Item | Value |
---|---|
geneid | 27250 |
ensemblid | ENSG00000150593.18 |
hgncid | 8763 |
symbol | PDCD4 |
name | programmed cell death 4 |
refseq_nuc | NM_014456.5 |
refseq_prot | NP_055271.2 |
ensembl_nuc | ENST00000280154.12 |
ensembl_prot | ENSP00000280154.7 |
mane_status | MANE Select |
chr | chr10 |
start | 110871928 |
end | 110900006 |
strand | + |
ver | v1.2 |
region | chr10:110871928-110900006 |
region5000 | chr10:110866928-110905006 |
regionname0 | PDCD4_chr10_110871928_110900006 |
regionname5000 | PDCD4_chr10_110866928_110905006 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 469 | 398 | 78 | 64 | 205 | 11 | 40 | 164 | PDCD4_chr10_110866928_110905006 | PDCD4 | MDVEN others(464): Show |
chr10 | 110866928 | 110905006 |
a0002 | 0/0 | 469 | 16 | 11 | 2 | 0 | 1 | 2 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | MDVEN others(464): Show |
chr10 | 110866928 | 110905006 |
a0003 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | MDVEN others(464): Show |
chr10 | 110866928 | 110905006 |
a0004 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | MDVEN others(464): Show |
chr10 | 110866928 | 110905006 |
a0005 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | MDVEN others(464): Show |
chr10 | 110866928 | 110905006 |
a0006 | 0/0 | 469 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | MDVEN others(464): Show |
chr10 | 110866928 | 110905006 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1407 | 396 | 77 | 64 | 204 | 11 | 40 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0001c0006 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0001c0007 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0002c0002 | 0/0 | 1407 | 12 | 9 | 2 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0002c0003 | 0/0 | 1407 | 3 | 1 | 0 | 0 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0002c0004 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0003c0008 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0004c0010 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0005c0009 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 | ||
a0006c0005 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | ATGGA others(1402): Show |
chr10 | 110866928 | 110905006 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3479 | 100 | 10 | 30 | 40 | 9 | 11 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0002 | 0/0 | 3480 | 83 | 2 | 14 | 62 | 0 | 5 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0003 | 0/0 | 3481 | 58 | 10 | 3 | 39 | 2 | 4 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0004 | 0/0 | 3480 | 21 | 13 | 1 | 3 | 0 | 4 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0005 | 0/0 | 3480 | 19 | 4 | 3 | 10 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0006 | 0/0 | 3477 | 18 | 0 | 0 | 16 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3472): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0007 | 0/0 | 3481 | 14 | 3 | 2 | 4 | 0 | 5 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0008 | 0/0 | 3480 | 12 | 12 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0009 | 0/0 | 3480 | 12 | 0 | 5 | 6 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0010 | 0/0 | 3481 | 9 | 3 | 3 | 0 | 0 | 3 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0011 | 0/0 | 3480 | 9 | 9 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0013 | 0/0 | 3481 | 5 | 0 | 0 | 5 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0014 | 0/0 | 3481 | 5 | 0 | 0 | 5 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0015 | 0/0 | 3482 | 5 | 3 | 1 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3477): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0016 | 0/0 | 3480 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0018 | 0/0 | 3480 | 2 | 0 | 1 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0019 | 0/0 | 3481 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0021 | 0/0 | 3481 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0022 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3461): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0023 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3471): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0024 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0025 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0026 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0027 | 0/0 | 3478 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3473): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0028 | 0/0 | 3479 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0029 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3472): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0030 | 0/0 | 3476 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3471): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0031 | 0/0 | 3480 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0032 | 0/0 | 3479 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0033 | 0/0 | 3481 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0034 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0035 | 0/0 | 3478 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3473): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0036 | 0/0 | 3503 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3498): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0040 | 0/0 | 3482 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3477): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0041 | 0/0 | 3481 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0001t0042 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0001c0006t0007 | 0/0 | 3481 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0001c0007t0037 | 0/0 | 3481 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0002c0002t0012 | 0/0 | 3477 | 6 | 3 | 2 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3472): Show |
chr10 | 110866928 | 110905006 |
a0002c0002t0017 | 0/0 | 3482 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3477): Show |
chr10 | 110866928 | 110905006 |
a0002c0002t0020 | 0/0 | 3482 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3477): Show |
chr10 | 110866928 | 110905006 |
a0002c0002t0038 | 0/0 | 3482 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3477): Show |
chr10 | 110866928 | 110905006 |
a0002c0003t0004 | 0/0 | 3480 | 2 | 0 | 0 | 0 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3475): Show |
chr10 | 110866928 | 110905006 |
a0002c0003t0039 | 0/0 | 3481 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0002c0004t0010 | 0/0 | 3481 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0003c0008t0001 | 0/0 | 3479 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0004c0010t0001 | 0/0 | 3479 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3474): Show |
chr10 | 110866928 | 110905006 |
a0005c0009t0007 | 0/0 | 3481 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3476): Show |
chr10 | 110866928 | 110905006 |
a0006c0005t0012 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | AGAGA others(3472): Show |
chr10 | 110866928 | 110905006 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 24 | 1 | 3 | 18 | 1 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0005 | 0/0 | 14 | 0 | 1 | 11 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0006 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0001 | 0/0 | 36 | 2 | 8 | 24 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0009 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 3 | 2 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0004 | 0/0 | 12 | 4 | 2 | 5 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0006g0003 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0015 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0009g0002 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0009g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0009g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0009g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0010g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0010g0024 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0011g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0011g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0013g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0013g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0014g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0014g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0014g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0014g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0014g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0015g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0015g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0016g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0016g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0018g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0019g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0021g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0022g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0023g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0024g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0025g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0026g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0027g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0028g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0029g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0031g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0032g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0033g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0034g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0035g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0036g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0040g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0041g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0001t0042g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0006t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0001c0007t0037g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0012g0030 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0012g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0012g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0017g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0017g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0020g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0002t0038g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0003t0004g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0003t0039g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0002c0004t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0003c0008t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0004c0010t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0005c0009t0007g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
