Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80380 |
| ensemblid | ENSG00000197646.8 |
| hgncid | 18731 |
| symbol | PDCD1LG2 |
| name | programmed cell death 1 ligand 2 |
| refseq_nuc | NM_025239.4 |
| refseq_prot | NP_079515.2 |
| ensembl_nuc | ENST00000397747.5 |
| ensembl_prot | ENSP00000380855.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 5510531 |
| end | 5571282 |
| strand | + |
| ver | v1.2 |
| region | chr9:5510531-5571282 |
| region5000 | chr9:5505531-5576282 |
| regionname0 | PDCD1LG2_chr9_5510531_5571282 |
| regionname5000 | PDCD1LG2_chr9_5505531_5576282 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 273 | 286 | 28 | 56 | 160 | 10 | 31 | 123 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0002 | 0/0 | 273 | 108 | 57 | 10 | 30 | 0 | 11 | 22 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0003 | 0/0 | 273 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0004 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0005 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0006 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0007 | 0/0 | 273 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0008 | 0/0 | 273 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0009 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| a0010 | 0/1 | 273 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | MIFLL others(268): Show |
chr9 | 5505531 | 5576282 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 819 | 286 | 28 | 56 | 160 | 10 | 31 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0002c0002 | 0/0 | 819 | 104 | 53 | 10 | 30 | 0 | 11 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0002c0004 | 0/0 | 819 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0003c0003 | 0/0 | 819 | 5 | 5 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0004c0007 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0005c0006 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0006c0005 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0007c0008 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0008c0011 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0009c0010 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 | ||
| a0010c0009 | 0/1 | 819 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ATGAT others(814): Show |
chr9 | 5505531 | 5576282 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2432 | 162 | 23 | 28 | 86 | 4 | 20 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0002 | 0/0 | 2432 | 69 | 1 | 25 | 31 | 4 | 8 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0003 | 0/0 | 2432 | 23 | 2 | 1 | 16 | 1 | 3 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0004 | 0/0 | 2432 | 18 | 0 | 2 | 16 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0007 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0008 | 0/0 | 2432 | 5 | 0 | 0 | 5 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0010 | 0/0 | 2432 | 4 | 0 | 0 | 4 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0012 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0016 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0017 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0001c0001t0018 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0001 | 0/0 | 2432 | 48 | 22 | 2 | 19 | 0 | 5 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0002 | 0/0 | 2432 | 23 | 8 | 2 | 7 | 0 | 6 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0003 | 0/0 | 2432 | 6 | 1 | 1 | 4 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0005 | 0/0 | 2432 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0006 | 0/0 | 2432 | 6 | 6 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0007 | 0/0 | 2432 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0009 | 0/0 | 2432 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0011 | 0/0 | 2432 | 3 | 2 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0012 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0013 | 0/0 | 2432 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0014 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0015 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0020 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0021 | 0/0 | 2432 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0022 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0002t0023 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0002c0004t0005 | 0/0 | 2432 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0003c0003t0001 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0003c0003t0003 | 0/0 | 2432 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0003c0003t0009 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0004c0007t0003 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0005c0006t0019 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0006c0005t0007 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0007c0008t0001 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0008c0011t0001 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0009c0010t0001 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| a0010c0009t0001 | 0/1 | 2432 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | ACTCT others(2427): Show |
chr9 | 5505531 | 5576282 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0003g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0008g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0016g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0017g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0001c0001t0018g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0003g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0007g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0009g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0009g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0011g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0011g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0012g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0013g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0014g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0020g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0021g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0022g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0002t0023g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0004t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0004t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0002c0004t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0003c0003t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0004c0007t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0005c0006t0019g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0006c0005t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0007c0008t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0008c0011t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0009c0010t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| a0010c0009t0001g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0018 | g0321 | EUR | GBR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0351 | EUR | GBR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00408 | hp2 | a0001 | c0001 | t0010 | g0085 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00423 | hp1 | a0004 | c0007 | t0003 | g0365 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0367 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0361 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | CHS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0384 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0159 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01109 | hp1 | a0002 | c0002 | t0012 | g0330 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01192 | hp1 | a0002 | c0002 | t0011 | g0107 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01243 | hp1 | a0002 | c0002 | t0005 | g0233 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0305 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0319 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0316 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01884 | hp2 | a0002 | c0002 | t0009 | g0332 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01978 | hp1 | a0002 | c0002 | t0021 | g0374 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0371 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02027 | hp2 | a0001 | c0001 | t0010 | g0039 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02055 | hp2 | a0002 | c0002 | t0006 | g0024 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0364 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0379 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0329 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0368 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CDX | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02257 | hp2 | a0002 | c0004 | t0005 | g0228 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0373 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02572 | hp1 | a0002 | c0004 | t0005 | g0230 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02615 | hp1 | a0002 | c0002 | t0014 | g0339 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02615 | hp2 | a0002 | c0002 | t0006 | g0105 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0071 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02630 | hp1 | a0002 | c0002 | t0006 | g0068 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02647 | hp2 | a0003 | c0003 | t0003 | g0248 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0360 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02717 | hp1 | a0005 | c0006 | t0019 | g0104 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0247 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02809 | hp1 | a0002 | c0002 | t0007 | g0001 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02809 | hp2 | a0002 | c0002 | t0006 | g0072 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0341 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0252 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02922 | hp2 | a0006 | c0005 | t0007 | g0117 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0331 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02970 | hp1 | a0003 | c0003 | t0003 | g0250 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02976 | hp1 | a0002 | c0004 | t0005 | g0006 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0231 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03041 | hp1 | a0002 | c0002 | t0020 | g0110 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0267 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03139 | hp1 | a0002 | c0002 | t0011 | g0043 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03139 | hp2 | a0003 | c0003 | t0009 | g0324 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03195 | hp1 | a0002 | c0002 | t0015 | g0145 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03209 | hp1 | a0002 | c0004 | t0005 | g0006 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03209 | hp2 | a0002 | c0002 | t0009 | g0335 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0381 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0347 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0375 | AFR | ESN | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0348 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0333 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0380 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | PJL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0187 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03927 | hp2 | a0007 | c0008 | t0001 | g0245 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04115 | hp2 | a0008 | c0011 | t0001 | g0189 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18522 | hp1 | a0002 | c0002 | t0007 | g0116 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18522 | hp2 | a0002 | c0002 | t0013 | g0015 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18906 | hp1 | a0002 | c0002 | t0007 | g0001 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18952 | hp2 | a0002 | c0002 | t0003 | g0340 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0352 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0362 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18969 | hp1 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18977 | hp1 | a0001 | c0001 | t0016 | g0221 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0377 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0366 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0378 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0358 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0370 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0383 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0249 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19057 | hp2 | a0001 | c0001 | t0017 | g0309 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19077 | hp1 | a0009 | c0010 | t0001 | g0274 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0376 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | YRI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ASW | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20129 | hp2 | a0002 | c0002 | t0007 | g0001 | AFR | ASW | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0106 | EUR | TSI | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0320 | SAS | GIH | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0272 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG02559 | hp2 | a0002 | c0002 | t0011 | g0086 | AFR | ACB | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03471 | hp1 | a0002 | c0002 | t0009 | g0334 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| HG06807 | hp2 | a0002 | c0002 | t0013 | g0015 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0323 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA20300 | hp2 | a0002 | c0002 | t0023 | g0118 | AFR | USA | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| NA21309 | hp2 | a0002 | c0002 | t0022 | g0355 | AFR | LWK | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| homoSapiens | chm13v2 | a0010 | c0009 | t0001 | g0240 | REF | REF | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0178 | REF | REF | PDCD1LG2_chr9_5505531_5576282 | PDCD1LG2 | chr9 | 5505531 | 5576282 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5534862 | G | C | 2 | a0003 a0006 |
6 | HG02647.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
missense_variant | MODERATE | c.173G>C | p.Ser58Thr | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/7 | 460/2432 | 173/822 | 58/273 | chr9 | 5534862 | |||
| chr9:5549451 | G | A | 1 | a0006 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.478G>A | p.Val160Ile | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 765/2432 | 478/822 | 160/273 | chr9 | 5549451 | |||
| chr9:5549507 | T | A | 1 | a0005 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.534T>A | p.Ser178Arg | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 821/2432 | 534/822 | 178/273 | chr9 | 5549507 | |||
| chr9:5549514 | C | T | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.541C>T | p.Arg181Cys | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 828/2432 | 541/822 | 181/273 | chr9 | 5549514 | |||
| chr9:5549568 | G | A | 1 | a0004 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.595G>A | p.Val199Met | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 882/2432 | 595/822 | 199/273 | chr9 | 5549568 | |||
| chr9:5549574 | G | A | 1 | a0007 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.601G>A | p.Glu201Lys | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 888/2432 | 601/822 | 201/273 | chr9 | 5549574 | |||
| chr9:5557708 | T | C | 5 | a0002 a0003 a0005 others(2): Show |
116 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(113): Show |
missense_variant | MODERATE | c.722T>C | p.Ile241Thr | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/7 | 1009/2432 | 722/822 | 241/273 | chr9 | 5557708 | |||
| chr9:5557716 | A | G | 1 | a0009 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.730A>G | p.Arg244Gly | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/7 | 1017/2432 | 730/822 | 244/273 | chr9 | 5557716 | |||
| chr9:5557717 | G | A | 1 | a0009 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.731G>A | p.Arg244Lys | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/7 | 1018/2432 | 731/822 | 244/273 | chr9 | 5557717 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5549540 | C | T | 1 | a0002c0004 | 4 | HG02257.hp2 HG02572.hp1 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.567C>T | p.Asn189Asn | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/7 | 854/2432 | 567/822 | 189/273 | chr9 | 5549540 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5510544 | G | A | 1 | a0002c0002t0014 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-274G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 12003 | chr9 | 5510544 | ||||||
| chr9:5510601 | A | G | 7 | a0001c0001t0007 a0001c0001t0012 a0002c0002t0007 others(4): Show |
11 | HG01109.hp1 HG02717.hp2 HG02809.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-217A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 11946 | chr9 | 5510601 | ||||||
| chr9:5510631 | A | G | 7 | a0001c0001t0003 a0001c0001t0008 a0002c0002t0003 others(4): Show |
40 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-187A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 11916 | chr9 | 5510631 | ||||||
| chr9:5510644 | A | G | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(8): Show |
109 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(106): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-174A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | chr9 | 5510644 | |||||||
| chr9:5510679 | T | C | 2 | a0001c0001t0012 a0002c0002t0012 |
2 | HG01109.hp1 HG02717.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-139T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | chr9 | 5510679 | |||||||
| chr9:5510742 | A | G | 4 | a0002c0002t0009 a0002c0002t0011 a0002c0002t0020 others(1): Show |
8 | HG01192.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-76A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/7 | 11805 | chr9 | 5510742 | ||||||
| chr9:5570463 | T | C | 2 | a0002c0002t0015 a0002c0002t0021 |
2 | HG01978.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*504T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 504 | chr9 | 5570463 | ||||||
| chr9:5570584 | T | C | 1 | a0001c0001t0016 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 625 | chr9 | 5570584 | ||||||
| chr9:5570777 | A | C | 3 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 |
27 | HG00408.hp2 HG01261.hp1 HG01496.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*818A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 818 | chr9 | 5570777 | ||||||
| chr9:5570824 | C | T | 4 | a0002c0002t0006 a0002c0002t0020 a0002c0002t0022 others(1): Show |
9 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*865C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 865 | chr9 | 5570824 | ||||||
| chr9:5570887 | C | T | 1 | a0002c0002t0013 | 2 | HG06807.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*928C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 928 | chr9 | 5570887 | ||||||
| chr9:5570940 | A | C | 1 | a0001c0001t0017 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 981 | chr9 | 5570940 | ||||||
| chr9:5570944 | C | T | 3 | a0002c0002t0005 a0002c0002t0023 a0002c0004t0005 |
7 | HG00741.hp2 HG01243.hp1 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*985C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 985 | chr9 | 5570944 | ||||||
| chr9:5571105 | A | G | 1 | a0001c0001t0018 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1146A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 7/7 | 1146 | chr9 | 5571105 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:5510837 | T | TG | 143 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0253 others(140): Show |
148 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-15+34_-15+35insG | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5510837 | |||||||
| chr9:5510838 | A | T | 143 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0253 others(140): Show |
148 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-15+35A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5510838 | |||||||
| chr9:5510948 | C | T | 1 | a0002c0002t0003g0384 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-15+145C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5510948 | |||||||
| chr9:5511111 | G | A | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15+308G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511111 | |||||||
| chr9:5511143 | T | C | 3 | a0003c0003t0003g0248 a0003c0003t0003g0249 a0003c0003t0003g0250 |
3 | HG02647.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+340T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511143 | |||||||
| chr9:5511190 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+387T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511190 | |||||||
| chr9:5511203 | C | G | 1 | a0001c0001t0010g0246 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-15+400C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511203 | |||||||
| chr9:5511373 | G | A | 3 | a0003c0003t0003g0248 a0003c0003t0003g0249 a0003c0003t0003g0250 |
