | |||||||
| chr1:108911799 | A | AT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(143): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1193-2515dupT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | ||||||
| chr1:108911799 | A | ATT | 48 | a0001c0001t0001g0085 a0001c0001t0001g0103 a0001c0001t0001g0123 others(45): Show |
54 | HG01099.hp2 HG01123.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1193-2516_1193-251 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | ||||||
| chr1:108911799 | A | ATTT | 31 | a0001c0001t0002g0117 a0002c0002t0006g0005 a0002c0002t0006g0038 others(28): Show |
33 | HG01099.hp1 HG01109.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.1193-2517_1193-251 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | ||||||
| chr1:108911799 | A | ATTTT | 5 | a0002c0010t0030g0193 a0004c0004t0022g0073 a0004c0004t0022g0074 others(2): Show |
5 | HG02055.hp1 HG02615.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1193-2518_1193-251 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108911799 | ||||||
| chr1:108911853 | G | A | 1 | a0001c0001t0050g0105 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1193-2485G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911853 | |||||||
| chr1:108911949 | G | C | 5 | a0003c0003t0003g0212 a0003c0003t0021g0209 a0003c0003t0021g0210 others(2): Show |
5 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-2389G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108911949 | |||||||
| chr1:108912343 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1193-1995G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912343 | |||||||
| chr1:108912476 | G | C | 7 | a0002c0005t0008g0008 a0002c0005t0008g0064 a0002c0005t0008g0065 others(4): Show |
8 | HG01433.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193-1862G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912476 | |||||||
| chr1:108912577 | T | TA | 12 | a0001c0001t0001g0015 a0001c0001t0001g0199 a0002c0002t0005g0019 others(9): Show |
16 | HG00738.hp2 HG01123.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1193-1743dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912577 | ||||||
| chr1:108912577 | TA | T | 24 | a0002c0002t0006g0063 a0002c0005t0014g0070 a0002c0005t0014g0071 others(21): Show |
24 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1193-1743delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912577 | ||||||
| chr1:108912577 | TAA | T | 10 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(7): Show |
11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1193-1744_1193-174 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912577 | ||||||
| chr1:108912718 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1193-1620T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912718 | |||||||
| chr1:108912757 | G | A | 46 | a0001c0001t0001g0176 a0001c0001t0001g0206 a0001c0001t0023g0059 others(43): Show |
49 | HG00140.hp1 HG00280.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1193-1581G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912757 | |||||||
| chr1:108912872 | C | G | 1 | a0001c0001t0002g0096 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1193-1466C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912872 | |||||||
| chr1:108912884 | T | TA | 12 | a0001c0001t0015g0093 a0001c0001t0044g0078 a0002c0002t0020g0006 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-1442dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108912884 | ||||||
| chr1:108912916 | C | T | 16 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0041 others(13): Show |
16 | HG01109.hp1 HG01346.hp2 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.1193-1422C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108912916 | |||||||
| chr1:108913001 | A | AG | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1336dupG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 108913001 | ||||||
| chr1:108913003 | T | A | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1335T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913003 | |||||||
| chr1:108913004 | G | A | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1334G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913004 | |||||||
| chr1:108913006 | A | T | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1332A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913006 | |||||||
| chr1:108913013 | G | T | 125 | a0001c0001t0001g0149 a0001c0001t0001g0176 a0001c0001t0001g0194 others(122): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1193-1325G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913013 | |||||||
| chr1:108913035 | A | G | 3 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0083 |
3 | NA18944.hp2 NA18974.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1193-1303A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913035 | |||||||
| chr1:108913064 | G | A | 11 | a0002c0002t0006g0033 a0002c0002t0006g0038 a0004c0004t0004g0018 others(8): Show |
13 | HG01515.hp2 HG01517.hp1 HG02970.hp1 others(10): Show |
intron_variant | MODIFIER | c.1193-1274G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913064 | |||||||
| chr1:108913155 | C | T | 2 | a0002c0006t0010g0007 a0002c0006t0010g0053 |
3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1193-1183C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913155 | |||||||
| chr1:108913203 | T | C | 2 | a0002c0006t0010g0007 a0002c0006t0010g0053 |
3 | HG01884.hp2 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1193-1135T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913203 | |||||||
| chr1:108913216 | C | T | 2 | a0001c0001t0023g0059 a0001c0001t0023g0060 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1193-1122C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913216 | |||||||
| chr1:108913237 | C | T | 2 | a0001c0001t0023g0059 a0001c0001t0023g0060 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1193-1101C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913237 | |||||||
| chr1:108913250 | A | T | 12 | a0002c0010t0030g0193 a0004c0004t0004g0018 a0004c0004t0004g0181 others(9): Show |
14 | HG02055.hp1 HG02886.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.1193-1088A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913250 | |||||||
| chr1:108913311 | A | C | 1 | a0004c0004t0032g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1193-1027A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913311 | |||||||
