Item | Value |
---|---|
geneid | 5678 |
ensemblid | ENSG00000183668.18 |
hgncid | 9526 |
symbol | PSG9 |
name | pregnancy specific beta-1-glycoprotein 9 |
refseq_nuc | NM_002784.5 |
refseq_prot | NP_002775.3 |
ensembl_nuc | ENST00000270077.8 |
ensembl_prot | ENSP00000270077.3 |
mane_status | MANE Select |
chr | chr19 |
start | 43253282 |
end | 43269530 |
strand | - |
ver | v1.2 |
region | chr19:43253282-43269530 |
region5000 | chr19:43248282-43274530 |
regionname0 | PSG9_chr19_43253282_43269530 |
regionname5000 | PSG9_chr19_43248282_43274530 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 426 | 140 | 28 | 39 | 44 | 4 | 23 | 29 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0002 | 0/0 | 426 | 21 | 10 | 0 | 10 | 0 | 1 | 6 | PSG9_chr19_43248282_43274530 | PSG9 | MGPFP others(421): Show |
chr19 | 43248282 | 43274530 |
a0003 | 0/0 | 426 | 8 | 0 | 4 | 0 | 3 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0004 | 0/0 | 426 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0005 | 0/0 | 426 | 5 | 0 | 0 | 2 | 0 | 3 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0006 | 0/0 | 426 | 4 | 0 | 1 | 0 | 1 | 2 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0007 | 0/0 | 426 | 4 | 1 | 0 | 0 | 0 | 3 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPFP others(421): Show |
chr19 | 43248282 | 43274530 |
a0008 | 0/0 | 426 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0009 | 0/0 | 426 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0010 | 0/0 | 426 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0011 | 0/0 | 426 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0012 | 0/0 | 426 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0013 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0014 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0015 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0016 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPFP others(421): Show |
chr19 | 43248282 | 43274530 |
a0017 | 0/0 | 126 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(121): Show |
chr19 | 43248282 | 43274530 |
a0018 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPFP others(421): Show |
chr19 | 43248282 | 43274530 |
a0019 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0020 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0021 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPFP others(421): Show |
chr19 | 43248282 | 43274530 |
a0022 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0023 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0024 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
a0025 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | MGPLP others(421): Show |
chr19 | 43248282 | 43274530 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1278 | 134 | 25 | 37 | 44 | 4 | 22 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0001c0012 | 0/0 | 1278 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0001c0013 | 0/0 | 1278 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0001c0014 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0001c0021 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0002c0002 | 0/0 | 1278 | 20 | 9 | 0 | 10 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0002c0029 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0003c0003 | 0/0 | 1278 | 8 | 0 | 4 | 0 | 3 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0004c0005 | 0/0 | 1278 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0005c0004 | 0/0 | 1278 | 5 | 0 | 0 | 2 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0006c0006 | 0/0 | 1278 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0007c0007 | 0/0 | 1278 | 4 | 1 | 0 | 0 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0008c0010 | 0/0 | 1278 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0009c0009 | 0/0 | 1278 | 3 | 0 | 1 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0010c0008 | 0/0 | 1278 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0011c0011 | 0/0 | 1278 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0012c0023 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0013c0025 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0014c0016 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0015c0015 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0016c0030 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0017c0024 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0018c0028 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0019c0020 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0020c0017 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0021c0027 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0022c0018 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0023c0026 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0024c0022 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 | ||
a0025c0019 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ATGGG others(1273): Show |
chr19 | 43248282 | 43274530 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1707 | 80 | 8 | 14 | 42 | 1 | 14 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0001t0002 | 1/0 | 1707 | 45 | 12 | 22 | 2 | 2 | 6 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0001t0003 | 0/0 | 1707 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0001t0004 | 0/0 | 1707 | 3 | 0 | 0 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0001t0005 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0001t0008 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0001t0010 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0012t0001 | 0/0 | 1707 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0013t0001 | 0/0 | 1707 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0014t0006 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0001c0021t0003 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0002c0002t0001 | 0/0 | 1707 | 18 | 7 | 0 | 10 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0002c0002t0009 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0002c0002t0011 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0002c0029t0001 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0003c0003t0001 | 0/0 | 1707 | 4 | 0 | 3 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0003c0003t0002 | 0/0 | 1707 | 4 | 0 | 1 | 0 | 3 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0004c0005t0001 | 0/0 | 1707 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0005c0004t0001 | 0/0 | 1707 | 4 | 0 | 0 | 1 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0005c0004t0002 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0006c0006t0002 | 0/0 | 1707 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0007c0007t0001 | 0/0 | 1707 | 4 | 1 | 0 | 0 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0008c0010t0002 | 0/0 | 1707 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0009c0009t0001 | 0/0 | 1707 | 3 | 0 | 1 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0010c0008t0001 | 0/0 | 1707 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0011c0011t0002 | 0/0 | 1707 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0012c0023t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0013c0025t0001 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0014c0016t0002 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0015c0015t0002 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0016c0030t0001 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0017c0024t0007 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0018c0028t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0019c0020t0002 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0020c0017t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0021c0027t0001 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0022c0018t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0023c0026t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0024c0022t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
a0025c0019t0001 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | ACAGA others(1702): Show |