3 | HG02647.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+570G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511373 | |||||||
| chr9:5511625 | A | G | 2 | a0001c0001t0001g0382 a0002c0002t0001g0383 |
2 | NA18998.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-15+822A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511625 | |||||||
| chr9:5511646 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-15+843G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511646 | |||||||
| chr9:5511723 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-15+920G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511723 | |||||||
| chr9:5511824 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+1021T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511824 | |||||||
| chr9:5511865 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-15+1062C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511865 | |||||||
| chr9:5511921 | C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-15+1118C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511921 | |||||||
| chr9:5511940 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | HG00558.hp2 NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-15+1137G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511940 | |||||||
| chr9:5511986 | A | G | 2 | a0001c0001t0012g0247 a0002c0002t0001g0381 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+1183A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5511986 | |||||||
| chr9:5512089 | C | T | 1 | a0001c0001t0001g0380 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+1286C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512089 | |||||||
| chr9:5512129 | C | A | 1 | a0002c0002t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-15+1326C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512129 | |||||||
| chr9:5512203 | C | G | 5 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(2): Show |
6 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1400C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512203 | |||||||
| chr9:5512204 | G | A | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15+1401G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512204 | |||||||
| chr9:5512270 | C | G | 35 | a0001c0001t0003g0020 a0001c0001t0003g0257 a0001c0001t0003g0349 others(32): Show |
36 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-15+1467C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512270 | |||||||
| chr9:5512369 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+1566G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512369 | |||||||
| chr9:5512459 | T | C | 72 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0258 others(69): Show |
75 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-15+1656T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512459 | |||||||
| chr9:5512484 | G | A | 1 | a0002c0002t0002g0027 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-15+1681G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512484 | |||||||
| chr9:5512486 | G | A | 105 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(102): Show |
109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-15+1683G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512486 | |||||||
| chr9:5512505 | C | A | 2 | a0001c0001t0012g0247 a0002c0002t0001g0381 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+1702C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512505 | |||||||
| chr9:5512507 | A | G | 6 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(3): Show |
7 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+1704A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512507 | |||||||
| chr9:5512522 | T | G | 148 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(145): Show |
154 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-15+1719T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512522 | |||||||
| chr9:5512534 | C | G | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-15+1731C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512534 | |||||||
| chr9:5512655 | A | G | 1 | a0007c0008t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-15+1852A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512655 | |||||||
| chr9:5512656 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15+1853T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512656 | |||||||
| chr9:5512731 | A | G | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+1928A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512731 | |||||||
| chr9:5512786 | C | A | 104 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(101): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+1983C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512786 | |||||||
| chr9:5512818 | C | T | 102 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(99): Show |
106 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.-15+2015C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512818 | |||||||
| chr9:5512849 | G | C | 5 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(2): Show |
6 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+2046G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5512849 | |||||||
| chr9:5513057 | C | T | 3 | a0002c0002t0001g0347 a0003c0003t0003g0249 a0003c0003t0003g0250 |
3 | HG02970.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+2254C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513057 | |||||||
| chr9:5513080 | A | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-15+2277A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513080 | |||||||
| chr9:5513290 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | HG00558.hp2 NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-15+2487G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513290 | |||||||
| chr9:5513529 | A | G | 5 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0001g0345 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+2726A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513529 | |||||||
| chr9:5513545 | T | C | 7 | a0001c0001t0007g0119 a0001c0001t0012g0247 a0002c0002t0001g0381 others(4): Show |
9 | HG02717.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+2742T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513545 | |||||||
| chr9:5513546 | G | A | 2 | a0001c0001t0012g0247 a0002c0002t0001g0381 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+2743G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513546 | |||||||
| chr9:5513563 | T | A | 1 | a0002c0002t0009g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-15+2760T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513563 | |||||||
| chr9:5513578 | T | C | 1 | a0002c0002t0001g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+2775T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513578 | |||||||
| chr9:5513619 | A | C | 1 | a0001c0001t0003g0379 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+2816A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513619 | |||||||
| chr9:5513671 | G | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-15+2868G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513671 | |||||||
| chr9:5513897 | T | C | 1 | a0002c0002t0002g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+3094T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513897 | |||||||
| chr9:5513988 | T | C | 1 | a0001c0001t0001g0380 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+3185T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513988 | |||||||
| chr9:5513992 | T | C | 2 | a0001c0001t0001g0120 a0002c0002t0001g0333 |
2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-15+3189T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5513992 | |||||||
| chr9:5514167 | A | C | 1 | a0001c0001t0001g0258 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-15+3364A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514167 | |||||||
| chr9:5514199 | G | A | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0002c0002t0002g0033 |
3 | NA18612.hp2 NA18964.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-15+3396G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514199 | |||||||
| chr9:5514331 | T | A | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+3528T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514331 | |||||||
| chr9:5514351 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+3548T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514351 | |||||||
| chr9:5514372 | A | C | 120 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(117): Show |
125 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-15+3569A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514372 | |||||||
| chr9:5514375 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+3572G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514375 | |||||||
| chr9:5514575 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+3772T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514575 | |||||||
| chr9:5514772 | G | GA | 16 | a0001c0001t0001g0034 a0001c0001t0001g0122 a0001c0001t0001g0123 others(13): Show |
16 | HG01106.hp2 HG01358.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+3991dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5514772 | ||||||
| chr9:5514772 | GA | G | 28 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0226 others(25): Show |
29 | HG00597.hp2 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15+3991delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5514772 | ||||||
| chr9:5514772 | GAAA | G | 35 | a0001c0001t0003g0020 a0001c0001t0003g0257 a0001c0001t0003g0350 others(32): Show |
36 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-15+3989_-15+3991d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5514772 | ||||||
| chr9:5514839 | T | C | 261 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0034 others(258): Show |
273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.-15+4036T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514839 | |||||||
| chr9:5514841 | G | A | 2 | a0001c0001t0004g0260 a0002c0002t0001g0261 |
2 | NA18612.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-15+4038G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514841 | |||||||
| chr9:5514869 | G | A | 1 | a0003c0003t0009g0324 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+4066G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514869 | |||||||
| chr9:5514882 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+4079T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514882 | |||||||
| chr9:5514919 | T | C | 121 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(118): Show |
126 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-15+4116T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5514919 | |||||||
| chr9:5515054 | C | T | 1 | a0002c0002t0014g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-15+4251C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515054 | |||||||
| chr9:5515111 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-15+4308G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515111 | |||||||
| chr9:5515177 | T | C | 1 | a0002c0002t0001g0347 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-15+4374T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515177 | |||||||
| chr9:5515207 | A | C | 121 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(118): Show |
126 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-15+4404A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515207 | |||||||
| chr9:5515247 | C | G | 1 | a0002c0002t0002g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-15+4444C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515247 | |||||||
| chr9:5515251 | A | G | 121 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(118): Show |
126 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-15+4448A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515251 | |||||||
| chr9:5515640 | A | G | 1 | a0002c0002t0002g0341 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15+4837A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515640 | |||||||
| chr9:5515710 | G | T | 1 | a0001c0001t0001g0322 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-15+4907G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515710 | |||||||
| chr9:5515816 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-15+5013A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515816 | |||||||
| chr9:5515922 | C | CA | 28 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0120 others(25): Show |
32 | HG00438.hp2 HG00733.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-15+5146dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | C | CAA | 68 | a0001c0001t0001g0034 a0001c0001t0001g0067 a0001c0001t0001g0069 others(65): Show |
70 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+5145_-15+5146d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | C | CAAA | 42 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0049 others(39): Show |
44 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.-15+5144_-15+5146d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | C | CAAAA | 9 | a0001c0001t0001g0322 a0001c0001t0002g0022 a0001c0001t0002g0036 others(6): Show |
10 | HG00544.hp1 HG01109.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+5143_-15+5146d others(6): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | CA | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0222 a0001c0001t0001g0223 others(6): Show |
10 | HG02735.hp1 HG03225.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+5146delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | CAA | C | 34 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0232 others(31): Show |
35 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15+5145_-15+5146d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | CAAA | C | 55 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0258 others(52): Show |
57 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-15+5144_-15+5146d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | CAAAA | C | 5 | a0001c0001t0001g0224 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
6 | HG01993.hp1 NA18939.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5143_-15+5146d others(6): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515922 | CAAAAAAA | C | 35 | a0001c0001t0003g0020 a0001c0001t0003g0257 a0001c0001t0003g0349 others(32): Show |
36 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-15+5140_-15+5146d others(9): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5515922 | ||||||
| chr9:5515941 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-15+5138A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515941 | |||||||
| chr9:5515944 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-15+5141A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515944 | |||||||
| chr9:5515990 | G | C | 154 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(151): Show |
160 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.-15+5187G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5515990 | |||||||
| chr9:5516007 | G | C | 15 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG02027.hp1 HG02055.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+5204G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516007 | |||||||
| chr9:5516067 | T | C | 120 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(117): Show |
125 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-15+5264T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516067 | |||||||
| chr9:5516084 | C | G | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-15+5281C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516084 | |||||||
| chr9:5516145 | G | A | 5 | a0002c0002t0002g0019 a0002c0002t0002g0329 a0002c0002t0002g0331 others(2): Show |
6 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+5342G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516145 | |||||||
| chr9:5516176 | C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-15+5373C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516176 | |||||||
| chr9:5516182 | G | C | 31 | a0001c0001t0003g0020 a0001c0001t0003g0257 a0001c0001t0003g0350 others(28): Show |
32 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-15+5379G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516182 | |||||||
| chr9:5516197 | A | G | 155 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(152): Show |
161 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-15+5394A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516197 | |||||||
| chr9:5516208 | C | T | 1 | a0002c0002t0002g0064 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+5405C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516208 | |||||||
| chr9:5516265 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-15+5462C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516265 | |||||||
| chr9:5516268 | G | A | 2 | a0001c0001t0003g0349 a0002c0002t0003g0377 |
2 | HG02135.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-15+5465G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516268 | |||||||
| chr9:5516349 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15+5546C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516349 | |||||||
| chr9:5516395 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-15+5592A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516395 | |||||||
| chr9:5516461 | A | G | 2 | a0001c0001t0012g0247 a0002c0002t0001g0381 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+5658A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516461 | |||||||
| chr9:5516463 | T | C | 3 | a0002c0002t0001g0348 a0002c0002t0013g0015 a0002c0002t0014g0339 |
4 | HG02615.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5660T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516463 | |||||||
| chr9:5516559 | C | T | 1 | a0002c0002t0001g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15+5756C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516559 | |||||||
| chr9:5516612 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-15+5809C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516612 | |||||||
| chr9:5516703 | C | T | 2 | a0002c0002t0002g0019 a0002c0002t0002g0331 |
3 | HG02258.hp1 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-14-5830C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516703 | |||||||
| chr9:5516779 | C | G | 1 | a0001c0001t0001g0311 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-14-5754C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516779 | |||||||
| chr9:5516866 | G | T | 1 | a0001c0001t0002g0063 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-5667G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516866 | |||||||
| chr9:5516956 | G | A | 20 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(17): Show |
20 | HG00140.hp2 HG00735.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-5577G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516956 | |||||||
| chr9:5516980 | C | T | 26 | a0001c0001t0001g0115 a0001c0001t0001g0226 a0001c0001t0001g0232 others(23): Show |
28 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-5553C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5516980 | |||||||
| chr9:5517046 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-14-5487C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517046 | |||||||
| chr9:5517090 | C | T | 1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-14-5443C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517090 | |||||||
| chr9:5517265 | G | A | 82 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0148 others(79): Show |
84 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-14-5268G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517265 | |||||||
| chr9:5517559 | C | T | 163 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0041 others(160): Show |
170 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-14-4974C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517559 | |||||||
| chr9:5517568 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0224 a0001c0001t0004g0014 |
4 | NA18991.hp1 NA18998.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-4965C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517568 | |||||||
| chr9:5517589 | G | A | 1 | a0003c0003t0009g0324 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-4944G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517589 | |||||||
| chr9:5517662 | C | T | 3 | a0002c0002t0001g0131 a0002c0002t0001g0146 a0002c0002t0015g0145 |
3 | HG02258.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-14-4871C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517662 | |||||||
| chr9:5517719 | G | A | 27 | a0001c0001t0003g0020 a0001c0001t0003g0353 a0001c0001t0003g0354 others(24): Show |
28 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-4814G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517719 | |||||||
| chr9:5517880 | G | A | 1 | a0001c0001t0010g0149 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-14-4653G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5517880 | |||||||
| chr9:5518008 | A | G | 9 | a0001c0001t0001g0115 a0001c0001t0001g0226 a0001c0001t0001g0232 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-4525A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518008 | |||||||