| chr1:108913354 | A | C | 1 | a0001c0001t0039g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1193-984A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913354 | |||||||
| chr1:108913558 | C | T | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1193-780C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913558 | |||||||
| chr1:108913559 | T | C | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1193-779T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913559 | |||||||
| chr1:108913678 | T | C | 1 | a0004c0004t0022g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1193-660T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913678 | |||||||
| chr1:108913759 | C | G | 6 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(3): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1193-579C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913759 | |||||||
| chr1:108913839 | T | C | 1 | a0003c0003t0003g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1193-499T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913839 | |||||||
| chr1:108913936 | C | T | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1193-402C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913936 | |||||||
| chr1:108913989 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1193-349T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108913989 | |||||||
| chr1:108914228 | G | A | 76 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(73): Show |
84 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1193-110G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 10/14 | chr1 | 108914228 | |||||||
| chr1:108914511 | G | C | 1 | a0001c0001t0007g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1263+103G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914511 | |||||||
| chr1:108914516 | A | C | 1 | a0001c0001t0036g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1263+108A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914516 | |||||||
| chr1:108914529 | C | T | 51 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(48): Show |
55 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.1263+121C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914529 | |||||||
| chr1:108914629 | T | G | 5 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+221T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914629 | |||||||
| chr1:108914809 | A | G | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+401A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914809 | |||||||
| chr1:108914819 | C | T | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1263+411C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914819 | |||||||
| chr1:108914888 | G | A | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1263+480G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108914888 | |||||||
| chr1:108915007 | G | A | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1263+599G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915007 | |||||||
| chr1:108915151 | T | A | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+743T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915151 | |||||||
| chr1:108915303 | G | A | 11 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0144 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.1263+895G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915303 | |||||||
| chr1:108915368 | C | CA | 15 | a0001c0001t0001g0114 a0001c0001t0001g0131 a0001c0001t0001g0147 others(12): Show |
15 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.1263+979dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | ||||||
| chr1:108915368 | CA | C | 29 | a0001c0001t0001g0201 a0001c0001t0002g0107 a0001c0001t0002g0119 others(26): Show |
29 | HG01099.hp1 HG01516.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.1263+979delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | ||||||
| chr1:108915368 | CAA | C | 51 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(48): Show |
57 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.1263+978_1263+979d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | ||||||
| chr1:108915368 | CAAA | C | 14 | a0002c0002t0005g0191 a0002c0002t0020g0006 a0002c0002t0020g0049 others(11): Show |
16 | HG01433.hp2 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1263+977_1263+979d others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108915368 | ||||||
| chr1:108915489 | C | T | 5 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1081C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915489 | |||||||
| chr1:108915522 | G | A | 4 | a0002c0002t0005g0020 a0002c0002t0005g0190 a0002c0002t0005g0191 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+1114G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915522 | |||||||
| chr1:108915552 | G | A | 18 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(15): Show |
21 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1263+1144G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915552 | |||||||
| chr1:108915666 | C | T | 5 | a0002c0002t0018g0026 a0002c0002t0043g0029 a0002c0008t0018g0028 others(2): Show |
5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+1258C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915666 | |||||||
| chr1:108915716 | C | A | 4 | a0002c0002t0005g0020 a0002c0002t0005g0190 a0002c0002t0005g0191 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+1308C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915716 | |||||||
| chr1:108915770 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0177 |
3 | HG01081.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1263+1362A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915770 | |||||||
| chr1:108915967 | C | T | 1 | a0004c0013t0048g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1263+1559C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915967 | |||||||
| chr1:108915968 | G | A | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1263+1560G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108915968 | |||||||
| chr1:108916078 | C | CA | 68 | a0001c0001t0001g0200 a0001c0001t0023g0059 a0001c0001t0023g0060 others(65): Show |
74 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.1263+1686dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916078 | ||||||
| chr1:108916078 | C | CAA | 22 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(19): Show |
23 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1263+1685_1263+168 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916078 | ||||||