chr19 | 43248282 | 43274530 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 4 | 10 | 1 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0002 | 0/0 | 11 | 1 | 1 | 7 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0003 | 0/0 | 9 | 1 | 5 | 1 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0004 | 1/0 | 8 | 0 | 4 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0007 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0012t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0013t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0014t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0021t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0029t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0002g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0004c0005t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0005c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0005c0004t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0005c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0006c0006t0002g0009 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0007c0007t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0007c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0007c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0008c0010t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0009c0009t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0009c0009t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0010c0008t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0010c0008t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0011c0011t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0011c0011t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0012c0023t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0013c0025t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0014c0016t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0015c0015t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0016c0030t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0017c0024t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0018c0028t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0019c0020t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0020c0017t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0021c0027t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0022c0018t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0023c0026t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0024c0022t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0025c0019t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0002 | g0034 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00099 | hp2 | a0003 | c0003 | t0002 | g0012 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00140 | hp1 | a0006 | c0006 | t0002 | g0009 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0057 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00280 | hp1 | a0012 | c0023 | t0001 | g0085 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00280 | hp2 | a0011 | c0011 | t0002 | g0044 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00609 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00621 | hp2 | a0004 | c0005 | t0001 | g0008 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00735 | hp2 | a0013 | c0025 | t0001 | g0090 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00738 | hp1 | a0001 | c0012 | t0001 | g0030 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01070 | hp2 | a0006 | c0006 | t0002 | g0009 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01168 | hp1 | a0014 | c0016 | t0002 | g0036 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01168 | hp2 | a0008 | c0010 | t0002 | g0014 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01175 | hp2 | a0011 | c0011 | t0002 | g0043 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01192 | hp1 | a0003 | c0003 | t0002 | g0012 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01192 | hp2 | a0015 | c0015 | t0002 | g0035 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01496 | hp1 | a0001 | c0013 | t0001 | g0026 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01515 | hp2 | a0003 | c0003 | t0002 | g0012 | EUR | IBS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01934 | hp1 | a0008 | c0010 | t0002 | g0014 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ACB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02129 | hp1 | a0005 | c0004 | t0002 | g0041 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02300 | hp1 | a0009 | c0009 | t0001 | g0078 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02572 | hp2 | a0016 | c0030 | t0001 | g0097 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02622 | hp2 | a0017 | c0024 | t0007 | g0040 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02630 | hp1 | a0007 | c0007 | t0001 | g0099 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02683 | hp1 | a0018 | c0028 | t0001 | g0106 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02698 | hp1 | a0001 | c0013 | t0001 | g0026 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02717 | hp1 | a0019 | c0020 | t0002 | g0048 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02723 | hp2 | a0010 | c0008 | t0001 | g0055 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02735 | hp2 | a0020 | c0017 | t0001 | g0071 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02809 | hp2 | a0010 | c0008 | t0001 | g0021 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02818 | hp1 | a0001 | c0012 | t0001 | g0030 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0060 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0079 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03041 | hp1 | a0002 | c0002 | t0011 | g0101 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03195 | hp1 | a0001 | c0021 | t0003 | g0058 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03225 | hp1 | a0010 | c0008 | t0001 | g0021 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03490 | hp2 | a0009 | c0009 | t0001 | g0024 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03491 | hp2 | a0006 | c0006 | t0002 | g0009 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03492 | hp1 | a0009 | c0009 | t0001 | g0024 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03492 | hp2 | a0006 | c0006 | t0002 | g0009 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03710 | hp2 | a0022 | c0018 | t0001 | g0080 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03831 | hp2 | a0005 | c0004 | t0001 | g0025 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03834 | hp1 | a0023 | c0026 | t0001 | g0091 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03927 | hp1 | a0007 | c0007 | t0001 | g0031 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03927 | hp2 | a0007 | c0007 | t0001 | g0100 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03942 | hp1 | a0024 | c0022 | t0001 | g0076 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03942 | hp2 | a0005 | c0004 | t0001 | g0023 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04115 | hp2 | a0007 | c0007 | t0001 | g0031 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04204 | hp2 | a0005 | c0004 | t0001 | g0025 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0062 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18612 | hp1 | a0025 | c0019 | t0001 | g0072 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18747 | hp1 | a0005 | c0004 | t0001 | g0023 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18993 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19043 | hp2 | a0002 | c0002 | t0009 | g0112 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19056 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19090 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | YRI | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA20129 | hp1 | a0001 | c0014 | t0006 | g0046 | AFR | ASW | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ASW | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01123 | hp1 | a0008 | c0010 | t0002 | g0014 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03471 | hp2 | a0021 | c0027 | t0001 | g0098 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | USA | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA21309 | hp2 | a0002 | c0029 | t0001 | g0103 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0084 | REF | REF | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0004 | REF | REF | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43258277 | C | T | 1 | a0008 | 3 | HG01123.hp1 HG01168.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.1168G>A | p.Gly390Arg | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1267/1707 | 1168/1281 | 390/426 | chr19 | 43258277 | |||
chr19:43258288 | C | G | 1 | a0019 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1157G>C | p.Arg386Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1256/1707 | 1157/1281 | 386/426 | chr19 | 43258288 | |||
chr19:43258399 | T | A | 1 | a0010 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.1046A>T | p.Asn349Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1145/1707 | 1046/1281 | 349/426 | chr19 | 43258399 | |||
chr19:43258871 | A | G | 6 | a0005 a0006 a0014 others(3): Show |
13 | HG00140.hp1 HG01070.hp2 HG01168.hp1 others(10): Show |
missense_variant | MODERATE | c.974T>C | p.Ile325Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1073/1707 | 974/1281 | 325/426 | chr19 | 43258871 | |||
chr19:43258881 | T | A | 3 | a0006 a0009 a0022 |