| chr9:5518169 | G | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0001t0001g0150 others(6): Show |
11 | HG01123.hp1 HG01255.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-4364G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518169 | |||||||
| chr9:5518211 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14-4322C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518211 | |||||||
| chr9:5518260 | C | T | 69 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(66): Show |
70 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-14-4273C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518260 | |||||||
| chr9:5518265 | G | A | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-4268G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518265 | |||||||
| chr9:5518500 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-14-4033G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518500 | |||||||
| chr9:5518553 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-14-3980G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518553 | |||||||
| chr9:5518633 | C | G | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-14-3900C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518633 | |||||||
| chr9:5518718 | C | A | 1 | a0001c0001t0002g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-14-3815C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518718 | |||||||
| chr9:5518780 | C | T | 31 | a0001c0001t0003g0020 a0001c0001t0003g0353 a0001c0001t0003g0354 others(28): Show |
32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-3753C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518780 | |||||||
| chr9:5518989 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-14-3544G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5518989 | |||||||
| chr9:5519076 | A | C | 1 | a0001c0001t0002g0026 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-14-3457A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519076 | |||||||
| chr9:5519100 | G | C | 32 | a0001c0001t0003g0020 a0001c0001t0003g0353 a0001c0001t0003g0354 others(29): Show |
33 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.-14-3433G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519100 | |||||||
| chr9:5519201 | AG | A | 27 | a0001c0001t0003g0020 a0001c0001t0003g0353 a0001c0001t0003g0354 others(24): Show |
28 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-3328delG | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5519201 | ||||||
| chr9:5519238 | G | A | 4 | a0001c0001t0003g0376 a0001c0001t0003g0379 a0002c0002t0003g0375 others(1): Show |
4 | HG01978.hp1 HG02145.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3295G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519238 | |||||||
| chr9:5519257 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-14-3276A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519257 | |||||||
| chr9:5519343 | C | G | 2 | a0002c0002t0001g0348 a0002c0002t0014g0339 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-3190C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519343 | |||||||
| chr9:5519369 | T | C | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-14-3164T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519369 | |||||||
| chr9:5519370 | T | C | 2 | a0001c0001t0002g0326 a0001c0001t0002g0327 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-14-3163T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519370 | |||||||
| chr9:5519594 | A | G | 14 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0226 others(11): Show |
15 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-2939A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519594 | |||||||
| chr9:5519626 | A | G | 1 | a0002c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-14-2907A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519626 | |||||||
| chr9:5519707 | C | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01106.hp1 HG02602.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2826C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519707 | |||||||
| chr9:5519716 | C | G | 1 | a0001c0001t0001g0336 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-14-2817C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519716 | |||||||
| chr9:5519738 | T | C | 57 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(54): Show |
58 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-14-2795T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519738 | |||||||
| chr9:5519786 | C | T | 51 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(48): Show |
52 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14-2747C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519786 | |||||||
| chr9:5519944 | C | T | 51 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(48): Show |
52 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14-2589C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5519944 | |||||||
| chr9:5520215 | G | A | 50 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(47): Show |
51 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-14-2318G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520215 | |||||||
| chr9:5520317 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0157 |
5 | NA18955.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-2216G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520317 | |||||||
| chr9:5520404 | T | G | 2 | a0001c0001t0012g0247 a0002c0002t0001g0381 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-2129T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520404 | |||||||
| chr9:5520415 | T | C | 2 | a0001c0001t0012g0247 a0002c0002t0001g0381 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-2118T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520415 | |||||||
| chr9:5520427 | G | T | 31 | a0001c0001t0003g0020 a0001c0001t0003g0353 a0001c0001t0003g0354 others(28): Show |
32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-2106G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520427 | |||||||
| chr9:5520761 | A | C | 1 | a0002c0002t0001g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14-1772A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520761 | |||||||
| chr9:5520800 | G | C | 1 | a0002c0002t0001g0333 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-14-1733G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520800 | |||||||
| chr9:5520876 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0157 |
5 | NA18955.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1657G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520876 | |||||||
| chr9:5520921 | A | C | 1 | a0001c0001t0002g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-14-1612A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520921 | |||||||
| chr9:5520929 | T | A | 11 | a0001c0001t0007g0119 a0001c0001t0012g0247 a0002c0002t0001g0381 others(8): Show |
13 | HG02647.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-1604T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5520929 | |||||||
| chr9:5521094 | G | A | 101 | a0001c0001t0001g0016 a0001c0001t0001g0148 a0001c0001t0001g0253 others(98): Show |
104 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-1439G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521094 | |||||||
| chr9:5521109 | C | A | 101 | a0001c0001t0001g0016 a0001c0001t0001g0148 a0001c0001t0001g0253 others(98): Show |
104 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-1424C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521109 | |||||||
| chr9:5521367 | T | G | 17 | a0001c0001t0001g0268 a0001c0001t0007g0119 a0002c0002t0001g0269 others(14): Show |
19 | HG01099.hp2 HG01243.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-1166T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521367 | |||||||
| chr9:5521407 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-14-1126G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521407 | |||||||
| chr9:5521435 | T | C | 1 | a0002c0004t0005g0228 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-14-1098T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521435 | |||||||
| chr9:5521655 | G | T | 106 | a0001c0001t0001g0016 a0001c0001t0001g0148 a0001c0001t0001g0253 others(103): Show |
109 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-14-878G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521655 | |||||||
| chr9:5521736 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0002t0001g0251 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-797T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521736 | |||||||
| chr9:5521740 | T | C | 1 | a0001c0001t0002g0325 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-14-793T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521740 | |||||||
| chr9:5521974 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG02027.hp1 HG02056.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-559C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5521974 | |||||||
| chr9:5522039 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-14-494C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522039 | |||||||
| chr9:5522167 | T | C | 36 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(33): Show |
37 | HG00140.hp2 HG00735.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-14-366T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522167 | |||||||
| chr9:5522173 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-360G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522173 | |||||||
| chr9:5522173 | GACAA | G | 69 | a0001c0001t0001g0016 a0001c0001t0001g0148 a0001c0001t0001g0259 others(66): Show |
71 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-14-354_-14-351del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 5522173 | ||||||
| chr9:5522290 | C | T | 1 | a0002c0002t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-14-243C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 1/6 | chr9 | 5522290 | |||||||
| chr9:5522617 | G | C | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+16G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522617 | |||||||
| chr9:5522630 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.55+29G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522630 | |||||||
| chr9:5522654 | T | C | 1 | a0002c0002t0005g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.55+53T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522654 | |||||||
| chr9:5522711 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0002c0002t0001g0347 |
3 | HG02451.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.55+110C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522711 | |||||||
| chr9:5522712 | G | A | 4 | a0001c0001t0003g0376 a0001c0001t0003g0379 a0002c0002t0003g0375 others(1): Show |
4 | HG01978.hp1 HG02145.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+111G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522712 | |||||||
| chr9:5522741 | C | CA | 42 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(39): Show |
44 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.55+151dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5522741 | ||||||
| chr9:5522909 | G | A | 5 | a0001c0001t0007g0119 a0002c0002t0007g0001 a0002c0002t0007g0116 others(2): Show |
7 | HG02809.hp1 HG02922.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+308G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522909 | |||||||
| chr9:5522943 | C | T | 50 | a0001c0001t0001g0016 a0001c0001t0001g0148 a0001c0001t0001g0259 others(47): Show |
51 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.55+342C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5522943 | |||||||
| chr9:5523085 | G | A | 1 | a0001c0001t0004g0313 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.55+484G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523085 | |||||||
| chr9:5523239 | C | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0223 |
2 | NA19062.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.55+638C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523239 | |||||||
| chr9:5523308 | C | G | 29 | a0001c0001t0001g0258 a0001c0001t0003g0020 a0001c0001t0003g0337 others(26): Show |
30 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+707C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523308 | |||||||
| chr9:5523469 | G | T | 6 | a0002c0002t0002g0019 a0002c0002t0002g0329 a0002c0002t0002g0331 others(3): Show |
7 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+868G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523469 | |||||||
| chr9:5523512 | T | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0235 a0002c0002t0001g0011 others(1): Show |
5 | HG00609.hp2 NA18945.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+911T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523512 | |||||||
| chr9:5523722 | T | C | 1 | a0001c0001t0008g0352 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.55+1121T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523722 | |||||||
| chr9:5523773 | C | T | 34 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(31): Show |
34 | HG00140.hp2 HG00735.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.55+1172C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523773 | |||||||
| chr9:5523850 | C | T | 28 | a0001c0001t0001g0258 a0001c0001t0003g0020 a0001c0001t0003g0353 others(25): Show |
29 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.55+1249C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523850 | |||||||
| chr9:5523951 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.55+1350C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5523951 | |||||||
| chr9:5524037 | T | C | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.55+1436T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524037 | |||||||
| chr9:5524353 | C | T | 6 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0003c0003t0001g0029 others(3): Show |
6 | HG02451.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1752C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524353 | |||||||
| chr9:5524389 | A | G | 10 | a0002c0002t0001g0070 a0002c0002t0001g0266 a0002c0002t0001g0267 others(7): Show |
11 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.55+1788A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524389 | |||||||
| chr9:5524447 | C | T | 1 | a0002c0002t0002g0064 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.55+1846C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524447 | |||||||
| chr9:5524571 | T | A | 18 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
18 | HG00140.hp2 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+1970T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524571 | |||||||
| chr9:5524682 | T | C | 1 | a0002c0002t0001g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55+2081T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524682 | |||||||
| chr9:5524749 | C | T | 1 | a0005c0006t0019g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.55+2148C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524749 | |||||||
| chr9:5524812 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.55+2211A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524812 | |||||||
| chr9:5524904 | A | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0059 |
3 | NA18965.hp2 NA18969.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.55+2303A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524904 | |||||||
| chr9:5524915 | A | G | 83 | a0001c0001t0001g0016 a0001c0001t0001g0125 a0001c0001t0001g0148 others(80): Show |
86 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.55+2314A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524915 | |||||||
| chr9:5524967 | T | C | 3 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0323 |
3 | HG02723.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.55+2366T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524967 | |||||||
| chr9:5524993 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.55+2392T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5524993 | |||||||
| chr9:5525031 | T | C | 4 | a0002c0002t0007g0001 a0002c0002t0007g0116 a0002c0002t0023g0118 others(1): Show |
6 | HG02809.hp1 HG02922.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2430T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525031 | |||||||
| chr9:5525034 | T | C | 3 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0323 |
3 | HG02723.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.55+2433T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525034 | |||||||
| chr9:5525073 | C | T | 6 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0003c0003t0001g0029 others(3): Show |
6 | HG02451.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+2472C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525073 | |||||||
| chr9:5525192 | G | C | 6 | a0002c0002t0002g0019 a0002c0002t0002g0329 a0002c0002t0002g0331 others(3): Show |
7 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2591G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525192 | |||||||
| chr9:5525292 | C | A | 1 | a0002c0002t0003g0377 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.55+2691C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525292 | |||||||
| chr9:5525343 | TA | T | 273 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(270): Show |
288 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.55+2757delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5525343 | ||||||
| chr9:5525351 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.55+2750A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525351 | |||||||
| chr9:5525355 | A | G | 6 | a0002c0002t0002g0019 a0002c0002t0002g0329 a0002c0002t0002g0331 others(3): Show |
7 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2754A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525355 | |||||||
| chr9:5525358 | A | G | 1 | a0002c0002t0003g0377 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.55+2757A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525358 | |||||||
| chr9:5525359 | G | A | 1 | a0002c0002t0003g0377 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.55+2758G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525359 | |||||||
| chr9:5525363 | A | G | 2 | a0001c0001t0001g0338 a0002c0002t0001g0347 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.55+2762A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525363 | |||||||
| chr9:5525370 | A | T | 4 | a0002c0002t0001g0266 a0002c0002t0001g0267 a0002c0002t0001g0323 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+2769A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525370 | |||||||
| chr9:5525388 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.55+2787A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525388 | |||||||
| chr9:5525608 | A | T | 26 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0115 others(23): Show |
26 | HG01081.hp1 HG01109.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.55+3007A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525608 | |||||||
| chr9:5525733 | T | C | 8 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0003c0003t0001g0029 others(5): Show |
8 | HG02647.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.55+3132T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525733 | |||||||
| chr9:5525744 | T | C | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0268 others(2): Show |
5 | HG01099.hp2 HG01192.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+3143T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525744 | |||||||
| chr9:5525768 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.55+3167G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525768 | |||||||
| chr9:5525771 | G | A | 3 | a0001c0001t0002g0075 a0001c0001t0004g0260 a0002c0002t0001g0261 |
3 | NA18612.hp1 NA18979.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.55+3170G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525771 | |||||||
| chr9:5525774 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.55+3173C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525774 | |||||||
| chr9:5525775 | A | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0042 others(113): Show |
121 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.55+3174A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525775 | |||||||
| chr9:5525776 | T | C | 15 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0001g0224 others(12): Show |
16 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.55+3175T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525776 | |||||||
| chr9:5525781 | G | T | 1 | a0001c0001t0002g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.55+3180G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525781 | |||||||
| chr9:5525787 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.55+3186G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525787 | |||||||
| chr9:5525819 | T | C | 1 | a0002c0002t0001g0252 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55+3218T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525819 | |||||||
| chr9:5525823 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.55+3222C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525823 | |||||||
| chr9:5525828 | C | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(53): Show |
61 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.55+3227C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525828 | |||||||