| chr1:108916078 | C | CAAAA | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1683_1263+168 others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916078 | ||||||
| chr1:108916260 | G | GAA | 6 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(3): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1263+1863_1263+186 others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108916260 | ||||||
| chr1:108916393 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00280.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1263+1985A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916393 | |||||||
| chr1:108916457 | T | C | 7 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(4): Show |
10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1263+2049T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916457 | |||||||
| chr1:108916674 | A | T | 17 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(14): Show |
20 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1264-1939A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916674 | |||||||
| chr1:108916832 | T | A | 1 | a0001c0001t0002g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1264-1781T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108916832 | |||||||
| chr1:108917033 | C | T | 1 | a0002c0005t0014g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1264-1580C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917033 | |||||||
| chr1:108917057 | T | G | 3 | a0002c0005t0014g0070 a0002c0005t0014g0071 a0002c0005t0014g0072 |
3 | HG02109.hp2 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1264-1556T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917057 | |||||||
| chr1:108917290 | G | A | 15 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(12): Show |
17 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(14): Show |
intron_variant | MODIFIER | c.1264-1323G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917290 | |||||||
| chr1:108917334 | G | A | 1 | a0004c0004t0031g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1264-1279G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917334 | |||||||
| chr1:108917513 | G | A | 1 | a0002c0010t0030g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1264-1100G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917513 | |||||||
| chr1:108917525 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1264-1088C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917525 | |||||||
| chr1:108917609 | CACATATA others(29): Show |
C | 8 | a0002c0002t0020g0006 a0002c0002t0020g0049 a0002c0005t0008g0008 others(5): Show |
10 | HG01433.hp2 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-1002_1264-967 others(39): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917609 | ||||||
| chr1:108917609 | CACATATA others(31): Show |
C | 68 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(65): Show |
74 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.1264-1002_1264-965 others(41): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917609 | ||||||
| chr1:108917609 | CACATATA others(33): Show |
C | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264-1002_1264-963 others(43): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917609 | ||||||
| chr1:108917611 | C | CACACACA others(21): Show |
1 | a0001c0001t0002g0113 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(32): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(13): Show |
1 | a0001c0001t0001g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(15): Show |
1 | a0001c0001t0002g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(13): Show |
1 | a0001c0001t0002g0104 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(17): Show |
1 | a0001c0001t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(28): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(7): Show |
1 | a0001c0001t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(15): Show |
1 | a0001c0001t0001g0086 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(7): Show |
1 | a0008c0012t0016g0157 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(11): Show |
1 | a0001c0001t0029g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(13): Show |
1 | a0001c0001t0015g0092 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(15): Show |
1 | a0001c0001t0002g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(17): Show |
2 | a0001c0001t0002g0009 a0001c0001t0015g0009 |
2 | HG01952.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(28): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACACA others(23): Show |
1 | a0001c0001t0002g0003 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(34): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACATA others(9): Show |
4 | a0001c0001t0001g0208 a0001c0001t0002g0094 a0001c0001t0002g0141 others(1): Show |
4 | HG00741.hp2 HG02056.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACATA others(11): Show |
1 | a0001c0001t0039g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACATA others(19): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0023 |
2 | NA18939.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(30): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACACATA others(25): Show |
1 | a0001c0001t0001g0129 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(36): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACATATA others(3): Show |
2 | a0001c0001t0001g0174 a0001c0001t0002g0084 |
2 | NA18978.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACATATA others(5): Show |
2 | a0001c0001t0001g0085 a0006c0009t0001g0154 |
2 | HG01071.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACATATA others(7): Show |
1 | a0001c0001t0001g0199 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1264-1001_1264-100 others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACATATA others(9): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0149 a0001c0001t0002g0096 |
3 | HG04204.hp2 NA18956.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CACATATA others(11): Show |
3 | a0001c0001t0001g0153 a0001c0001t0002g0089 a0001c0001t0007g0004 |
3 | HG01346.hp1 HG03195.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1264-1001_1264-100 others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CAT | 4 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0136 others(1): Show |
4 | HG01243.hp1 HG01515.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-948_1264-947d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATACATA others(3): Show |