8 | HG00140.hp1 HG01070.hp2 HG02300.hp1 others(5): Show |
missense_variant | MODERATE | c.964A>T | p.Asn322Tyr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1063/1707 | 964/1281 | 322/426 | chr19 | 43258881 | |||
chr19:43258881 | T | C | 2 | a0018 a0020 |
2 | HG02683.hp1 HG02735.hp2 |
missense_variant | MODERATE | c.964A>G | p.Asn322Asp | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1063/1707 | 964/1281 | 322/426 | chr19 | 43258881 | |||
chr19:43258883 | C | G | 1 | a0025 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.962G>C | p.Ser321Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1061/1707 | 962/1281 | 321/426 | chr19 | 43258883 | |||
chr19:43258886 | C | T | 1 | a0020 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.959G>A | p.Arg320His | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1058/1707 | 959/1281 | 320/426 | chr19 | 43258886 | |||
chr19:43258890 | G | T | 7 | a0006 a0009 a0014 others(4): Show |
12 | HG00140.hp1 HG01070.hp2 HG01168.hp1 others(9): Show |
missense_variant | MODERATE | c.955C>A | p.Leu319Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1054/1707 | 955/1281 | 319/426 | chr19 | 43258890 | |||
chr19:43258907 | C | T | 4 | a0003 a0009 a0014 others(1): Show |
13 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(10): Show |
missense_variant | MODERATE | c.938G>A | p.Arg313Gln | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1037/1707 | 938/1281 | 313/426 | chr19 | 43258907 | |||
chr19:43258920 | G | C | 1 | a0024 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.925C>G | p.Gln309Glu | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1024/1707 | 925/1281 | 309/426 | chr19 | 43258920 | |||
chr19:43258992 | C | T | 1 | a0011 | 2 | HG00280.hp2 HG01175.hp2 |
missense_variant | MODERATE | c.853G>A | p.Gly285Arg | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 952/1707 | 853/1281 | 285/426 | chr19 | 43258992 | |||
chr19:43261892 | C | A | 3 | a0007 a0016 a0021 |
6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
missense_variant | MODERATE | c.677G>T | p.Ser226Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 776/1707 | 677/1281 | 226/426 | chr19 | 43261892 | |||
chr19:43261936 | A | C | 1 | a0015 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.633T>G | p.Ile211Met | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 732/1707 | 633/1281 | 211/426 | chr19 | 43261936 | |||
chr19:43261961 | T | C | 1 | a0004 | 5 | HG00609.hp1 HG00621.hp2 NA18993.hp1 others(2): Show |
missense_variant | MODERATE | c.608A>G | p.Tyr203Cys | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 707/1707 | 608/1281 | 203/426 | chr19 | 43261961 | |||
chr19:43262072 | C | T | 1 | a0021 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.497G>A | p.Arg166His | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 596/1707 | 497/1281 | 166/426 | chr19 | 43262072 | |||
chr19:43262120 | T | G | 1 | a0012 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.449A>C | p.Tyr150Ser | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 548/1707 | 449/1281 | 150/426 | chr19 | 43262120 | |||
chr19:43267835 | G | A | 1 | a0017 | 1 | HG02622.hp2 | stop_gained | HIGH | c.379C>T | p.Arg127* | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 478/1707 | 379/1281 | 127/426 | chr19 | 43267835 | |||
chr19:43267874 | G | A | 1 | a0013 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.340C>T | p.Arg114Trp | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 439/1707 | 340/1281 | 114/426 | chr19 | 43267874 | |||
chr19:43268125 | G | A | 1 | a0023 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.89C>T | p.Pro30Leu | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 188/1707 | 89/1281 | 30/426 | chr19 | 43268125 | |||
chr19:43269422 | G | A | 5 | a0002 a0007 a0016 others(2): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
missense_variant | MODERATE | c.10C>T | p.Leu4Phe | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/6 | 109/1707 | 10/1281 | 4/426 | chr19 | 43269422 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43258431 | G | A | 1 | a0001c0021 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1014C>T | p.Tyr338Tyr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1113/1707 | 1014/1281 | 338/426 | chr19 | 43258431 | |||
chr19:43258867 | T | C | 6 | a0005c0004 a0006c0006 a0014c0016 others(3): Show |
13 | HG00140.hp1 HG01070.hp2 HG01168.hp1 others(10): Show |
synonymous_variant | LOW | c.978A>G | p.Leu326Leu | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1077/1707 | 978/1281 | 326/426 | chr19 | 43258867 | |||
chr19:43258918 | T | C | 1 | a0001c0014 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.927A>G | p.Gln309Gln | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1026/1707 | 927/1281 | 309/426 | chr19 | 43258918 | |||
chr19:43258963 | T | G | 3 | a0001c0012 a0002c0029 a0024c0022 |
4 | HG00738.hp1 HG02818.hp1 HG03942.hp1 others(1): Show |
synonymous_variant | LOW | c.882A>C | p.Ile294Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 981/1707 | 882/1281 | 294/426 | chr19 | 43258963 | |||
chr19:43259038 | G | A | 1 | a0001c0013 | 2 | HG01496.hp1 HG02698.hp1 |
synonymous_variant | LOW | c.807C>T | p.Tyr269Tyr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 906/1707 | 807/1281 | 269/426 | chr19 | 43259038 | |||
chr19:43261930 | T | C | 1 | a0010c0008 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.639A>G | p.Gly213Gly | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 738/1707 | 639/1281 | 213/426 | chr19 | 43261930 | |||
chr19:43268118 | G | T | 1 | a0010c0008 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.96C>A | p.Thr32Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 195/1707 | 96/1281 | 32/426 | chr19 | 43268118 | |||
chr19:43268124 | C | T | 1 | a0001c0014 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.90G>A | p.Pro30Pro | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 189/1707 | 90/1281 | 30/426 | chr19 | 43268124 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43253285 | C | T | 1 | a0001c0001t0008 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*324G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 324 | chr19 | 43253285 | ||||||
chr19:43253313 | A | G | 2 | a0002c0002t0009 a0017c0024t0007 |
2 | HG02622.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 296 | chr19 | 43253313 | ||||||
chr19:43253321 | A | G | 1 | a0001c0001t0004 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*288T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 288 | chr19 | 43253321 | ||||||
chr19:43253461 | A | C | 1 | a0001c0014t0006 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*148T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 148 | chr19 | 43253461 | ||||||
chr19:43253508 | T | G | 1 | a0001c0001t0010 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 101 | chr19 | 43253508 | ||||||
chr19:43253516 | T | C | 2 | a0001c0001t0003 a0001c0021t0003 |
4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*93A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 93 | chr19 | 43253516 | ||||||
chr19:43253602 | G | T | 1 | a0001c0001t0005 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 7 | chr19 | 43253602 | ||||||
chr19:43253606 | C | A | 1 | a0002c0002t0011 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 3 | chr19 | 43253606 | ||||||
chr19:43269447 | T | C | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(24): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/6 | 16 | chr19 | 43269447 | ||||||
chr19:43269474 | G | A | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(24): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-43C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/6 | 43 | chr19 | 43269474 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43253877 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1244-231C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253877 | |||||||
chr19:43253943 | T | A | 3 | a0002c0002t0001g0096 a0002c0002t0001g0108 a0002c0029t0001g0103 |
3 | HG02055.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1244-297A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253943 | |||||||
chr19:43253962 | C | T | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1244-316G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253962 | |||||||
chr19:43253963 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1244-317G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253963 | |||||||
chr19:43253965 | T | C | 11 | a0002c0002t0001g0017 a0002c0002t0001g0096 a0002c0002t0001g0102 others(8): Show |
14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244-319A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253965 | |||||||
