Item | Value |
---|---|
geneid | 26086 |
ensemblid | ENSG00000160360.13 |
hgncid | 17858 |
symbol | GPSM1 |
name | G protein signaling modulator 1 |
refseq_nuc | NM_001145638.3 |
refseq_prot | NP_001139110.2 |
ensembl_nuc | ENST00000440944.6 |
ensembl_prot | ENSP00000392828.1 |
mane_status | MANE Select |
chr | chr9 |
start | 136327539 |
end | 136359601 |
strand | + |
ver | v1.2 |
region | chr9:136327539-136359601 |
region5000 | chr9:136322539-136364601 |
regionname0 | GPSM1_chr9_136327539_136359601 |
regionname5000 | GPSM1_chr9_136322539_136364601 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 675 | 321 | 71 | 59 | 135 | 15 | 39 | 93 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0002 | 0/0 | 675 | 64 | 22 | 21 | 15 | 1 | 5 | 13 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0003 | 0/0 | 675 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0004 | 0/0 | 675 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0005 | 0/0 | 675 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0006 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0007 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0008 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0009 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0010 | 0/0 | 675 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0011 | 0/0 | 675 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0012 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
a0013 | 0/0 | 671 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(666): Show |
chr9 | 136322539 | 136364601 |
a0014 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | MAGPA others(670): Show |
chr9 | 136322539 | 136364601 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2025 | 259 | 52 | 36 | 125 | 13 | 32 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0003 | 1/0 | 2025 | 26 | 3 | 17 | 0 | 1 | 4 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0005 | 0/0 | 2025 | 9 | 7 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0006 | 0/0 | 2025 | 7 | 6 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0007 | 0/0 | 2025 | 5 | 0 | 2 | 0 | 1 | 2 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0008 | 0/0 | 2025 | 4 | 0 | 0 | 4 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0010 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0011 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0012 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0013 | 0/0 | 2025 | 2 | 0 | 1 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0016 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0029 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0001c0031 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0002c0002 | 0/0 | 2025 | 47 | 10 | 18 | 13 | 1 | 5 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0002c0004 | 0/0 | 2025 | 11 | 7 | 3 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0002c0014 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0002c0015 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0002c0027 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0002c0030 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0003c0009 | 0/0 | 2025 | 4 | 0 | 0 | 4 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0004c0019 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0005c0026 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0006c0018 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0007c0025 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0008c0023 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0009c0022 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0010c0024 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0011c0028 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0012c0017 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 | ||
a0013c0021 | 0/0 | 2015 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2010): Show |
chr9 | 136322539 | 136364601 | ||
a0014c0020 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ATGGC others(2020): Show |
chr9 | 136322539 | 136364601 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3566 | 180 | 37 | 30 | 82 | 9 | 22 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0003 | 0/1 | 3566 | 32 | 1 | 5 | 22 | 3 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0004 | 0/0 | 3566 | 23 | 3 | 0 | 14 | 1 | 5 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0006 | 0/0 | 3566 | 5 | 3 | 1 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0007 | 0/0 | 3566 | 4 | 0 | 0 | 1 | 0 | 3 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0011 | 0/0 | 3566 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0012 | 0/0 | 3566 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0014 | 0/0 | 3566 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0015 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0016 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0018 | 0/0 | 3566 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0020 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0024 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0025 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0026 | 0/0 | 3566 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0027 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0028 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0001t0029 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0003t0001 | 1/0 | 3566 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0003t0002 | 0/0 | 3566 | 23 | 1 | 17 | 0 | 1 | 4 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0003t0004 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0003t0019 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0005t0005 | 0/0 | 3566 | 9 | 7 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0006t0001 | 0/0 | 3566 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0006t0004 | 0/0 | 3566 | 3 | 3 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0006t0023 | 0/0 | 3566 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0007t0001 | 0/0 | 3566 | 5 | 0 | 2 | 0 | 1 | 2 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0008t0001 | 0/0 | 3566 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0008t0004 | 0/0 | 3566 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0010t0001 | 0/0 | 3566 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0011t0013 | 0/0 | 3566 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0012t0004 | 0/0 | 3566 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0013t0009 | 0/0 | 3566 | 2 | 0 | 1 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0016t0001 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0001c0029t0010 | 0/0 | 3554 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3549): Show |
chr9 | 136322539 | 136364601 |
a0001c0031t0008 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0002t0002 | 0/0 | 3566 | 44 | 8 | 17 | 13 | 1 | 5 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0002t0017 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0002t0021 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0002t0022 | 0/0 | 3566 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0004t0001 | 0/0 | 3566 | 7 | 5 | 1 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0004t0003 | 0/0 | 3566 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0004t0006 | 0/0 | 3566 | 3 | 2 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0014t0010 | 0/0 | 3554 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3549): Show |
chr9 | 136322539 | 136364601 |
a0002c0015t0008 | 0/0 | 3566 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0027t0002 | 0/0 | 3566 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0002c0030t0030 | 0/0 | 3554 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3549): Show |
chr9 | 136322539 | 136364601 |
a0003c0009t0001 | 0/0 | 3566 | 4 | 0 | 0 | 4 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0004c0019t0003 | 0/0 | 3566 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0005c0026t0001 | 0/0 | 3566 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0006c0018t0009 | 0/0 | 3566 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0007c0025t0001 | 0/0 | 3566 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0008c0023t0001 | 0/0 | 3566 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0009c0022t0001 | 0/0 | 3566 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0010c0024t0002 | 0/0 | 3566 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0011c0028t0001 | 0/0 | 3566 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0012c0017t0001 | 0/0 | 3566 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
a0013c0021t0004 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3551): Show |
chr9 | 136322539 | 136364601 |
a0014c0020t0001 | 0/0 | 3566 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | ACTTC others(3561): Show |
chr9 | 136322539 | 136364601 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0007g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0012g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0014g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0015g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0016g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0018g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0020g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0024g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0025g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0026g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0027g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0028g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0001t0029g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0001g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0003t0019g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0005t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0006t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0006t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0006t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0006t0023g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0007t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0007t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0007t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0008t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0008t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0008t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0008t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0010t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0011t0013g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0011t0013g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0012t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0012t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0013t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0013t0009g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0016t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0029t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0001c0031t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0021g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0002t0022g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0006g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0004t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0014t0010g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0015t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0015t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0027t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0002c0030t0030g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0003c0009t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0003c0009t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0003c0009t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0004c0019t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0005c0026t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0006c0018t0009g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0007c0025t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0008c0023t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0009c0022t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0010c0024t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0011c0028t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0012c0017t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0013c0021t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
a0014c0020t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00140 | hp1 | a0004 | c0019 | t0003 | g0104 | EUR | GBR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00140 | hp2 | a0005 | c0026 | t0001 | g0258 | EUR | GBR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00280 | hp1 | a0001 | c0007 | t0001 | g0328 | EUR | FIN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00408 | hp1 | a0001 | c0010 | t0001 | g0247 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00597 | hp1 | a0001 | c0012 | t0004 | g0217 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00673 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00733 | hp1 | a0001 | c0003 | t0002 | g0255 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0174 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0220 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01074 | hp2 | a0002 | c0004 | t0006 | g0014 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0108 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0305 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01167 | hp1 | a0001 | c0005 | t0005 | g0084 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01169 | hp1 | a0001 | c0005 | t0005 | g0078 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01175 | hp1 | a0001 | c0007 | t0001 | g0140 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0272 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0054 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01243 | hp2 | a0001 | c0006 | t0023 | g0072 | AMR | PUR | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01261 | hp1 | a0002 | c0004 | t0001 | g0030 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01261 | hp2 | a0001 | c0003 | t0002 | g0207 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01358 | hp1 | a0001 | c0003 | t0002 | g0312 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01361 | hp2 | a0007 | c0025 | t0001 | g0037 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01433 | hp2 | a0002 | c0002 | t0022 | g0148 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0146 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | IBS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0110 | EUR | IBS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0259 | EUR | IBS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0179 | EUR | IBS | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01884 | hp1 | a0002 | c0015 | t0008 | g0086 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0004 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01934 | hp1 | a0001 | c0003 | t0002 | g0106 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01943 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0225 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0115 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01975 | hp2 | a0001 | c0003 | t0002 | g0291 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01978 | hp1 | a0001 | c0003 | t0002 | g0004 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01978 | hp2 | a0001 | c0003 | t0002 | g0297 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01981 | hp2 | a0001 | c0003 | t0002 | g0311 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01993 | hp2 | a0001 | c0007 | t0001 | g0171 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02004 | hp1 | a0002 | c0004 | t0003 | g0313 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02015 | hp1 | a0001 | c0011 | t0013 | g0035 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02027 | hp1 | a0008 | c0023 | t0001 | g0249 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02083 | hp2 | a0001 | c0001 | t0012 | g0288 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02129 | hp2 | a0001 | c0008 | t0001 | g0009 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02135 | hp2 | a0001 | c0001 | t0018 | g0197 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0256 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02145 | hp2 | a0001 | c0006 | t0004 | g0089 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | CDX | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CDX | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0177 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02257 | hp2 | a0002 | c0014 | t0010 | g0018 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02258 | hp2 | a0001 | c0001 | t0015 | g0323 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02273 | hp1 | a0001 | c0003 | t0002 | g0105 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02273 | hp2 | a0001 | c0013 | t0009 | g0056 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02280 | hp1 | a0001 | c0003 | t0019 | g0129 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02280 | hp2 | a0001 | c0005 | t0005 | g0085 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02293 | hp1 | a0001 | c0003 | t0002 | g0109 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02293 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0107 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PEL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02451 | hp2 | a0001 | c0005 | t0005 | g0076 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02572 | hp1 | a0002 | c0004 | t0001 | g0029 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02572 | hp2 | a0001 | c0003 | t0002 | g0099 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02602 | hp2 | a0001 | c0001 | t0007 | g0053 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0181 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02647 | hp1 | a0001 | c0006 | t0004 | g0153 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02698 | hp1 | a0001 | c0007 | t0001 | g0065 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02698 | hp2 | a0001 | c0003 | t0002 | g0015 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02717 | hp1 | a0001 | c0005 | t0005 | g0080 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02723 | hp2 | a0001 | c0001 | t0027 | g0236 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02809 | hp1 | a0001 | c0001 | t0029 | g0124 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02886 | hp1 | a0001 | c0006 | t0004 | g0152 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02886 | hp2 | a0002 | c0030 | t0030 | g0155 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0131 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02922 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02965 | hp1 | a0002 | c0004 | t0001 | g0321 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02965 | hp2 | a0002 | c0015 | t0008 | g0082 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0073 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02976 | hp1 | a0002 | c0004 | t0006 | g0014 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02976 | hp2 | a0001 | c0001 | t0020 | g0006 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0223 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03041 | hp1 | a0001 | c0005 | t0005 | g0079 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03041 | hp2 | a0009 | c0022 | t0001 | g0326 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03130 | hp2 | a0002 | c0014 | t0010 | g0018 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0333 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0103 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03209 | hp2 | a0001 | c0003 | t0004 | g0158 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03239 | hp1 | a0001 | c0013 | t0009 | g0335 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0119 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03453 | hp2 | a0001 | c0001 | t0028 | g0091 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03516 | hp2 | a0002 | c0004 | t0001 | g0029 | AFR | ESN | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03540 | hp2 | a0001 | c0005 | t0005 | g0077 | AFR | GWD | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0196 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03669 | hp2 | a0010 | c0024 | t0002 | g0167 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0284 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0195 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0281 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03927 | hp2 | a0001 | c0001 | t0014 | g0296 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04115 | hp1 | a0011 | c0028 | t0001 | g0128 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04184 | hp2 | a0001 | c0007 | t0001 | g0149 | SAS | BEB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0339 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04204 | hp2 | a0001 | c0003 | t0002 | g0161 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0015 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0293 | AFR | YRI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18612 | hp1 | a0012 | c0017 | t0001 | g0276 | EAS | CHB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18906 | hp1 | a0001 | c0005 | t0005 | g0075 | AFR | YRI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18906 | hp2 | a0002 | c0004 | t0001 | g0322 | AFR | YRI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18942 | hp1 | a0013 | c0021 | t0004 | g0238 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0338 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18946 | hp1 | a0003 | c0009 | t0001 | g0116 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18948 | hp2 | a0002 | c0004 | t0001 | g0064 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18959 | hp1 | a0003 | c0009 | t0001 | g0210 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18961 | hp1 | a0001 | c0012 | t0004 | g0008 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18964 | hp2 | a0001 | c0001 | t0026 | g0166 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0340 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18970 | hp2 | a0003 | c0009 | t0001 | g0023 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18975 | hp1 | a0003 | c0009 | t0001 | g0023 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18983 | hp1 | a0001 | c0001 | t0011 | g0130 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18984 | hp2 | a0002 | c0027 | t0002 | g0141 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19000 | hp1 | a0001 | c0008 | t0001 | g0194 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19000 | hp2 | a0001 | c0001 | t0012 | g0034 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19005 | hp1 | a0014 | c0020 | t0001 | g0138 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19009 | hp2 | a0001 | c0011 | t0013 | g0033 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19030 | hp1 | a0002 | c0004 | t0006 | g0309 | AFR | LWK | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | LWK | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0102 | AFR | LWK | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19043 | hp2 | a0001 | c0006 | t0001 | g0087 | AFR | LWK | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19060 | hp2 | a0001 | c0010 | t0001 | g0001 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19070 | hp1 | a0001 | c0008 | t0004 | g0228 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19085 | hp1 | a0001 | c0008 | t0004 | g0008 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19240 | hp1 | a0001 | c0029 | t0010 | g0189 | AFR | YRI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0205 | EUR | TSI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0204 | EUR | TSI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0257 | SAS | GIH | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | GIH | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG01123 | hp2 | a0006 | c0018 | t0009 | g0260 | AMR | CLM | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02109 | hp1 | a0001 | c0016 | t0001 | g0188 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02559 | hp1 | a0002 | c0002 | t0017 | g0117 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG03471 | hp2 | a0002 | c0002 | t0021 | g0074 | AFR | MSL | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG06807 | hp1 | a0001 | c0006 | t0001 | g0088 | AFR | USA | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
HG06807 | hp2 | a0001 | c0001 | t0024 | g0006 | AFR | USA | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20300 | hp1 | a0001 | c0031 | t0008 | g0081 | AFR | USA | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA20300 | hp2 | a0001 | c0005 | t0005 | g0083 | AFR | USA | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | LWK | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
NA21309 | hp2 | a0001 | c0001 | t0025 | g0300 | AFR | LWK | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0222 | REF | REF | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0275 | REF | REF | GPSM1_chr9_136322539_136364601 | GPSM1 | chr9 | 136322539 | 136364601 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136336950 | C | G | 1 | a0005 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.456C>G | p.Ile152Met | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/14 | 613/3566 | 456/2028 | 152/675 | chr9 | 136336950 | |||
chr9:136337479 | C | T | 1 | a0007 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.617C>T | p.Ala206Val | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/14 | 774/3566 | 617/2028 | 206/675 | chr9 | 136337479 | |||
chr9:136338656 | G | A | 1 | a0003 | 4 | NA18946.hp1 NA18959.hp1 NA18970.hp2 others(1): Show |
missense_variant | MODERATE | c.920G>A | p.Arg307His | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/14 | 1077/3566 | 920/2028 | 307/675 | chr9 | 136338656 | |||
chr9:136340958 | C | T | 2 | a0002 a0010 |
65 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(62): Show |
missense_variant | MODERATE | c.1172C>T | p.Ser391Leu | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/14 | 1329/3566 | 1172/2028 | 391/675 | chr9 | 136340958 | |||
chr9:136348715 | C | T | 1 | a0008 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1226C>T | p.Thr409Met | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/14 | 1383/3566 | 1226/2028 | 409/675 | chr9 | 136348715 | |||
chr9:136348766 | G | A | 1 | a0012 | 1 | NA18612.hp1 | missense_variant&splice_region_variant | MODERATE | c.1277G>A | p.Arg426Gln | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/14 | 1434/3566 | 1277/2028 | 426/675 | chr9 | 136348766 | |||
chr9:136349650 | C | A | 1 | a0006 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.1342C>A | p.Leu448Ile | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/14 | 1499/3566 | 1342/2028 | 448/675 | chr9 | 136349650 | |||
chr9:136356351 | C | T | 1 | a0009 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1622C>T | p.Ser541Leu | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/14 | 1779/3566 | 1622/2028 | 541/675 | chr9 | 136356351 | |||
chr9:136356429 | G | A | 1 | a0011 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1700G>A | p.Arg567Gln | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/14 | 1857/3566 | 1700/2028 | 567/675 | chr9 | 136356429 | |||
chr9:136356503 | C | A | 1 | a0004 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1774C>A | p.Pro592Thr | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/14 | 1931/3566 | 1774/2028 | 592/675 | chr9 | 136356503 | |||
chr9:136356508 | G | C | 1 | a0010 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1779G>C | p.Gln593His | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/14 | 1936/3566 | 1779/2028 | 593/675 | chr9 | 136356508 | |||
chr9:136356540 | TCAAGTAC others(15): Show |
T | 1 | a0013 | 1 | NA18942.hp1 | splice_donor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1813_1821+13delAAG others(19): Show |
p.Lys605_Gln607del | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/14 | 1970/3566 | 1813/2028 | 605/675 | INFO_REALIGN_3_PRIME | chr9 | 136356540 | ||
chr9:136358057 | T | C | 1 | a0014 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1865T>C | p.Leu622Pro | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 2022/3566 | 1865/2028 | 622/675 | chr9 | 136358057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136327716 | C | T | 3 | a0001c0005 a0001c0031 a0002c0015 |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
synonymous_variant | LOW | c.21C>T | p.Pro7Pro | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/14 | 178/3566 | 21/2028 | 7/675 | chr9 | 136327716 | |||
chr9:136327734 | G | A | 1 | a0001c0008 | 4 | HG02129.hp2 NA19000.hp1 NA19070.hp1 others(1): Show |
synonymous_variant | LOW | c.39G>A | p.Pro13Pro | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/14 | 196/3566 | 39/2028 | 13/675 | chr9 | 136327734 | |||
chr9:136334474 | G | A | 1 | a0001c0016 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.96G>A | p.Ala32Ala | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/14 | 253/3566 | 96/2028 | 32/675 | chr9 | 136334474 | |||
chr9:136334501 | G | A | 1 | a0001c0010 | 2 | HG00408.hp1 NA19060.hp2 |
synonymous_variant | LOW | c.123G>A | p.Ala41Ala | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/14 | 280/3566 | 123/2028 | 41/675 | chr9 | 136334501 | |||
chr9:136334612 | C | T | 3 | a0001c0029 a0002c0014 a0002c0030 |
4 | HG02257.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.234C>T | p.Tyr78Tyr | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/14 | 391/3566 | 234/2028 | 78/675 | chr9 | 136334612 | |||
chr9:136334624 | C | T | 1 | a0011c0028 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.246C>T | p.His82His | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/14 | 403/3566 | 246/2028 | 82/675 | chr9 | 136334624 | |||
chr9:136336950 | C | T | 1 | a0002c0027 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.456C>T | p.Ile152Ile | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/14 | 613/3566 | 456/2028 | 152/675 | chr9 | 136336950 | |||
chr9:136337471 | C | A | 1 | a0001c0006 | 7 | HG01243.hp2 HG02145.hp2 HG02647.hp1 others(4): Show |
synonymous_variant | LOW | c.609C>A | p.Gly203Gly | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/14 | 766/3566 | 609/2028 | 203/675 | chr9 | 136337471 | |||
chr9:136355734 | C | T | 1 | a0001c0013 | 2 | HG02273.hp2 HG03239.hp1 |
synonymous_variant | LOW | c.1500C>T | p.Asp500Asp | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/14 | 1657/3566 | 1500/2028 | 500/675 | chr9 | 136355734 | |||
chr9:136356352 | G | A | 1 | a0001c0011 | 2 | HG02015.hp1 NA19009.hp2 |
synonymous_variant | LOW | c.1623G>A | p.Ser541Ser | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/14 | 1780/3566 | 1623/2028 | 541/675 | chr9 | 136356352 | |||
chr9:136358043 | G | A | 22 | a0001c0001 a0001c0005 a0001c0006 others(19): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
synonymous_variant | LOW | c.1851G>A | p.Pro617Pro | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 2008/3566 | 1851/2028 | 617/675 | chr9 | 136358043 | |||
chr9:136358151 | C | T | 1 | a0001c0007 | 5 | HG00280.hp1 HG01175.hp1 HG01993.hp2 others(2): Show |
synonymous_variant | LOW | c.1959C>T | p.Ala653Ala | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 2116/3566 | 1959/2028 | 653/675 | chr9 | 136358151 | |||
chr9:136358214 | G | A | 1 | a0001c0012 | 2 | HG00597.hp1 NA18961.hp1 |
synonymous_variant | LOW | c.2022G>A | p.Ala674Ala | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 2179/3566 | 2022/2028 | 674/675 | chr9 | 136358214 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136327558 | G | A | 1 | a0001c0001t0014 | 1 | HG03927.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/14 | 138 | chr9 | 136327558 | ||||||
chr9:136327606 | CGGACAGC others(5): Show |
C | 3 | a0001c0029t0010 a0002c0014t0010 a0002c0030t0030 |
4 | HG02257.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-78_-67delAGGACAGC others(4): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/14 | 67 | INFO_REALIGN_3_PRIME | chr9 | 136327606 | |||||
chr9:136327640 | G | A | 3 | a0001c0005t0005 a0001c0031t0008 a0002c0015t0008 |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-56G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/14 | 56 | chr9 | 136327640 | ||||||
chr9:136327645 | C | G | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/14 | 51 | chr9 | 136327645 | ||||||
chr9:136327661 | G | C | 1 | a0001c0001t0015 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/14 | 35 | chr9 | 136327661 | ||||||
chr9:136358268 | C | T | 3 | a0001c0001t0015 a0001c0001t0027 a0001c0001t0028 |
3 | HG02258.hp2 HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*48C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 48 | chr9 | 136358268 | ||||||
chr9:136358297 | G | C | 2 | a0001c0013t0009 a0006c0018t0009 |
3 | HG01123.hp2 HG02273.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*77G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 77 | chr9 | 136358297 | ||||||
chr9:136358308 | C | T | 1 | a0001c0001t0026 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 88 | chr9 | 136358308 | ||||||
chr9:136358338 | G | A | 1 | a0001c0001t0016 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*118G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 118 | chr9 | 136358338 | ||||||
chr9:136358379 | C | T | 1 | a0001c0001t0025 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 159 | chr9 | 136358379 | ||||||
chr9:136358384 | T | C | 1 | a0002c0002t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 164 | chr9 | 136358384 | ||||||
chr9:136358426 | C | G | 7 | a0001c0001t0004 a0001c0001t0026 a0001c0003t0004 others(4): Show |
33 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 206 | chr9 | 136358426 | ||||||
chr9:136358427 | A | G | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(24): Show |
152 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*207A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 207 | chr9 | 136358427 | ||||||
chr9:136358471 | G | A | 1 | a0001c0001t0011 | 2 | HG00673.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*251G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 251 | chr9 | 136358471 | ||||||
chr9:136358507 | G | A | 2 | a0001c0013t0009 a0006c0018t0009 |
3 | HG01123.hp2 HG02273.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*287G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 287 | chr9 | 136358507 | ||||||
chr9:136358602 | G | A | 1 | a0002c0002t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 382 | chr9 | 136358602 | ||||||
chr9:136358616 | C | T | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0026 others(7): Show |
66 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*396C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 396 | chr9 | 136358616 | ||||||
chr9:136358731 | C | T | 1 | a0001c0011t0013 | 2 | HG02015.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*511C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 511 | chr9 | 136358731 | ||||||
chr9:136358862 | G | A | 1 | a0001c0001t0007 | 4 | HG02602.hp2 HG03239.hp2 HG03831.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*642G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 642 | chr9 | 136358862 | ||||||
chr9:136359101 | C | T | 2 | a0001c0001t0020 a0001c0001t0024 |
2 | HG02976.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*881C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 881 | chr9 | 136359101 | ||||||
chr9:136359274 | A | T | 1 | a0001c0006t0023 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 1054 | chr9 | 136359274 | ||||||
chr9:136359291 | C | G | 1 | a0001c0003t0019 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1071C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 1071 | chr9 | 136359291 | ||||||
chr9:136359385 | G | A | 1 | a0001c0001t0018 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 1165 | chr9 | 136359385 | ||||||
chr9:136359387 | T | C | 32 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(29): Show |
163 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1167T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 1167 | chr9 | 136359387 | ||||||
chr9:136359463 | C | T | 1 | a0002c0002t0022 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1243C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 14/14 | 1243 | chr9 | 136359463 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:136327770 | C | CGGGCCG | 3 | a0001c0006t0001g0073 a0001c0006t0023g0072 a0002c0002t0021g0074 |
3 | HG01243.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68+30_68+35dupCGGG others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136327770 | ||||||
chr9:136327770 | CGGGCCG | C | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
50 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.68+30_68+35delCGGG others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136327770 | ||||||
chr9:136327776 | G | A | 14 | a0001c0001t0001g0031 a0001c0001t0001g0324 a0001c0001t0001g0325 others(11): Show |
15 | HG00280.hp1 HG00408.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.68+13G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327776 | |||||||
chr9:136327782 | G | A | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
50 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.68+19G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327782 | |||||||
chr9:136327793 | C | CGGGGCT | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
50 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.68+34_68+39dupGCTG others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136327793 | ||||||
chr9:136327793 | C | T | 21 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0324 others(18): Show |
23 | HG00280.hp1 HG00408.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.68+30C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327793 | |||||||
chr9:136327839 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(15): Show |
24 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.68+76C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327839 | |||||||
chr9:136327934 | G | T | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.68+171G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327934 | |||||||
chr9:136327969 | G | C | 12 | a0001c0005t0005g0075 a0001c0005t0005g0076 a0001c0005t0005g0077 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+206G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327969 | |||||||
chr9:136327974 | G | A | 2 | a0001c0001t0001g0308 a0002c0004t0006g0309 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68+211G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327974 | |||||||
chr9:136327998 | A | C | 2 | a0001c0001t0001g0308 a0002c0004t0006g0309 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68+235A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136327998 | |||||||
chr9:136328144 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.68+381T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328144 | |||||||
chr9:136328145 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.68+382C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328145 | |||||||
chr9:136328167 | G | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0090 others(64): Show |
77 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.68+404G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328167 | |||||||
chr9:136328246 | G | A | 1 | a0001c0001t0011g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.68+483G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328246 | |||||||
chr9:136328250 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.68+487A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328250 | |||||||
chr9:136328329 | A | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(10): Show |
17 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+566A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328329 | |||||||
chr9:136328336 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.68+573C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328336 | |||||||
chr9:136328364 | G | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0308 a0001c0001t0001g0316 others(12): Show |
19 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.68+601G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328364 | |||||||
chr9:136328403 | A | G | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68+640A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328403 | |||||||
chr9:136328439 | A | C | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.68+676A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328439 | |||||||
chr9:136328442 | C | T | 6 | a0001c0001t0015g0323 a0002c0002t0002g0306 a0002c0004t0001g0029 others(3): Show |
8 | HG00735.hp1 HG01261.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+679C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328442 | |||||||
chr9:136328446 | C | T | 6 | a0001c0001t0015g0323 a0002c0002t0002g0306 a0002c0004t0001g0029 others(3): Show |
8 | HG00735.hp1 HG01261.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+683C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328446 | |||||||
chr9:136328495 | G | T | 1 | a0001c0001t0006g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.68+732G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328495 | |||||||
chr9:136328497 | C | T | 5 | a0001c0001t0015g0323 a0002c0004t0001g0029 a0002c0004t0001g0030 others(2): Show |
7 | HG01261.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+734C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328497 | |||||||
chr9:136328501 | G | C | 1 | a0002c0002t0002g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.68+738G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328501 | |||||||
chr9:136328576 | C | T | 1 | a0001c0001t0015g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.68+813C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328576 | |||||||
chr9:136328682 | C | T | 2 | a0001c0001t0001g0308 a0002c0004t0006g0309 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68+919C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328682 | |||||||
chr9:136328683 | G | A | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.68+920G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328683 | |||||||