1 | a0001c0001t0002g0090 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1264-999_1264-998i others(12): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATAT | 4 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0200 others(1): Show |
4 | HG02809.hp2 NA18972.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-950_1264-947d others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATAT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0147 others(4): Show |
8 | HG01123.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-952_1264-947d others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(3): Show |
4 | a0001c0001t0001g0138 a0001c0001t0002g0107 a0001c0001t0002g0130 others(1): Show |
4 | HG01433.hp1 HG02040.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-956_1264-947d others(12): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(5): Show |
9 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0077 others(6): Show |
9 | HG00738.hp2 HG01257.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264-958_1264-947d others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(7): Show |
5 | a0001c0001t0001g0109 a0001c0001t0002g0081 a0001c0001t0002g0150 others(2): Show |
5 | HG00140.hp2 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264-960_1264-947d others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(9): Show |
5 | a0001c0001t0001g0123 a0001c0001t0002g0083 a0001c0001t0024g0097 others(2): Show |
5 | HG02027.hp1 HG02559.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-962_1264-947d others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(11): Show |
4 | a0001c0001t0001g0125 a0001c0001t0002g0010 a0001c0001t0007g0108 others(1): Show |
4 | HG01081.hp1 HG01175.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-964_1264-947d others(20): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(13): Show |
9 | a0001c0001t0001g0110 a0001c0001t0001g0170 a0001c0001t0001g0177 others(6): Show |
9 | HG00544.hp1 HG00544.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1264-966_1264-947d others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(15): Show |
1 | a0001c0001t0001g0201 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1264-968_1264-947d others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(17): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0101 a0001c0001t0007g0004 |
3 | HG02622.hp1 NA18943.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1264-970_1264-947d others(26): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(21): Show |
1 | a0001c0001t0002g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1264-974_1264-947d others(30): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | C | CATATATA others(27): Show |
1 | a0001c0001t0002g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1264-980_1264-947d others(36): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CAT | C | 5 | a0001c0001t0001g0145 a0001c0001t0002g0112 a0001c0001t0002g0196 others(2): Show |
5 | HG01109.hp2 HG02074.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264-948_1264-947d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATAT | C | 10 | a0001c0001t0001g0024 a0001c0001t0001g0122 a0001c0001t0001g0137 others(7): Show |
10 | HG00438.hp1 HG00741.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-950_1264-947d others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATAT | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG02145.hp2 HG02148.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264-952_1264-947d others(8): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG00099.hp2 HG01496.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264-954_1264-947d others(10): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(3): Show |
C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0002g0099 |
3 | HG02486.hp1 HG03130.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1264-956_1264-947d others(12): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1264-958_1264-947d others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(7): Show |
C | 1 | a0001c0001t0002g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1264-960_1264-947d others(16): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(9): Show |
C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0098 |
2 | HG00099.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1264-962_1264-947d others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(13): Show |
C | 3 | a0001c0001t0001g0175 a0001c0001t0002g0003 a0001c0001t0002g0115 |
3 | HG01978.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1264-966_1264-947d others(22): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0103 |
3 | HG01496.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1264-968_1264-947d others(24): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(23): Show |
C | 1 | a0001c0001t0012g0164 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1264-976_1264-947d others(32): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(25): Show |
C | 4 | a0001c0001t0002g0116 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-978_1264-947d others(34): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917611 | CATATATA others(33): Show |
C | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1264-986_1264-947d others(42): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917611 | ||||||
| chr1:108917613 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0133 a0001c0001t0001g0168 others(1): Show |
4 | HG00408.hp1 HG02040.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1000T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917613 | |||||||
| chr1:108917615 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0145 a0001c0001t0002g0112 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264-998T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917615 | |||||||
| chr1:108917617 | T | C | 10 | a0001c0001t0001g0122 a0001c0001t0001g0137 a0001c0001t0001g0140 others(7): Show |
10 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-996T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917617 | |||||||
| chr1:108917619 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0127 a0001c0001t0001g0137 others(5): Show |
8 | HG00438.hp1 HG01109.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-994T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917619 | |||||||
| chr1:108917621 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0127 a0001c0001t0001g0152 others(5): Show |
8 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-992T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917621 | |||||||