chr19:43253968 | A | C | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1244-322T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253968 | |||||||
chr19:43254118 | A | G | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1244-472T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254118 | |||||||
chr19:43254213 | C | G | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-567G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254213 | |||||||
chr19:43254215 | C | G | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-569G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254215 | |||||||
chr19:43254216 | A | G | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-570T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254216 | |||||||
chr19:43254224 | T | C | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-578A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254224 | |||||||
chr19:43254259 | G | T | 2 | a0011c0011t0002g0043 a0011c0011t0002g0044 |
2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1244-613C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254259 | |||||||
chr19:43254431 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1244-785T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254431 | |||||||
chr19:43254700 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1244-1054T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254700 | |||||||
chr19:43254799 | G | C | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-1153C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254799 | |||||||
chr19:43254807 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1244-1161T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254807 | |||||||
chr19:43254809 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1244-1163A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254809 | |||||||
chr19:43254932 | TA | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
128 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1244-1287delT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254932 | |||||||
chr19:43254969 | TAGTCCTA others(9): Show |
T | 1 | a0012c0023t0001g0085 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1244-1339_1244-132 others(20): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254969 | |||||||
chr19:43255040 | G | A | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1244-1394C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255040 | |||||||
chr19:43255117 | A | G | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0062 |
3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1244-1471T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255117 | |||||||
chr19:43255117 | AAAAG | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(51): Show |
113 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1244-1475_1244-147 others(8): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255117 | |||||||
chr19:43255230 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(89): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1244-1584C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255230 | |||||||
chr19:43255412 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1244-1766C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255412 | |||||||
chr19:43255476 | T | A | 3 | a0002c0002t0001g0096 a0002c0002t0001g0108 a0002c0029t0001g0103 |
3 | HG02055.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1244-1830A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255476 | |||||||
chr19:43255481 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(51): Show |
113 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1244-1835A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255481 | |||||||
chr19:43255487 | G | T | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1244-1841C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255487 | |||||||
chr19:43255688 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1244-2042A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255688 | |||||||
chr19:43255848 | T | G | 11 | a0002c0002t0001g0017 a0002c0002t0001g0096 a0002c0002t0001g0102 others(8): Show |
14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244-2202A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255848 | |||||||
chr19:43255884 | T | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1244-2238A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255884 | |||||||
chr19:43255903 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
128 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1244-2257G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255903 | |||||||
chr19:43255939 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(86): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1243+2263A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255939 | |||||||
chr19:43256145 | G | T | 1 | a0001c0001t0001g0006 | 8 | NA18949.hp2 NA18983.hp1 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243+2057C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256145 | |||||||
chr19:43256284 | C | A | 1 | a0002c0002t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1243+1918G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256284 | |||||||
chr19:43256367 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1243+1835T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256367 | |||||||
chr19:43256482 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0004g0056 a0001c0001t0004g0057 others(2): Show |
6 | HG00140.hp2 HG00738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243+1720C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256482 | |||||||
chr19:43256492 | A | G | 3 | a0001c0001t0001g0067 a0001c0001t0002g0045 a0001c0001t0002g0047 |
3 | HG02055.hp2 HG04115.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243+1710T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256492 | |||||||
chr19:43256579 | C | T | 2 | a0001c0001t0003g0015 a0001c0021t0003g0058 |
4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243+1623G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256579 | |||||||
chr19:43256608 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1243+1594G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256608 | |||||||
chr19:43256712 | G | T | 5 | a0007c0007t0001g0031 a0007c0007t0001g0099 a0007c0007t0001g0100 others(2): Show |
6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+1490C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256712 | |||||||
chr19:43256811 | A | C | 11 | a0002c0002t0001g0017 a0002c0002t0001g0096 a0002c0002t0001g0102 others(8): Show |
14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1243+1391T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256811 | |||||||
chr19:43256885 | C | G | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0062 |
3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1243+1317G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256885 | |||||||
chr19:43257016 | C | A | 11 | a0002c0002t0001g0017 a0002c0002t0001g0096 a0002c0002t0001g0102 others(8): Show |
14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1243+1186G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257016 | |||||||
chr19:43257047 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0086 |
2 | HG02273.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1243+1155A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257047 | |||||||
chr19:43257244 | G | A | 2 | a0001c0001t0001g0095 a0001c0012t0001g0030 |
3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1243+958C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257244 | |||||||
chr19:43257353 | T | G | 5 | a0007c0007t0001g0031 a0007c0007t0001g0099 a0007c0007t0001g0100 others(2): Show |
6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+849A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257353 | |||||||
chr19:43257440 | C | T | 1 | a0010c0008t0001g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1243+762G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257440 | |||||||
chr19:43257473 | C | T | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0062 |
3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1243+729G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257473 | |||||||
chr19:43257545 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1243+657A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257545 | |||||||
chr19:43257546 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0024c0022t0001g0076 |
3 | HG03490.hp1 HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1243+656C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257546 | |||||||
chr19:43257697 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
115 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1243+505C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257697 | |||||||