chr9:136328918 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.68+1155C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328918 | |||||||
chr9:136328934 | G | A | 1 | a0002c0002t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.68+1171G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136328934 | |||||||
chr9:136328974 | AGTGTGTG others(17): Show |
A | 6 | a0001c0001t0001g0132 a0001c0001t0015g0323 a0002c0004t0001g0029 others(3): Show |
8 | HG01261.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+1232_68+1255del others(24): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136328974 | ||||||
chr9:136329049 | G | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0092 others(45): Show |
54 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.68+1286G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329049 | |||||||
chr9:136329066 | T | C | 154 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(151): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.68+1303T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329066 | |||||||
chr9:136329126 | G | A | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(103): Show |
120 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.68+1363G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329126 | |||||||
chr9:136329160 | G | A | 93 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.68+1397G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329160 | |||||||
chr9:136329260 | G | A | 1 | a0014c0020t0001g0138 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.68+1497G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329260 | |||||||
chr9:136329288 | C | G | 81 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
93 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.68+1525C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329288 | |||||||
chr9:136329292 | GT | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(10): Show |
17 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+1530delT | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329292 | |||||||
chr9:136329299 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(10): Show |
17 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+1536C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329299 | |||||||
chr9:136329317 | C | A | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.68+1554C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329317 | |||||||
chr9:136329333 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68+1570G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329333 | |||||||
chr9:136329411 | C | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0092 others(42): Show |
51 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.68+1648C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329411 | |||||||
chr9:136329542 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0092 others(48): Show |
57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.68+1779C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329542 | |||||||
chr9:136329562 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.68+1799C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329562 | |||||||
chr9:136329649 | A | G | 1 | a0002c0002t0002g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.68+1886A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329649 | |||||||
chr9:136329819 | TCTGGGTC others(51): Show |
T | 1 | a0001c0007t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.68+2134_68+2191del others(58): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136329819 | ||||||
chr9:136329825 | T | G | 1 | a0001c0001t0015g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.68+2062T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329825 | |||||||
chr9:136329839 | GCCCTGGG others(22): Show |
G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0192 |
4 | HG00597.hp2 HG00609.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+2105_68+2133del others(29): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136329839 | ||||||
chr9:136329868 | CCCCTGGG others(22): Show |
C | 1 | a0002c0002t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.68+2134_68+2162del others(29): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136329868 | ||||||
chr9:136329922 | C | T | 13 | a0001c0003t0019g0129 a0001c0005t0005g0075 a0001c0005t0005g0076 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.68+2159C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329922 | |||||||
chr9:136329986 | C | T | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(57): Show |
68 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.68+2223C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136329986 | |||||||
chr9:136330025 | C | G | 4 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(1): Show |
4 | HG03130.hp1 HG03453.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+2262C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330025 | |||||||
chr9:136330133 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+2370G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330133 | |||||||
chr9:136330216 | G | A | 17 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(14): Show |
23 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.68+2453G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330216 | |||||||
chr9:136330280 | T | C | 153 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(150): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.68+2517T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330280 | |||||||
chr9:136330348 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | NA18947.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.68+2585C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330348 | |||||||
chr9:136330362 | ACCTTCAC others(5): Show |
A | 2 | a0001c0001t0001g0070 a0002c0002t0002g0071 |
2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.68+2605_68+2616del others(12): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136330362 | ||||||
chr9:136330368 | A | G | 2 | a0001c0001t0001g0308 a0002c0004t0006g0309 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68+2605A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330368 | |||||||
chr9:136330428 | G | A | 12 | a0001c0005t0005g0075 a0001c0005t0005g0076 a0001c0005t0005g0077 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+2665G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330428 | |||||||
chr9:136330499 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.68+2736C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330499 | |||||||
chr9:136330683 | G | A | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.68+2920G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330683 | |||||||
chr9:136330755 | G | A | 12 | a0001c0005t0005g0075 a0001c0005t0005g0076 a0001c0005t0005g0077 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+2992G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330755 | |||||||
chr9:136330776 | G | A | 17 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(14): Show |
23 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.68+3013G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330776 | |||||||
chr9:136330788 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.68+3025G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330788 | |||||||
chr9:136330894 | C | T | 127 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.68+3131C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330894 | |||||||
chr9:136330895 | G | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.68+3132G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330895 | |||||||
chr9:136330896 | C | G | 23 | a0001c0001t0001g0009 a0001c0001t0001g0308 a0001c0001t0001g0316 others(20): Show |
29 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+3133C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330896 | |||||||
chr9:136330956 | C | T | 2 | a0001c0001t0014g0296 a0001c0003t0002g0297 |
2 | HG01978.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.68+3193C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136330956 | |||||||
chr9:136331026 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(127): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.68+3263C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331026 | |||||||
chr9:136331067 | C | G | 4 | a0002c0004t0001g0029 a0002c0004t0001g0030 a0002c0004t0001g0321 others(1): Show |
6 | HG01261.hp1 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+3304C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331067 | |||||||
chr9:136331108 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.69-3339G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331108 | |||||||
chr9:136331155 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.69-3292C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331155 | |||||||
chr9:136331156 | G | A | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.69-3291G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331156 | |||||||
chr9:136331269 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0142 |
3 | HG02818.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.69-3178G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331269 | |||||||
chr9:136331291 | C | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(15): Show |
24 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.69-3156C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331291 | |||||||
chr9:136331341 | G | C | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.69-3106G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331341 | |||||||
chr9:136331364 | G | GC | 95 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0019 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.69-3071dupC | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136331364 | ||||||
chr9:136331364 | G | GCC | 29 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0156 others(26): Show |
29 | HG00280.hp2 HG00738.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-3072_69-3071dup others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136331364 | ||||||
chr9:136331364 | G | GCCC | 17 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0001g0143 others(14): Show |
18 | HG00099.hp2 HG00642.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.69-3073_69-3071dup others(3): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136331364 | ||||||
chr9:136331366 | C | T | 20 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(17): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.69-3081C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331366 | |||||||
chr9:136331367 | C | G | 43 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0093 others(40): Show |
49 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.69-3080C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331367 | |||||||
chr9:136331439 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.69-3008C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331439 | |||||||
chr9:136331556 | G | A | 3 | a0001c0006t0001g0087 a0001c0006t0001g0088 a0001c0006t0004g0089 |
3 | HG02145.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.69-2891G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331556 | |||||||
chr9:136331571 | A | T | 1 | a0002c0002t0002g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.69-2876A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331571 | |||||||
chr9:136331581 | C | T | 1 | a0002c0002t0002g0126 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.69-2866C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331581 | |||||||
chr9:136331622 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0093 others(41): Show |
50 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.69-2825G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331622 | |||||||
chr9:136331632 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.69-2815G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331632 | |||||||
chr9:136331652 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.69-2795C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331652 | |||||||
chr9:136331682 | G | C | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.69-2765G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331682 | |||||||
chr9:136331701 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.69-2746C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331701 | |||||||
chr9:136331706 | G | A | 1 | a0001c0008t0004g0228 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.69-2741G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331706 | |||||||
chr9:136331763 | G | T | 1 | a0001c0001t0006g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69-2684G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331763 | |||||||
chr9:136331771 | C | A | 1 | a0001c0001t0001g0229 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.69-2676C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331771 | |||||||
chr9:136331774 | C | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(6): Show |
9 | HG00408.hp2 HG01243.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.69-2673C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331774 | |||||||
chr9:136331784 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.69-2663G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331784 | |||||||
chr9:136331880 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
21 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.69-2567G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331880 | |||||||
chr9:136331902 | C | G | 1 | a0001c0001t0003g0226 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.69-2545C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136331902 | |||||||
chr9:136332010 | C | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-2437C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332010 | |||||||
chr9:136332085 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.69-2362G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332085 | |||||||
chr9:136332097 | C | T | 3 | a0001c0001t0004g0304 a0001c0001t0028g0091 a0002c0002t0002g0306 |
3 | HG00735.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.69-2350C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332097 | |||||||
chr9:136332186 | A | G | 133 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.69-2261A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332186 | |||||||
chr9:136332238 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG00741.hp1 HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.69-2209G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332238 | |||||||
chr9:136332296 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(16): Show |
25 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.69-2151G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332296 | |||||||
chr9:136332335 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18947.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.69-2112C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332335 | |||||||
chr9:136332350 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.69-2097G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332350 | |||||||
chr9:136332352 | C | G | 3 | a0001c0001t0004g0304 a0001c0001t0028g0091 a0002c0002t0002g0306 |
3 | HG00735.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.69-2095C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332352 | |||||||
chr9:136332422 | T | C | 152 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(149): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.69-2025T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332422 | |||||||
chr9:136332450 | C | A | 141 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.69-1997C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332450 | |||||||
chr9:136332479 | G | C | 1 | a0001c0001t0004g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.69-1968G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332479 | |||||||
chr9:136332484 | A | G | 143 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(140): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.69-1963A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332484 | |||||||
chr9:136332612 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.69-1835C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332612 | |||||||
chr9:136332617 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.69-1830G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332617 | |||||||
chr9:136332666 | G | A | 1 | a0002c0004t0006g0309 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.69-1781G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332666 | |||||||
chr9:136332839 | C | CA | 28 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0142 others(25): Show |
28 | HG00408.hp2 HG00423.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.69-1585dupA | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136332839 | ||||||
chr9:136332839 | CA | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0031 others(46): Show |
57 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.69-1585delA | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136332839 | ||||||
chr9:136332839 | CAA | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(61): Show |
70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.69-1586_69-1585del others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136332839 | ||||||
chr9:136332839 | CAAA | C | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG00099.hp1 HG01169.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-1587_69-1585del others(3): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 136332839 | ||||||
chr9:136332884 | C | G | 66 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(63): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.69-1563C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332884 | |||||||
chr9:136332963 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(59): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.69-1484C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332963 | |||||||
chr9:136332975 | C | T | 2 | a0001c0003t0002g0099 a0002c0004t0006g0309 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.69-1472C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136332975 | |||||||
chr9:136333030 | A | G | 2 | a0001c0001t0003g0169 a0001c0001t0003g0179 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.69-1417A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333030 | |||||||
chr9:136333087 | G | A | 16 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(13): Show |
22 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.69-1360G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333087 | |||||||
chr9:136333101 | C | T | 1 | a0002c0015t0008g0086 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69-1346C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333101 | |||||||
chr9:136333104 | G | A | 7 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0227 others(4): Show |
7 | HG01109.hp2 HG01891.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-1343G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333104 | |||||||
chr9:136333218 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0003g0183 |
2 | HG00438.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.69-1229G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333218 | |||||||
chr9:136333258 | C | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(157): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.69-1189C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333258 | |||||||
chr9:136333291 | C | T | 1 | a0001c0001t0012g0288 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.69-1156C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333291 | |||||||
chr9:136333305 | C | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.69-1142C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333305 | |||||||
chr9:136333417 | T | TTGCTGGC others(250): Show |
7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-1030_69-1029ins others(257): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333417 | |||||||
chr9:136333418 | G | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-1029G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333418 | |||||||
chr9:136333423 | C | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-1024C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333423 | |||||||
chr9:136333424 | A | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-1023A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333424 | |||||||
chr9:136333440 | G | A | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
104 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.69-1007G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333440 | |||||||
chr9:136333468 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.69-979C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333468 | |||||||
chr9:136333488 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.69-959G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333488 | |||||||
chr9:136333772 | C | T | 29 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0142 others(26): Show |