| chr1:108917623 | T | C | 5 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-990T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917623 | |||||||
| chr1:108917629 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1264-984T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917629 | |||||||
| chr1:108917631 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1264-982T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917631 | |||||||
| chr1:108917633 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0098 |
2 | NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1264-980T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917633 | |||||||
| chr1:108917635 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1264-978T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917635 | |||||||
| chr1:108917645 | T | C | 1 | a0001c0001t0012g0164 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1264-968T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917645 | |||||||
| chr1:108917647 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1264-951_1264-950i others(18): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917647 | ||||||
| chr1:108917663 | T | A | 17 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(14): Show |
19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1264-950T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917663 | |||||||
| chr1:108917665 | T | A | 78 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(75): Show |
85 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(82): Show |
intron_variant | MODIFIER | c.1264-948T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917665 | |||||||
| chr1:108917666 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0151 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1264-947_1264-946i others(19): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917666 | |||||||
| chr1:108917667 | A | T | 1 | a0001c0001t0002g0107 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1264-946A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917667 | |||||||
| chr1:108917691 | G | A | 8 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(5): Show |
8 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-922G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917691 | |||||||
| chr1:108917830 | TG | T | 4 | a0002c0002t0018g0026 a0002c0008t0018g0028 a0002c0008t0018g0202 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-779delG | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 108917830 | ||||||
| chr1:108917960 | A | G | 11 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(8): Show |
11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1264-653A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108917960 | |||||||
| chr1:108918160 | A | C | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264-453A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918160 | |||||||
| chr1:108918186 | G | A | 27 | a0002c0002t0020g0006 a0002c0002t0020g0049 a0002c0005t0008g0008 others(24): Show |
29 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264-427G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918186 | |||||||
| chr1:108918214 | A | T | 1 | a0002c0002t0006g0041 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1264-399A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918214 | |||||||
| chr1:108918215 | T | A | 1 | a0002c0002t0006g0041 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1264-398T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918215 | |||||||
| chr1:108918220 | T | A | 1 | a0002c0002t0006g0041 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1264-393T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918220 | |||||||
| chr1:108918341 | C | T | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1264-272C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918341 | |||||||
| chr1:108918487 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1264-126T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918487 | |||||||
| chr1:108918509 | A | G | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264-104A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918509 | |||||||
| chr1:108918510 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1264-103A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 11/14 | chr1 | 108918510 | |||||||
| chr1:108918882 | G | A | 1 | a0002c0002t0020g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1440+93G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108918882 | |||||||
| chr1:108918911 | A | C | 1 | a0003c0003t0045g0216 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1440+122A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108918911 | |||||||
| chr1:108919056 | G | A | 1 | a0004c0004t0031g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1440+267G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919056 | |||||||
| chr1:108919136 | T | C | 1 | a0002c0002t0020g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1440+347T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919136 | |||||||
| chr1:108919196 | C | T | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1440+407C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919196 | |||||||
| chr1:108919210 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1440+421G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919210 | |||||||
| chr1:108919423 | C | G | 6 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(3): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+634C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919423 | |||||||
| chr1:108919511 | T | C | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1440+722T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919511 | |||||||
| chr1:108919817 | C | T | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1440+1028C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919817 | |||||||
| chr1:108919938 | G | A | 7 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(4): Show |
10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1440+1149G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919938 | |||||||
| chr1:108919950 | G | C | 92 | a0001c0001t0001g0176 a0002c0002t0002g0034 a0002c0002t0005g0019 others(89): Show |
100 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(97): Show |
intron_variant | MODIFIER | c.1440+1161G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108919950 | |||||||