a0006c0005t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00438 | hp1 | a0003 | c0008 | t0001 | g0005 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00609 | hp1 | a0001 | c0001 | t0026 | g0173 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00741 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG00741 | hp2 | a0001 | c0001 | t0010 | g0106 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01069 | hp1 | a0001 | c0001 | t0027 | g0010 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01074 | hp1 | a0002 | c0002 | t0012 | g0175 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0004 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01168 | hp1 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01168 | hp2 | a0002 | c0002 | t0012 | g0030 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0022 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0052 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0079 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01261 | hp1 | a0001 | c0001 | t0010 | g0024 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0078 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01884 | hp2 | a0002 | c0002 | t0017 | g0051 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01891 | hp2 | a0002 | c0002 | t0017 | g0174 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0022 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02004 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02040 | hp2 | a0001 | c0001 | t0018 | g0057 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02135 | hp2 | a0001 | c0001 | t0029 | g0003 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CDX | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0013 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02273 | hp1 | a0001 | c0001 | t0009 | g0104 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0071 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02451 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02451 | hp2 | a0002 | c0002 | t0012 | g0178 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02523 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | KHV | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0067 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02602 | hp1 | a0001 | c0001 | t0010 | g0024 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0153 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02615 | hp2 | a0001 | c0001 | t0033 | g0141 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02630 | hp2 | a0002 | c0002 | t0020 | g0177 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02647 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0003 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02683 | hp2 | a0001 | c0001 | t0007 | g0015 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02698 | hp2 | a0002 | c0003 | t0004 | g0041 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02717 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02717 | hp2 | a0001 | c0001 | t0022 | g0004 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0152 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02735 | hp1 | a0001 | c0001 | t0010 | g0189 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0112 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02818 | hp1 | a0001 | c0001 | t0042 | g0185 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02896 | hp1 | a0001 | c0001 | t0028 | g0110 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02922 | hp1 | a0002 | c0003 | t0039 | g0053 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0070 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03139 | hp2 | a0001 | c0001 | t0016 | g0180 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03195 | hp1 | a0002 | c0002 | t0017 | g0051 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0069 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03225 | hp2 | a0001 | c0001 | t0016 | g0179 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03486 | hp1 | a0002 | c0002 | t0038 | g0031 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03490 | hp2 | a0001 | c0001 | t0007 | g0015 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03491 | hp1 | a0001 | c0001 | t0030 | g0003 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0015 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0003 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03516 | hp1 | a0001 | c0007 | t0037 | g0188 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03540 | hp2 | a0002 | c0002 | t0012 | g0031 | AFR | GWD | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03579 | hp2 | a0002 | c0002 | t0020 | g0176 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03654 | hp1 | a0001 | c0001 | t0010 | g0155 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03688 | hp1 | a0004 | c0010 | t0001 | g0095 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03831 | hp1 | a0001 | c0001 | t0040 | g0118 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03834 | hp2 | a0001 | c0001 | t0009 | g0002 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03927 | hp1 | a0005 | c0009 | t0007 | g0111 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04115 | hp2 | a0001 | c0001 | t0032 | g0157 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0022 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04199 | hp1 | a0002 | c0003 | t0004 | g0041 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | STU | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | YRI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18522 | hp2 | a0001 | c0001 | t0016 | g0142 | AFR | YRI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0034 | AFR | YRI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18942 | hp2 | a0001 | c0001 | t0014 | g0134 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18943 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18944 | hp2 | a0001 | c0001 | t0031 | g0007 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18947 | hp2 | a0001 | c0001 | t0013 | g0018 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18948 | hp1 | a0001 | c0001 | t0013 | g0018 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18953 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18953 | hp2 | a0001 | c0001 | t0009 | g0087 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18959 | hp1 | a0001 | c0001 | t0014 | g0139 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18959 | hp2 | a0001 | c0006 | t0007 | g0042 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18961 | hp2 | a0001 | c0001 | t0035 | g0128 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18970 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18972 | hp2 | a0001 | c0001 | t0014 | g0127 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18977 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0115 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18980 | hp2 | a0001 | c0001 | t0013 | g0018 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18981 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18986 | hp1 | a0001 | c0001 | t0025 | g0007 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18987 | hp1 | a0001 | c0001 | t0023 | g0011 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18987 | hp2 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18991 | hp2 | a0001 | c0001 | t0014 | g0126 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18992 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18994 | hp2 | a0001 | c0001 | t0034 | g0074 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18997 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18999 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19009 | hp2 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19010 | hp1 | a0001 | c0001 | t0013 | g0190 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19011 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19030 | hp1 | a0002 | c0004 | t0010 | g0169 | AFR | LWK | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19030 | hp2 | a0001 | c0001 | t0041 | g0151 | AFR | LWK | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | LWK | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0154 | AFR | LWK | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19055 | hp1 | a0001 | c0001 | t0007 | g0113 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19058 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19062 | hp2 | a0001 | c0001 | t0013 | g0018 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19076 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19078 | hp1 | a0001 | c0001 | t0021 | g0019 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19079 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19080 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19083 | hp1 | a0001 | c0001 | t0015 | g0008 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19085 | hp2 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19087 | hp1 | a0001 | c0001 | t0036 | g0007 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19240 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | YRI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | YRI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20129 | hp1 | a0006 | c0005 | t0012 | g0031 | AFR | ASW | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ASW | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20752 | hp2 | a0002 | c0002 | t0012 | g0030 | EUR | TSI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | GIH | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0007 | SAS | GIH | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0047 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02486 | hp1 | a0002 | c0002 | t0012 | g0030 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0066 | AFR | ACB | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | USA | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18955 | hp1 | a0001 | c0001 | t0024 | g0191 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | USA | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
NA21309 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | LWK | PDCD4_chr10_110866928_110905006 | PDCD4 | chr10 | 110866928 | 110905006 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:110881295 | A | G | 4 | a0001 a0003 a0004 others(1): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
missense_variant | MODERATE | c.106A>G | p.Ile36Val | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/12 | 259/3481 | 106/1410 | 36/469 | chr10 | 110881295 | |||
chr10:110881424 | G | A | 1 | a0003 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.235G>A | p.Asp79Asn | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/12 | 388/3481 | 235/1410 | 79/469 | chr10 | 110881424 | |||
chr10:110887675 | G | A | 1 | a0005 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.566G>A | p.Arg189Lys | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/12 | 719/3481 | 566/1410 | 189/469 | chr10 | 110887675 | |||
chr10:110887807 | C | T | 1 | a0006 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.698C>T | p.Thr233Ile | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/12 | 851/3481 | 698/1410 | 233/469 | chr10 | 110887807 | |||
chr10:110896020 | C | T | 1 | a0004 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1282C>T | p.Arg428Trp | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/12 | 1435/3481 | 1282/1410 | 428/469 | chr10 | 110896020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:110881291 | G | A | 1 | a0002c0004 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.102G>A | p.Glu34Glu | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/12 | 255/3481 | 102/1410 | 34/469 | chr10 | 110881291 | |||
chr10:110881300 | G | A | 1 | a0001c0006 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.111G>A | p.Lys37Lys | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/12 | 264/3481 | 111/1410 | 37/469 | chr10 | 110881300 | |||
chr10:110881342 | C | T | 1 | a0004c0010 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.153C>T | p.Asn51Asn | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/12 | 306/3481 | 153/1410 | 51/469 | chr10 | 110881342 | |||
chr10:110881417 | G | A | 1 | a0001c0007 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.228G>A | p.Ser76Ser | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/12 | 381/3481 | 228/1410 | 76/469 | chr10 | 110881417 | |||
chr10:110885330 | G | A | 2 | a0002c0002 a0006c0005 |
13 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(10): Show |
synonymous_variant | LOW | c.519G>A | p.Gln173Gln | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/12 | 672/3481 | 519/1410 | 173/469 | chr10 | 110885330 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:110871966 | G | T | 1 | a0001c0001t0042 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-115G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/12 | 4062 | chr10 | 110871966 | ||||||
chr10:110875975 | G | A | 1 | a0001c0001t0021 | 1 | NA19078.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/12 | 53 | chr10 | 110875975 | ||||||
chr10:110898123 | A | T | 2 | a0001c0001t0011 a0001c0001t0041 |
10 | HG02109.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*35A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 35 | chr10 | 110898123 | ||||||
chr10:110898158 | GT | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(23): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*90delT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 90 | INFO_REALIGN_3_PRIME | chr10 | 110898158 | |||||
chr10:110898158 | GTT | G | 6 | a0001c0001t0018 a0001c0001t0023 a0001c0001t0024 others(3): Show |
7 | HG00609.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*89_*90delTT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 89 | INFO_REALIGN_3_PRIME | chr10 | 110898158 | |||||
chr10:110898158 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0022 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75_*90delTTTTTTTT others(8): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 75 | INFO_REALIGN_3_PRIME | chr10 | 110898158 | |||||
chr10:110898240 | T | G | 1 | a0001c0001t0028 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 152 | chr10 | 110898240 | ||||||
chr10:110898260 | CTTTT | C | 5 | a0001c0001t0006 a0001c0001t0023 a0001c0001t0029 others(2): Show |
22 | HG00544.hp2 HG02071.hp1 HG02083.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*179_*182delTTTT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 179 | INFO_REALIGN_3_PRIME | chr10 | 110898260 | |||||
chr10:110898269 | T | C | 6 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0024 others(3): Show |
28 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*181T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 181 | chr10 | 110898269 | ||||||
chr10:110898302 | G | A | 7 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0014 others(4): Show |
102 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*214G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 214 | chr10 | 110898302 | ||||||
chr10:110898310 | T | C | 1 | a0001c0001t0029 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 222 | chr10 | 110898310 | ||||||
chr10:110898390 | G | A | 4 | a0001c0001t0016 a0001c0007t0037 a0002c0002t0012 others(1): Show |
11 | HG01074.hp1 HG01168.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*302G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 302 | chr10 | 110898390 | ||||||
chr10:110898945 | T | C | 1 | a0001c0001t0008 | 12 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*857T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 857 | chr10 | 110898945 | ||||||
chr10:110898959 | A | ATCTGACC others(15): Show |
1 | a0001c0001t0036 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873_*894dupCTGACC others(16): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 895 | INFO_REALIGN_3_PRIME | chr10 | 110898959 | |||||
chr10:110898977 | TTAAG | T | 2 | a0002c0002t0012 a0006c0005t0012 |
7 | HG01074.hp1 HG01168.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*891_*894delAAGT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 891 | INFO_REALIGN_3_PRIME | chr10 | 110898977 | |||||
chr10:110899206 | G | T | 3 | a0001c0001t0007 a0001c0006t0007 a0005c0009t0007 |
16 | HG01175.hp2 HG01978.hp2 HG02258.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1118G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1118 | chr10 | 110899206 | ||||||
chr10:110899291 | T | C | 5 | a0001c0001t0042 a0002c0002t0017 a0002c0002t0020 others(2): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1203T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1203 | chr10 | 110899291 | ||||||
chr10:110899372 | T | G | 1 | a0001c0001t0042 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1284T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1284 | chr10 | 110899372 | ||||||
chr10:110899525 | C | T | 1 | a0001c0001t0034 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1437C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1437 | chr10 | 110899525 | ||||||
chr10:110899526 | G | A | 1 | a0001c0001t0040 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1438G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1438 | chr10 | 110899526 | ||||||
chr10:110899705 | G | C | 5 | a0001c0001t0033 a0002c0002t0012 a0002c0002t0017 others(2): Show |
12 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1617G>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1617 | chr10 | 110899705 | ||||||
chr10:110899719 | C | T | 4 | a0001c0001t0033 a0002c0002t0012 a0002c0002t0038 others(1): Show |
9 | HG01074.hp1 HG01168.hp2 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1631C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1631 | chr10 | 110899719 | ||||||
chr10:110899796 | C | CA | 20 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(17): Show |
115 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1723dupA | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1724 | INFO_REALIGN_3_PRIME | chr10 | 110899796 | |||||
chr10:110899796 | CA | C | 8 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0027 others(5): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1723delA | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1723 | INFO_REALIGN_3_PRIME | chr10 | 110899796 | |||||