30 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.69-675C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333772 | |||||||
chr9:136333776 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.69-671C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333776 | |||||||
chr9:136333863 | G | A | 1 | a0001c0005t0005g0080 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69-584G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136333863 | |||||||
chr9:136334021 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.69-426G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334021 | |||||||
chr9:136334085 | C | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-362C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334085 | |||||||
chr9:136334093 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-354T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334093 | |||||||
chr9:136334109 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.69-338G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334109 | |||||||
chr9:136334200 | G | A | 2 | a0001c0001t0001g0308 a0002c0004t0006g0309 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.69-247G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334200 | |||||||
chr9:136334305 | G | A | 2 | a0002c0002t0002g0017 a0002c0027t0002g0141 |
3 | NA18954.hp2 NA18975.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.69-142G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334305 | |||||||
chr9:136334329 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69-118G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334329 | |||||||
chr9:136334403 | G | A | 2 | a0001c0006t0001g0087 a0001c0006t0001g0088 |
2 | HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.69-44G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 1/13 | chr9 | 136334403 | |||||||
chr9:136334718 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+50G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136334718 | |||||||
chr9:136334733 | GGCCCTGC others(45): Show |
G | 13 | a0001c0005t0005g0075 a0001c0005t0005g0076 a0001c0005t0005g0077 others(10): Show |
13 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.290+89_290+140delC others(51): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 136334733 | ||||||
chr9:136334859 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.290+191G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136334859 | |||||||
chr9:136335007 | G | C | 4 | a0001c0003t0019g0129 a0001c0006t0001g0087 a0001c0006t0001g0088 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+339G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335007 | |||||||
chr9:136335199 | C | T | 1 | a0012c0017t0001g0276 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.290+531C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335199 | |||||||
chr9:136335200 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.290+532G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335200 | |||||||
chr9:136335334 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(342): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.291-632T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335334 | |||||||
chr9:136335353 | G | A | 1 | a0001c0003t0002g0297 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.291-613G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335353 | |||||||
chr9:136335391 | G | A | 1 | a0002c0002t0002g0186 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.291-575G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335391 | |||||||
chr9:136335400 | G | A | 12 | a0001c0005t0005g0075 a0001c0005t0005g0076 a0001c0005t0005g0077 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-566G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335400 | |||||||
chr9:136335435 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.291-531G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335435 | |||||||
chr9:136335535 | A | G | 155 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(152): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.291-431A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335535 | |||||||
chr9:136335610 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
107 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.291-356A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335610 | |||||||
chr9:136335633 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-333G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335633 | |||||||
chr9:136335696 | G | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0090 others(48): Show |
60 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-270G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335696 | |||||||
chr9:136335822 | A | G | 8 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0273 others(5): Show |
8 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-144A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335822 | |||||||
chr9:136335835 | G | T | 4 | a0001c0001t0003g0169 a0001c0001t0003g0179 a0002c0002t0002g0174 others(1): Show |
4 | HG00735.hp2 HG01099.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-131G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335835 | |||||||
chr9:136335898 | A | G | 22 | a0001c0001t0001g0229 a0001c0001t0001g0262 a0001c0001t0001g0285 others(19): Show |
23 | HG00544.hp2 HG00597.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.291-68A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335898 | |||||||
chr9:136335924 | A | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0324 others(4): Show |
7 | HG00408.hp2 HG02015.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-42A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 2/13 | chr9 | 136335924 | |||||||
chr9:136336128 | T | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.426+27T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336128 | |||||||
chr9:136336206 | T | C | 1 | a0002c0004t0006g0014 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.426+105T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336206 | |||||||
chr9:136336227 | C | T | 2 | a0001c0006t0004g0152 a0001c0006t0004g0153 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.426+126C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336227 | |||||||
chr9:136336363 | A | G | 1 | a0006c0018t0009g0260 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.426+262A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336363 | |||||||
chr9:136336413 | A | C | 76 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0022 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.426+312A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336413 | |||||||
chr9:136336437 | G | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0048 others(56): Show |
71 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.426+336G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336437 | |||||||
chr9:136336525 | C | G | 1 | a0001c0001t0001g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.427-396C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336525 | |||||||
chr9:136336603 | A | G | 130 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(127): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.427-318A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336603 | |||||||
chr9:136336697 | C | T | 1 | a0001c0003t0002g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.427-224C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336697 | |||||||
chr9:136336751 | G | A | 1 | a0001c0003t0002g0196 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.427-170G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336751 | |||||||
chr9:136336836 | G | T | 1 | a0002c0004t0001g0030 | 2 | HG01261.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.427-85G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336836 | |||||||
chr9:136336855 | T | C | 6 | a0001c0001t0001g0133 a0001c0001t0001g0324 a0001c0001t0001g0325 others(3): Show |
6 | HG00408.hp2 HG02015.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-66T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 3/13 | chr9 | 136336855 | |||||||
chr9:136337128 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.578+56C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/13 | chr9 | 136337128 | |||||||
chr9:136337273 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.579-168A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/13 | chr9 | 136337273 | |||||||
chr9:136337331 | C | A | 1 | a0001c0001t0001g0011 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.579-110C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/13 | chr9 | 136337331 | |||||||
chr9:136337347 | A | AG | 10 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0308 others(7): Show |
10 | HG00408.hp2 HG02015.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-92dupG | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 136337347 | ||||||
chr9:136337362 | C | T | 1 | a0003c0009t0001g0210 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.579-79C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/13 | chr9 | 136337362 | |||||||
chr9:136337427 | C | T | 31 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0045 others(28): Show |
35 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.579-14C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 4/13 | chr9 | 136337427 | |||||||
chr9:136337571 | C | T | 1 | a0002c0002t0002g0195 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.702+7C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/13 | chr9 | 136337571 | |||||||
chr9:136337576 | A | G | 70 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0090 others(67): Show |
78 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.702+12A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/13 | chr9 | 136337576 | |||||||
chr9:136337592 | G | A | 1 | a0002c0002t0002g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.702+28G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/13 | chr9 | 136337592 | |||||||
chr9:136337723 | T | C | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.703-123T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/13 | chr9 | 136337723 | |||||||
chr9:136337786 | C | T | 2 | a0001c0013t0009g0056 a0001c0013t0009g0335 |
2 | HG02273.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.703-60C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/13 | chr9 | 136337786 | |||||||
chr9:136337810 | C | T | 2 | a0001c0001t0001g0252 a0002c0002t0021g0074 |
2 | HG02080.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703-36C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/13 | chr9 | 136337810 | |||||||
chr9:136337815 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.703-31T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 5/13 | chr9 | 136337815 | |||||||
chr9:136338099 | G | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0294 a0001c0006t0001g0073 others(1): Show |
5 | HG01243.hp2 HG02615.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.818+138G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338099 | |||||||
chr9:136338142 | G | A | 1 | a0001c0013t0009g0335 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.818+181G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338142 | |||||||
chr9:136338206 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.818+245G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338206 | |||||||
chr9:136338236 | G | A | 63 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0016 others(60): Show |
69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.818+275G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338236 | |||||||
chr9:136338330 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.819-225A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338330 | |||||||
chr9:136338343 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0015g0323 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.819-212A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338343 | |||||||
chr9:136338456 | G | A | 7 | a0001c0001t0003g0290 a0001c0003t0002g0220 a0001c0003t0002g0255 others(4): Show |
7 | HG00733.hp1 HG00741.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.819-99G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338456 | |||||||
chr9:136338542 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.819-13C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 6/13 | chr9 | 136338542 | |||||||
chr9:136338732 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.974+22G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338732 | |||||||
chr9:136338776 | G | A | 1 | a0002c0002t0021g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.974+66G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338776 | |||||||
chr9:136338816 | C | G | 1 | a0001c0001t0025g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.974+106C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338816 | |||||||
chr9:136338869 | T | C | 2 | a0001c0001t0001g0308 a0002c0004t0006g0014 |
3 | HG01074.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.974+159T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338869 | |||||||
chr9:136338881 | C | T | 1 | a0001c0008t0001g0194 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.974+171C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338881 | |||||||
chr9:136338935 | G | A | 2 | a0001c0001t0004g0261 a0001c0008t0004g0228 |
2 | NA19067.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.974+225G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338935 | |||||||
chr9:136338957 | C | T | 1 | a0002c0002t0002g0115 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.974+247C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338957 | |||||||
chr9:136338975 | A | T | 6 | a0001c0005t0005g0077 a0001c0005t0005g0078 a0001c0005t0005g0080 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.974+265A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136338975 | |||||||
chr9:136339015 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.974+305C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339015 | |||||||
chr9:136339161 | G | A | 1 | a0001c0001t0007g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.974+451G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339161 | |||||||
chr9:136339195 | T | C | 1 | a0001c0001t0027g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.974+485T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339195 | |||||||
chr9:136339290 | C | A | 3 | a0001c0001t0001g0163 a0005c0026t0001g0258 a0011c0028t0001g0128 |
3 | HG00140.hp2 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.975-417C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339290 | |||||||
chr9:136339295 | C | A | 1 | a0001c0001t0007g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.975-412C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339295 | |||||||
chr9:136339367 | GGCTTGCC others(7): Show |
G | 1 | a0001c0001t0001g0187 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.975-339_975-326del others(14): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339367 | |||||||
chr9:136339418 | G | A | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.975-289G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339418 | |||||||
chr9:136339482 | A | G | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(340): Show |
392 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.975-225A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339482 | |||||||
chr9:136339594 | C | T | 1 | a0001c0001t0004g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.975-113C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339594 | |||||||
chr9:136339673 | G | T | 2 | a0001c0013t0009g0056 a0001c0013t0009g0335 |
2 | HG02273.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.975-34G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 7/13 | chr9 | 136339673 | |||||||
chr9:136339869 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+54G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136339869 | |||||||
chr9:136339905 | T | TGCCTGGG others(47): Show |
13 | a0001c0001t0001g0237 a0001c0001t0001g0295 a0001c0006t0001g0073 others(10): Show |
15 | HG01243.hp2 HG01261.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1083+97_1083+150du others(55): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr9 | 136339905 | ||||||
chr9:136339914 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1083+99C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136339914 | |||||||
chr9:136340003 | A | G | 1 | a0001c0001t0004g0304 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1083+188A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340003 | |||||||
chr9:136340055 | T | G | 85 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(82): Show |
89 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1083+240T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340055 | |||||||
chr9:136340095 | C | G | 10 | a0001c0006t0001g0073 a0001c0006t0023g0072 a0001c0029t0010g0189 others(7): Show |
12 | HG01243.hp2 HG01261.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083+280C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340095 | |||||||
chr9:136340142 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1083+327G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340142 | |||||||
chr9:136340309 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(12): Show |
16 | HG00741.hp1 HG01074.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1083+494C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340309 | |||||||
chr9:136340310 | G | A | 1 | a0002c0002t0021g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1083+495G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340310 | |||||||
chr9:136340374 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0095 others(13): Show |
17 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1084-496C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340374 | |||||||
chr9:136340502 | G | T | 1 | a0001c0001t0004g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1084-368G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340502 | |||||||
chr9:136340503 | T | G | 1 | a0001c0001t0004g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1084-367T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340503 | |||||||
chr9:136340505 | C | T | 1 | a0001c0001t0004g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1084-365C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340505 | |||||||
chr9:136340507 | C | T | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1084-363C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340507 | |||||||
chr9:136340508 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | NA18947.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1084-362G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340508 | |||||||
chr9:136340564 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0004g0039 a0013c0021t0004g0238 |
3 | HG00741.hp1 HG02738.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1084-306C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340564 | |||||||
chr9:136340565 | G | C | 1 | a0009c0022t0001g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1084-305G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340565 | |||||||
chr9:136340569 | G | C | 1 | a0009c0022t0001g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1084-301G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340569 | |||||||
chr9:136340735 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1084-135G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 8/13 | chr9 | 136340735 | |||||||
chr9:136341024 | TC | T | 55 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0156 others(52): Show |
56 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1207+35delC | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136341024 | ||||||
chr9:136341069 | C | A | 82 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0156 others(79): Show |
87 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1207+76C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341069 | |||||||
chr9:136341088 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1207+95C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341088 | |||||||
chr9:136341089 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0092 |
2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1207+96G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341089 | |||||||
chr9:136341102 | G | A | 2 | a0001c0029t0010g0189 a0001c0031t0008g0081 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1207+109G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341102 | |||||||
chr9:136341117 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1207+124C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341117 | |||||||
chr9:136341149 | G | C | 31 | a0001c0001t0001g0123 a0001c0001t0001g0156 a0001c0001t0001g0307 others(28): Show |
33 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1207+156G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341149 | |||||||
chr9:136341171 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1207+178G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341171 | |||||||
chr9:136341207 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1207+214G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341207 | |||||||