| chr1:108920123 | C | T | 6 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(3): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+1334C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920123 | |||||||
| chr1:108920168 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1440+1379A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920168 | |||||||
| chr1:108920186 | T | C | 3 | a0002c0002t0009g0043 a0002c0002t0009g0050 a0002c0002t0009g0051 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1440+1397T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920186 | |||||||
| chr1:108920228 | G | T | 6 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(3): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+1439G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920228 | |||||||
| chr1:108920382 | T | C | 1 | a0002c0002t0043g0029 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1440+1593T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920382 | |||||||
| chr1:108920458 | G | A | 1 | a0004c0004t0004g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1440+1669G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920458 | |||||||
| chr1:108920622 | C | T | 1 | a0004c0004t0004g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1441-1795C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920622 | |||||||
| chr1:108920951 | T | A | 17 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(14): Show |
19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1441-1466T>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920951 | |||||||
| chr1:108920994 | G | A | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1441-1423G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108920994 | |||||||
| chr1:108921052 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1441-1365C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921052 | |||||||
| chr1:108921084 | A | T | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-1333A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921084 | |||||||
| chr1:108921240 | C | T | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-1177C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921240 | |||||||
| chr1:108921256 | T | C | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-1161T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921256 | |||||||
| chr1:108921416 | CA | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1441-986delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108921416 | ||||||
| chr1:108921416 | CAA | C | 13 | a0001c0001t0001g0013 a0001c0001t0002g0084 a0002c0002t0009g0043 others(10): Show |
14 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1441-987_1441-986d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108921416 | ||||||
| chr1:108921416 | CAAA | C | 80 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(77): Show |
88 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(85): Show |
intron_variant | MODIFIER | c.1441-988_1441-986d others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108921416 | ||||||
| chr1:108921606 | C | G | 27 | a0002c0002t0020g0006 a0002c0002t0020g0049 a0002c0005t0008g0008 others(24): Show |
29 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1441-811C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921606 | |||||||
| chr1:108921653 | A | C | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-764A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921653 | |||||||
| chr1:108921660 | T | C | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1441-757T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921660 | |||||||
| chr1:108921725 | T | G | 5 | a0002c0002t0018g0026 a0002c0002t0043g0029 a0002c0008t0018g0028 others(2): Show |
5 | HG01109.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-692T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108921725 | |||||||
| chr1:108922005 | T | TA | 36 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(33): Show |
39 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(36): Show |
intron_variant | MODIFIER | c.1441-404dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108922005 | ||||||
| chr1:108922043 | A | G | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-374A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108922043 | |||||||
| chr1:108922060 | T | TAGAC | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1441-355_1441-354i others(6): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 108922060 | ||||||
| chr1:108922077 | T | G | 4 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 others(1): Show |
5 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441-340T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108922077 | |||||||
| chr1:108922121 | A | G | 6 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(3): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1441-296A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 12/14 | chr1 | 108922121 | |||||||
| chr1:108922692 | GTA | G | 13 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(10): Show |
15 | HG02886.hp1 HG02970.hp1 HG03098.hp2 others(12): Show |
intron_variant | MODIFIER | c.1600+120_1600+121d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 108922692 | ||||||
| chr1:108922772 | A | G | 1 | a0004c0004t0013g0002 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1600+196A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922772 | |||||||
| chr1:108922842 | A | G | 1 | a0004c0004t0004g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1600+266A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922842 | |||||||
| chr1:108922877 | C | T | 1 | a0001c0014t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1600+301C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922877 | |||||||
| chr1:108922879 | C | T | 1 | a0001c0014t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1600+303C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108922879 | |||||||
| chr1:108923253 | T | C | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1600+677T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923253 | |||||||
| chr1:108923259 | C | T | 1 | a0004c0004t0004g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1600+683C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923259 | |||||||
| chr1:108923304 | T | C | 1 | a0004c0004t0031g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1601-696T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923304 | |||||||
| chr1:108923376 | T | TGTA | 17 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(14): Show |