| chr9:5525831 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(183): Show |
196 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.55+3230G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525831 | |||||||
| chr9:5525852 | G | T | 176 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(173): Show |
186 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.55+3251G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525852 | |||||||
| chr9:5525859 | C | T | 8 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0215 others(5): Show |
8 | HG01081.hp1 HG02027.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+3258C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525859 | |||||||
| chr9:5525860 | C | A | 8 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0215 others(5): Show |
8 | HG01081.hp1 HG02027.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+3259C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525860 | |||||||
| chr9:5525861 | G | A | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0215 others(10): Show |
15 | HG01081.hp1 HG02027.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.55+3260G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525861 | |||||||
| chr9:5525864 | T | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0002g0325 others(1): Show |
4 | HG01081.hp1 HG02083.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+3263T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525864 | |||||||
| chr9:5525874 | T | C | 28 | a0001c0001t0001g0133 a0001c0001t0001g0163 a0001c0001t0001g0164 others(25): Show |
28 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.55+3273T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525874 | |||||||
| chr9:5525884 | A | T | 5 | a0001c0001t0001g0115 a0002c0002t0001g0219 a0002c0002t0001g0381 others(2): Show |
6 | HG03139.hp2 HG03453.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+3283A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525884 | |||||||
| chr9:5525901 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.55+3300G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525901 | |||||||
| chr9:5525907 | C | T | 2 | a0001c0001t0002g0103 a0002c0002t0002g0097 |
2 | HG01981.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.55+3306C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525907 | |||||||
| chr9:5525908 | A | G | 2 | a0001c0001t0002g0103 a0002c0002t0002g0097 |
2 | HG01981.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.55+3307A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525908 | |||||||
| chr9:5525941 | G | A | 17 | a0001c0001t0001g0069 a0001c0001t0001g0115 a0001c0001t0001g0156 others(14): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+3340G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5525941 | |||||||
| chr9:5526004 | G | A | 1 | a0001c0001t0004g0304 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.55+3403G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526004 | |||||||
| chr9:5526041 | C | T | 6 | a0001c0001t0001g0147 a0003c0003t0001g0029 a0003c0003t0003g0248 others(3): Show |
6 | HG01109.hp2 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+3440C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526041 | |||||||
| chr9:5526046 | C | CA | 77 | a0001c0001t0001g0115 a0001c0001t0001g0134 a0001c0001t0001g0147 others(74): Show |
81 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.55+3462dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5526046 | ||||||
| chr9:5526046 | C | CAA | 214 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(211): Show |
222 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.55+3461_55+3462dup others(2): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5526046 | ||||||
| chr9:5526077 | T | C | 143 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(140): Show |
149 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.55+3476T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526077 | |||||||
| chr9:5526087 | G | A | 1 | a0001c0001t0001g0382 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.55+3486G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526087 | |||||||
| chr9:5526124 | C | T | 305 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(302): Show |
318 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.55+3523C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526124 | |||||||
| chr9:5526165 | A | T | 2 | a0002c0002t0007g0001 a0002c0002t0007g0116 |
4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+3564A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526165 | |||||||
| chr9:5526211 | T | G | 7 | a0001c0001t0002g0111 a0001c0001t0004g0140 a0001c0001t0004g0190 others(4): Show |
7 | NA18942.hp1 NA18944.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+3610T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526211 | |||||||
| chr9:5526434 | T | A | 52 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0156 others(49): Show |
54 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.55+3833T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526434 | |||||||
| chr9:5526473 | T | C | 1 | a0002c0002t0001g0333 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.55+3872T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526473 | |||||||
| chr9:5526502 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.55+3901A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526502 | |||||||
| chr9:5526516 | C | G | 1 | a0002c0002t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.55+3915C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526516 | |||||||
| chr9:5526667 | G | A | 1 | a0002c0002t0002g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.55+4066G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526667 | |||||||
| chr9:5526880 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0018g0321 |
2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.55+4279T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5526880 | |||||||
| chr9:5527014 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.55+4413A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527014 | |||||||
| chr9:5527351 | A | G | 16 | a0001c0001t0001g0067 a0001c0001t0001g0156 a0001c0001t0001g0255 others(13): Show |
16 | HG00140.hp2 HG00733.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.55+4750A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527351 | |||||||
| chr9:5527429 | G | C | 1 | a0002c0004t0005g0228 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.55+4828G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527429 | |||||||
| chr9:5527525 | T | C | 8 | a0001c0001t0001g0211 a0001c0001t0002g0089 a0001c0001t0004g0304 others(5): Show |
8 | HG00408.hp2 HG00621.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.55+4924T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527525 | |||||||
| chr9:5527837 | C | CTT | 12 | a0001c0001t0001g0122 a0001c0001t0001g0226 a0001c0001t0002g0018 others(9): Show |
13 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.55+5244_55+5245dup others(2): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5527837 | ||||||
| chr9:5527878 | A | G | 33 | a0001c0001t0001g0069 a0001c0001t0001g0193 a0001c0001t0001g0197 others(30): Show |
36 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.55+5277A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527878 | |||||||
| chr9:5527888 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.55+5287C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527888 | |||||||
| chr9:5527922 | G | A | 5 | a0003c0003t0001g0029 a0003c0003t0003g0248 a0003c0003t0003g0249 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+5321G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527922 | |||||||
| chr9:5527945 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.55+5344C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5527945 | |||||||
| chr9:5528045 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.55+5444G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528045 | |||||||
| chr9:5528061 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.55+5460C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528061 | |||||||
| chr9:5528121 | C | T | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.55+5520C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528121 | |||||||
| chr9:5528152 | G | C | 1 | a0001c0001t0004g0260 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.55+5551G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528152 | |||||||
| chr9:5528155 | G | A | 5 | a0002c0002t0006g0024 a0002c0002t0006g0068 a0002c0002t0006g0071 others(2): Show |
5 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+5554G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528155 | |||||||
| chr9:5528198 | T | C | 21 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0206 others(18): Show |
22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.55+5597T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528198 | |||||||
| chr9:5528276 | T | TTA | 7 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0001g0272 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+5686_55+5687dup others(2): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5528276 | ||||||
| chr9:5528289 | C | T | 86 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(83): Show |
88 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.55+5688C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528289 | |||||||
| chr9:5528440 | T | C | 1 | a0001c0001t0004g0304 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.55+5839T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528440 | |||||||
| chr9:5528595 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+5994G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528595 | |||||||
| chr9:5528599 | C | T | 7 | a0001c0001t0001g0232 a0002c0002t0001g0229 a0002c0002t0005g0233 others(4): Show |
8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.55+5998C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528599 | |||||||
| chr9:5528658 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(81): Show |
86 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.55+6057A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528658 | |||||||
| chr9:5528796 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.56-5949C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528796 | |||||||
| chr9:5528818 | C | A | 2 | a0001c0001t0001g0115 a0002c0002t0013g0015 |
3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-5927C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528818 | |||||||
| chr9:5528832 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0264 a0001c0001t0003g0354 others(1): Show |
4 | NA18957.hp1 NA18978.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-5913C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528832 | |||||||
| chr9:5528882 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.56-5863A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528882 | |||||||
| chr9:5528899 | T | A | 7 | a0001c0001t0001g0232 a0002c0002t0001g0229 a0002c0002t0005g0233 others(4): Show |
8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.56-5846T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528899 | |||||||
| chr9:5528908 | T | G | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.56-5837T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528908 | |||||||
| chr9:5528912 | T | C | 22 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0206 others(19): Show |
23 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-5833T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528912 | |||||||
| chr9:5528915 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.56-5830A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528915 | |||||||
| chr9:5528923 | T | A | 9 | a0001c0001t0001g0122 a0001c0001t0001g0226 a0001c0001t0002g0018 others(6): Show |
10 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-5822T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528923 | |||||||
| chr9:5528957 | G | C | 8 | a0001c0001t0002g0103 a0002c0002t0002g0045 a0003c0003t0001g0029 others(5): Show |
8 | HG01981.hp1 HG02647.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-5788G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528957 | |||||||
| chr9:5528966 | T | A | 1 | a0001c0001t0001g0345 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-5779T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5528966 | |||||||
| chr9:5529023 | C | T | 2 | a0001c0001t0002g0106 a0002c0002t0002g0329 |
2 | HG02145.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.56-5722C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529023 | |||||||
| chr9:5529027 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.56-5718C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529027 | |||||||
| chr9:5529126 | G | A | 1 | a0001c0001t0001g0382 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.56-5619G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529126 | |||||||
| chr9:5529138 | G | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-5607G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529138 | |||||||
| chr9:5529158 | G | A | 2 | a0001c0001t0002g0075 a0001c0001t0002g0124 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.56-5587G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529158 | |||||||
| chr9:5529219 | T | C | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.56-5526T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529219 | |||||||
| chr9:5529225 | C | G | 1 | a0001c0001t0001g0380 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-5520C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529225 | |||||||
| chr9:5529294 | T | C | 9 | a0001c0001t0001g0122 a0001c0001t0001g0226 a0001c0001t0002g0018 others(6): Show |
10 | HG01106.hp1 HG01261.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-5451T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529294 | |||||||
| chr9:5529324 | T | C | 1 | a0002c0002t0014g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.56-5421T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529324 | |||||||
| chr9:5529650 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0308 |
2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.56-5095A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529650 | |||||||
| chr9:5529705 | A | C | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-5040A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529705 | |||||||
| chr9:5529737 | G | T | 7 | a0001c0001t0002g0103 a0003c0003t0001g0029 a0003c0003t0003g0248 others(4): Show |
7 | HG01981.hp1 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-5008G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529737 | |||||||
| chr9:5529843 | G | C | 3 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0005c0006t0019g0104 |
3 | HG02647.hp1 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.56-4902G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529843 | |||||||
| chr9:5529973 | G | T | 1 | a0001c0001t0004g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.56-4772G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529973 | |||||||
| chr9:5529982 | C | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-4763C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5529982 | |||||||
| chr9:5530017 | A | G | 183 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(180): Show |
192 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.56-4728A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530017 | |||||||
| chr9:5530082 | A | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.56-4663A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530082 | |||||||
| chr9:5530248 | A | G | 35 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(32): Show |
38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.56-4497A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530248 | |||||||
| chr9:5530264 | C | T | 1 | a0002c0002t0022g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.56-4481C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530264 | |||||||
| chr9:5530473 | C | CA | 14 | a0001c0001t0001g0144 a0001c0001t0001g0176 a0001c0001t0001g0277 others(11): Show |
14 | HG00544.hp1 HG00642.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.56-4256dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5530473 | ||||||
| chr9:5530473 | CA | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0123 a0001c0001t0001g0132 others(7): Show |
11 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-4256delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 5530473 | ||||||
| chr9:5530487 | A | AC | 30 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(27): Show |
33 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.56-4258_56-4257ins others(1): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530487 | |||||||
| chr9:5530487 | A | C | 5 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0001g0272 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-4258A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530487 | |||||||
| chr9:5530500 | G | A | 6 | a0001c0001t0001g0226 a0002c0002t0001g0065 a0002c0002t0001g0251 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-4245G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530500 | |||||||
| chr9:5530716 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.56-4029G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530716 | |||||||
| chr9:5530840 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02056.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.56-3905T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530840 | |||||||
| chr9:5530983 | G | A | 6 | a0001c0001t0001g0226 a0002c0002t0001g0065 a0002c0002t0001g0251 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-3762G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5530983 | |||||||
| chr9:5531068 | T | C | 10 | a0001c0001t0001g0191 a0001c0001t0001g0205 a0001c0001t0003g0376 others(7): Show |
11 | HG01109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-3677T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531068 | |||||||
| chr9:5531293 | T | C | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-3452T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531293 | |||||||
| chr9:5531311 | A | G | 6 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0001g0272 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-3434A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531311 | |||||||
| chr9:5531311 | A | T | 1 | a0003c0003t0003g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56-3434A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531311 | |||||||
| chr9:5531328 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.56-3417A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531328 | |||||||
| chr9:5531499 | A | T | 1 | a0002c0002t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.56-3246A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531499 | |||||||
| chr9:5531647 | T | C | 1 | a0002c0002t0001g0237 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.56-3098T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531647 | |||||||
| chr9:5531754 | A | G | 2 | a0002c0002t0001g0162 a0002c0002t0001g0333 |
2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.56-2991A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531754 | |||||||
| chr9:5531763 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.56-2982G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531763 | |||||||
| chr9:5531841 | C | A | 1 | a0002c0002t0003g0384 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.56-2904C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531841 | |||||||
| chr9:5531861 | A | T | 12 | a0001c0001t0001g0122 a0001c0001t0001g0226 a0001c0001t0002g0018 others(9): Show |
13 | HG01106.hp1 HG01516.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.56-2884A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531861 | |||||||
| chr9:5531878 | A | G | 1 | a0002c0002t0002g0320 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.56-2867A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5531878 | |||||||
| chr9:5532122 | A | C | 2 | a0001c0001t0001g0115 a0002c0002t0013g0015 |
3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-2623A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532122 | |||||||
| chr9:5532212 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.56-2533C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532212 | |||||||
| chr9:5532593 | C | T | 5 | a0002c0002t0006g0024 a0002c0002t0006g0068 a0002c0002t0006g0071 others(2): Show |
5 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-2152C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532593 | |||||||
| chr9:5532633 | T | G | 2 | a0001c0001t0001g0115 a0002c0002t0013g0015 |
3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-2112T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532633 | |||||||
| chr9:5532694 | G | A | 1 | a0002c0002t0007g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.56-2051G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532694 | |||||||
| chr9:5532821 | C | T | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.56-1924C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532821 | |||||||
| chr9:5532871 | T | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(127): Show |