chr9:136341329 | G | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0040 others(2): Show |
6 | HG00323.hp2 HG02683.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+336G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341329 | |||||||
chr9:136341348 | C | T | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG00544.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1207+355C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341348 | |||||||
chr9:136341366 | A | AGGGCTGG others(3): Show |
1 | a0001c0001t0001g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1207+395_1207+404d others(12): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136341366 | ||||||
chr9:136341366 | AGGGCT | A | 147 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(144): Show |
160 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1207+400_1207+404d others(7): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136341366 | ||||||
chr9:136341386 | T | C | 1 | a0001c0001t0007g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1207+393T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341386 | |||||||
chr9:136341416 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0142 |
3 | HG02818.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1207+423G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341416 | |||||||
chr9:136341491 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207+498C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341491 | |||||||
chr9:136341787 | C | T | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+794C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341787 | |||||||
chr9:136341861 | G | A | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1207+868G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341861 | |||||||
chr9:136341892 | C | T | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+899C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341892 | |||||||
chr9:136341930 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1207+937C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341930 | |||||||
chr9:136341949 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(79): Show |
104 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1207+956C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136341949 | |||||||
chr9:136342103 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1207+1110G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342103 | |||||||
chr9:136342184 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1207+1191G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342184 | |||||||
chr9:136342210 | C | T | 1 | a0002c0002t0021g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1207+1217C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342210 | |||||||
chr9:136342305 | G | A | 9 | a0002c0002t0017g0117 a0002c0002t0021g0074 a0002c0004t0001g0029 others(6): Show |
12 | HG01074.hp2 HG01261.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207+1312G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342305 | |||||||
chr9:136342311 | C | T | 67 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0156 others(64): Show |
69 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1207+1318C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342311 | |||||||
chr9:136342414 | G | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(12): Show |
15 | HG00741.hp1 HG01884.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1207+1421G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342414 | |||||||
chr9:136342446 | C | G | 7 | a0001c0001t0003g0021 a0001c0001t0003g0159 a0001c0001t0003g0160 others(4): Show |
8 | NA18939.hp1 NA18951.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+1453C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342446 | |||||||
chr9:136342474 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1207+1481G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342474 | |||||||
chr9:136342485 | T | G | 3 | a0001c0005t0005g0075 a0001c0005t0005g0076 a0001c0005t0005g0079 |
3 | HG02451.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1207+1492T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342485 | |||||||
chr9:136342502 | G | GA | 7 | a0002c0004t0001g0029 a0002c0004t0001g0030 a0002c0004t0001g0321 others(4): Show |
10 | HG01074.hp2 HG01261.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1207+1509_1207+151 others(5): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342502 | |||||||
chr9:136342516 | C | T | 1 | a0001c0001t0003g0221 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1207+1523C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342516 | |||||||
chr9:136342561 | C | T | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+1568C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342561 | |||||||
chr9:136342566 | G | A | 3 | a0001c0005t0005g0075 a0001c0005t0005g0076 a0001c0005t0005g0079 |
3 | HG02451.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1207+1573G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342566 | |||||||
chr9:136342602 | G | T | 42 | a0001c0001t0001g0118 a0001c0001t0001g0143 a0001c0001t0001g0163 others(39): Show |
42 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1207+1609G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342602 | |||||||
chr9:136342607 | T | C | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+1614T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342607 | |||||||
chr9:136342646 | G | A | 1 | a0001c0007t0001g0065 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1207+1653G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342646 | |||||||
chr9:136342720 | T | C | 8 | a0002c0002t0017g0117 a0002c0004t0001g0029 a0002c0004t0001g0030 others(5): Show |
11 | HG01074.hp2 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207+1727T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342720 | |||||||
chr9:136342870 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1207+1877G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342870 | |||||||
chr9:136342877 | GGAGGTGG others(20): Show |
G | 39 | a0001c0001t0001g0118 a0001c0001t0001g0235 a0001c0001t0001g0264 others(36): Show |
39 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1207+1886_1207+191 others(31): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136342877 | ||||||
chr9:136342899 | G | T | 1 | a0002c0002t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1207+1906G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136342899 | |||||||
chr9:136343001 | G | A | 1 | a0001c0003t0002g0106 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1207+2008G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343001 | |||||||
chr9:136343204 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1207+2211C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343204 | |||||||
chr9:136343206 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1207+2213T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343206 | |||||||
chr9:136343207 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1207+2214C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343207 | |||||||
chr9:136343384 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1207+2391C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343384 | |||||||
chr9:136343398 | C | A | 1 | a0001c0001t0004g0280 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1207+2405C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343398 | |||||||
chr9:136343398 | C | T | 2 | a0001c0001t0004g0261 a0001c0008t0004g0228 |
2 | NA19067.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1207+2405C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343398 | |||||||
chr9:136343450 | C | T | 61 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(58): Show |
69 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1207+2457C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343450 | |||||||
chr9:136343485 | C | T | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+2492C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343485 | |||||||
chr9:136343561 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1207+2568C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343561 | |||||||
chr9:136343794 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+2801G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343794 | |||||||
chr9:136343802 | T | C | 2 | a0001c0006t0001g0073 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+2809T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343802 | |||||||
chr9:136343820 | C | T | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1207+2827C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343820 | |||||||
chr9:136343825 | G | C | 8 | a0002c0002t0017g0117 a0002c0004t0001g0029 a0002c0004t0001g0030 others(5): Show |
11 | HG01074.hp2 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207+2832G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343825 | |||||||
chr9:136343828 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+2835C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136343828 | |||||||
chr9:136344028 | A | G | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1207+3035A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344028 | |||||||
chr9:136344043 | C | T | 1 | a0001c0003t0002g0312 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1207+3050C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344043 | |||||||
chr9:136344153 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1207+3160T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344153 | |||||||
chr9:136344153 | T | TGCGGACA others(15): Show |
1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1207+3171_1207+319 others(26): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136344153 | ||||||
chr9:136344164 | T | TCGGGGGG others(15): Show |
1 | a0001c0001t0001g0277 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1207+3199_1207+322 others(26): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136344164 | ||||||
chr9:136344164 | TCGGGGGG others(15): Show |
T | 1 | a0001c0001t0001g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1207+3199_1207+322 others(26): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136344164 | ||||||
chr9:136344200 | G | A | 1 | a0001c0003t0002g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1207+3207G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344200 | |||||||
chr9:136344206 | GAGCGGGG others(16): Show |
G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0332 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+3226_1207+324 others(27): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136344206 | ||||||
chr9:136344233 | G | A | 1 | a0002c0002t0002g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1207+3240G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344233 | |||||||
chr9:136344255 | A | G | 148 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(145): Show |
162 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1207+3262A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344255 | |||||||
chr9:136344264 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1207+3271G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344264 | |||||||
chr9:136344266 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1207+3273G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344266 | |||||||
chr9:136344312 | A | G | 8 | a0002c0002t0017g0117 a0002c0004t0001g0029 a0002c0004t0001g0030 others(5): Show |
11 | HG01074.hp2 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207+3319A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344312 | |||||||
chr9:136344332 | C | A | 1 | a0001c0001t0004g0280 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1207+3339C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344332 | |||||||
chr9:136344354 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0294 |
3 | HG02615.hp2 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1207+3361G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344354 | |||||||
chr9:136344372 | G | A | 46 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(43): Show |
54 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1207+3379G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344372 | |||||||
chr9:136344474 | G | C | 7 | a0002c0002t0017g0117 a0002c0004t0001g0029 a0002c0004t0001g0030 others(4): Show |
9 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207+3481G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344474 | |||||||
chr9:136344579 | C | T | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1207+3586C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344579 | |||||||
chr9:136344714 | A | AT | 49 | a0001c0003t0019g0129 a0001c0029t0010g0189 a0001c0031t0008g0081 others(46): Show |
57 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.1207+3722dupT | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136344714 | ||||||
chr9:136344751 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1207+3758C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344751 | |||||||
chr9:136344791 | G | C | 8 | a0002c0002t0017g0117 a0002c0004t0001g0029 a0002c0004t0001g0030 others(5): Show |
11 | HG01074.hp2 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207+3798G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344791 | |||||||
chr9:136344994 | C | T | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1208-3703C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344994 | |||||||
chr9:136344995 | G | A | 8 | a0002c0002t0017g0117 a0002c0004t0001g0029 a0002c0004t0001g0030 others(5): Show |
11 | HG01074.hp2 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1208-3702G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136344995 | |||||||
chr9:136345104 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-3593G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345104 | |||||||
chr9:136345125 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1208-3572A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345125 | |||||||
chr9:136345132 | C | T | 45 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0017 others(42): Show |
53 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1208-3565C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345132 | |||||||
chr9:136345229 | G | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-3468G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345229 | |||||||
chr9:136345271 | G | A | 2 | a0001c0029t0010g0189 a0001c0031t0008g0081 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1208-3426G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345271 | |||||||
chr9:136345285 | C | A | 1 | a0001c0001t0001g0022 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1208-3412C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345285 | |||||||
chr9:136345354 | G | A | 38 | a0001c0001t0001g0118 a0001c0001t0001g0235 a0001c0001t0001g0317 others(35): Show |
38 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1208-3343G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345354 | |||||||
chr9:136345414 | C | G | 118 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0156 others(115): Show |
128 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1208-3283C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345414 | |||||||
chr9:136345448 | G | C | 68 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0156 others(65): Show |
70 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1208-3249G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345448 | |||||||
chr9:136345449 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1208-3248G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345449 | |||||||
chr9:136345467 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0307 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1208-3230C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345467 | |||||||
chr9:136345536 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1208-3161G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345536 | |||||||
chr9:136345551 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1208-3146G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345551 | |||||||
chr9:136345560 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1208-3137T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345560 | |||||||
chr9:136345572 | G | A | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1208-3125G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345572 | |||||||
chr9:136345627 | C | A | 1 | a0006c0018t0009g0260 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1208-3070C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345627 | |||||||
chr9:136345654 | T | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(143): Show |
159 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1208-3043T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345654 | |||||||
chr9:136345666 | C | T | 8 | a0002c0002t0017g0117 a0002c0004t0001g0029 a0002c0004t0001g0030 others(5): Show |
11 | HG01074.hp2 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1208-3031C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345666 | |||||||
chr9:136345721 | T | C | 1 | a0001c0001t0003g0265 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1208-2976T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345721 | |||||||
chr9:136345733 | T | C | 1 | a0001c0001t0003g0202 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1208-2964T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345733 | |||||||
chr9:136345744 | G | A | 1 | a0001c0001t0004g0314 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1208-2953G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345744 | |||||||
chr9:136345829 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1208-2868C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345829 | |||||||
chr9:136345907 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-2790G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345907 | |||||||
chr9:136345944 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
22 | HG00741.hp1 HG01074.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1208-2753C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345944 | |||||||
chr9:136345945 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1208-2752G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345945 | |||||||
chr9:136345982 | C | T | 1 | a0012c0017t0001g0276 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1208-2715C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136345982 | |||||||
chr9:136346001 | G | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
22 | HG00741.hp1 HG01074.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1208-2696G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346001 | |||||||
chr9:136346044 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1208-2653G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346044 | |||||||
chr9:136346177 | T | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0095 others(147): Show |
164 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.1208-2520T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346177 | |||||||
chr9:136346191 | G | A | 1 | a0001c0006t0004g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1208-2506G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346191 | |||||||
chr9:136346279 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1208-2418C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346279 | |||||||
chr9:136346304 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1208-2393G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346304 | |||||||
chr9:136346367 | TC | T | 71 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0156 others(68): Show |
73 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1208-2324delC | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136346367 | ||||||
chr9:136346433 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-2264G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346433 | |||||||
chr9:136346493 | A | G | 1 | a0002c0004t0006g0014 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1208-2204A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346493 | |||||||
chr9:136346518 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1208-2179A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346518 | |||||||
chr9:136346563 | G | A | 1 | a0002c0004t0006g0014 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1208-2134G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346563 | |||||||
chr9:136346577 | G | A | 48 | a0001c0003t0002g0099 a0001c0029t0010g0189 a0001c0031t0008g0081 others(45): Show |
56 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1208-2120G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346577 | |||||||
chr9:136346633 | C | A | 1 | a0001c0001t0004g0279 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1208-2064C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346633 | |||||||
chr9:136346782 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1208-1915G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346782 | |||||||