19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1601-624_1601-623i others(5): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923376 | |||||||
| chr1:108923377 | A | T | 17 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(14): Show |
19 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.1601-623A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923377 | |||||||
| chr1:108923441 | A | C | 7 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(4): Show |
10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1601-559A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923441 | |||||||
| chr1:108923464 | TGGCTAAG others(5): Show |
T | 76 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(73): Show |
84 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1601-526_1601-515d others(14): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 108923464 | ||||||
| chr1:108923734 | G | C | 1 | a0001c0001t0002g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1601-266G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923734 | |||||||
| chr1:108923940 | TTTTTTTG | T | 19 | a0003c0003t0003g0212 a0003c0003t0003g0214 a0003c0003t0003g0215 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1601-39_1601-33del others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 108923940 | ||||||
| chr1:108923975 | T | C | 12 | a0004c0004t0004g0018 a0004c0004t0004g0181 a0004c0004t0004g0182 others(9): Show |
14 | HG02886.hp1 HG02970.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.1601-25T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 13/14 | chr1 | 108923975 | |||||||
| chr1:108924236 | G | A | 75 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(72): Show |
83 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1815+22G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924236 | |||||||
| chr1:108924360 | G | A | 15 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(12): Show |
15 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1815+146G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924360 | |||||||
| chr1:108924447 | G | A | 22 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(19): Show |
25 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1815+233G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924447 | |||||||
| chr1:108924456 | T | G | 1 | a0002c0002t0006g0041 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1815+242T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924456 | |||||||
| chr1:108924458 | G | T | 25 | a0001c0001t0001g0148 a0001c0001t0001g0156 a0002c0002t0011g0054 others(22): Show |
27 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1815+244G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924458 | |||||||
| chr1:108924548 | G | A | 2 | a0001c0001t0023g0059 a0001c0001t0023g0060 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1815+334G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924548 | |||||||
| chr1:108924651 | G | T | 11 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(8): Show |
11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1815+437G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924651 | |||||||
| chr1:108924956 | T | C | 3 | a0004c0004t0022g0073 a0004c0004t0022g0074 a0004c0004t0032g0042 |
3 | HG02615.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1815+742T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924956 | |||||||
| chr1:108924990 | A | G | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1815+776A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108924990 | |||||||
| chr1:108925044 | T | C | 1 | a0004c0004t0032g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1815+830T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925044 | |||||||
| chr1:108925239 | T | C | 4 | a0002c0002t0018g0026 a0002c0008t0018g0028 a0002c0008t0018g0202 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+1025T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925239 | |||||||
| chr1:108925378 | T | C | 1 | a0002c0002t0043g0029 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1815+1164T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925378 | |||||||
| chr1:108925392 | G | C | 1 | a0001c0001t0001g0016 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1815+1178G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925392 | |||||||
| chr1:108925498 | C | G | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1815+1284C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925498 | |||||||
| chr1:108925624 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1815+1410C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925624 | |||||||
| chr1:108925785 | G | T | 5 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+1571G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925785 | |||||||
| chr1:108925824 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1815+1610G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925824 | |||||||
| chr1:108925824 | GT | G | 5 | a0001c0001t0001g0177 a0001c0001t0002g0081 a0002c0006t0010g0007 others(2): Show |
6 | HG01081.hp2 HG01884.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1815+1621delT | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108925824 | ||||||
| chr1:108925866 | C | A | 1 | a0004c0004t0004g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1815+1652C>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925866 | |||||||
| chr1:108925878 | G | A | 1 | a0002c0010t0030g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1815+1664G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108925878 | |||||||
| chr1:108926031 | G | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0107 |
2 | NA18747.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1815+1817G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926031 | |||||||
| chr1:108926086 | G | A | 75 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(72): Show |
83 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1815+1872G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926086 | |||||||
| chr1:108926202 | C | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
64 | HG00408.hp2 HG00544.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1815+1988C>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926202 | |||||||
| chr1:108926577 | G | C | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1815+2363G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926577 | |||||||
| chr1:108926685 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1815+2471G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926685 | |||||||