135 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.56-1874T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532871 | |||||||
| chr9:5532964 | C | T | 8 | a0001c0001t0002g0031 a0001c0001t0003g0362 a0001c0001t0003g0363 others(5): Show |
8 | NA18961.hp2 NA18962.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-1781C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5532964 | |||||||
| chr9:5533280 | A | G | 174 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(171): Show |
183 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.56-1465A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533280 | |||||||
| chr9:5533310 | C | G | 1 | a0002c0002t0001g0199 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.56-1435C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533310 | |||||||
| chr9:5533325 | C | T | 1 | a0002c0002t0001g0187 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.56-1420C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533325 | |||||||
| chr9:5533450 | A | G | 48 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0156 others(45): Show |
51 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.56-1295A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533450 | |||||||
| chr9:5533511 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.56-1234C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533511 | |||||||
| chr9:5533698 | C | T | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.56-1047C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533698 | |||||||
| chr9:5533831 | T | C | 48 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0156 others(45): Show |
51 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.56-914T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533831 | |||||||
| chr9:5533935 | C | T | 6 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0001g0272 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-810C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5533935 | |||||||
| chr9:5534068 | A | C | 2 | a0001c0001t0001g0115 a0002c0002t0013g0015 |
3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.56-677A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534068 | |||||||
| chr9:5534087 | T | G | 52 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0130 others(49): Show |
55 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.56-658T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534087 | |||||||
| chr9:5534243 | C | T | 118 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(115): Show |
124 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.56-502C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534243 | |||||||
| chr9:5534301 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.56-444A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534301 | |||||||
| chr9:5534424 | T | C | 24 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(21): Show |
25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.56-321T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534424 | |||||||
| chr9:5534432 | G | T | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-313G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534432 | |||||||
| chr9:5534590 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.56-155G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534590 | |||||||
| chr9:5534608 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56-137G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534608 | |||||||
| chr9:5534727 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0315 |
3 | NA18962.hp2 NA19066.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.56-18A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 2/6 | chr9 | 5534727 | |||||||
| chr9:5535123 | T | C | 36 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(33): Show |
39 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.361+73T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535123 | |||||||
| chr9:5535236 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.361+186G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535236 | |||||||
| chr9:5535274 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.361+224A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535274 | |||||||
| chr9:5535535 | G | C | 24 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(21): Show |
25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.361+485G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535535 | |||||||
| chr9:5535599 | C | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+549C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535599 | |||||||
| chr9:5535825 | T | G | 5 | a0003c0003t0001g0029 a0003c0003t0003g0248 a0003c0003t0003g0249 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+775T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535825 | |||||||
| chr9:5535884 | T | C | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0103 others(3): Show |
6 | HG00741.hp2 HG01981.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+834T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535884 | |||||||
| chr9:5535939 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.361+889T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535939 | |||||||
| chr9:5535946 | C | A | 1 | a0001c0001t0004g0304 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.361+896C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5535946 | |||||||
| chr9:5536058 | G | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0300 a0001c0001t0001g0314 others(11): Show |
15 | HG01993.hp1 HG02004.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.361+1008G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536058 | |||||||
| chr9:5536161 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.361+1111G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536161 | |||||||
| chr9:5536167 | A | G | 35 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(32): Show |
38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+1117A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536167 | |||||||
| chr9:5536288 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+1238A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536288 | |||||||
| chr9:5536307 | G | A | 1 | a0009c0010t0001g0274 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.361+1257G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536307 | |||||||
| chr9:5536361 | G | A | 1 | a0001c0001t0004g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.361+1311G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536361 | |||||||
| chr9:5536385 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361+1335C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536385 | |||||||
| chr9:5536494 | T | C | 1 | a0001c0001t0002g0022 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.361+1444T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536494 | |||||||
| chr9:5536780 | T | C | 1 | a0002c0002t0002g0095 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.361+1730T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536780 | |||||||
| chr9:5536846 | C | T | 1 | a0002c0002t0001g0347 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+1796C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536846 | |||||||
| chr9:5536849 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.361+1799G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536849 | |||||||
| chr9:5536904 | C | T | 2 | a0002c0002t0001g0131 a0002c0002t0001g0146 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.361+1854C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5536904 | |||||||
| chr9:5537066 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0123 a0001c0001t0001g0141 |
4 | HG01167.hp1 HG01192.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+2016G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537066 | |||||||
| chr9:5537071 | T | A | 35 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(32): Show |
38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+2021T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537071 | |||||||
| chr9:5537099 | G | A | 1 | a0001c0001t0003g0372 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.361+2049G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537099 | |||||||
| chr9:5537326 | G | C | 168 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(165): Show |
177 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.361+2276G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537326 | |||||||
| chr9:5537344 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.361+2294T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537344 | |||||||
| chr9:5537493 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.361+2443C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537493 | |||||||
| chr9:5537530 | C | T | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG01074.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+2480C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537530 | |||||||
| chr9:5537575 | C | T | 169 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(166): Show |
178 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.361+2525C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537575 | |||||||
| chr9:5537581 | G | C | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+2531G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537581 | |||||||
| chr9:5537646 | G | A | 35 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0115 others(32): Show |
39 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.361+2596G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537646 | |||||||
| chr9:5537688 | A | G | 36 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(33): Show |
39 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.361+2638A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537688 | |||||||
| chr9:5537761 | G | T | 3 | a0001c0001t0001g0147 a0001c0001t0002g0101 a0001c0001t0002g0106 |
3 | HG01109.hp2 HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.361+2711G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537761 | |||||||
| chr9:5537871 | C | G | 173 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(170): Show |
182 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.361+2821C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537871 | |||||||
| chr9:5537901 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0276 a0001c0001t0002g0114 others(1): Show |
4 | HG01081.hp1 HG01358.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+2851A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537901 | |||||||
| chr9:5537930 | G | A | 1 | a0002c0002t0006g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.361+2880G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537930 | |||||||
| chr9:5537952 | T | A | 1 | a0001c0001t0010g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.361+2902T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537952 | |||||||
| chr9:5537973 | G | C | 7 | a0001c0001t0001g0232 a0002c0002t0001g0229 a0002c0002t0005g0233 others(4): Show |
8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+2923G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5537973 | |||||||
| chr9:5538298 | G | T | 1 | a0001c0001t0002g0102 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.361+3248G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538298 | |||||||
| chr9:5538354 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.361+3304G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538354 | |||||||
| chr9:5538407 | C | T | 115 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(112): Show |
119 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.361+3357C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538407 | |||||||
| chr9:5538411 | C | T | 30 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(27): Show |
31 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.361+3361C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538411 | |||||||
| chr9:5538428 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.361+3378G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538428 | |||||||
| chr9:5538440 | C | T | 120 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(117): Show |
126 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.361+3390C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538440 | |||||||
| chr9:5538501 | T | A | 1 | a0001c0001t0001g0310 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.361+3451T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538501 | |||||||
| chr9:5538512 | T | C | 35 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(32): Show |
38 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.361+3462T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538512 | |||||||
| chr9:5538545 | G | A | 1 | a0002c0002t0020g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.361+3495G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538545 | |||||||
| chr9:5538607 | T | G | 33 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0115 others(30): Show |
37 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.361+3557T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538607 | |||||||
| chr9:5538610 | G | C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0115 others(30): Show |
37 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.361+3560G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538610 | |||||||
| chr9:5538628 | T | C | 2 | a0001c0001t0001g0115 a0002c0002t0013g0015 |
3 | HG03453.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+3578T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538628 | |||||||
| chr9:5538637 | G | A | 32 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(29): Show |
35 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.361+3587G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538637 | |||||||
| chr9:5538667 | G | A | 77 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(74): Show |
79 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.361+3617G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538667 | |||||||
| chr9:5538775 | A | T | 3 | a0001c0001t0001g0226 a0002c0002t0001g0065 a0002c0002t0014g0339 |
3 | HG02615.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.361+3725A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538775 | |||||||
| chr9:5538793 | G | A | 22 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(19): Show |
23 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.361+3743G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538793 | |||||||
| chr9:5538879 | A | G | 175 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(172): Show |
184 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.361+3829A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538879 | |||||||
| chr9:5538998 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361+3948G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5538998 | |||||||
| chr9:5539033 | A | G | 6 | a0001c0001t0001g0226 a0002c0002t0001g0065 a0002c0002t0001g0251 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+3983A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539033 | |||||||
| chr9:5539057 | T | C | 2 | a0001c0001t0003g0362 a0001c0001t0003g0363 |
2 | NA18961.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.361+4007T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539057 | |||||||
| chr9:5539151 | T | G | 94 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(91): Show |
97 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.361+4101T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539151 | |||||||
| chr9:5539175 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.361+4125T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539175 | |||||||
| chr9:5539247 | G | C | 94 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(91): Show |
97 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.361+4197G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539247 | |||||||
| chr9:5539256 | A | G | 1 | a0002c0002t0001g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.361+4206A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539256 | |||||||
| chr9:5539451 | G | A | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG00733.hp2 HG01496.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+4401G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539451 | |||||||
| chr9:5539536 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.361+4486C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539536 | |||||||
| chr9:5539537 | G | A | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG00733.hp2 HG01496.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+4487G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539537 | |||||||
| chr9:5539627 | G | C | 2 | a0002c0002t0001g0131 a0002c0002t0001g0146 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.361+4577G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539627 | |||||||
| chr9:5539866 | T | A | 22 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(19): Show |
24 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.361+4816T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539866 | |||||||
| chr9:5539929 | C | T | 92 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(89): Show |
94 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.361+4879C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539929 | |||||||
| chr9:5539988 | T | C | 1 | a0002c0002t0002g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.361+4938T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5539988 | |||||||
| chr9:5540154 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+5104T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540154 | |||||||
| chr9:5540167 | T | G | 53 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0156 others(50): Show |
57 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.361+5117T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540167 | |||||||
| chr9:5540183 | C | T | 10 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(7): Show |
10 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+5133C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540183 | |||||||
| chr9:5540202 | C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+5152C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540202 | |||||||
| chr9:5540215 | C | G | 93 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(90): Show |
95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.361+5165C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540215 | |||||||
| chr9:5540249 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.361+5199C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540249 | |||||||
| chr9:5540252 | T | A | 3 | a0002c0002t0001g0066 a0002c0002t0009g0334 a0002c0002t0009g0335 |
3 | HG02257.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.361+5202T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540252 | |||||||
| chr9:5540326 | C | A | 93 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(90): Show |
95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.361+5276C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540326 | |||||||
| chr9:5540350 | C | T | 46 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0042 others(43): Show |
48 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.361+5300C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540350 | |||||||
| chr9:5540364 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.361+5314A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540364 | |||||||
| chr9:5540528 | G | C | 1 | a0002c0002t0002g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.361+5478G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540528 | |||||||
| chr9:5540600 | A | C | 1 | a0002c0002t0005g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.361+5550A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540600 | |||||||
| chr9:5540651 | C | CTA | 95 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(92): Show |
97 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.361+5601_361+5602i others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540651 | |||||||
| chr9:5540697 | G | C | 2 | a0001c0001t0001g0256 a0002c0002t0011g0107 |
2 | HG01192.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.361+5647G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540697 | |||||||
| chr9:5540782 | A | T | 3 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0005c0006t0019g0104 |
3 | HG02647.hp1 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.361+5732A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540782 | |||||||
| chr9:5540838 | A | C | 1 | a0001c0001t0001g0194 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.361+5788A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540838 | |||||||
| chr9:5540891 | C | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.361+5841C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540891 | |||||||
| chr9:5540893 | A | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(10): Show |
16 | HG00438.hp1 NA18939.hp2 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.361+5843A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5540893 | |||||||
| chr9:5541255 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.361+6205T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541255 | |||||||
