Item | Value |
---|---|
geneid | 203197 |
ensemblid | ENSG00000157693.15 |
hgncid | 24513 |
symbol | TMEM268 |
name | transmembrane protein 268 |
refseq_nuc | NM_153045.4 |
refseq_prot | NP_694590.2 |
ensembl_nuc | ENST00000288502.9 |
ensembl_prot | ENSP00000288502.4 |
mane_status | MANE Select |
chr | chr9 |
start | 114611291 |
end | 114646422 |
strand | + |
ver | v1.2 |
region | chr9:114611291-114646422 |
region5000 | chr9:114606291-114651422 |
regionname0 | TMEM268_chr9_114611291_114646422 |
regionname5000 | TMEM268_chr9_114606291_114651422 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 342 | 396 | 85 | 75 | 178 | 14 | 42 | 143 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
a0002 | 0/0 | 342 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
a0003 | 0/0 | 342 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
a0004 | 0/0 | 342 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
a0005 | 0/0 | 342 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
a0006 | 0/0 | 342 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
a0007 | 0/0 | 342 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
a0008 | 0/0 | 342 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | MACEP others(337): Show |
chr9 | 114606291 | 114651422 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1026 | 363 | 83 | 74 | 150 | 14 | 40 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0001c0002 | 0/0 | 1026 | 23 | 0 | 0 | 21 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0001c0003 | 0/0 | 1026 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0001c0005 | 0/0 | 1026 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0001c0007 | 0/0 | 1026 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0001c0009 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0001c0012 | 0/0 | 1026 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0001c0015 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0002c0004 | 0/0 | 1026 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0003c0006 | 0/0 | 1026 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0004c0008 | 0/0 | 1026 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0005c0013 | 0/0 | 1026 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0006c0014 | 0/0 | 1026 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0007c0011 | 0/0 | 1026 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 | ||
a0008c0010 | 0/0 | 1026 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | ATGGC others(1021): Show |
chr9 | 114606291 | 114651422 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4493 | 118 | 30 | 28 | 45 | 5 | 10 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0002 | 1/1 | 4490 | 70 | 7 | 14 | 34 | 4 | 9 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0003 | 0/0 | 4493 | 33 | 1 | 1 | 24 | 0 | 7 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0004 | 0/0 | 4503 | 27 | 2 | 1 | 23 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4498): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0006 | 0/0 | 4490 | 11 | 10 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0007 | 0/0 | 4492 | 11 | 2 | 4 | 1 | 2 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4487): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0008 | 0/0 | 4497 | 10 | 0 | 8 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4492): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0009 | 0/0 | 4491 | 9 | 5 | 3 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4486): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0010 | 0/0 | 4496 | 9 | 1 | 2 | 6 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4491): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0011 | 0/0 | 4481 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4476): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0012 | 0/0 | 4497 | 5 | 0 | 0 | 0 | 0 | 5 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4492): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0013 | 0/0 | 4490 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0015 | 0/0 | 4490 | 4 | 0 | 3 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0016 | 0/0 | 4493 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0017 | 0/0 | 4490 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0018 | 0/0 | 4493 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0019 | 0/0 | 4499 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4494): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0020 | 0/0 | 4496 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4491): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0022 | 0/0 | 4491 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4486): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0023 | 0/0 | 4502 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4497): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0024 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0025 | 0/0 | 4493 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0026 | 0/0 | 4493 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0027 | 0/0 | 4497 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4492): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0028 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0030 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4491): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0031 | 0/0 | 4496 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4491): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0032 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4494): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0034 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0035 | 0/0 | 4491 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4486): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0036 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0037 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0038 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0039 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0040 | 0/0 | 4502 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4497): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0041 | 0/0 | 4495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4490): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0042 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0043 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0044 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4489): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0045 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0046 | 0/0 | 4493 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0047 | 0/0 | 4496 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4491): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0048 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4492): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0049 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0050 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4487): Show |