| chr1:108926692 | A | C | 27 | a0002c0002t0020g0006 a0002c0002t0020g0049 a0002c0005t0008g0008 others(24): Show |
29 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1815+2478A>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926692 | |||||||
| chr1:108926709 | A | G | 19 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(16): Show |
22 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1815+2495A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926709 | |||||||
| chr1:108926714 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1815+2500G>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926714 | |||||||
| chr1:108926947 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1815+2733A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108926947 | |||||||
| chr1:108927301 | A | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0199 |
2 | NA19000.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1816-2400A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927301 | |||||||
| chr1:108927311 | T | C | 7 | a0002c0002t0005g0019 a0002c0002t0005g0020 a0002c0002t0005g0021 others(4): Show |
10 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1816-2390T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927311 | |||||||
| chr1:108927459 | T | C | 1 | a0001c0001t0044g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1816-2242T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927459 | |||||||
| chr1:108927504 | A | G | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2197A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927504 | |||||||
| chr1:108927563 | T | C | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2138T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927563 | |||||||
| chr1:108927624 | C | T | 2 | a0002c0002t0006g0041 a0007c0011t0006g0035 |
2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1816-2077C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927624 | |||||||
| chr1:108927646 | G | A | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2055G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927646 | |||||||
| chr1:108927647 | C | T | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-2054C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927647 | |||||||
| chr1:108927813 | A | T | 1 | a0002c0006t0010g0053 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1816-1888A>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927813 | |||||||
| chr1:108927977 | A | G | 2 | a0004c0004t0022g0073 a0004c0004t0022g0074 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1816-1724A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108927977 | |||||||
| chr1:108928038 | G | A | 91 | a0002c0002t0002g0034 a0002c0002t0005g0019 a0002c0002t0005g0020 others(88): Show |
99 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-1663G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928038 | |||||||
| chr1:108928303 | T | C | 10 | a0002c0002t0011g0054 a0002c0002t0011g0055 a0002c0002t0011g0056 others(7): Show |
10 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1816-1398T>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928303 | |||||||
| chr1:108928398 | T | TGGA | 11 | a0002c0002t0009g0043 a0002c0002t0009g0046 a0002c0002t0009g0048 others(8): Show |
11 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1816-1299_1816-129 others(7): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108928398 | ||||||
| chr1:108928477 | G | A | 1 | a0002c0005t0008g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1816-1224G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928477 | |||||||
| chr1:108928847 | A | G | 119 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(116): Show |
129 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1816-854A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928847 | |||||||
| chr1:108928867 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(221): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1816-834A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928867 | |||||||
| chr1:108928986 | C | T | 55 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(52): Show |
59 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1816-715C>T | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108928986 | |||||||
| chr1:108928988 | C | CA | 18 | a0001c0001t0001g0153 a0001c0001t0001g0172 a0002c0005t0014g0072 others(15): Show |
20 | HG01346.hp1 HG01891.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1816-694dupA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108928988 | ||||||
| chr1:108928988 | CA | C | 62 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0174 others(59): Show |
66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1816-694delA | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108928988 | ||||||
| chr1:108929012 | T | G | 128 | a0001c0001t0001g0011 a0001c0001t0002g0003 a0001c0001t0002g0009 others(125): Show |
141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1816-689T>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929012 | |||||||
| chr1:108929023 | TTC | T | 55 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0010 others(52): Show |
59 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1816-676_1816-675d others(4): Show |
GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 108929023 | ||||||
| chr1:108929107 | G | A | 16 | a0002c0002t0002g0034 a0002c0002t0006g0005 a0002c0002t0006g0033 others(13): Show |
16 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1816-594G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929107 | |||||||
| chr1:108929227 | G | A | 3 | a0002c0006t0010g0007 a0002c0006t0010g0030 a0002c0006t0010g0031 |
4 | HG01884.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-474G>A | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929227 | |||||||
| chr1:108929298 | G | C | 56 | a0001c0001t0001g0011 a0001c0001t0002g0003 a0001c0001t0002g0009 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1816-403G>C | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929298 | |||||||
| chr1:108929670 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1816-31A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929670 | |||||||
| chr1:108929693 | A | G | 3 | a0002c0002t0019g0044 a0002c0002t0019g0045 a0002c0002t0019g0047 |
3 | HG01099.hp1 HG02965.hp1 HG03540.hp1 |
splice_region_variant&intron_variant | LOW | c.1816-8A>G | GPSM2 | ENSG00000121957.15 | transcript | ENST00000264126.9 | protein_coding | 14/14 | chr1 | 108929693 |