| chr9:5541461 | G | T | 2 | a0001c0001t0001g0226 a0002c0002t0014g0339 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.361+6411G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541461 | |||||||
| chr9:5541526 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
8 | HG01981.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.361+6476T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541526 | |||||||
| chr9:5541539 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.361+6489G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541539 | |||||||
| chr9:5541558 | A | G | 1 | a0002c0002t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.361+6508A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541558 | |||||||
| chr9:5541603 | T | C | 1 | a0002c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.361+6553T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541603 | |||||||
| chr9:5541607 | T | C | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.361+6557T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541607 | |||||||
| chr9:5541797 | C | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG01074.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+6747C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541797 | |||||||
| chr9:5541877 | G | A | 91 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(88): Show |
93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.361+6827G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541877 | |||||||
| chr9:5541931 | C | G | 30 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0193 others(27): Show |
34 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.361+6881C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541931 | |||||||
| chr9:5541984 | C | G | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | NA18984.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.361+6934C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5541984 | |||||||
| chr9:5542030 | A | G | 47 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0001g0156 others(44): Show |
50 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.361+6980A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542030 | |||||||
| chr9:5542032 | A | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0170 a0001c0001t0003g0350 |
4 | HG00642.hp1 HG01928.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+6982A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542032 | |||||||
| chr9:5542119 | T | C | 1 | a0002c0002t0001g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.361+7069T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542119 | |||||||
| chr9:5542339 | A | T | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-6996A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542339 | |||||||
| chr9:5542364 | C | G | 1 | a0002c0002t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.362-6971C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542364 | |||||||
| chr9:5542367 | AG | A | 91 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(88): Show |
93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.362-6967delG | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542367 | |||||||
| chr9:5542369 | C | A | 91 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(88): Show |
93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.362-6966C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542369 | |||||||
| chr9:5542535 | T | C | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-6800T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542535 | |||||||
| chr9:5542552 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.362-6783G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542552 | |||||||
| chr9:5542570 | A | T | 1 | a0001c0001t0002g0037 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.362-6765A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542570 | |||||||
| chr9:5542636 | G | A | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-6699G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542636 | |||||||
| chr9:5542749 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.362-6586C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542749 | |||||||
| chr9:5542813 | C | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG01074.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-6522C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542813 | |||||||
| chr9:5542848 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.362-6487A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542848 | |||||||
| chr9:5542859 | C | CA | 89 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(86): Show |
91 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.362-6468dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5542859 | ||||||
| chr9:5542881 | G | A | 10 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0002c0002t0006g0024 others(7): Show |
10 | HG01192.hp1 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.362-6454G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5542881 | |||||||
| chr9:5542987 | CAT | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0154 a0001c0001t0001g0202 others(13): Show |
19 | HG00642.hp2 HG00735.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.362-6339_362-6338d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5542987 | ||||||
| chr9:5543028 | A | G | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG00733.hp2 HG01496.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.362-6307A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543028 | |||||||
| chr9:5543087 | A | G | 1 | a0001c0001t0004g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.362-6248A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543087 | |||||||
| chr9:5543142 | C | T | 10 | a0001c0001t0001g0226 a0002c0002t0001g0065 a0002c0002t0001g0251 others(7): Show |
13 | HG02145.hp2 HG02615.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-6193C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543142 | |||||||
| chr9:5543241 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-6094A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543241 | |||||||
| chr9:5543271 | T | G | 3 | a0001c0001t0001g0147 a0001c0001t0002g0101 a0001c0001t0002g0106 |
3 | HG01109.hp2 HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.362-6064T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543271 | |||||||
| chr9:5543310 | T | C | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-6025T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543310 | |||||||
| chr9:5543311 | G | T | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-6024G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543311 | |||||||
| chr9:5543315 | A | G | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-6020A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543315 | |||||||
| chr9:5543330 | G | A | 46 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0115 others(43): Show |
50 | HG00741.hp1 HG00741.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.362-6005G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543330 | |||||||
| chr9:5543336 | A | G | 1 | a0002c0002t0011g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.362-5999A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543336 | |||||||
| chr9:5543340 | T | C | 2 | a0002c0002t0002g0329 a0002c0002t0011g0043 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.362-5995T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543340 | |||||||
| chr9:5543346 | T | C | 1 | a0001c0001t0002g0319 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.362-5989T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543346 | |||||||
| chr9:5543367 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.362-5968G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543367 | |||||||
| chr9:5543395 | C | T | 7 | a0001c0001t0001g0208 a0001c0001t0004g0140 a0001c0001t0004g0190 others(4): Show |
7 | NA18942.hp1 NA18944.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.362-5940C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543395 | |||||||
| chr9:5543400 | G | T | 1 | a0001c0001t0010g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.362-5935G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543400 | |||||||
| chr9:5543434 | G | T | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | HG00558.hp2 NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.362-5901G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543434 | |||||||
| chr9:5543534 | G | C | 15 | a0001c0001t0001g0130 a0001c0001t0001g0188 a0001c0001t0001g0276 others(12): Show |
15 | HG01081.hp1 HG01358.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.362-5801G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543534 | |||||||
| chr9:5543538 | C | CA | 134 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0083 others(131): Show |
139 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.362-5775dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5543538 | ||||||
| chr9:5543538 | C | CAA | 15 | a0001c0001t0001g0049 a0001c0001t0001g0132 a0001c0001t0001g0164 others(12): Show |
15 | HG01074.hp2 HG01192.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.362-5776_362-5775d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5543538 | ||||||
| chr9:5543538 | CA | C | 21 | a0001c0001t0001g0067 a0001c0001t0001g0160 a0001c0001t0001g0193 others(18): Show |
23 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.362-5775delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5543538 | ||||||
| chr9:5543616 | A | T | 11 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(8): Show |
11 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-5719A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543616 | |||||||
| chr9:5543690 | G | T | 2 | a0001c0001t0001g0226 a0002c0002t0014g0339 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.362-5645G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5543690 | |||||||
| chr9:5544027 | A | C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0115 a0001c0001t0001g0193 others(30): Show |
35 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.362-5308A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544027 | |||||||
| chr9:5544191 | G | A | 1 | a0002c0002t0002g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.362-5144G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544191 | |||||||
| chr9:5544235 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.362-5100G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544235 | |||||||
| chr9:5544405 | A | G | 155 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(152): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.362-4930A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544405 | |||||||
| chr9:5544437 | G | C | 2 | a0003c0003t0001g0029 a0003c0003t0003g0249 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.362-4898G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544437 | |||||||
| chr9:5544502 | C | T | 1 | a0002c0002t0009g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.362-4833C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544502 | |||||||
| chr9:5544740 | G | GT | 145 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(142): Show |
152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4595_362-4594i others(3): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544740 | |||||||
| chr9:5544742 | C | T | 145 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(142): Show |
152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4593C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544742 | |||||||
| chr9:5544744 | C | G | 145 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(142): Show |
152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4591C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544744 | |||||||
| chr9:5544769 | G | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-4566G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544769 | |||||||
| chr9:5544976 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.362-4359A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544976 | |||||||
| chr9:5544992 | G | A | 87 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(84): Show |
89 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.362-4343G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5544992 | |||||||
| chr9:5545117 | C | A | 6 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
8 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.362-4218C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545117 | |||||||
| chr9:5545163 | A | G | 1 | a0002c0002t0001g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.362-4172A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545163 | |||||||
| chr9:5545183 | G | C | 88 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(85): Show |
91 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.362-4152G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545183 | |||||||
| chr9:5545198 | T | C | 145 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(142): Show |
152 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.362-4137T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545198 | |||||||
| chr9:5545273 | G | T | 2 | a0002c0002t0006g0072 a0002c0002t0022g0355 |
2 | HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.362-4062G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545273 | |||||||
| chr9:5545430 | G | T | 2 | a0001c0001t0001g0179 a0002c0002t0001g0180 |
2 | NA18975.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.362-3905G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545430 | |||||||
| chr9:5545431 | C | A | 1 | a0001c0001t0003g0360 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.362-3904C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545431 | |||||||
| chr9:5545849 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.362-3486T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545849 | |||||||
| chr9:5545911 | G | A | 1 | a0008c0011t0001g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.362-3424G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545911 | |||||||
| chr9:5545922 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.362-3413T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5545922 | |||||||
| chr9:5546030 | T | C | 180 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(177): Show |
189 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.362-3305T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546030 | |||||||
| chr9:5546496 | A | C | 91 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(88): Show |
93 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.362-2839A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546496 | |||||||
| chr9:5546571 | T | C | 183 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(180): Show |
192 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.362-2764T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546571 | |||||||
| chr9:5546599 | T | G | 3 | a0001c0001t0001g0188 a0002c0002t0001g0171 a0002c0002t0001g0187 |
3 | HG03491.hp1 HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.362-2736T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546599 | |||||||
| chr9:5546602 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.362-2733G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546602 | |||||||
| chr9:5546616 | C | T | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.362-2719C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546616 | |||||||
| chr9:5546664 | C | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.362-2671C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546664 | |||||||
| chr9:5546775 | C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-2560C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546775 | |||||||
| chr9:5546857 | G | A | 156 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(153): Show |
165 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.362-2478G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546857 | |||||||
| chr9:5546882 | C | T | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-2453C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546882 | |||||||
| chr9:5546993 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.362-2342G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5546993 | |||||||
| chr9:5547148 | A | G | 2 | a0002c0002t0007g0001 a0002c0002t0007g0116 |
4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.362-2187A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547148 | |||||||
| chr9:5547288 | C | T | 24 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(21): Show |
25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-2047C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547288 | |||||||
| chr9:5547408 | C | T | 25 | a0001c0001t0001g0126 a0001c0001t0001g0156 a0001c0001t0001g0214 others(22): Show |
27 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.362-1927C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547408 | |||||||
| chr9:5547421 | T | G | 4 | a0002c0002t0002g0329 a0002c0002t0009g0332 a0002c0002t0009g0334 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-1914T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547421 | |||||||
| chr9:5547659 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.362-1676G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547659 | |||||||
| chr9:5547688 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-1647G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547688 | |||||||
| chr9:5547927 | ACT | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(18): Show |
22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.362-1405_362-1404d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5547927 | ||||||
| chr9:5547936 | C | CA | 20 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0151 others(17): Show |
22 | HG01074.hp1 HG01169.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.362-1378dupA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5547936 | ||||||
| chr9:5547936 | CA | C | 35 | a0001c0001t0001g0067 a0001c0001t0001g0130 a0001c0001t0001g0193 others(32): Show |
36 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.362-1378delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 5547936 | ||||||
| chr9:5547950 | A | G | 1 | a0002c0002t0001g0282 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.362-1385A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547950 | |||||||
| chr9:5547960 | A | T | 1 | a0002c0002t0001g0282 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.362-1375A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5547960 | |||||||
| chr9:5548121 | C | T | 1 | a0002c0002t0015g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.362-1214C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5548121 | |||||||
| chr9:5548484 | A | G | 1 | a0002c0002t0013g0015 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.362-851A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5548484 | |||||||
| chr9:5548542 | T | C | 24 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(21): Show |
25 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-793T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5548542 | |||||||
| chr9:5549063 | T | C | 6 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0001g0272 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-272T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5549063 | |||||||
| chr9:5549080 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0144 others(17): Show |
23 | HG00438.hp2 HG00673.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.362-255T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5549080 | |||||||
| chr9:5549099 | G | A | 130 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(127): Show |
137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.362-236G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 3/6 | chr9 | 5549099 | |||||||
| chr9:5549743 | G | C | 14 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(11): Show |
14 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.631+139G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5549743 | |||||||
| chr9:5549884 | C | G | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.631+280C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5549884 | |||||||
| chr9:5549952 | T | A | 2 | a0001c0001t0003g0020 a0001c0001t0004g0217 |
3 | NA18951.hp2 NA18961.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.631+348T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5549952 | |||||||
| chr9:5550135 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+531A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550135 | |||||||
| chr9:5550288 | A | G | 2 | a0002c0002t0007g0001 a0002c0002t0007g0116 |
4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+684A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550288 | |||||||
| chr9:5550320 | T | C | 1 | a0006c0005t0007g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.631+716T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550320 | |||||||
| chr9:5550351 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.631+747T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550351 | |||||||