chr19:43257782 | TG | T | 11 | a0002c0002t0001g0017 a0002c0002t0001g0096 a0002c0002t0001g0102 others(8): Show |
14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1243+419delC | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257782 | |||||||
chr19:43257790 | A | C | 2 | a0001c0001t0001g0095 a0001c0012t0001g0030 |
3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1243+412T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257790 | |||||||
chr19:43257821 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1243+381G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257821 | |||||||
chr19:43257830 | C | G | 1 | a0001c0001t0002g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1243+372G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257830 | |||||||
chr19:43258164 | A | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0049 a0006c0006t0002g0009 others(1): Show |
13 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1243+38T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43258164 | |||||||
chr19:43258189 | G | T | 1 | a0001c0001t0008g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1243+13C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43258189 | |||||||
chr19:43258534 | T | TGACCCTC others(16): Show |
5 | a0007c0007t0001g0031 a0007c0007t0001g0099 a0007c0007t0001g0100 others(2): Show |
6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.989-101_989-79dupG others(22): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258534 | |||||||
chr19:43258665 | A | G | 1 | a0001c0001t0001g0006 | 8 | NA18949.hp2 NA18983.hp1 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.988+192T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258665 | |||||||
chr19:43258730 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.988+127A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258730 | |||||||
chr19:43258743 | T | G | 1 | a0025c0019t0001g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.988+114A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258743 | |||||||
chr19:43258757 | G | A | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.988+100C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258757 | |||||||
chr19:43258840 | G | T | 19 | a0002c0002t0001g0011 a0002c0002t0001g0017 a0002c0002t0001g0032 others(16): Show |
26 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.988+17C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258840 | |||||||
chr19:43258847 | A | G | 1 | a0014c0016t0002g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.988+10T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258847 | |||||||
chr19:43258855 | A | T | 1 | a0009c0009t0001g0078 | 1 | HG02300.hp1 | splice_donor_variant&intron_variant | HIGH | c.988+2T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258855 | |||||||
chr19:43259171 | G | A | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.710-36C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259171 | |||||||
chr19:43259192 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710-57C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259192 | |||||||
chr19:43259317 | G | T | 1 | a0001c0001t0002g0049 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.710-182C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259317 | |||||||
chr19:43259394 | C | T | 5 | a0007c0007t0001g0031 a0007c0007t0001g0099 a0007c0007t0001g0100 others(2): Show |
6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.710-259G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259394 | |||||||
chr19:43259400 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0008g0039 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.710-265C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259400 | |||||||
chr19:43259411 | C | T | 1 | a0001c0001t0001g0022 | 2 | NA18991.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.710-276G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259411 | |||||||
chr19:43259419 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.710-284G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259419 | |||||||
chr19:43259489 | G | A | 21 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(18): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.710-354C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259489 | |||||||
chr19:43259526 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710-391G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259526 | |||||||
chr19:43259529 | T | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710-394A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259529 | |||||||
chr19:43259581 | T | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0027 others(18): Show |
51 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.710-446A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259581 | |||||||
chr19:43259637 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.710-502T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259637 | |||||||
chr19:43259692 | AGTTC | A | 21 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(18): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.710-561_710-558del others(4): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259692 | |||||||
chr19:43259737 | G | A | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0062 |
3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.710-602C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259737 | |||||||
chr19:43259823 | A | T | 1 | a0001c0001t0004g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.710-688T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259823 | |||||||
chr19:43259837 | G | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710-702C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259837 | |||||||
chr19:43259854 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.710-719G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259854 | |||||||
chr19:43259939 | T | C | 5 | a0007c0007t0001g0031 a0007c0007t0001g0099 a0007c0007t0001g0100 others(2): Show |
6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.710-804A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259939 | |||||||
chr19:43259960 | A | C | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.710-825T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259960 | |||||||
chr19:43260043 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.710-908G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260043 | |||||||
chr19:43260089 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710-954A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260089 | |||||||
chr19:43260114 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.710-979A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260114 | |||||||
chr19:43260142 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.710-1007C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260142 | |||||||
chr19:43260167 | G | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0033 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.710-1032C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260167 | |||||||
chr19:43260349 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(44): Show |
102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.710-1214A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260349 | |||||||
chr19:43260351 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.710-1216A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260351 | |||||||
chr19:43260369 | A | G | 1 | a0002c0002t0001g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.710-1234T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260369 | |||||||
chr19:43260411 | C | G | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.710-1276G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260411 | |||||||
chr19:43260421 | T | C | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.710-1286A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260421 | |||||||
chr19:43260439 | C | T | 21 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(18): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.710-1304G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260439 | |||||||
chr19:43260514 | T | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.709+1346A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260514 | |||||||
chr19:43260593 | G | A | 1 | a0002c0002t0001g0107 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.709+1267C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260593 | |||||||
chr19:43260619 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.709+1241A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260619 | |||||||
chr19:43260725 | C | A | 2 | a0002c0002t0001g0108 a0002c0029t0001g0103 |