chr9 | 114606291 | 114651422 |
a0001c0001t0051 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0002t0005 | 0/0 | 4497 | 17 | 0 | 0 | 17 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4492): Show |
chr9 | 114606291 | 114651422 |
a0001c0002t0014 | 0/0 | 4496 | 4 | 0 | 0 | 3 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4491): Show |
chr9 | 114606291 | 114651422 |
a0001c0002t0024 | 0/0 | 4493 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0002t0033 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4494): Show |
chr9 | 114606291 | 114651422 |
a0001c0003t0002 | 0/0 | 4490 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0005t0002 | 0/0 | 4490 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0001c0007t0023 | 0/0 | 4502 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4497): Show |
chr9 | 114606291 | 114651422 |
a0001c0009t0001 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0012t0001 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0001c0015t0001 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0002c0004t0013 | 0/0 | 4490 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0002c0004t0029 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0003c0006t0021 | 0/0 | 4481 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4476): Show |
chr9 | 114606291 | 114651422 |
a0004c0008t0002 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0005c0013t0003 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
a0006c0014t0002 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0007c0011t0002 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4485): Show |
chr9 | 114606291 | 114651422 |
a0008c0010t0001 | 0/0 | 4493 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | GATGA others(4488): Show |
chr9 | 114606291 | 114651422 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 10 | 5 | 16 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0011 | 0/0 | 5 | 2 | 1 | 1 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0002 | 0/0 | 11 | 0 | 1 | 8 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0007 | 0/0 | 6 | 0 | 3 | 1 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0012 | 1/0 | 4 | 0 | 1 | 0 | 1 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0023 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0009 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0008g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0001 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0010g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0011g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0012g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0012g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0012g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0015g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0015g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0015g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0016g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0017g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0017g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0017g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0018g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0018g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0018g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0019g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0020g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0022g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0022g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0023g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0025g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0025g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0026g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0026g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0027g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0027g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0028g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0030g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0031g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0032g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0034g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0035g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0036g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0037g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0038g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0039g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0040g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0041g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0042g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0043g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0044g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0045g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0046g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0047g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0048g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0049g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0050g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0001t0051g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0014g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0014g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0014g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0024g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0002t0033g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0003t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0005t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0005t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0007t0023g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0009t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0012t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0001c0015t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0002c0004t0013g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0002c0004t0013g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0002c0004t0029g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0003c0006t0021g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0003c0006t0021g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0004c0008t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0005c0013t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0006c0014t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0007c0011t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