chr10:110899946 | T | C | 1 | a0001c0001t0042 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1858T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1858 | chr10 | 110899946 | ||||||
chr10:110899948 | T | A | 1 | a0001c0001t0031 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1860T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 12/12 | 1860 | chr10 | 110899948 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:110872026 | C | T | 3 | a0001c0001t0013g0018 a0001c0001t0013g0190 a0001c0001t0024g0191 |
6 | NA18947.hp2 NA18948.hp1 NA18955.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.-63+8C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872026 | |||||||
chr10:110872208 | C | G | 1 | a0001c0001t0010g0189 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-63+190C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872208 | |||||||
chr10:110872493 | C | G | 1 | a0001c0007t0037g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-63+475C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872493 | |||||||
chr10:110872501 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-63+483C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872501 | |||||||
chr10:110872519 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-63+501C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872519 | |||||||
chr10:110872607 | A | G | 1 | a0001c0001t0042g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-63+589A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872607 | |||||||
chr10:110872622 | G | A | 1 | a0001c0001t0005g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-63+604G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872622 | |||||||
chr10:110872631 | C | A | 1 | a0002c0003t0039g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-63+613C>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872631 | |||||||
chr10:110872649 | G | A | 22 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0013 others(19): Show |
42 | HG00408.hp2 HG00642.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-63+631G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872649 | |||||||
chr10:110872711 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-63+693G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872711 | |||||||
chr10:110872712 | T | C | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-63+694T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872712 | |||||||
chr10:110872891 | T | G | 1 | a0001c0001t0007g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-63+873T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872891 | |||||||
chr10:110872924 | G | T | 1 | a0001c0001t0002g0184 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-63+906G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110872924 | |||||||
chr10:110873003 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-63+985C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873003 | |||||||
chr10:110873052 | C | G | 1 | a0001c0001t0007g0182 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-63+1034C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873052 | |||||||
chr10:110873144 | T | A | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-63+1126T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873144 | |||||||
chr10:110873219 | G | GA | 3 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0028g0110 |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-63+1207dupA | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 110873219 | ||||||
chr10:110873323 | A | C | 1 | a0001c0001t0003g0181 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-63+1305A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873323 | |||||||
chr10:110873388 | C | T | 1 | a0001c0001t0003g0062 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-63+1370C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873388 | |||||||
chr10:110873414 | G | A | 11 | a0001c0001t0007g0015 a0001c0001t0007g0022 a0001c0001t0007g0042 others(8): Show |
16 | HG01175.hp2 HG01978.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-63+1396G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873414 | |||||||
chr10:110873454 | G | A | 1 | a0001c0001t0003g0116 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-63+1436G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873454 | |||||||
chr10:110873503 | C | A | 1 | a0001c0001t0006g0117 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-63+1485C>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873503 | |||||||
chr10:110873574 | C | G | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-63+1556C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873574 | |||||||
chr10:110873913 | T | C | 55 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(52): Show |
101 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-63+1895T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110873913 | |||||||
chr10:110874160 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-62-1806T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110874160 | |||||||
chr10:110874226 | A | G | 1 | a0001c0001t0007g0115 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-62-1740A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110874226 | |||||||
chr10:110874265 | A | G | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-62-1701A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110874265 | |||||||
chr10:110874276 | T | C | 1 | a0001c0001t0002g0044 | 2 | NA18960.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-62-1690T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110874276 | |||||||
chr10:110874307 | C | G | 11 | a0001c0001t0007g0015 a0001c0001t0007g0022 a0001c0001t0007g0042 others(8): Show |
16 | HG01175.hp2 HG01978.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-62-1659C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110874307 | |||||||
chr10:110874695 | A | C | 14 | a0001c0001t0016g0142 a0001c0001t0016g0179 a0001c0001t0016g0180 others(11): Show |
17 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-62-1271A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110874695 | |||||||
chr10:110875224 | T | G | 18 | a0001c0001t0005g0007 a0001c0001t0005g0045 a0001c0001t0005g0046 others(15): Show |
28 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-62-742T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875224 | |||||||
chr10:110875317 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-62-649A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875317 | |||||||
chr10:110875371 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-62-595A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875371 | |||||||
chr10:110875581 | C | A | 1 | a0001c0001t0040g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-62-385C>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875581 | |||||||
chr10:110875690 | A | G | 13 | a0001c0001t0016g0142 a0001c0001t0016g0179 a0001c0001t0016g0180 others(10): Show |
16 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-62-276A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875690 | |||||||
chr10:110875739 | C | G | 1 | a0001c0001t0026g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-62-227C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875739 | |||||||
chr10:110875744 | AT | A | 12 | a0001c0001t0004g0065 a0001c0001t0004g0068 a0001c0001t0008g0020 others(9): Show |
16 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-62-211delT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 110875744 | ||||||
chr10:110875867 | GT | G | 10 | a0002c0002t0012g0030 a0002c0002t0012g0031 a0002c0002t0012g0175 others(7): Show |
13 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-62-98delT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875867 | |||||||
chr10:110875871 | T | G | 1 | a0001c0001t0003g0061 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-62-95T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | chr10 | 110875871 | |||||||
chr10:110875889 | TTAAG | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0004g0028 others(5): Show |
15 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-62-71_-62-68delAA others(2): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 110875889 | ||||||
chr10:110876309 | A | T | 1 | a0001c0001t0010g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.43+239A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110876309 | |||||||
chr10:110876374 | G | T | 1 | a0002c0003t0039g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.43+304G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110876374 | |||||||
chr10:110876391 | T | A | 5 | a0001c0001t0011g0012 a0001c0001t0011g0047 a0001c0001t0011g0152 others(2): Show |
10 | HG02109.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+321T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110876391 | |||||||
chr10:110876502 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.43+432C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110876502 | |||||||
chr10:110876911 | A | G | 2 | a0001c0001t0008g0070 a0001c0001t0008g0071 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.43+841A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110876911 | |||||||
chr10:110877095 | A | T | 1 | a0001c0001t0003g0060 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.43+1025A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877095 | |||||||
chr10:110877312 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.43+1242T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877312 | |||||||
chr10:110877318 | C | T | 2 | a0001c0001t0008g0034 a0001c0001t0008g0069 |
3 | HG03225.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.43+1248C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877318 | |||||||