2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.709+1135G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260725 | |||||||
chr19:43260742 | G | A | 2 | a0001c0001t0003g0015 a0001c0021t0003g0058 |
4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+1118C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260742 | |||||||
chr19:43260763 | G | T | 1 | a0001c0001t0002g0019 | 2 | HG01175.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.709+1097C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260763 | |||||||
chr19:43260786 | T | C | 5 | a0001c0001t0001g0095 a0001c0001t0004g0056 a0001c0001t0004g0057 others(2): Show |
6 | HG00140.hp2 HG00738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+1074A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260786 | |||||||
chr19:43260863 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.709+997T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260863 | |||||||
chr19:43261099 | G | T | 1 | a0002c0002t0001g0111 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.709+761C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261099 | |||||||
chr19:43261123 | T | G | 21 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(18): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.709+737A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261123 | |||||||
chr19:43261220 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.709+640G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261220 | |||||||
chr19:43261278 | A | AC | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(89): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.709+581dupG | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261278 | |||||||
chr19:43261306 | G | T | 1 | a0007c0007t0001g0031 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.709+554C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261306 | |||||||
chr19:43261327 | G | T | 2 | a0002c0002t0001g0105 a0007c0007t0001g0031 |
3 | HG03927.hp1 HG04115.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.709+533C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261327 | |||||||
chr19:43261461 | G | C | 1 | a0010c0008t0001g0021 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.709+399C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261461 | |||||||
chr19:43261613 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.709+247T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261613 | |||||||
chr19:43261648 | A | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.709+212T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261648 | |||||||
chr19:43261678 | C | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.709+182G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261678 | |||||||
chr19:43261786 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.709+74T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261786 | |||||||
chr19:43261850 | A | G | 1 | a0003c0003t0001g0016 | 3 | HG00741.hp2 HG01081.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.709+10T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261850 | |||||||
chr19:43261851 | G | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0051 |
5 | HG00323.hp1 HG01074.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+9C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261851 | |||||||
chr19:43262231 | A | G | 14 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0033 others(11): Show |
19 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.431-93T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262231 | |||||||
chr19:43262240 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.431-102G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262240 | |||||||
chr19:43262290 | G | A | 2 | a0002c0002t0009g0112 a0017c0024t0007g0040 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.431-152C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262290 | |||||||
chr19:43262373 | G | A | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.431-235C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262373 | |||||||
chr19:43262422 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.431-284G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262422 | |||||||
chr19:43262426 | T | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.431-288A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262426 | |||||||
chr19:43262453 | A | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.431-315T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262453 | |||||||
chr19:43262462 | A | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.431-324T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262462 | |||||||
chr19:43262492 | C | T | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.431-354G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262492 | |||||||
chr19:43262507 | T | G | 21 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(18): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.431-369A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262507 | |||||||
chr19:43262527 | C | A | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-389G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262527 | |||||||
chr19:43262652 | G | T | 1 | a0003c0003t0002g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.431-514C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262652 | |||||||
chr19:43262683 | G | A | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.431-545C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262683 | |||||||
chr19:43262733 | G | A | 21 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(18): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.431-595C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262733 | |||||||
chr19:43262828 | C | T | 1 | a0011c0011t0002g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.431-690G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262828 | |||||||
chr19:43262898 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.431-760G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262898 | |||||||
chr19:43262901 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.431-763A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262901 | |||||||
chr19:43262919 | C | G | 1 | a0002c0002t0001g0032 | 2 | HG02074.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.431-781G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262919 | |||||||
chr19:43263017 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.431-879T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263017 | |||||||
chr19:43263066 | T | C | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.431-928A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263066 | |||||||
chr19:43263316 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431-1178C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263316 | |||||||
chr19:43263429 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0027 |
10 | NA18949.hp2 NA18956.hp2 NA18983.hp1 others(7): Show |
intron_variant | MODIFIER | c.431-1291C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263429 | |||||||
chr19:43263575 | G | A | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.431-1437C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263575 | |||||||
chr19:43263591 | C | CA | 9 | a0001c0001t0002g0013 a0001c0001t0002g0033 a0001c0001t0008g0039 others(6): Show |
12 | HG00280.hp2 HG01123.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-1454dupT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263591 | |||||||
chr19:43263591 | CA | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0059 others(10): Show |
21 | HG00642.hp2 HG00735.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-1454delT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263591 | |||||||
chr19:43263778 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.431-1640C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263778 | |||||||
chr19:43263823 | C | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.431-1685G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263823 | |||||||
chr19:43263960 | T | C | 2 | a0001c0001t0001g0028 a0013c0025t0001g0090 |
3 | HG00735.hp2 HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.431-1822A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263960 | |||||||
chr19:43263973 | G | T | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431-1835C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263973 | |||||||
chr19:43264030 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.431-1892G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264030 | |||||||
chr19:43264166 | T | G | 8 | a0002c0002t0001g0011 a0002c0002t0001g0032 a0002c0002t0001g0104 others(5): Show |