a0008c0010t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00140 | hp1 | a0001 | c0001 | t0019 | g0045 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00408 | hp2 | a0001 | c0001 | t0011 | g0013 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00423 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0009 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00544 | hp1 | a0004 | c0008 | t0002 | g0008 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0209 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00733 | hp1 | a0001 | c0001 | t0009 | g0100 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00738 | hp2 | a0001 | c0001 | t0043 | g0190 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01074 | hp1 | a0001 | c0001 | t0015 | g0197 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0211 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0018 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0057 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01168 | hp2 | a0001 | c0001 | t0007 | g0212 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0056 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01243 | hp1 | a0001 | c0001 | t0035 | g0018 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01243 | hp2 | a0001 | c0001 | t0028 | g0174 | AMR | PUR | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0145 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0043 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01257 | hp2 | a0001 | c0001 | t0040 | g0062 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01258 | hp1 | a0001 | c0001 | t0015 | g0043 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0099 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0023 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01515 | hp2 | a0001 | c0001 | t0046 | g0168 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01517 | hp2 | a0001 | c0001 | t0007 | g0023 | EUR | IBS | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01884 | hp1 | a0001 | c0001 | t0027 | g0054 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01891 | hp1 | a0001 | c0001 | t0017 | g0044 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01891 | hp2 | a0001 | c0001 | t0016 | g0196 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0053 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01928 | hp2 | a0001 | c0001 | t0044 | g0038 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01975 | hp2 | a0001 | c0001 | t0023 | g0061 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01978 | hp1 | a0001 | c0001 | t0019 | g0045 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01978 | hp2 | a0001 | c0001 | t0042 | g0121 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01981 | hp1 | a0001 | c0001 | t0041 | g0171 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01981 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02004 | hp1 | a0005 | c0013 | t0003 | g0162 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02004 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02027 | hp2 | a0001 | c0002 | t0014 | g0231 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02056 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02080 | hp1 | a0001 | c0001 | t0007 | g0213 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02132 | hp1 | a0001 | c0001 | t0030 | g0229 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02148 | hp1 | a0001 | c0012 | t0001 | g0122 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02155 | hp1 | a0001 | c0001 | t0010 | g0142 | EAS | CDX | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02155 | hp2 | a0001 | c0002 | t0014 | g0048 | EAS | CDX | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02257 | hp1 | a0001 | c0001 | t0026 | g0137 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0051 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0178 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02273 | hp2 | a0001 | c0001 | t0008 | g0055 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02280 | hp1 | a0001 | c0001 | t0025 | g0154 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0052 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0215 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02523 | hp2 | a0001 | c0001 | t0022 | g0094 | EAS | KHV | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02602 | hp1 | a0001 | c0001 | t0031 | g0235 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02602 | hp2 | a0001 | c0001 | t0007 | g0210 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0200 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0225 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02622 | hp2 | a0001 | c0001 | t0018 | g0219 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0134 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0098 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02647 | hp2 | a0002 | c0004 | t0013 | g0224 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02698 | hp2 | a0001 | c0001 | t0012 | g0230 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02717 | hp1 | a0001 | c0001 | t0013 | g0204 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02735 | hp1 | a0001 | c0001 | t0009 | g0088 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02738 | hp1 | a0001 | c0001 | t0036 | g0106 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02809 | hp2 | a0001 | c0001 | t0017 | g0044 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0216 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02886 | hp2 | a0001 | c0001 | t0025 | g0113 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0217 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0247 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02896 | hp1 | a0001 | c0001 | t0027 | g0058 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0218 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0198 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03017 | hp1 | a0001 | c0002 | t0024 | g0120 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03098 | hp1 | a0002 | c0004 | t0013 | g0222 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03098 | hp2 | a0001 | c0009 | t0001 | g0001 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03130 | hp1 | a0003 | c0006 | t0021 | g0169 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03139 | hp2 | a0001 | c0001 | t0049 | g0205 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0102 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0206 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03453 | hp2 | a0001 | c0001 | t0048 | g0249 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03491 | hp2 | a0001 | c0001 | t0012 | g0047 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0047 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0238 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03654 | hp1 | a0001 | c0001 | t0008 | g0009 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03654 | hp2 | a0006 | c0014 | t0002 | g0245 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03669 | hp1 | a0001 | c0001 | t0012 | g0046 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03688 | hp2 | a0001 | c0001 | t0007 | g0214 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03704 | hp1 | a0001 | c0001 | t0051 | g0208 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03942 | hp1 | a0001 | c0001 | t0050 | g0207 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0046 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04199 | hp2 | a0007 | c0011 | t0002 | g0097 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | STU | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18612 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18906 | hp1 | a0001 | c0001 | t0038 | g0103 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18951 | hp2 | a0001 | c0002 | t0005 | g0049 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18956 | hp2 | a0001 | c0001 | t0022 | g0080 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18964 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18965 | hp1 | a0001 | c0005 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18966 | hp1 | a0001 | c0005 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18979 | hp2 | a0001 | c0001 | t0010 | g0191 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18982 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18987 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18988 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18989 | hp1 | a0001 | c0001 | t0032 | g0234 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18994 | hp2 | a0001 | c0002 | t0033 | g0232 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18995 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18995 | hp2 | a0001 | c0001 | t0010 | g0163 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18997 | hp1 | a0001 | c0001 | t0034 | g0193 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18997 | hp2 | a0001 | c0001 | t0037 | g0244 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18999 | hp2 | a0001 | c0001 | t0010 | g0158 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19001 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19002 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19003 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19005 | hp1 | a0001 | c0001 | t0011 | g0130 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19009 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19010 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19011 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0104 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19055 | hp2 | a0001 | c0007 | t0023 | g0074 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19056 | hp2 | a0001 | c0002 | t0005 | g0049 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19057 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19057 | hp2 | a0008 | c0010 | t0001 | g0136 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19058 | hp1 | a0001 | c0001 | t0011 | g0151 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19058 | hp2 | a0001 | c0002 | t0005 | g0236 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19060 | hp2 | a0001 | c0002 | t0005 | g0233 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19063 | hp2 | a0001 | c0002 | t0005 | g0237 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19064 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19068 | hp1 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19079 | hp1 | a0001 | c0005 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19081 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19084 | hp1 | a0001 | c0001 | t0039 | g0087 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19085 | hp1 | a0001 | c0001 | t0047 | g0004 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19085 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19086 | hp1 | a0001 | c0002 | t0005 | g0227 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA19091 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ASW | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20129 | hp2 | a0002 | c0004 | t0029 | g0223 | AFR | ASW | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20805 | hp1 | a0001 | c0001 | t0015 | g0202 | EUR | TSI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20905 | hp1 | a0001 | c0002 | t0014 | g0228 | SAS | GIH | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | GIH | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02109 | hp1 | a0001 | c0001 | t0045 | g0112 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0050 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG03471 | hp2 | a0001 | c0001 | t0024 | g0226 | AFR | MSL | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG06807 | hp1 | a0001 | c0015 | t0001 | g0140 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
HG06807 | hp2 | a0003 | c0006 | t0021 | g0221 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA18955 | hp2 | a0001 | c0002 | t0014 | g0048 | EAS | JPT | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | USA | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
NA21309 | hp2 | a0001 | c0001 | t0026 | g0138 | AFR | LWK | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0105 | REF | REF | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0012 | REF | REF | TMEM268_chr9_114606291_114651422 | TMEM268 | chr9 | 114606291 | 114651422 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114628140 | A | G | 1 | a0006 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.364A>G | p.Ser122Gly | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/9 | 716/4490 | 364/1029 | 122/342 | chr9 | 114628140 | |||