| chr9:5550430 | T | G | 1 | a0002c0002t0001g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.631+826T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550430 | |||||||
| chr9:5550534 | T | A | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.631+930T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550534 | |||||||
| chr9:5550685 | ATC | A | 15 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(12): Show |
16 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.631+1095_631+1096d others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5550685 | ||||||
| chr9:5550698 | TC | T | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0103 others(3): Show |
6 | HG00741.hp2 HG01981.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1095delC | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550698 | |||||||
| chr9:5550699 | C | CT | 28 | a0001c0001t0001g0126 a0001c0001t0001g0156 a0001c0001t0001g0214 others(25): Show |
30 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.631+1107dupT | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5550699 | ||||||
| chr9:5550699 | CT | C | 88 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(85): Show |
90 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.631+1107delT | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5550699 | ||||||
| chr9:5550762 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.631+1158C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550762 | |||||||
| chr9:5550763 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.631+1159G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550763 | |||||||
| chr9:5550786 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+1182C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550786 | |||||||
| chr9:5550882 | T | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(127): Show |
135 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.631+1278T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550882 | |||||||
| chr9:5550973 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1369G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5550973 | |||||||
| chr9:5551037 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.631+1433A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551037 | |||||||
| chr9:5551261 | C | T | 151 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(148): Show |
159 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.631+1657C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551261 | |||||||
| chr9:5551380 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.631+1776C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551380 | |||||||
| chr9:5551385 | G | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(18): Show |
22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.631+1781G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551385 | |||||||
| chr9:5551413 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.631+1809T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551413 | |||||||
| chr9:5551451 | A | T | 130 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(127): Show |
137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.631+1847A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551451 | |||||||
| chr9:5551529 | T | G | 1 | a0001c0001t0001g0312 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.631+1925T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551529 | |||||||
| chr9:5551602 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.631+1998G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551602 | |||||||
| chr9:5551795 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.631+2191G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551795 | |||||||
| chr9:5551864 | C | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0197 others(18): Show |
22 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.631+2260C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551864 | |||||||
| chr9:5551945 | G | A | 130 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(127): Show |
137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.631+2341G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5551945 | |||||||
| chr9:5552030 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.631+2426G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552030 | |||||||
| chr9:5552152 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+2548G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552152 | |||||||
| chr9:5552166 | T | C | 6 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0001g0272 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+2562T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552166 | |||||||
| chr9:5552514 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
7 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.631+2910G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552514 | |||||||
| chr9:5552588 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.631+2984T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552588 | |||||||
| chr9:5552753 | T | G | 1 | a0005c0006t0019g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.631+3149T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552753 | |||||||
| chr9:5552786 | A | G | 2 | a0001c0001t0001g0115 a0002c0002t0002g0045 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.631+3182A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552786 | |||||||
| chr9:5552884 | C | T | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.631+3280C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552884 | |||||||
| chr9:5552900 | T | G | 1 | a0002c0002t0001g0347 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.631+3296T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552900 | |||||||
| chr9:5552910 | G | A | 1 | a0002c0002t0001g0383 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.631+3306G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5552910 | |||||||
| chr9:5553068 | T | C | 1 | a0001c0001t0012g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.631+3464T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553068 | |||||||
| chr9:5553162 | A | C | 1 | a0002c0002t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.631+3558A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553162 | |||||||
| chr9:5553191 | A | C | 2 | a0002c0002t0006g0024 a0002c0002t0006g0231 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.631+3587A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553191 | |||||||
| chr9:5553237 | A | C | 8 | a0001c0001t0001g0115 a0002c0002t0001g0270 a0002c0002t0001g0271 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+3633A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553237 | |||||||
| chr9:5553251 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.631+3647C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553251 | |||||||
| chr9:5553441 | A | G | 1 | a0002c0002t0006g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.631+3837A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553441 | |||||||
| chr9:5553703 | C | A | 2 | a0001c0001t0001g0308 a0002c0002t0001g0381 |
2 | HG03486.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.632-3915C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553703 | |||||||
| chr9:5553710 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.632-3908G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553710 | |||||||
| chr9:5553765 | T | A | 69 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0122 others(66): Show |
76 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.632-3853T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553765 | |||||||
| chr9:5553843 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.632-3775C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553843 | |||||||
| chr9:5553957 | G | A | 6 | a0001c0001t0001g0226 a0001c0001t0001g0343 a0001c0001t0001g0344 others(3): Show |
6 | HG02615.hp1 HG03225.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.632-3661G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553957 | |||||||
| chr9:5553991 | C | T | 25 | a0001c0001t0001g0067 a0001c0001t0001g0182 a0001c0001t0001g0193 others(22): Show |
26 | HG00741.hp1 HG00741.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.632-3627C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5553991 | |||||||
| chr9:5554035 | T | C | 139 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(136): Show |
147 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.632-3583T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554035 | |||||||
| chr9:5554095 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.632-3523C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554095 | |||||||
| chr9:5554109 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
7 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.632-3509T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554109 | |||||||
| chr9:5554219 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.632-3399A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554219 | |||||||
| chr9:5554274 | C | T | 1 | a0001c0001t0010g0149 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.632-3344C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554274 | |||||||
| chr9:5554275 | G | A | 2 | a0001c0001t0001g0256 a0002c0002t0011g0107 |
2 | HG01192.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.632-3343G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554275 | |||||||
| chr9:5554401 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632-3217C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554401 | |||||||
| chr9:5554430 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.632-3188A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554430 | |||||||
| chr9:5554770 | C | T | 88 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(85): Show |
90 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.632-2848C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554770 | |||||||
| chr9:5554773 | G | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(134): Show |
145 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.632-2845G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554773 | |||||||
| chr9:5554977 | G | A | 5 | a0003c0003t0001g0029 a0003c0003t0003g0248 a0003c0003t0003g0249 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-2641G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5554977 | |||||||
| chr9:5555007 | TA | T | 94 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(91): Show |
96 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.632-2602delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5555007 | ||||||
| chr9:5555023 | A | C | 142 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(139): Show |
150 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.632-2595A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555023 | |||||||
| chr9:5555130 | A | T | 1 | a0001c0001t0017g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.632-2488A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555130 | |||||||
| chr9:5555160 | A | C | 72 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0122 others(69): Show |
79 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.632-2458A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555160 | |||||||
| chr9:5555200 | A | T | 5 | a0003c0003t0001g0029 a0003c0003t0003g0248 a0003c0003t0003g0249 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-2418A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555200 | |||||||
| chr9:5555304 | C | A | 87 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(84): Show |
89 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.632-2314C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555304 | |||||||
| chr9:5555348 | C | T | 92 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(89): Show |
94 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.632-2270C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555348 | |||||||
| chr9:5555451 | C | T | 1 | a0002c0004t0005g0228 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.632-2167C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555451 | |||||||
| chr9:5555452 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.632-2166G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555452 | |||||||
| chr9:5555489 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0144 others(14): Show |
20 | HG00673.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.632-2129G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555489 | |||||||
| chr9:5555554 | G | A | 92 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(89): Show |
94 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.632-2064G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555554 | |||||||
| chr9:5555572 | G | A | 15 | a0001c0001t0001g0067 a0001c0001t0001g0182 a0001c0001t0001g0193 others(12): Show |
15 | HG00741.hp1 HG00741.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.632-2046G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555572 | |||||||
| chr9:5555572 | G | T | 93 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(90): Show |
95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.632-2046G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555572 | |||||||
| chr9:5555831 | G | A | 93 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(90): Show |
95 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.632-1787G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555831 | |||||||
| chr9:5555897 | C | T | 89 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(86): Show |
91 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.632-1721C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555897 | |||||||
| chr9:5555942 | C | T | 1 | a0001c0001t0003g0361 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.632-1676C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5555942 | |||||||
| chr9:5556024 | G | A | 380 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(377): Show |
402 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.632-1594G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556024 | |||||||
| chr9:5556034 | T | C | 173 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0067 others(170): Show |
182 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.632-1584T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556034 | |||||||
| chr9:5556122 | T | G | 94 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(91): Show |
96 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.632-1496T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556122 | |||||||
| chr9:5556129 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.632-1489C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556129 | |||||||
| chr9:5556272 | A | G | 2 | a0001c0001t0001g0115 a0002c0002t0002g0045 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.632-1346A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556272 | |||||||
| chr9:5556372 | CCTT | C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
10 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.632-1245_632-1243d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556372 | |||||||
| chr9:5556406 | T | C | 1 | a0001c0001t0004g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.632-1212T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556406 | |||||||
| chr9:5556434 | G | A | 94 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0083 others(91): Show |
96 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.632-1184G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556434 | |||||||
| chr9:5556444 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.632-1174G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556444 | |||||||
| chr9:5556514 | A | C | 1 | a0002c0002t0001g0288 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.632-1104A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556514 | |||||||
| chr9:5556532 | T | C | 2 | a0001c0001t0001g0115 a0002c0002t0002g0045 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.632-1086T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556532 | |||||||
| chr9:5556677 | C | T | 7 | a0001c0001t0001g0232 a0002c0002t0001g0229 a0002c0002t0005g0233 others(4): Show |
8 | HG01243.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.632-941C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556677 | |||||||
| chr9:5556700 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.632-918T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556700 | |||||||
| chr9:5556786 | A | G | 186 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(183): Show |
198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.632-832A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556786 | |||||||
| chr9:5556822 | T | C | 99 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0069 others(96): Show |
103 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.632-796T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556822 | |||||||
| chr9:5556999 | A | C | 1 | a0009c0010t0001g0274 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.632-619A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5556999 | |||||||
| chr9:5557104 | G | C | 1 | a0001c0001t0003g0360 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.632-514G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557104 | |||||||
| chr9:5557108 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.632-510T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557108 | |||||||
| chr9:5557249 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0194 a0001c0001t0001g0239 |
4 | NA18939.hp2 NA18943.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-369G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557249 | |||||||
| chr9:5557251 | TGATA | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0042 others(100): Show |
110 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.632-363_632-360del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5557251 | ||||||
| chr9:5557255 | A | G | 38 | a0001c0001t0001g0012 a0001c0001t0001g0122 a0001c0001t0001g0130 others(35): Show |
41 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.632-363A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557255 | |||||||
| chr9:5557255 | AGATG | A | 4 | a0001c0001t0001g0203 a0001c0001t0002g0047 a0002c0002t0002g0097 others(1): Show |
4 | HG01978.hp1 HG02572.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.632-355_632-352del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5557255 | ||||||
| chr9:5557263 | G | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0312 |
2 | HG02074.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.632-355G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557263 | |||||||
| chr9:5557267 | T | G | 3 | a0001c0001t0001g0302 a0001c0001t0001g0312 a0001c0001t0002g0061 |
3 | HG02074.hp1 HG04228.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.632-351T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557267 | |||||||
| chr9:5557267 | TGATG | T | 2 | a0001c0001t0003g0367 a0001c0001t0004g0014 |
3 | HG00544.hp2 NA19077.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.632-340_632-337del others(4): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 5557267 | ||||||
| chr9:5557302 | G | A | 1 | a0001c0001t0003g0337 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.632-316G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557302 | |||||||
| chr9:5557422 | T | C | 25 | a0001c0001t0001g0120 a0001c0001t0001g0130 a0001c0001t0001g0132 others(22): Show |
25 | HG00735.hp1 HG01081.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.632-196T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557422 | |||||||
| chr9:5557451 | G | A | 1 | a0002c0002t0002g0320 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.632-167G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557451 | |||||||
| chr9:5557561 | G | A | 2 | a0002c0002t0001g0347 a0002c0002t0002g0097 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.632-57G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557561 | |||||||
| chr9:5557562 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0262 |
3 | HG00438.hp2 NA18949.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.632-56T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557562 | |||||||
| chr9:5557608 | C | T | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.632-10C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557608 | |||||||
| chr9:5557611 | T | C | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.632-7T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 4/6 | chr9 | 5557611 | |||||||
| chr9:5557768 | T | G | 1 | a0003c0003t0003g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766+16T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557768 | |||||||
| chr9:5557793 | T | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0345 a0001c0001t0001g0346 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+41T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557793 | |||||||
| chr9:5557825 | G | C | 13 | a0002c0002t0001g0229 a0002c0002t0001g0270 a0002c0002t0001g0271 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+73G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557825 | |||||||
| chr9:5557926 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.766+174C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557926 | |||||||