12 | HG00544.hp1 HG02074.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-2028A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264166 | |||||||
chr19:43264178 | C | T | 8 | a0002c0002t0001g0011 a0002c0002t0001g0032 a0002c0002t0001g0104 others(5): Show |
12 | HG00544.hp1 HG02074.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-2040G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264178 | |||||||
chr19:43264220 | T | C | 1 | a0019c0020t0002g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-2082A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264220 | |||||||
chr19:43264473 | T | TC | 2 | a0001c0001t0001g0095 a0001c0012t0001g0030 |
3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.431-2336dupG | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264473 | |||||||
chr19:43264602 | C | T | 2 | a0007c0007t0001g0099 a0021c0027t0001g0098 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.431-2464G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264602 | |||||||
chr19:43264619 | G | A | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-2481C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264619 | |||||||
chr19:43264704 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431-2566C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264704 | |||||||
chr19:43264833 | C | A | 1 | a0019c0020t0002g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-2695G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264833 | |||||||
chr19:43265004 | G | C | 22 | a0001c0001t0001g0054 a0001c0001t0001g0087 a0002c0002t0001g0011 others(19): Show |
29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.430+2780C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265004 | |||||||
chr19:43265094 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.430+2690A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265094 | |||||||
chr19:43265192 | A | G | 2 | a0001c0001t0004g0057 a0001c0001t0004g0062 |
2 | HG00140.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.430+2592T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265192 | |||||||
chr19:43265285 | T | C | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0062 |
3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.430+2499A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265285 | |||||||
chr19:43265291 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.430+2493G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265291 | |||||||
chr19:43265529 | CA | C | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+2254delT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265529 | |||||||
chr19:43265634 | A | C | 4 | a0001c0001t0001g0065 a0001c0001t0004g0056 a0001c0001t0004g0057 others(1): Show |
4 | HG00140.hp2 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2150T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265634 | |||||||
chr19:43265637 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.430+2147G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265637 | |||||||
chr19:43265661 | A | C | 1 | a0001c0001t0004g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.430+2123T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265661 | |||||||
chr19:43265711 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.430+2073A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265711 | |||||||
chr19:43265711 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(44): Show |
102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.430+2073A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265711 | |||||||
chr19:43265721 | G | A | 1 | a0001c0021t0003g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+2063C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265721 | |||||||
chr19:43265749 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.430+2035G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265749 | |||||||
chr19:43265791 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.430+1993A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265791 | |||||||
chr19:43265829 | A | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.430+1955T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265829 | |||||||
chr19:43265862 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.430+1922A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265862 | |||||||
chr19:43265970 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.430+1814C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265970 | |||||||
chr19:43265997 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.430+1787A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265997 | |||||||
chr19:43266005 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.430+1779T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266005 | |||||||
chr19:43266109 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.430+1675C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266109 | |||||||
chr19:43266131 | G | A | 1 | a0001c0001t0004g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.430+1653C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266131 | |||||||
chr19:43266141 | A | T | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+1643T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266141 | |||||||
chr19:43266142 | G | T | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+1642C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266142 | |||||||
chr19:43266167 | C | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(52): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.430+1617G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266167 | |||||||
chr19:43266232 | G | A | 21 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(18): Show |
28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.430+1552C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266232 | |||||||
chr19:43266243 | A | G | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.430+1541T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266243 | |||||||
chr19:43266267 | G | T | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.430+1517C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266267 | |||||||
chr19:43266292 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.430+1492C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266292 | |||||||
chr19:43266343 | G | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1441C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266343 | |||||||
chr19:43266344 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0008g0039 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.430+1440C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266344 | |||||||
chr19:43266354 | G | C | 5 | a0001c0001t0001g0029 a0001c0001t0002g0007 a0001c0001t0002g0049 others(2): Show |
15 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+1430C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266354 | |||||||
chr19:43266357 | A | AC | 5 | a0001c0001t0001g0029 a0001c0001t0002g0007 a0001c0001t0002g0049 others(2): Show |
15 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+1426_430+1427i others(3): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266357 | |||||||
chr19:43266360 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0002g0007 a0001c0001t0002g0049 others(2): Show |
15 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+1424A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266360 | |||||||
chr19:43266385 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.430+1399T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266385 | |||||||
chr19:43266401 | A | C | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1383T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266401 | |||||||
chr19:43266403 | G | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1381C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266403 | |||||||
chr19:43266405 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1379A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266405 | |||||||
chr19:43266413 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1371G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266413 | |||||||
chr19:43266414 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(101): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.430+1370T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266414 | |||||||
chr19:43266439 | G | C | 1 | a0001c0001t0002g0013 | 3 | HG01123.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.430+1345C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266439 | |||||||
chr19:43266446 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.430+1338C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266446 | |||||||
chr19:43266464 | T | C | 2 | a0001c0001t0001g0029 a0002c0002t0001g0109 |