chr10:110877437 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.43+1367A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877437 | |||||||
chr10:110877510 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.43+1440T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877510 | |||||||
chr10:110877619 | T | C | 1 | a0001c0001t0004g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.43+1549T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877619 | |||||||
chr10:110877716 | A | G | 1 | a0001c0001t0042g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43+1646A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877716 | |||||||
chr10:110877874 | A | G | 1 | a0002c0004t0010g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.43+1804A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110877874 | |||||||
chr10:110878027 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.43+1957A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878027 | |||||||
chr10:110878053 | A | C | 1 | a0001c0001t0042g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43+1983A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878053 | |||||||
chr10:110878143 | G | T | 1 | a0001c0001t0016g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43+2073G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878143 | |||||||
chr10:110878205 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.43+2135C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878205 | |||||||
chr10:110878270 | T | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.43+2200T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878270 | |||||||
chr10:110878626 | T | C | 1 | a0002c0003t0039g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.43+2556T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878626 | |||||||
chr10:110878635 | A | G | 43 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0017 others(40): Show |
102 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.43+2565A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878635 | |||||||
chr10:110878746 | T | G | 42 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0017 others(39): Show |
101 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.44-2487T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110878746 | |||||||
chr10:110878824 | GCTAATAG others(19): Show |
G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0028g0110 |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-2383_44-2358del others(26): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 110878824 | ||||||
chr10:110879001 | C | T | 1 | a0001c0001t0003g0062 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.44-2232C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879001 | |||||||
chr10:110879057 | A | G | 4 | a0002c0002t0012g0031 a0002c0002t0012g0178 a0002c0002t0038g0031 others(1): Show |
4 | HG02451.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-2176A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879057 | |||||||
chr10:110879090 | T | G | 1 | a0001c0001t0005g0143 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44-2143T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879090 | |||||||
chr10:110879182 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.44-2051A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879182 | |||||||
chr10:110879308 | TAGC | T | 42 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0017 others(39): Show |
101 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.44-1922_44-1920del others(3): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 110879308 | ||||||
chr10:110879639 | C | T | 1 | a0001c0001t0040g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.44-1594C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879639 | |||||||
chr10:110879640 | G | A | 1 | a0001c0001t0004g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.44-1593G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879640 | |||||||
chr10:110879652 | C | CA | 43 | a0001c0001t0001g0075 a0001c0001t0002g0001 a0001c0001t0002g0009 others(40): Show |
100 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.44-1563dupA | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 110879652 | ||||||
chr10:110879652 | CA | C | 7 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
7 | HG00323.hp1 HG00323.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-1563delA | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 110879652 | ||||||
chr10:110879847 | T | C | 30 | a0001c0001t0003g0003 a0001c0001t0003g0011 a0001c0001t0003g0016 others(27): Show |
54 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.44-1386T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879847 | |||||||
chr10:110879853 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0028g0110 |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-1380C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879853 | |||||||
chr10:110879877 | G | A | 3 | a0001c0001t0013g0018 a0001c0001t0013g0190 a0001c0001t0024g0191 |
6 | NA18947.hp2 NA18948.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-1356G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879877 | |||||||
chr10:110879880 | T | G | 1 | a0002c0003t0039g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.44-1353T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110879880 | |||||||
chr10:110880133 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.44-1100C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880133 | |||||||
chr10:110880220 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.44-1013C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880220 | |||||||
chr10:110880221 | T | G | 1 | a0001c0001t0005g0045 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.44-1012T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880221 | |||||||
chr10:110880251 | A | C | 1 | a0001c0001t0001g0040 | 2 | HG01516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44-982A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880251 | |||||||
chr10:110880607 | G | C | 1 | a0001c0001t0003g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.44-626G>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880607 | |||||||
chr10:110880836 | T | C | 1 | a0002c0004t0010g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.44-397T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880836 | |||||||
chr10:110880953 | T | G | 13 | a0001c0001t0016g0179 a0001c0001t0016g0180 a0001c0001t0033g0141 others(10): Show |
16 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.44-280T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880953 | |||||||
chr10:110880978 | G | T | 1 | a0002c0004t0010g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.44-255G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110880978 | |||||||
chr10:110881124 | C | T | 10 | a0001c0001t0004g0065 a0001c0001t0004g0068 a0001c0001t0008g0020 others(7): Show |
14 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-109C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 2/11 | chr10 | 110881124 | |||||||
chr10:110881607 | C | T | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.346+72C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | chr10 | 110881607 | |||||||
chr10:110881702 | T | TCTCACTT others(2786): Show |
1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.346+181_346+182ins others(2793): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 110881702 | ||||||
chr10:110881975 | T | C | 2 | a0001c0001t0010g0154 a0001c0007t0037g0188 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.346+440T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | chr10 | 110881975 | |||||||
chr10:110882170 | A | G | 1 | a0001c0001t0042g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346+635A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | chr10 | 110882170 | |||||||
chr10:110882584 | T | G | 1 | a0001c0001t0005g0145 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.347-419T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | chr10 | 110882584 | |||||||
chr10:110882621 | A | G | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.347-382A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | chr10 | 110882621 | |||||||
chr10:110882636 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.347-367G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | chr10 | 110882636 | |||||||
chr10:110882902 | A | AT | 43 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0017 others(40): Show |
103 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.347-92dupT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 110882902 | ||||||
chr10:110882991 | A | C | 1 | a0001c0001t0003g0016 | 4 | HG00558.hp1 NA18972.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-12A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 3/11 | chr10 | 110882991 | |||||||
chr10:110883194 | A | G | 3 | a0001c0001t0010g0024 a0001c0001t0010g0155 a0001c0001t0010g0189 |
5 | HG01261.hp1 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+97A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883194 | |||||||
chr10:110883217 | C | T | 1 | a0001c0001t0002g0163 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.441+120C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883217 | |||||||
chr10:110883279 | G | C | 3 | a0001c0001t0010g0024 a0001c0001t0010g0155 a0001c0001t0010g0189 |
5 | HG01261.hp1 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+182G>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883279 | |||||||
chr10:110883402 | T | C | 1 | a0001c0001t0002g0043 | 2 | NA18992.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.441+305T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883402 | |||||||