chr9:136346785 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG00741.hp1 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-1912A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346785 | |||||||
chr9:136346835 | G | A | 1 | a0001c0003t0002g0054 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1208-1862G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346835 | |||||||
chr9:136346899 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1208-1798G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346899 | |||||||
chr9:136346953 | A | G | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1208-1744A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136346953 | |||||||
chr9:136347028 | T | C | 73 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(70): Show |
75 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1208-1669T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347028 | |||||||
chr9:136347142 | G | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(57): Show |
68 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1208-1555G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347142 | |||||||
chr9:136347143 | G | A | 1 | a0001c0001t0027g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1208-1554G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347143 | |||||||
chr9:136347145 | G | A | 1 | a0001c0006t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1208-1552G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347145 | |||||||
chr9:136347154 | G | A | 2 | a0001c0001t0004g0178 a0001c0001t0004g0216 |
2 | NA18954.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1208-1543G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347154 | |||||||
chr9:136347158 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0307 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1208-1539G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347158 | |||||||
chr9:136347375 | C | T | 47 | a0001c0003t0002g0099 a0001c0029t0010g0189 a0001c0031t0008g0081 others(44): Show |
55 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1208-1322C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347375 | |||||||
chr9:136347412 | A | G | 76 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(73): Show |
78 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1208-1285A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347412 | |||||||
chr9:136347431 | T | C | 1 | a0002c0002t0021g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1208-1266T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347431 | |||||||
chr9:136347569 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1208-1128G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347569 | |||||||
chr9:136347572 | C | T | 2 | a0001c0029t0010g0189 a0001c0031t0008g0081 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1208-1125C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347572 | |||||||
chr9:136347575 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0240 |
2 | NA19079.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1208-1122T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347575 | |||||||
chr9:136347578 | G | C | 3 | a0001c0001t0001g0193 a0003c0009t0001g0023 a0003c0009t0001g0210 |
4 | NA18959.hp1 NA18970.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-1119G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347578 | |||||||
chr9:136347619 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0267 |
2 | NA18963.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1208-1078G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347619 | |||||||
chr9:136347622 | T | G | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1208-1075T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347622 | |||||||
chr9:136347667 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1208-1030G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347667 | |||||||
chr9:136347716 | C | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-981C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347716 | |||||||
chr9:136347717 | C | G | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-980C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347717 | |||||||
chr9:136347718 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1208-979G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347718 | |||||||
chr9:136347718 | G | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-979G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347718 | |||||||
chr9:136347719 | G | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-978G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347719 | |||||||
chr9:136347720 | A | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-977A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347720 | |||||||
chr9:136347723 | C | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-974C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347723 | |||||||
chr9:136347724 | C | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-973C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347724 | |||||||
chr9:136347725 | A | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-972A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347725 | |||||||
chr9:136347727 | C | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-970C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347727 | |||||||
chr9:136347728 | C | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-969C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347728 | |||||||
chr9:136347729 | C | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-968C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347729 | |||||||
chr9:136347729 | CA | C | 7 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 others(4): Show |
7 | HG01123.hp2 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208-967delA | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347729 | |||||||
chr9:136347730 | A | T | 1 | a0002c0027t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1208-967A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347730 | |||||||
chr9:136347730 | AT | A | 124 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(121): Show |
135 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1208-961delT | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 136347730 | ||||||
chr9:136347731 | T | G | 7 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 others(4): Show |
7 | HG01123.hp2 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208-966T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347731 | |||||||
chr9:136347773 | C | T | 133 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(130): Show |
144 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1208-924C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347773 | |||||||
chr9:136347815 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1208-882T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347815 | |||||||
chr9:136347885 | G | A | 2 | a0001c0001t0004g0261 a0001c0008t0004g0228 |
2 | NA19067.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1208-812G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347885 | |||||||
chr9:136347996 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0170 others(1): Show |
6 | HG00280.hp2 HG00642.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-701G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136347996 | |||||||
chr9:136348136 | G | A | 1 | a0001c0003t0002g0220 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1208-561G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348136 | |||||||
chr9:136348204 | T | C | 131 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(128): Show |
142 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1208-493T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348204 | |||||||
chr9:136348211 | C | G | 2 | a0002c0002t0002g0333 a0002c0015t0008g0086 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1208-486C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348211 | |||||||
chr9:136348213 | C | A | 10 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(7): Show |
10 | HG01106.hp1 HG02451.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-484C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348213 | |||||||
chr9:136348234 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0070 others(2): Show |
5 | HG02602.hp1 HG02735.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-463G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348234 | |||||||
chr9:136348353 | G | T | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1208-344G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348353 | |||||||
chr9:136348388 | G | C | 3 | a0002c0002t0017g0117 a0002c0004t0006g0014 a0002c0004t0006g0309 |
4 | HG01074.hp2 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-309G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348388 | |||||||
chr9:136348402 | C | T | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1208-295C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348402 | |||||||
chr9:136348574 | G | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0170 others(1): Show |
6 | HG00280.hp2 HG00642.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-123G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348574 | |||||||
chr9:136348603 | G | A | 1 | a0002c0002t0002g0195 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1208-94G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 9/13 | chr9 | 136348603 | |||||||
chr9:136348774 | C | T | 35 | a0001c0001t0001g0118 a0001c0001t0004g0008 a0001c0001t0004g0039 others(32): Show |
35 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.1278+7C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/13 | chr9 | 136348774 | |||||||
chr9:136348882 | A | T | 50 | a0001c0003t0002g0099 a0001c0011t0013g0033 a0001c0011t0013g0035 others(47): Show |
58 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1278+115A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/13 | chr9 | 136348882 | |||||||
chr9:136348895 | G | A | 1 | a0001c0001t0004g0281 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1278+128G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/13 | chr9 | 136348895 | |||||||
chr9:136348952 | G | A | 1 | a0001c0003t0002g0196 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1278+185G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/13 | chr9 | 136348952 | |||||||
chr9:136349036 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1278+269G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/13 | chr9 | 136349036 | |||||||
chr9:136349338 | A | C | 74 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(71): Show |
76 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1279-249A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 10/13 | chr9 | 136349338 | |||||||
chr9:136349924 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1455+161G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136349924 | |||||||
chr9:136349924 | G | T | 37 | a0001c0003t0002g0110 a0001c0029t0010g0189 a0001c0031t0008g0081 others(34): Show |
41 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1455+161G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136349924 | |||||||
chr9:136349987 | G | A | 1 | a0002c0002t0021g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1455+224G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136349987 | |||||||
chr9:136349988 | G | A | 1 | a0001c0003t0002g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1455+225G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136349988 | |||||||
chr9:136349999 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1455+236G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136349999 | |||||||
chr9:136350163 | A | G | 2 | a0001c0003t0019g0129 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1455+400A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350163 | |||||||
chr9:136350171 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1455+408G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350171 | |||||||
chr9:136350186 | G | A | 3 | a0001c0013t0009g0056 a0001c0013t0009g0335 a0002c0002t0002g0306 |
3 | HG00735.hp1 HG02273.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1455+423G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350186 | |||||||
chr9:136350186 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1455+423G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350186 | |||||||
chr9:136350187 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1455+424T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350187 | |||||||
chr9:136350226 | G | A | 2 | a0001c0005t0005g0075 a0001c0005t0005g0079 |
2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1455+463G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350226 | |||||||
chr9:136350244 | G | A | 41 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0156 others(38): Show |
43 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1455+481G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350244 | |||||||
chr9:136350381 | C | T | 1 | a0002c0004t0006g0014 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1455+618C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350381 | |||||||
chr9:136350541 | C | T | 1 | a0003c0009t0001g0210 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1455+778C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350541 | |||||||
chr9:136350571 | A | G | 5 | a0001c0003t0019g0129 a0001c0006t0023g0072 a0002c0002t0017g0117 others(2): Show |
6 | HG01074.hp2 HG01243.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+808A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350571 | |||||||
chr9:136350742 | C | T | 34 | a0001c0001t0001g0133 a0001c0001t0004g0008 a0001c0001t0004g0039 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1455+979C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350742 | |||||||
chr9:136350760 | C | T | 4 | a0001c0001t0003g0165 a0001c0001t0003g0169 a0001c0001t0003g0179 others(1): Show |
4 | HG00738.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1455+997C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350760 | |||||||
chr9:136350810 | G | A | 2 | a0001c0013t0009g0056 a0001c0013t0009g0335 |
2 | HG02273.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1455+1047G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350810 | |||||||
chr9:136350815 | C | T | 4 | a0001c0001t0001g0251 a0001c0001t0004g0292 a0001c0029t0010g0189 others(1): Show |
4 | HG02040.hp2 HG02083.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455+1052C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350815 | |||||||
chr9:136350837 | G | A | 59 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(56): Show |
67 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1455+1074G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350837 | |||||||
chr9:136350852 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1455+1089A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350852 | |||||||
chr9:136350912 | A | G | 138 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(135): Show |
149 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1455+1149A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350912 | |||||||
chr9:136350937 | G | A | 33 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0044 others(30): Show |
33 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1455+1174G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350937 | |||||||
chr9:136350938 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1455+1175C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136350938 | |||||||
chr9:136351008 | C | T | 50 | a0001c0003t0002g0099 a0001c0003t0002g0110 a0001c0029t0010g0189 others(47): Show |
58 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1455+1245C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351008 | |||||||
chr9:136351058 | G | C | 8 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0182 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1455+1295G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351058 | |||||||
chr9:136351073 | A | C | 33 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0044 others(30): Show |
33 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1455+1310A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351073 | |||||||
chr9:136351150 | C | T | 1 | a0002c0002t0021g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1455+1387C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351150 | |||||||
chr9:136351181 | C | T | 1 | a0001c0001t0026g0166 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1455+1418C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351181 | |||||||
chr9:136351188 | C | G | 1 | a0001c0001t0003g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1455+1425C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351188 | |||||||
chr9:136351197 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(264): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1455+1434T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351197 | |||||||
chr9:136351247 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1455+1484C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351247 | |||||||
chr9:136351248 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0213 a0001c0001t0001g0268 others(3): Show |
6 | HG02083.hp2 NA18939.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+1485G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351248 | |||||||
chr9:136351278 | G | A | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1455+1515G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351278 | |||||||
chr9:136351291 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1455+1528C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351291 | |||||||
chr9:136351449 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(206): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1455+1686C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351449 | |||||||
chr9:136351578 | A | G | 3 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 |
3 | HG02258.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1455+1815A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351578 | |||||||
chr9:136351752 | A | G | 3 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 |
3 | HG02258.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1455+1989A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351752 | |||||||
chr9:136351797 | C | T | 1 | a0002c0002t0002g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1455+2034C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351797 | |||||||
chr9:136351798 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1455+2035G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351798 | |||||||
chr9:136351932 | G | A | 39 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(36): Show |
41 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1455+2169G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351932 | |||||||
chr9:136351954 | A | AGTGGCCG others(1): Show |
210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(207): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1455+2196_1455+220 others(12): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136351954 | ||||||
chr9:136351967 | G | C | 1 | a0001c0001t0003g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1455+2204G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136351967 | |||||||
chr9:136352047 | ATACCAAT others(19): Show |
A | 29 | a0001c0001t0001g0121 a0001c0001t0001g0303 a0001c0001t0003g0020 others(26): Show |
31 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1455+2286_1455+231 others(30): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352047 | ||||||
chr9:136352048 | T | C | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1455+2285T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352048 | |||||||
chr9:136352048 | T | TACCAATA others(225): Show |
1 | a0001c0011t0013g0035 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1455+2349_1455+235 others(236): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352048 | ||||||
chr9:136352048 | T | TGAC | 10 | a0001c0001t0001g0120 a0001c0001t0001g0123 a0001c0001t0001g0156 others(7): Show |
10 | HG01106.hp1 HG01256.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1455+2285_1455+228 others(7): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352048 | |||||||
chr9:136352048 | TACCAATA others(22): Show |
T | 1 | a0001c0003t0002g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1455+2321_1455+234 others(33): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352048 | ||||||
chr9:136352064 | T | C | 7 | a0001c0001t0001g0193 a0001c0001t0001g0243 a0001c0005t0005g0075 others(4): Show |
8 | HG02451.hp2 HG03041.hp1 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.1455+2301T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352064 | |||||||
chr9:136352081 | A | AATGCTGC others(22): Show |
1 | a0001c0031t0008g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1455+2320_1455+232 others(33): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352081 | ||||||
chr9:136352081 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1455+2318A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352081 | |||||||