3 | HG02717.hp2 HG02965.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.430+1320A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266464 | |||||||
chr19:43266618 | G | C | 1 | a0010c0008t0001g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.430+1166C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266618 | |||||||
chr19:43266690 | G | A | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+1094C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266690 | |||||||
chr19:43266716 | C | T | 7 | a0001c0001t0001g0095 a0001c0001t0003g0015 a0001c0001t0004g0056 others(4): Show |
10 | HG00140.hp2 HG00738.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+1068G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266716 | |||||||
chr19:43266962 | G | C | 1 | a0002c0002t0001g0110 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.430+822C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266962 | |||||||
chr19:43267122 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.430+662T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267122 | |||||||
chr19:43267130 | A | C | 1 | a0016c0030t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.430+654T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267130 | |||||||
chr19:43267197 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.430+587G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267197 | |||||||
chr19:43267230 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.430+554T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267230 | |||||||
chr19:43267258 | A | G | 2 | a0001c0001t0003g0015 a0001c0021t0003g0058 |
4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+526T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267258 | |||||||
chr19:43267260 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.430+524T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267260 | |||||||
chr19:43267274 | C | T | 1 | a0001c0001t0002g0010 | 4 | HG02723.hp1 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+510G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267274 | |||||||
chr19:43267386 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.430+398C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267386 | |||||||
chr19:43267418 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
101 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.430+366A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267418 | |||||||
chr19:43267422 | TGA | T | 2 | a0001c0001t0003g0015 a0001c0021t0003g0058 |
4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+360_430+361del others(2): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267422 | |||||||
chr19:43267509 | T | G | 1 | a0002c0002t0001g0111 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.430+275A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267509 | |||||||
chr19:43267517 | G | T | 2 | a0001c0001t0001g0095 a0001c0012t0001g0030 |
3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.430+267C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267517 | |||||||
chr19:43267549 | C | T | 1 | a0002c0029t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.430+235G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267549 | |||||||
chr19:43267634 | TGTGTGTG others(26): Show |
T | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430+117_430+149del others(33): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267634 | |||||||
chr19:43268157 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0010g0060 |
2 | HG02886.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.65-8C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268157 | |||||||
chr19:43268211 | G | A | 1 | a0002c0002t0009g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-62C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268211 | |||||||
chr19:43268237 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.65-88G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268237 | |||||||
chr19:43268237 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.65-88G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268237 | |||||||
chr19:43268246 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-97G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268246 | |||||||
chr19:43268263 | C | T | 13 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0033 others(10): Show |
18 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-114G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268263 | |||||||
chr19:43268267 | C | CACAT | 12 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0033 others(9): Show |
17 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-122_65-119dupAT others(2): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268267 | |||||||
chr19:43268321 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.65-172C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268321 | |||||||
chr19:43268332 | C | G | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0062 |
3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.65-183G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268332 | |||||||
chr19:43268484 | A | C | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.65-335T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268484 | |||||||
chr19:43268519 | G | A | 22 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(19): Show |
29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-370C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268519 | |||||||
chr19:43268591 | C | G | 2 | a0001c0001t0002g0042 a0005c0004t0002g0041 |
2 | HG02129.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.65-442G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268591 | |||||||
chr19:43268599 | C | T | 2 | a0001c0001t0002g0042 a0005c0004t0002g0041 |
2 | HG02129.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.65-450G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268599 | |||||||
chr19:43268600 | G | A | 16 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(13): Show |
22 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-451C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268600 | |||||||
chr19:43268636 | C | G | 22 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(19): Show |
29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-487G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268636 | |||||||
chr19:43268724 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.65-575G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268724 | |||||||
chr19:43268780 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+588A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268780 | |||||||
chr19:43268783 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+585A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268783 | |||||||
chr19:43268784 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+584C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268784 | |||||||
chr19:43268865 | G | T | 2 | a0010c0008t0001g0021 a0010c0008t0001g0055 |
3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.64+503C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268865 | |||||||
chr19:43268940 | C | A | 2 | a0001c0001t0002g0010 a0001c0001t0003g0015 |
7 | HG02723.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+428G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268940 | |||||||
chr19:43269026 | A | G | 1 | a0002c0002t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64+342T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269026 | |||||||
chr19:43269056 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64+312C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269056 | |||||||
chr19:43269064 | G | A | 11 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0033 others(8): Show |
16 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.64+304C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269064 | |||||||
chr19:43269067 | G | T | 11 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0033 others(8): Show |
16 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.64+301C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269067 | |||||||
chr19:43269078 | A | C | 22 | a0001c0001t0001g0054 a0002c0002t0001g0011 a0002c0002t0001g0017 others(19): Show |
29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+290T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269078 | |||||||
chr19:43269151 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(44): Show |
102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.64+217A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269151 | |||||||
chr19:43269292 | C | A | 2 | a0001c0001t0001g0095 a0001c0012t0001g0030 |
3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64+76G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269292 |