chr10:110883536 | T | A | 1 | a0001c0001t0042g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+439T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883536 | |||||||
chr10:110883659 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.441+562C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883659 | |||||||
chr10:110883667 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.441+570A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883667 | |||||||
chr10:110883998 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.441+901T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110883998 | |||||||
chr10:110884634 | T | G | 1 | a0001c0001t0002g0136 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.442-619T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110884634 | |||||||
chr10:110884651 | T | G | 1 | a0001c0001t0002g0163 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.442-602T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110884651 | |||||||
chr10:110884709 | T | G | 8 | a0001c0001t0008g0020 a0001c0001t0008g0033 a0001c0001t0008g0034 others(5): Show |
12 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-544T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110884709 | |||||||
chr10:110884845 | A | G | 1 | a0004c0010t0001g0095 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.442-408A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110884845 | |||||||
chr10:110885019 | C | T | 1 | a0001c0001t0002g0050 | 2 | NA18988.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.442-234C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110885019 | |||||||
chr10:110885110 | A | G | 1 | a0001c0001t0003g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.442-143A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110885110 | |||||||
chr10:110885200 | T | C | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.442-53T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 4/11 | chr10 | 110885200 | |||||||
chr10:110885536 | T | A | 1 | a0001c0001t0006g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.555+170T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885536 | |||||||
chr10:110885627 | G | A | 8 | a0001c0001t0008g0020 a0001c0001t0008g0033 a0001c0001t0008g0034 others(5): Show |
12 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.555+261G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885627 | |||||||
chr10:110885654 | A | G | 53 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(50): Show |
96 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.555+288A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885654 | |||||||
chr10:110885699 | C | T | 1 | a0002c0004t0010g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.555+333C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885699 | |||||||
chr10:110885739 | C | T | 1 | a0002c0002t0012g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.555+373C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885739 | |||||||
chr10:110885854 | A | G | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.555+488A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885854 | |||||||
chr10:110885930 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.555+564G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885930 | |||||||
chr10:110885978 | A | T | 1 | a0001c0001t0011g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.555+612A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110885978 | |||||||
chr10:110886183 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.555+817C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886183 | |||||||
chr10:110886217 | T | G | 1 | a0001c0001t0004g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.555+851T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886217 | |||||||
chr10:110886337 | T | G | 4 | a0001c0001t0001g0099 a0001c0001t0009g0078 a0001c0001t0009g0079 others(1): Show |
4 | HG00323.hp2 HG00741.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+971T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886337 | |||||||
chr10:110886375 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.555+1009T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886375 | |||||||
chr10:110886497 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0004g0028 others(5): Show |
15 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.555+1131C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886497 | |||||||
chr10:110886593 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.556-1072C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886593 | |||||||
chr10:110886698 | T | G | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.556-967T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886698 | |||||||
chr10:110886757 | G | A | 2 | a0002c0003t0039g0053 a0002c0004t0010g0169 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.556-908G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110886757 | |||||||
chr10:110887009 | C | T | 11 | a0001c0001t0007g0015 a0001c0001t0007g0022 a0001c0001t0007g0042 others(8): Show |
16 | HG01175.hp2 HG01978.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.556-656C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887009 | |||||||
chr10:110887100 | G | A | 1 | a0001c0001t0042g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.556-565G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887100 | |||||||
chr10:110887114 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
20 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.556-551C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887114 | |||||||
chr10:110887155 | A | G | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.556-510A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887155 | |||||||
chr10:110887355 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01261.hp2 HG01433.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.556-310C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887355 | |||||||
chr10:110887358 | A | G | 44 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0017 others(41): Show |
104 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.556-307A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887358 | |||||||
chr10:110887397 | A | T | 1 | a0001c0001t0004g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.556-268A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887397 | |||||||
chr10:110887437 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.556-228C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 5/11 | chr10 | 110887437 | |||||||
chr10:110888003 | C | T | 14 | a0001c0001t0007g0015 a0001c0001t0007g0022 a0001c0001t0007g0042 others(11): Show |
21 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.777+117C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888003 | |||||||
chr10:110888069 | G | T | 1 | a0001c0001t0011g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+183G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888069 | |||||||
chr10:110888083 | A | G | 1 | a0001c0001t0003g0059 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.777+197A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888083 | |||||||
chr10:110888228 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.777+342G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888228 | |||||||
chr10:110888241 | T | A | 1 | a0001c0001t0016g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.777+355T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888241 | |||||||
chr10:110888283 | T | C | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.777+397T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888283 | |||||||
chr10:110888421 | A | G | 1 | a0001c0001t0033g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+535A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888421 | |||||||
chr10:110888690 | T | G | 1 | a0001c0001t0001g0035 | 2 | HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.777+804T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888690 | |||||||
chr10:110888840 | T | C | 14 | a0001c0001t0007g0015 a0001c0001t0007g0022 a0001c0001t0007g0042 others(11): Show |
21 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.778-693T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888840 | |||||||
chr10:110888971 | C | T | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.778-562C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110888971 | |||||||
chr10:110888972 | GTTTAACC others(7): Show |
G | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.778-557_778-544del others(14): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 110888972 | ||||||
chr10:110889006 | C | T | 1 | a0002c0003t0039g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.778-527C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889006 | |||||||
chr10:110889007 | G | A | 12 | a0001c0001t0005g0007 a0001c0001t0005g0045 a0001c0001t0005g0046 others(9): Show |
19 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.778-526G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889007 | |||||||
chr10:110889013 | C | T | 3 | a0001c0001t0033g0141 a0002c0002t0012g0030 a0002c0002t0012g0175 |
5 | HG01074.hp1 HG01168.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-520C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889013 | |||||||
chr10:110889084 | G | A | 1 | a0002c0004t0010g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.778-449G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889084 | |||||||
chr10:110889114 | C | T | 1 | a0001c0001t0004g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.778-419C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889114 | |||||||
chr10:110889176 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.778-357C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889176 | |||||||