chr9:114633781 | C | T | 1 | a0005 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.488C>T | p.Thr163Met | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/9 | 840/4490 | 488/1029 | 163/342 | chr9 | 114633781 | |||
chr9:114633840 | G | C | 1 | a0003 | 2 | HG03130.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.547G>C | p.Val183Leu | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/9 | 899/4490 | 547/1029 | 183/342 | chr9 | 114633840 | |||
chr9:114638549 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.672G>T | p.Leu224Phe | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1024/4490 | 672/1029 | 224/342 | chr9 | 114638549 | |||
chr9:114638581 | T | C | 1 | a0004 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.704T>C | p.Val235Ala | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1056/4490 | 704/1029 | 235/342 | chr9 | 114638581 | |||
chr9:114638587 | A | T | 1 | a0008 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.710A>T | p.Glu237Val | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1062/4490 | 710/1029 | 237/342 | chr9 | 114638587 | |||
chr9:114638667 | A | G | 1 | a0002 | 3 | HG02647.hp2 HG03098.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.790A>G | p.Asn264Asp | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1142/4490 | 790/1029 | 264/342 | chr9 | 114638667 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114624426 | C | T | 1 | a0001c0015 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.183C>T | p.Ala61Ala | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/9 | 535/4490 | 183/1029 | 61/342 | chr9 | 114624426 | |||
chr9:114624439 | C | T | 1 | a0001c0002 | 23 | HG00423.hp2 HG02027.hp2 HG02155.hp2 others(20): Show |
synonymous_variant | LOW | c.196C>T | p.Leu66Leu | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/9 | 548/4490 | 196/1029 | 66/342 | chr9 | 114624439 | |||
chr9:114626901 | C | A | 1 | a0001c0007 | 1 | NA19055.hp2 | splice_region_variant&synonymous_variant | LOW | c.219C>A | p.Val73Val | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/9 | 571/4490 | 219/1029 | 73/342 | chr9 | 114626901 | |||
chr9:114626985 | T | C | 2 | a0001c0003 a0004c0008 |
4 | HG00544.hp1 NA18964.hp2 NA19001.hp1 others(1): Show |
synonymous_variant | LOW | c.303T>C | p.Pro101Pro | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/9 | 655/4490 | 303/1029 | 101/342 | chr9 | 114626985 | |||
chr9:114638546 | C | T | 1 | a0001c0012 | 1 | HG02148.hp1 | splice_region_variant&synonymous_variant | LOW | c.669C>T | p.Ser223Ser | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1021/4490 | 669/1029 | 223/342 | chr9 | 114638546 | |||
chr9:114638651 | C | T | 1 | a0001c0005 | 3 | NA18965.hp1 NA18966.hp1 NA19079.hp1 |
synonymous_variant | LOW | c.774C>T | p.Pro258Pro | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1126/4490 | 774/1029 | 258/342 | chr9 | 114638651 | |||
chr9:114638723 | G | A | 1 | a0001c0009 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.846G>A | p.Pro282Pro | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/9 | 1198/4490 | 846/1029 | 282/342 | chr9 | 114638723 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114611304 | C | T | 5 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0049 others(2): Show |
18 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-339C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5892 | chr9 | 114611304 | ||||||
chr9:114611395 | G | A | 1 | a0001c0001t0049 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-248G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5801 | chr9 | 114611395 | ||||||
chr9:114611426 | G | A | 1 | a0001c0001t0028 | 1 | HG01243.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-217G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | chr9 | 114611426 | |||||||
chr9:114611431 | G | A | 1 | a0002c0004t0029 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5765 | chr9 | 114611431 | ||||||
chr9:114611444 | G | C | 8 | a0001c0001t0012 a0001c0001t0019 a0001c0001t0030 others(5): Show |
32 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-199G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5752 | chr9 | 114611444 | ||||||
chr9:114611486 | G | C | 1 | a0001c0001t0020 | 2 | NA19010.hp2 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-157G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5710 | chr9 | 114611486 | ||||||
chr9:114611533 | T | C | 1 | a0001c0001t0034 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5663 | chr9 | 114611533 | ||||||
chr9:114611533 | T | TGGC | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0016 others(17): Show |
176 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(173): Show |
5_prime_UTR_variant | MODIFIER | c.-87_-85dupGCG | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | |||||
chr9:114611533 | T | TGGCGGC | 11 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0012 others(8): Show |
53 | HG00423.hp2 HG00438.hp1 HG01071.hp1 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-90_-85dupGCGGCG | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | |||||
chr9:114611533 | T | TGGCGGCG others(2): Show |
3 | a0001c0001t0019 a0001c0001t0032 a0001c0002t0033 |
4 | HG00140.hp1 HG01978.hp1 NA18989.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-85dupGCGGCGGC others(1): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | |||||
chr9:114611533 | TGGCGGCG others(2): Show |
T | 2 | a0001c0001t0011 a0003c0006t0021 |
8 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-85delGCGGCGGC others(1): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5638 | INFO_REALIGN_3_PRIME | chr9 | 114611533 | |||||
chr9:114611550 | G | GCGGCGGC others(5): Show |
4 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0040 others(1): Show |
30 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-85_-84insGCGCCGGC others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/9 | 5637 | INFO_REALIGN_3_PRIME | chr9 | 114611550 | |||||
chr9:114643365 | T | G | 5 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0035 others(2): Show |
23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*52T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 52 | chr9 | 114643365 | ||||||
chr9:114643888 | C | T | 1 | a0001c0001t0026 | 2 | HG02257.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 575 | chr9 | 114643888 | ||||||