chr9:136352084 | A | ACTGCGCC others(22): Show |
1 | a0002c0002t0002g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1455+2405_1455+243 others(33): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352084 | ||||||
chr9:136352084 | A | G | 3 | a0001c0029t0010g0189 a0001c0031t0008g0081 a0002c0002t0002g0127 |
3 | HG01981.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1455+2321A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352084 | |||||||
chr9:136352086 | T | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(211): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1455+2323T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352086 | |||||||
chr9:136352089 | G | A | 1 | a0002c0002t0002g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1455+2326G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352089 | |||||||
chr9:136352093 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(207): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1455+2330T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352093 | |||||||
chr9:136352110 | A | AATGCTGC others(22): Show |
1 | a0001c0029t0010g0189 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1455+2375_1455+237 others(33): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352110 | ||||||
chr9:136352110 | A | G | 15 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(12): Show |
15 | HG01106.hp1 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1455+2347A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352110 | |||||||
chr9:136352110 | AATGCTGC others(167): Show |
A | 34 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0044 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1455+2376_1455+254 others(4): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352110 | ||||||
chr9:136352110 | AATGCTGC others(196): Show |
A | 2 | a0001c0001t0001g0229 a0001c0006t0023g0072 |
2 | HG01243.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1455+2373_1455+257 others(4): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352110 | ||||||
chr9:136352111 | A | C | 2 | a0001c0001t0015g0323 a0001c0001t0028g0091 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1455+2348A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352111 | |||||||
chr9:136352113 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(260): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1455+2350G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352113 | |||||||
chr9:136352115 | T | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0308 a0001c0003t0002g0109 others(2): Show |
6 | HG02273.hp2 HG02293.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1455+2352T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352115 | |||||||
chr9:136352122 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(212): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1455+2359T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352122 | |||||||
chr9:136352136 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(28): Show |
32 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1455+2373A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352136 | |||||||
chr9:136352139 | A | G | 42 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(39): Show |
44 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1455+2376A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352139 | |||||||
chr9:136352140 | A | C | 3 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 |
3 | HG02258.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1455+2377A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352140 | |||||||
chr9:136352142 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(260): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1455+2379G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352142 | |||||||
chr9:136352151 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(212): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1455+2388T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352151 | |||||||
chr9:136352165 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(206): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1455+2402A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352165 | |||||||
chr9:136352168 | A | G | 42 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(39): Show |
44 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1455+2405A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352168 | |||||||
chr9:136352168 | AATGCTGC others(22): Show |
A | 3 | a0001c0003t0019g0129 a0002c0002t0002g0127 a0002c0002t0002g0272 |
3 | HG01192.hp1 HG01981.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1455+2547_1455+257 others(33): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352168 | ||||||
chr9:136352168 | AATGCTGC others(51): Show |
G | 1 | a0001c0001t0003g0159 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1455+2405_1455+246 others(62): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352168 | |||||||
chr9:136352168 | AATGCTGC others(80): Show |
A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1455+2489_1455+257 others(91): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352168 | ||||||
chr9:136352168 | AATGCTGC others(109): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0137 |
3 | HG01256.hp2 HG01258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1455+2460_1455+257 others(4): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352168 | ||||||
chr9:136352169 | A | C | 3 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 |
3 | HG02258.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1455+2406A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352169 | |||||||
chr9:136352171 | G | A | 46 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(43): Show |
49 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1455+2408G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352171 | |||||||
chr9:136352180 | TTGCTGTT others(25): Show |
T | 3 | a0002c0002t0017g0117 a0002c0004t0006g0014 a0002c0004t0006g0309 |
4 | HG01074.hp2 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455+2420_1455+245 others(36): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352180 | ||||||
chr9:136352197 | G | A | 34 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 others(31): Show |
39 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1455+2434G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352197 | |||||||
chr9:136352198 | A | CTACTGCG others(22): Show |
1 | a0001c0001t0027g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1455+2434_1455+243 others(33): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352198 | |||||||
chr9:136352198 | A | CTACTGCG others(51): Show |
2 | a0001c0001t0015g0323 a0001c0001t0028g0091 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1455+2434_1455+243 others(62): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352198 | |||||||
chr9:136352200 | G | A | 44 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(41): Show |
46 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1455+2437G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352200 | |||||||
chr9:136352226 | G | A | 6 | a0001c0003t0019g0129 a0001c0011t0013g0035 a0002c0002t0017g0117 others(3): Show |
7 | HG01074.hp2 HG02015.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1455+2463G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352226 | |||||||
chr9:136352226 | G | AATACTGC others(254): Show |
1 | a0001c0011t0013g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1455+2462_1455+246 others(265): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352226 | |||||||
chr9:136352229 | G | A | 48 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(45): Show |
51 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1455+2466G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352229 | |||||||
chr9:136352255 | G | A | 5 | a0001c0003t0019g0129 a0001c0011t0013g0035 a0002c0002t0017g0117 others(2): Show |
6 | HG01074.hp2 HG02015.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+2492G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352255 | |||||||
chr9:136352258 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(259): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1455+2495G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352258 | |||||||
chr9:136352263 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1455+2500G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352263 | |||||||
chr9:136352267 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1455+2504T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352267 | |||||||
chr9:136352281 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(207): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1455+2518A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352281 | |||||||
chr9:136352284 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(214): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1455+2521G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352284 | |||||||
chr9:136352287 | G | A | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(295): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1455+2524G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352287 | |||||||
chr9:136352310 | A | G | 2 | a0001c0013t0009g0056 a0001c0013t0009g0335 |
2 | HG02273.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1455+2547A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352310 | |||||||
chr9:136352313 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1455+2550G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352313 | |||||||
chr9:136352314 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(206): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1455+2551A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352314 | |||||||
chr9:136352316 | G | A | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(297): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1455+2553G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352316 | |||||||
chr9:136352330 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(214): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1455+2567G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352330 | |||||||
chr9:136352372 | A | C | 1 | a0001c0001t0001g0301 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1455+2609A>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352372 | |||||||
chr9:136352404 | C | T | 1 | a0002c0004t0001g0322 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1455+2641C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352404 | |||||||
chr9:136352405 | G | A | 2 | a0001c0001t0003g0239 a0001c0001t0007g0284 |
2 | HG03831.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1455+2642G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352405 | |||||||
chr9:136352444 | TG | T | 5 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 others(2): Show |
5 | HG02015.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455+2686delG | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352444 | ||||||
chr9:136352513 | G | A | 1 | a0001c0001t0007g0058 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1455+2750G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352513 | |||||||
chr9:136352565 | G | C | 1 | a0001c0003t0002g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1455+2802G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352565 | |||||||
chr9:136352638 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1455+2875G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352638 | |||||||
chr9:136352678 | C | A | 3 | a0002c0002t0002g0103 a0002c0002t0002g0111 a0002c0015t0008g0082 |
3 | HG02055.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1455+2915C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352678 | |||||||
chr9:136352777 | C | T | 28 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0151 others(25): Show |
30 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1456-2913C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352777 | |||||||
chr9:136352831 | G | A | 3 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 |
3 | HG02258.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1456-2859G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352831 | |||||||
chr9:136352848 | G | T | 3 | a0001c0001t0015g0323 a0001c0001t0027g0236 a0001c0001t0028g0091 |
3 | HG02258.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1456-2842G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352848 | |||||||
chr9:136352911 | G | A | 1 | a0001c0001t0016g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1456-2779G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352911 | |||||||
chr9:136352922 | CGT | C | 33 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0151 others(30): Show |
35 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1456-2760_1456-275 others(6): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352922 | ||||||
chr9:136352922 | CGTGT | C | 4 | a0001c0003t0002g0015 a0001c0003t0002g0099 a0001c0003t0002g0161 others(1): Show |
5 | HG02572.hp2 HG02698.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456-2762_1456-275 others(8): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136352922 | ||||||
chr9:136352949 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0219 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1456-2741G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352949 | |||||||
chr9:136352968 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0157 |
2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1456-2722C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352968 | |||||||
chr9:136352973 | G | A | 4 | a0001c0003t0019g0129 a0002c0002t0017g0117 a0002c0004t0006g0014 others(1): Show |
5 | HG01074.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456-2717G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136352973 | |||||||
chr9:136353037 | G | A | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1456-2653G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353037 | |||||||
chr9:136353121 | G | A | 1 | a0001c0001t0001g0337 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1456-2569G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353121 | |||||||
chr9:136353154 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0070 others(2): Show |
5 | HG02602.hp1 HG02735.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456-2536G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353154 | |||||||
chr9:136353156 | G | A | 1 | a0002c0002t0002g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1456-2534G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353156 | |||||||
chr9:136353156 | G | C | 2 | a0001c0001t0001g0125 a0001c0006t0023g0072 |
2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1456-2534G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353156 | |||||||
chr9:136353293 | A | G | 1 | a0002c0004t0006g0014 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1456-2397A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353293 | |||||||
chr9:136353365 | G | A | 2 | a0001c0029t0010g0189 a0001c0031t0008g0081 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1456-2325G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353365 | |||||||
chr9:136353502 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1456-2188T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353502 | |||||||
chr9:136353503 | T | C | 74 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0151 others(71): Show |
77 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1456-2187T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353503 | |||||||
chr9:136353545 | C | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0240 a0001c0001t0001g0245 others(2): Show |
5 | NA19003.hp2 NA19011.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456-2145C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353545 | |||||||
chr9:136353630 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(296): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1456-2060A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353630 | |||||||
chr9:136353642 | G | A | 1 | a0001c0001t0003g0206 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1456-2048G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353642 | |||||||
chr9:136353723 | C | T | 1 | a0001c0005t0005g0080 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1456-1967C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353723 | |||||||
chr9:136353764 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1456-1926A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353764 | |||||||
chr9:136353773 | G | A | 1 | a0001c0003t0002g0312 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1456-1917G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353773 | |||||||
chr9:136353811 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(344): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1456-1879T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353811 | |||||||
chr9:136353864 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1456-1826A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353864 | |||||||
chr9:136353956 | G | A | 2 | a0002c0002t0002g0136 a0002c0002t0002g0338 |
2 | NA18945.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1456-1734G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353956 | |||||||
chr9:136353973 | C | T | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-1717C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136353973 | |||||||
chr9:136354015 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1456-1675C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354015 | |||||||
chr9:136354052 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1456-1638G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354052 | |||||||
chr9:136354122 | G | A | 4 | a0001c0001t0027g0236 a0002c0002t0017g0117 a0002c0004t0006g0014 others(1): Show |
5 | HG01074.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456-1568G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354122 | |||||||
chr9:136354199 | G | A | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-1491G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354199 | |||||||
chr9:136354342 | G | C | 3 | a0002c0002t0002g0103 a0002c0002t0002g0111 a0002c0015t0008g0082 |
3 | HG02055.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1456-1348G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354342 | |||||||
chr9:136354409 | G | A | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-1281G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354409 | |||||||
chr9:136354445 | G | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(279): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1456-1245G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354445 | |||||||
chr9:136354476 | C | A | 2 | a0001c0029t0010g0189 a0001c0031t0008g0081 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1456-1214C>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354476 | |||||||
chr9:136354476 | C | T | 3 | a0001c0006t0023g0072 a0002c0002t0017g0117 a0002c0004t0006g0309 |
3 | HG01243.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1456-1214C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354476 | |||||||
chr9:136354477 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1456-1213G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354477 | |||||||
chr9:136354571 | C | G | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1456-1119C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354571 | |||||||
chr9:136354581 | C | T | 8 | a0001c0001t0001g0137 a0001c0001t0006g0154 a0001c0001t0006g0173 others(5): Show |
9 | HG01074.hp2 HG01109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1456-1109C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354581 | |||||||
chr9:136354650 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1456-1040T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354650 | |||||||
chr9:136354694 | TG | T | 7 | a0001c0001t0006g0154 a0001c0001t0006g0173 a0001c0001t0006g0181 others(4): Show |
8 | HG01074.hp2 HG01109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1456-990delG | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136354694 | ||||||
chr9:136354726 | T | A | 30 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0151 others(27): Show |
32 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1456-964T>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354726 | |||||||
chr9:136354829 | G | A | 2 | a0001c0029t0010g0189 a0001c0031t0008g0081 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1456-861G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354829 | |||||||
chr9:136354904 | G | A | 1 | a0001c0005t0005g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1456-786G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136354904 | |||||||
chr9:136355008 | C | T | 1 | a0010c0024t0002g0167 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1456-682C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355008 | |||||||
chr9:136355026 | A | AGTGACAC others(202): Show |