chr10:110889200 | C | T | 14 | a0001c0001t0007g0015 a0001c0001t0007g0022 a0001c0001t0007g0042 others(11): Show |
21 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.778-333C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889200 | |||||||
chr10:110889215 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.778-318C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889215 | |||||||
chr10:110889221 | CA | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.778-288delA | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 110889221 | ||||||
chr10:110889221 | CAA | C | 25 | a0001c0001t0001g0089 a0001c0001t0002g0026 a0001c0001t0002g0167 others(22): Show |
35 | HG01175.hp2 HG01261.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-289_778-288del others(2): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 110889221 | ||||||
chr10:110889253 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0004g0028 a0001c0001t0004g0029 others(5): Show |
15 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.778-280A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889253 | |||||||
chr10:110889399 | A | T | 1 | a0001c0001t0001g0002 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.778-134A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889399 | |||||||
chr10:110889405 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-128A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889405 | |||||||
chr10:110889406 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-127A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889406 | |||||||
chr10:110889410 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-123C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889410 | |||||||
chr10:110889411 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-122C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889411 | |||||||
chr10:110889413 | G | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-120G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889413 | |||||||
chr10:110889414 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-119C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889414 | |||||||
chr10:110889415 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-118A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889415 | |||||||
chr10:110889417 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-116C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889417 | |||||||
chr10:110889422 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-111A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889422 | |||||||
chr10:110889424 | G | A | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-109G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889424 | |||||||
chr10:110889427 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-106C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889427 | |||||||
chr10:110889429 | G | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-104G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889429 | |||||||
chr10:110889431 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-102C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889431 | |||||||
chr10:110889433 | G | A | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-100G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889433 | |||||||
chr10:110889435 | G | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-98G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889435 | |||||||
chr10:110889437 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-96A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889437 | |||||||
chr10:110889438 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-95C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889438 | |||||||
chr10:110889440 | T | A | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-93T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889440 | |||||||
chr10:110889441 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-92C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889441 | |||||||
chr10:110889442 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-91A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889442 | |||||||
chr10:110889443 | G | A | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-90G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889443 | |||||||
chr10:110889444 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-89C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889444 | |||||||
chr10:110889446 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-87A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889446 | |||||||
chr10:110889447 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-86A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889447 | |||||||
chr10:110889449 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-84C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889449 | |||||||
chr10:110889452 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-81C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889452 | |||||||
chr10:110889453 | A | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-80A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889453 | |||||||
chr10:110889455 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-78C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889455 | |||||||
chr10:110889457 | T | A | 1 | a0001c0001t0004g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-76T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 6/11 | chr10 | 110889457 | |||||||
chr10:110889717 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.875+87A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110889717 | |||||||
chr10:110889730 | CT | C | 9 | a0001c0001t0003g0008 a0001c0001t0003g0019 a0001c0001t0003g0054 others(6): Show |
14 | HG00408.hp2 HG02040.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.875+101delT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110889730 | |||||||
chr10:110889952 | A | G | 1 | a0001c0001t0003g0129 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.875+322A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110889952 | |||||||
chr10:110889997 | C | G | 5 | a0001c0001t0007g0042 a0001c0001t0007g0113 a0001c0001t0007g0114 others(2): Show |
5 | NA18951.hp2 NA18959.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.875+367C>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110889997 | |||||||
chr10:110890297 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.876-259T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110890297 | |||||||
chr10:110890344 | T | G | 1 | a0002c0003t0039g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.876-212T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110890344 | |||||||
chr10:110890451 | A | G | 55 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(52): Show |
101 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.876-105A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110890451 | |||||||
chr10:110890544 | C | A | 1 | a0001c0001t0003g0123 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.876-12C>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 7/11 | chr10 | 110890544 | |||||||
chr10:110890905 | A | G | 1 | a0001c0001t0035g0128 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.990+235A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110890905 | |||||||
chr10:110891011 | G | A | 42 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0017 others(39): Show |
101 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.990+341G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891011 | |||||||
chr10:110891013 | T | C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0184 |
3 | NA18978.hp1 NA18981.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.990+343T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891013 | |||||||
chr10:110891058 | A | G | 42 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0017 others(39): Show |
101 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.990+388A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891058 | |||||||
chr10:110891103 | A | G | 1 | a0001c0001t0005g0147 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.990+433A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891103 | |||||||
chr10:110891147 | G | A | 2 | a0002c0003t0039g0053 a0002c0004t0010g0169 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.990+477G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891147 | |||||||
chr10:110891175 | C | T | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.990+505C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891175 | |||||||
chr10:110891234 | G | A | 1 | a0001c0001t0042g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.990+564G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891234 | |||||||
chr10:110891278 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(66): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.990+608G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891278 | |||||||
chr10:110891362 | A | C | 14 | a0001c0001t0007g0015 a0001c0001t0007g0022 a0001c0001t0007g0042 others(11): Show |
21 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.990+692A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891362 | |||||||
chr10:110891370 | G | A | 1 | a0001c0001t0016g0142 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.990+700G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891370 | |||||||
chr10:110891406 | C | CA | 56 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0037 others(53): Show |
108 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.990+756dupA | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 110891406 | ||||||