chr9:114644018 | T | C | 1 | a0001c0001t0036 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 705 | chr9 | 114644018 | ||||||
chr9:114644101 | A | G | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(9): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*788A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 788 | chr9 | 114644101 | ||||||
chr9:114644236 | C | G | 1 | a0001c0001t0046 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*923C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 923 | chr9 | 114644236 | ||||||
chr9:114644321 | A | G | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(9): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1008A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1008 | chr9 | 114644321 | ||||||
chr9:114644557 | A | G | 1 | a0001c0001t0045 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1244A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1244 | chr9 | 114644557 | ||||||
chr9:114644594 | G | GA | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(9): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1290dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1291 | INFO_REALIGN_3_PRIME | chr9 | 114644594 | |||||
chr9:114644683 | C | T | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(9): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1370C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1370 | chr9 | 114644683 | ||||||
chr9:114644685 | G | A | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(9): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1372G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1372 | chr9 | 114644685 | ||||||
chr9:114644797 | A | AT | 4 | a0001c0001t0007 a0001c0001t0041 a0001c0001t0044 others(1): Show |
14 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1497dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1498 | INFO_REALIGN_3_PRIME | chr9 | 114644797 | |||||
chr9:114644879 | C | A | 1 | a0001c0001t0037 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1566C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1566 | chr9 | 114644879 | ||||||
chr9:114644885 | C | T | 2 | a0001c0001t0025 a0001c0001t0045 |
3 | HG02109.hp1 HG02280.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1572C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1572 | chr9 | 114644885 | ||||||
chr9:114644886 | A | G | 37 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(34): Show |
170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1573A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1573 | chr9 | 114644886 | ||||||
chr9:114644973 | T | G | 12 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0023 others(9): Show |
46 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1660T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1660 | chr9 | 114644973 | ||||||
chr9:114645044 | C | T | 2 | a0001c0001t0015 a0001c0001t0043 |
5 | HG00738.hp2 HG01074.hp1 HG01257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1731C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1731 | chr9 | 114645044 | ||||||
chr9:114645061 | G | C | 13 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0023 others(10): Show |
47 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1748G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 1748 | chr9 | 114645061 | ||||||
chr9:114645420 | A | G | 1 | a0001c0001t0038 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2107 | chr9 | 114645420 | ||||||
chr9:114645509 | G | T | 1 | a0001c0001t0031 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2196G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2196 | chr9 | 114645509 | ||||||
chr9:114645556 | G | A | 6 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0017 others(3): Show |
24 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2243G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2243 | chr9 | 114645556 | ||||||
chr9:114645579 | A | C | 2 | a0001c0001t0008 a0001c0001t0012 |
15 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2266A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2266 | chr9 | 114645579 | ||||||
chr9:114645643 | C | T | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(9): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2330C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2330 | chr9 | 114645643 | ||||||
chr9:114645644 | G | T | 10 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0031 others(7): Show |
42 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2331G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2331 | chr9 | 114645644 | ||||||
chr9:114645645 | G | T | 10 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0031 others(7): Show |
42 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2332G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2332 | chr9 | 114645645 | ||||||
chr9:114645781 | T | C | 1 | a0001c0001t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2468T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2468 | chr9 | 114645781 | ||||||
chr9:114645821 | A | G | 5 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0035 others(2): Show |
23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2508A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2508 | chr9 | 114645821 | ||||||
chr9:114645899 | G | T | 1 | a0001c0001t0048 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2586G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2586 | chr9 | 114645899 | ||||||
chr9:114645962 | A | T | 1 | a0001c0001t0050 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2649A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2649 | chr9 | 114645962 | ||||||
chr9:114645975 | T | A | 12 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0023 others(9): Show |
46 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2662T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2662 | chr9 | 114645975 | ||||||
chr9:114646180 | G | A | 1 | a0001c0001t0041 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2867G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 9/9 | 2867 | chr9 | 114646180 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:114611580 | C | G | 1 | a0001c0001t0002g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-79+16C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611580 | |||||||
chr9:114611626 | G | T | 1 | a0001c0001t0048g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-79+62G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611626 | |||||||