| chr9:5557962 | A | C | 2 | a0002c0002t0001g0323 a0002c0002t0002g0329 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.766+210A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557962 | |||||||
| chr9:5557975 | G | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0075 a0001c0001t0002g0124 others(1): Show |
4 | HG02523.hp2 NA18612.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+223G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5557975 | |||||||
| chr9:5558202 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.766+450G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558202 | |||||||
| chr9:5558224 | G | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0345 a0001c0001t0001g0346 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+472G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558224 | |||||||
| chr9:5558347 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.766+595G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558347 | |||||||
| chr9:5558360 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.766+608C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558360 | |||||||
| chr9:5558394 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.766+642T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558394 | |||||||
| chr9:5558464 | T | C | 1 | a0001c0001t0002g0325 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.766+712T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558464 | |||||||
| chr9:5558793 | CAGAG | C | 24 | a0002c0002t0001g0138 a0002c0002t0001g0227 a0002c0002t0001g0229 others(21): Show |
25 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.766+1042_766+1045d others(6): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558793 | |||||||
| chr9:5558794 | A | G | 5 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0002c0002t0001g0323 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+1042A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558794 | |||||||
| chr9:5558834 | G | C | 24 | a0002c0002t0001g0138 a0002c0002t0001g0227 a0002c0002t0001g0229 others(21): Show |
25 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.766+1082G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558834 | |||||||
| chr9:5558919 | T | C | 1 | a0002c0002t0015g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.766+1167T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5558919 | |||||||
| chr9:5559128 | C | G | 1 | a0002c0002t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.766+1376C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559128 | |||||||
| chr9:5559430 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.766+1678G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559430 | |||||||
| chr9:5559495 | T | G | 65 | a0001c0001t0001g0264 a0001c0001t0002g0114 a0001c0001t0003g0353 others(62): Show |
70 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.766+1743T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559495 | |||||||
| chr9:5559539 | T | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0083 |
2 | NA18981.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.766+1787T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559539 | |||||||
| chr9:5559835 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.766+2083C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559835 | |||||||
| chr9:5559893 | C | T | 90 | a0001c0001t0002g0114 a0001c0001t0003g0353 a0002c0002t0001g0011 others(87): Show |
96 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.766+2141C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559893 | |||||||
| chr9:5559937 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0153 a0001c0001t0001g0185 others(3): Show |
8 | NA18989.hp2 NA19001.hp1 NA19006.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+2185C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559937 | |||||||
| chr9:5559962 | C | G | 5 | a0002c0002t0001g0270 a0002c0002t0001g0271 a0002c0002t0001g0272 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+2210C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5559962 | |||||||
| chr9:5560232 | C | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0222 a0001c0001t0001g0308 others(1): Show |
4 | HG00140.hp2 HG02735.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+2480C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560232 | |||||||
| chr9:5560320 | C | A | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.766+2568C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560320 | |||||||
| chr9:5560372 | T | G | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.766+2620T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560372 | |||||||
| chr9:5560392 | C | T | 11 | a0002c0002t0001g0138 a0002c0002t0001g0227 a0002c0002t0001g0266 others(8): Show |
12 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.766+2640C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560392 | |||||||
| chr9:5560469 | C | T | 6 | a0002c0002t0005g0159 a0002c0002t0005g0233 a0002c0002t0023g0118 others(3): Show |
7 | HG00741.hp2 HG01243.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.767-2693C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560469 | |||||||
| chr9:5560581 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0002g0089 |
2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.767-2581C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560581 | |||||||
| chr9:5560607 | C | G | 1 | a0002c0002t0001g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.767-2555C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560607 | |||||||
| chr9:5560632 | G | C | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-2530G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560632 | |||||||
| chr9:5560635 | C | T | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.767-2527C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560635 | |||||||
| chr9:5560685 | T | TGGTATCC others(324): Show |
3 | a0002c0002t0001g0271 a0002c0002t0001g0273 a0002c0002t0011g0043 |
3 | HG03139.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.767-2460_767-2459i others(333): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | ||||||
| chr9:5560685 | T | TGGTATCC others(325): Show |
4 | a0002c0002t0001g0270 a0002c0002t0001g0272 a0003c0003t0003g0248 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.767-2460_767-2459i others(334): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | ||||||
| chr9:5560685 | T | TGGTATCC others(326): Show |
4 | a0002c0002t0002g0045 a0003c0003t0001g0029 a0003c0003t0003g0249 others(1): Show |
4 | HG03098.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-2460_767-2459i others(335): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | ||||||
| chr9:5560685 | T | TGGTATCC others(327): Show |
1 | a0002c0002t0014g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.767-2460_767-2459i others(336): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | ||||||
| chr9:5560685 | T | TGGTATCC others(329): Show |
1 | a0002c0002t0001g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.767-2460_767-2459i others(338): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5560685 | ||||||
| chr9:5560777 | C | A | 2 | a0002c0002t0001g0171 a0002c0002t0001g0187 |
2 | HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.767-2385C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560777 | |||||||
| chr9:5560822 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.767-2340G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560822 | |||||||
| chr9:5560892 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.767-2270T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560892 | |||||||
| chr9:5560922 | C | G | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-2240C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5560922 | |||||||
| chr9:5561225 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.767-1937C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561225 | |||||||
| chr9:5561356 | A | C | 1 | a0001c0001t0002g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.767-1806A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561356 | |||||||
| chr9:5561423 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.767-1739A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561423 | |||||||
| chr9:5561616 | G | C | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.767-1546G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561616 | |||||||
| chr9:5561755 | A | G | 3 | a0002c0002t0002g0329 a0002c0002t0007g0001 a0002c0002t0007g0116 |
5 | HG02145.hp2 HG02809.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-1407A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561755 | |||||||
| chr9:5561851 | T | C | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-1311T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561851 | |||||||
| chr9:5561962 | C | T | 55 | a0001c0001t0002g0114 a0001c0001t0003g0353 a0002c0002t0001g0011 others(52): Show |
59 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.767-1200C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5561962 | |||||||
| chr9:5562075 | G | A | 2 | a0002c0002t0006g0068 a0002c0002t0006g0071 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.767-1087G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562075 | |||||||
| chr9:5562252 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.767-910G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562252 | |||||||
| chr9:5562327 | G | A | 1 | a0002c0002t0022g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.767-835G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562327 | |||||||
| chr9:5562563 | T | A | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767-599T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562563 | |||||||
| chr9:5562642 | TA | T | 340 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(337): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.767-510delA | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 5562642 | ||||||
| chr9:5562713 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.767-449T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562713 | |||||||
| chr9:5562762 | C | A | 1 | a0002c0002t0001g0288 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.767-400C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5562762 | |||||||
| chr9:5563115 | A | T | 11 | a0002c0002t0001g0138 a0002c0002t0001g0227 a0002c0002t0001g0266 others(8): Show |
12 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.767-47A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 5/6 | chr9 | 5563115 | |||||||
| chr9:5563217 | T | C | 1 | a0002c0002t0001g0187 | 1 | HG03927.hp1 | splice_region_variant&intron_variant | LOW | c.816+6T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563217 | |||||||
| chr9:5563364 | C | G | 1 | a0001c0001t0002g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.816+153C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563364 | |||||||
| chr9:5563438 | C | A | 1 | a0001c0001t0002g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.816+227C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563438 | |||||||
| chr9:5563645 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.816+434G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563645 | |||||||
| chr9:5563769 | T | C | 1 | a0001c0001t0010g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.816+558T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563769 | |||||||
| chr9:5563881 | C | G | 13 | a0001c0001t0002g0114 a0001c0001t0017g0309 a0002c0002t0001g0171 others(10): Show |
13 | HG00735.hp1 HG01358.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+670C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563881 | |||||||
| chr9:5563942 | T | C | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.816+731T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563942 | |||||||
| chr9:5563988 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.816+777A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5563988 | |||||||
| chr9:5564596 | T | C | 1 | a0002c0002t0001g0196 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.816+1385T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564596 | |||||||
| chr9:5564616 | C | G | 1 | a0007c0008t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.816+1405C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564616 | |||||||
| chr9:5564668 | A | T | 1 | a0006c0005t0007g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.816+1457A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564668 | |||||||
| chr9:5564748 | A | C | 61 | a0001c0001t0001g0264 a0001c0001t0001g0336 a0001c0001t0002g0114 others(58): Show |
65 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.816+1537A>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564748 | |||||||
| chr9:5564817 | G | C | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.816+1606G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5564817 | |||||||
| chr9:5565172 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.816+1961T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565172 | |||||||
| chr9:5565316 | G | A | 1 | a0002c0002t0001g0348 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.816+2105G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565316 | |||||||
| chr9:5565412 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0225 a0001c0001t0002g0037 others(2): Show |
5 | NA18977.hp2 NA18980.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+2201C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565412 | |||||||
| chr9:5565413 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+2202G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565413 | |||||||
| chr9:5565472 | C | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0214 a0001c0001t0002g0005 others(2): Show |
6 | HG00639.hp1 HG01257.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+2261C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565472 | |||||||
| chr9:5565601 | G | A | 75 | a0001c0001t0002g0114 a0002c0002t0001g0011 a0002c0002t0001g0048 others(72): Show |
81 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.816+2390G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565601 | |||||||
| chr9:5565684 | C | A | 1 | a0002c0002t0001g0323 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.816+2473C>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565684 | |||||||
| chr9:5565716 | G | A | 17 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0173 others(14): Show |
17 | HG00423.hp2 HG01099.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.816+2505G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565716 | |||||||
| chr9:5565860 | G | C | 380 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(377): Show |
402 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.816+2649G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5565860 | |||||||
| chr9:5565866 | CAAT | C | 6 | a0002c0002t0005g0159 a0002c0002t0005g0233 a0002c0002t0023g0118 others(3): Show |
7 | HG00741.hp2 HG01243.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+2658_816+2660d others(5): Show |
PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 5565866 | ||||||
| chr9:5566069 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+2858A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566069 | |||||||
| chr9:5566113 | GC | G | 72 | a0001c0001t0002g0114 a0002c0002t0001g0011 a0002c0002t0001g0048 others(69): Show |
78 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.816+2905delC | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 5566113 | ||||||
| chr9:5566129 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.816+2918G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566129 | |||||||
| chr9:5566148 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+2937C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566148 | |||||||
| chr9:5566192 | C | G | 1 | a0002c0002t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.816+2981C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566192 | |||||||
| chr9:5566240 | C | T | 1 | a0002c0002t0006g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.816+3029C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566240 | |||||||
| chr9:5566249 | T | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.816+3038T>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566249 | |||||||
| chr9:5566281 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.816+3070C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566281 | |||||||
| chr9:5566334 | G | C | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+3123G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566334 | |||||||
| chr9:5566381 | A | T | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+3170A>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566381 | |||||||
| chr9:5566393 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.816+3182C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566393 | |||||||
| chr9:5566465 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.816+3254G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566465 | |||||||
| chr9:5566474 | G | C | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+3263G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566474 | |||||||
| chr9:5566868 | C | G | 1 | a0001c0001t0004g0305 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.817-3086C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566868 | |||||||
| chr9:5566929 | C | T | 380 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(377): Show |
402 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(399): Show |
intron_variant | MODIFIER | c.817-3025C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5566929 | |||||||
| chr9:5567073 | G | C | 6 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0167 others(3): Show |
6 | HG00738.hp1 HG01074.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-2881G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567073 | |||||||
| chr9:5567182 | G | A | 13 | a0002c0002t0001g0229 a0002c0002t0001g0270 a0002c0002t0001g0271 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-2772G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567182 | |||||||
| chr9:5567237 | C | T | 2 | a0001c0001t0002g0004 a0001c0001t0002g0059 |
3 | NA18965.hp2 NA18969.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.817-2717C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567237 | |||||||
| chr9:5567389 | G | C | 2 | a0002c0002t0007g0001 a0002c0002t0007g0116 |
4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-2565G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567389 | |||||||
| chr9:5567471 | C | G | 1 | a0001c0001t0010g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.817-2483C>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567471 | |||||||
| chr9:5567623 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-2331G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567623 | |||||||
| chr9:5567678 | C | T | 2 | a0002c0002t0007g0001 a0002c0002t0007g0116 |
4 | HG02809.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-2276C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567678 | |||||||
| chr9:5567808 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.817-2146C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5567808 | |||||||
| chr9:5568222 | C | T | 69 | a0001c0001t0001g0258 a0001c0001t0002g0114 a0002c0002t0001g0011 others(66): Show |
75 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.817-1732C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568222 | |||||||
| chr9:5568230 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.817-1724C>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568230 | |||||||
| chr9:5568338 | T | C | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.817-1616T>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568338 | |||||||
| chr9:5568737 | G | T | 45 | a0001c0001t0001g0258 a0001c0001t0002g0114 a0002c0002t0001g0011 others(42): Show |
47 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.817-1217G>T | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5568737 | |||||||
| chr9:5569155 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.817-799A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569155 | |||||||
| chr9:5569255 | G | C | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.817-699G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569255 | |||||||
| chr9:5569406 | G | A | 33 | a0002c0002t0001g0011 a0002c0002t0001g0070 a0002c0002t0001g0127 others(30): Show |
35 | HG00597.hp2 HG00609.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.817-548G>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569406 | |||||||
| chr9:5569495 | A | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-459A>G | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569495 | |||||||
| chr9:5569860 | T | A | 52 | a0001c0001t0001g0258 a0001c0001t0001g0264 a0001c0001t0002g0114 others(49): Show |
56 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.817-94T>A | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569860 | |||||||
| chr9:5569871 | G | C | 1 | a0002c0002t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817-83G>C | PDCD1LG2 | ENSG00000197646.8 | transcript | ENST00000397747.5 | protein_coding | 6/6 | chr9 | 5569871 |