1 | a0002c0004t0001g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1456-622_1456-621i others(211): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355026 | ||||||
chr9:136355026 | A | AGTGACAC others(244): Show |
2 | a0001c0001t0015g0323 a0001c0001t0028g0091 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1456-622_1456-621i others(253): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355026 | ||||||
chr9:136355042 | GGAGGGGT others(35): Show |
G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(191): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1456-621_1456-580d others(44): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355042 | ||||||
chr9:136355043 | G | GAGGGGTA others(35): Show |
1 | a0001c0001t0004g0292 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1456-630_1456-629i others(44): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355043 | ||||||
chr9:136355060 | CGAGGGTG others(76): Show |
C | 1 | a0001c0001t0001g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1456-621_1456-539d others(85): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355060 | ||||||
chr9:136355061 | G | A | 41 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0044 others(38): Show |
42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1456-629G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355061 | |||||||
chr9:136355068 | GA | G | 11 | a0001c0001t0001g0302 a0001c0001t0014g0296 a0001c0001t0027g0236 others(8): Show |
12 | HG01261.hp1 HG02723.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1456-621delA | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355068 | |||||||
chr9:136355069 | A | G | 4 | a0001c0001t0004g0292 a0001c0001t0015g0323 a0001c0001t0028g0091 others(1): Show |
4 | HG02083.hp1 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456-621A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355069 | |||||||
chr9:136355076 | A | G | 16 | a0001c0001t0001g0302 a0001c0001t0004g0292 a0001c0001t0014g0296 others(13): Show |
18 | HG01261.hp1 HG02015.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.1456-614A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355076 | |||||||
chr9:136355084 | A | G | 14 | a0001c0001t0001g0302 a0001c0001t0004g0292 a0001c0001t0014g0296 others(11): Show |
16 | HG01261.hp1 HG02083.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1456-606A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355084 | |||||||
chr9:136355095 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1456-595C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355095 | |||||||
chr9:136355102 | CGAGGGTG others(34): Show |
C | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-579_1456-539d others(43): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355102 | ||||||
chr9:136355108 | T | TG | 13 | a0001c0001t0001g0302 a0001c0001t0004g0292 a0001c0001t0014g0296 others(10): Show |
14 | HG01261.hp1 HG02083.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1456-580dupG | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355108 | ||||||
chr9:136355108 | T | TGGGTGAC others(870): Show |
1 | a0002c0030t0030g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1456-580_1456-579i others(879): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355108 | ||||||
chr9:136355126 | T | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(212): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.1456-564T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355126 | |||||||
chr9:136355126 | T | TAGGGGTA others(35): Show |
6 | a0001c0001t0004g0059 a0001c0001t0004g0060 a0001c0001t0004g0223 others(3): Show |
6 | HG02015.hp2 HG02257.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456-548_1456-547i others(44): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355126 | ||||||
chr9:136355126 | T | TAGGGGTA others(77): Show |
20 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0044 others(17): Show |
20 | HG00544.hp2 HG00597.hp1 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.1456-548_1456-547i others(86): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355126 | ||||||
chr9:136355126 | T | TAGGGGTA others(119): Show |
4 | a0001c0001t0004g0261 a0001c0001t0004g0304 a0001c0001t0018g0197 others(1): Show |
4 | HG02135.hp2 HG02258.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1456-548_1456-547i others(128): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355126 | ||||||
chr9:136355126 | TAGGGGTA others(35): Show |
T | 7 | a0001c0003t0019g0129 a0001c0029t0010g0189 a0001c0031t0008g0081 others(4): Show |
8 | HG02257.hp2 HG02280.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1456-547_1456-506d others(44): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355126 | ||||||
chr9:136355126 | TAGGGGTA others(245): Show |
T | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1456-547_1456-296d others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355126 | ||||||
chr9:136355143 | T | C | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(334): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1456-547T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355143 | |||||||
chr9:136355149 | TGGGTGAC others(36): Show |
T | 14 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0159 others(11): Show |
16 | HG02004.hp1 HG02004.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1456-538_1456-496d others(45): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355149 | ||||||
chr9:136355150 | G | GGGTGACA others(285): Show |
1 | a0002c0004t0001g0321 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1456-329_1456-328i others(294): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355150 | ||||||
chr9:136355150 | G | GGGTGACA others(243): Show |
4 | a0001c0006t0001g0073 a0002c0004t0001g0029 a0002c0004t0001g0030 others(1): Show |
5 | HG01261.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456-371_1456-370i others(252): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355150 | ||||||
chr9:136355152 | G | A | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-538G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355152 | |||||||
chr9:136355159 | G | A | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-531G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355159 | |||||||
chr9:136355167 | G | A | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-523G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355167 | |||||||
chr9:136355210 | G | GAGGGGTA others(76): Show |
1 | a0001c0003t0002g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1456-440_1456-439i others(85): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355210 | ||||||
chr9:136355210 | G | T | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-480G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355210 | |||||||
chr9:136355252 | G | C | 1 | a0001c0001t0003g0341 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1456-438G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355252 | |||||||
chr9:136355269 | C | T | 1 | a0002c0002t0002g0259 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1456-421C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355269 | |||||||
chr9:136355276 | G | GGGTGACA others(34): Show |
1 | a0002c0002t0017g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1456-411_1456-371d others(43): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355276 | ||||||
chr9:136355294 | G | GAGGGGTA others(34): Show |
1 | a0001c0001t0027g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1456-371_1456-370i others(43): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355294 | ||||||
chr9:136355297 | G | A | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1456-393G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355297 | |||||||
chr9:136355317 | TG | T | 3 | a0001c0001t0001g0302 a0001c0001t0014g0296 a0009c0022t0001g0326 |
3 | HG03041.hp2 HG03130.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1456-370delG | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355317 | ||||||
chr9:136355336 | G | T | 2 | a0001c0001t0001g0302 a0001c0001t0014g0296 |
2 | HG03130.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1456-354G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355336 | |||||||
chr9:136355359 | TG | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(189): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1456-328delG | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355359 | ||||||
chr9:136355371 | CCTGGGGG others(161): Show |
C | 1 | a0001c0006t0023g0072 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1456-300_1456-133d others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355371 | ||||||
chr9:136355378 | G | GAGGGGTA others(161): Show |
1 | a0001c0001t0027g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1456-164_1456-163i others(170): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355378 | ||||||
chr9:136355378 | G | GAGGGGTA others(34): Show |
5 | a0001c0006t0001g0073 a0002c0004t0001g0029 a0002c0004t0001g0030 others(2): Show |
7 | HG01261.hp1 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1456-287_1456-286i others(43): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355378 | ||||||
chr9:136355378 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(194): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1456-312G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355378 | |||||||
chr9:136355389 | G | A | 2 | a0001c0001t0004g0211 a0001c0001t0004g0263 |
2 | HG00423.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1456-301G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355389 | |||||||
chr9:136355395 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1456-295C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355395 | |||||||
chr9:136355402 | G | GGGTGACA others(34): Show |
1 | a0002c0002t0017g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1456-285_1456-245d others(43): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355402 | ||||||
chr9:136355402 | G | GGGTGACA others(369): Show |
1 | a0001c0001t0006g0154 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1456-152_1456-151i others(378): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355402 | ||||||
chr9:136355402 | G | GGGTGACA others(327): Show |
1 | a0001c0001t0006g0305 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1456-152_1456-151i others(336): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355402 | ||||||
chr9:136355402 | G | GGGTGACA others(327): Show |
4 | a0001c0001t0006g0173 a0001c0001t0006g0181 a0002c0004t0006g0014 others(1): Show |
5 | HG01074.hp2 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456-152_1456-151i others(336): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355402 | ||||||
chr9:136355413 | CCTGGGGG others(119): Show |
C | 2 | a0001c0001t0004g0211 a0001c0001t0004g0263 |
2 | HG00423.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1456-258_1456-133d others(2): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355413 | ||||||
chr9:136355437 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1456-253C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355437 | |||||||
chr9:136355438 | G | GAGGGTGG others(77): Show |
2 | a0001c0001t0004g0178 a0001c0001t0004g0216 |
2 | NA18954.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1456-169_1456-168i others(86): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355438 | ||||||
chr9:136355453 | G | A | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1456-237G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355453 | |||||||
chr9:136355472 | C | T | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1456-218C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355472 | |||||||
chr9:136355489 | T | C | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1456-201T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355489 | |||||||
chr9:136355497 | CCTGGGGG others(35): Show |
C | 18 | a0001c0001t0003g0151 a0001c0001t0003g0165 a0001c0001t0003g0169 others(15): Show |
18 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1456-174_1456-133d others(44): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr9 | 136355497 | ||||||
chr9:136355522 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0020g0006 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1456-168G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355522 | |||||||
chr9:136355539 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(260): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1456-151T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355539 | |||||||
chr9:136355557 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1456-133G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355557 | |||||||
chr9:136355594 | T | C | 33 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0044 others(30): Show |
33 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1456-96T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 11/13 | chr9 | 136355594 | |||||||
chr9:136355862 | A | G | 8 | a0001c0001t0004g0304 a0001c0001t0004g0314 a0001c0001t0004g0315 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1612+16A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136355862 | |||||||
chr9:136355894 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG00741.hp1 HG01884.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1612+48G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136355894 | |||||||
chr9:136355937 | G | C | 1 | a0002c0002t0002g0208 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1612+91G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136355937 | |||||||
chr9:136355984 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1612+138G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136355984 | |||||||
chr9:136355991 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0227 |
2 | HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1612+145G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136355991 | |||||||
chr9:136355996 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1612+150C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136355996 | |||||||
chr9:136356041 | C | T | 1 | a0002c0002t0002g0209 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1612+195C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136356041 | |||||||
chr9:136356102 | TTCTCCTC others(3): Show |
T | 7 | a0001c0003t0002g0054 a0001c0003t0002g0207 a0001c0003t0002g0220 others(4): Show |
7 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613-227_1613-218d others(12): Show |
GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 136356102 | ||||||
chr9:136356130 | C | T | 1 | a0001c0003t0019g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1613-212C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136356130 | |||||||
chr9:136356259 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0243 |
2 | NA19057.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1613-83G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136356259 | |||||||
chr9:136356294 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1613-48G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136356294 | |||||||
chr9:136356325 | C | T | 4 | a0002c0002t0002g0017 a0002c0002t0002g0208 a0002c0002t0002g0209 others(1): Show |
5 | NA18954.hp2 NA18971.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1613-17C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 12/13 | chr9 | 136356325 | |||||||
chr9:136356554 | G | A | 32 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0044 others(29): Show |
32 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.1821+4G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356554 | |||||||
chr9:136356570 | G | A | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1821+20G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356570 | |||||||
chr9:136356578 | C | T | 2 | a0001c0001t0015g0323 a0001c0001t0028g0091 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1821+28C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356578 | |||||||
chr9:136356611 | G | A | 1 | a0002c0002t0002g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1821+61G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356611 | |||||||
chr9:136356682 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1821+132G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356682 | |||||||
chr9:136356738 | C | G | 1 | a0002c0002t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1821+188C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356738 | |||||||
chr9:136356739 | T | G | 1 | a0002c0002t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1821+189T>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356739 | |||||||
chr9:136356880 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0219 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1821+330A>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356880 | |||||||
chr9:136356917 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1821+367C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356917 | |||||||
chr9:136356947 | G | A | 1 | a0001c0001t0003g0290 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1821+397G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356947 | |||||||
chr9:136356951 | G | A | 30 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0151 others(27): Show |
32 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1821+401G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136356951 | |||||||
chr9:136357028 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(195): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1821+478C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357028 | |||||||
chr9:136357029 | G | C | 1 | a0001c0003t0002g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1821+479G>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357029 | |||||||
chr9:136357063 | G | A | 7 | a0001c0001t0001g0308 a0001c0005t0005g0077 a0001c0005t0005g0078 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1821+513G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357063 | |||||||
chr9:136357135 | G | A | 2 | a0001c0001t0027g0236 a0002c0004t0001g0321 |
2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1821+585G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357135 | |||||||
chr9:136357274 | G | T | 1 | a0001c0001t0001g0027 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1821+724G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357274 | |||||||
chr9:136357456 | G | A | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1822-558G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357456 | |||||||
chr9:136357493 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(193): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1822-521T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357493 | |||||||
chr9:136357562 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1822-452C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357562 | |||||||
chr9:136357665 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(189): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1822-349G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357665 | |||||||
chr9:136357677 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1822-337C>G | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357677 | |||||||
chr9:136357696 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(276): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1822-318G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357696 | |||||||
chr9:136357736 | A | T | 1 | a0013c0021t0004g0238 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1822-278A>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357736 | |||||||
chr9:136357801 | G | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0133 others(21): Show |
33 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1822-213G>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357801 | |||||||
chr9:136357830 | C | T | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1822-184C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357830 | |||||||
chr9:136357841 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1822-173C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357841 | |||||||
chr9:136357867 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0150 |
2 | HG02080.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1822-147C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357867 | |||||||
chr9:136357895 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1822-119G>A | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357895 | |||||||
chr9:136357961 | C | T | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0151 others(28): Show |
33 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1822-53C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357961 | |||||||
chr9:136357969 | T | C | 1 | a0001c0005t0005g0083 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1822-45T>C | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357969 | |||||||
chr9:136357989 | C | T | 2 | a0001c0011t0013g0033 a0001c0011t0013g0035 |
2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1822-25C>T | GPSM1 | ENSG00000160360.13 | transcript | ENST00000440944.6 | protein_coding | 13/13 | chr9 | 136357989 |