chr10:110891406 | C | CAA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0035 others(30): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.990+755_990+756dup others(2): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 110891406 | ||||||
chr10:110891406 | C | CAAA | 7 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0081 others(4): Show |
11 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.990+754_990+756dup others(3): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 110891406 | ||||||
chr10:110891467 | A | AT | 25 | a0001c0001t0001g0086 a0001c0001t0003g0004 a0001c0001t0003g0008 others(22): Show |
47 | HG00408.hp2 HG00642.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.990+809dupT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 110891467 | ||||||
chr10:110891560 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0045 a0001c0001t0005g0046 others(12): Show |
22 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.990+890C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891560 | |||||||
chr10:110891566 | A | G | 11 | a0001c0001t0033g0141 a0002c0002t0012g0030 a0002c0002t0012g0031 others(8): Show |
14 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.990+896A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891566 | |||||||
chr10:110891570 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0083 |
4 | HG00140.hp1 HG00639.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+900G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110891570 | |||||||
chr10:110892137 | A | T | 50 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
93 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.990+1467A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110892137 | |||||||
chr10:110892218 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.990+1548A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110892218 | |||||||
chr10:110892257 | A | C | 1 | a0001c0001t0040g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.990+1587A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110892257 | |||||||
chr10:110892484 | A | G | 1 | a0001c0001t0016g0142 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.991-1607A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110892484 | |||||||
chr10:110893052 | G | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0025 others(31): Show |
90 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.991-1039G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893052 | |||||||
chr10:110893089 | ATACTC | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0072 |
3 | HG01074.hp2 HG01433.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.991-999_991-995del others(5): Show |
PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 110893089 | ||||||
chr10:110893115 | A | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.991-976A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893115 | |||||||
chr10:110893196 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.991-895T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893196 | |||||||
chr10:110893329 | G | A | 1 | a0001c0001t0003g0129 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.991-762G>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893329 | |||||||
chr10:110893494 | T | C | 14 | a0001c0001t0016g0142 a0001c0001t0016g0179 a0001c0001t0016g0180 others(11): Show |
17 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.991-597T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893494 | |||||||
chr10:110893515 | C | T | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.991-576C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893515 | |||||||
chr10:110893626 | A | G | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.991-465A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893626 | |||||||
chr10:110893839 | C | T | 35 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0025 others(32): Show |
91 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.991-252C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893839 | |||||||
chr10:110893906 | A | G | 18 | a0001c0001t0005g0007 a0001c0001t0005g0045 a0001c0001t0005g0046 others(15): Show |
28 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.991-185A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110893906 | |||||||
chr10:110894003 | A | C | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.991-88A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110894003 | |||||||
chr10:110894038 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.991-53C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 8/11 | chr10 | 110894038 | |||||||
chr10:110894395 | A | T | 1 | a0001c0001t0002g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1099-17A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 9/11 | chr10 | 110894395 | |||||||
chr10:110894719 | G | GT | 14 | a0001c0001t0001g0036 a0001c0001t0002g0158 a0001c0001t0003g0055 others(11): Show |
16 | HG00597.hp2 HG01257.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1209+214dupT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 110894719 | ||||||
chr10:110894719 | GT | G | 24 | a0001c0001t0004g0065 a0001c0001t0004g0068 a0001c0001t0005g0007 others(21): Show |
38 | HG00438.hp2 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1209+214delT | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 110894719 | ||||||
chr10:110894821 | G | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0100 |
2 | HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1209+299G>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | chr10 | 110894821 | |||||||
chr10:110895084 | A | T | 2 | a0001c0001t0016g0179 a0001c0001t0016g0180 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1209+562A>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | chr10 | 110895084 | |||||||
chr10:110895424 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0028g0110 |
6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-524G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | chr10 | 110895424 | |||||||
chr10:110895439 | A | G | 1 | a0001c0001t0010g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1210-509A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | chr10 | 110895439 | |||||||
chr10:110895530 | C | T | 15 | a0001c0001t0005g0007 a0001c0001t0005g0045 a0001c0001t0005g0046 others(12): Show |
22 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1210-418C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | chr10 | 110895530 | |||||||
chr10:110895609 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1210-339C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | chr10 | 110895609 | |||||||
chr10:110895732 | C | A | 1 | a0001c0001t0016g0142 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1210-216C>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 10/11 | chr10 | 110895732 | |||||||
chr10:110896259 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1349+172G>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110896259 | |||||||
chr10:110896359 | T | G | 1 | a0001c0001t0002g0164 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1349+272T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110896359 | |||||||
chr10:110896779 | A | C | 1 | a0001c0001t0004g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1349+692A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110896779 | |||||||
chr10:110896970 | C | T | 1 | a0001c0001t0007g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1349+883C>T | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110896970 | |||||||
chr10:110896994 | T | G | 1 | a0001c0001t0011g0047 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1349+907T>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110896994 | |||||||
chr10:110897233 | G | C | 1 | a0001c0001t0003g0124 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1350-795G>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897233 | |||||||
chr10:110897434 | T | A | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1350-594T>A | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897434 | |||||||
chr10:110897449 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1350-579A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897449 | |||||||
chr10:110897528 | A | G | 1 | a0001c0001t0014g0126 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1350-500A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897528 | |||||||
chr10:110897573 | T | C | 13 | a0001c0001t0016g0179 a0001c0001t0016g0180 a0001c0001t0033g0141 others(10): Show |
16 | HG01074.hp1 HG01168.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1350-455T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897573 | |||||||
chr10:110897676 | G | C | 1 | a0001c0001t0041g0151 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1350-352G>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897676 | |||||||
chr10:110897685 | T | C | 2 | a0002c0003t0039g0053 a0002c0004t0010g0169 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1350-343T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897685 | |||||||
chr10:110897741 | A | C | 1 | a0001c0001t0002g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1350-287A>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897741 | |||||||
chr10:110897748 | A | G | 1 | a0001c0001t0003g0125 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1350-280A>G | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897748 | |||||||
chr10:110897859 | T | C | 1 | a0002c0003t0004g0041 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1350-169T>C | PDCD4 | ENSG00000150593.18 | transcript | ENST00000280154.12 | protein_coding | 11/11 | chr10 | 110897859 |