chr9:114611742 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0016g0247 |
2 | HG02109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-79+178C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611742 | |||||||
chr9:114611800 | G | A | 2 | a0001c0001t0016g0050 a0001c0001t0016g0051 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-79+236G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611800 | |||||||
chr9:114611858 | A | G | 8 | a0001c0001t0002g0015 a0001c0001t0002g0240 a0001c0001t0002g0241 others(5): Show |
11 | HG02074.hp2 HG02129.hp1 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.-79+294A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114611858 | |||||||
chr9:114612032 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-79+468C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612032 | |||||||
chr9:114612127 | T | C | 9 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(6): Show |
13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-79+563T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612127 | |||||||
chr9:114612236 | C | T | 1 | a0001c0001t0009g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-79+672C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612236 | |||||||
chr9:114612434 | C | T | 17 | a0001c0001t0012g0046 a0001c0001t0012g0047 a0001c0001t0012g0230 others(14): Show |
32 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(29): Show |
intron_variant | MODIFIER | c.-79+870C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612434 | |||||||
chr9:114612453 | CCTT | C | 22 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(19): Show |
30 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-79+892_-79+894del others(3): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114612453 | ||||||
chr9:114612634 | C | G | 5 | a0001c0001t0009g0225 a0001c0001t0024g0226 a0002c0004t0013g0222 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-79+1070C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612634 | |||||||
chr9:114612690 | C | T | 1 | a0003c0006t0021g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-79+1126C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612690 | |||||||
chr9:114612745 | C | G | 1 | a0001c0001t0006g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-79+1181C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114612745 | |||||||
chr9:114613156 | C | T | 1 | a0001c0001t0024g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-79+1592C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613156 | |||||||
chr9:114613215 | A | G | 1 | a0001c0001t0024g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-79+1651A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613215 | |||||||
chr9:114613274 | G | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(199): Show |
311 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-79+1710G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613274 | |||||||
chr9:114613450 | A | T | 1 | a0001c0001t0018g0219 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-79+1886A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613450 | |||||||
chr9:114613496 | A | G | 1 | a0001c0001t0027g0058 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-79+1932A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613496 | |||||||
chr9:114613629 | C | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(118): Show |
196 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.-79+2065C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613629 | |||||||
chr9:114613745 | TTTTTGTT others(3): Show |
T | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-79+2198_-79+2207d others(12): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114613745 | ||||||
chr9:114613750 | G | T | 1 | a0001c0001t0034g0193 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-79+2186G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613750 | |||||||
chr9:114613933 | C | T | 20 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(17): Show |
28 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-79+2369C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613933 | |||||||
chr9:114613939 | T | G | 20 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(17): Show |
28 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-79+2375T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114613939 | |||||||
chr9:114614006 | C | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(251): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.-79+2442C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614006 | |||||||
chr9:114614116 | G | A | 1 | a0001c0001t0002g0027 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-79+2552G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614116 | |||||||
chr9:114614181 | T | G | 13 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(10): Show |
17 | HG01074.hp1 HG01192.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-79+2617T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614181 | |||||||
chr9:114614497 | C | T | 14 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(11): Show |
17 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78-2621C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614497 | |||||||
chr9:114614746 | A | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(253): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.-78-2372A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614746 | |||||||
chr9:114614892 | C | CT | 53 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(50): Show |
71 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.-78-2204dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | ||||||
chr9:114614892 | C | CTT | 8 | a0001c0001t0003g0014 a0001c0001t0003g0194 a0001c0001t0003g0195 others(5): Show |
11 | HG00544.hp2 HG00609.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78-2205_-78-2204d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | ||||||
chr9:114614892 | CT | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0016g0050 others(3): Show |
6 | HG02258.hp2 HG02486.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78-2204delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | ||||||
chr9:114614892 | CTTTT | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
10 | HG00438.hp1 HG01884.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-78-2207_-78-2204d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | ||||||
chr9:114614892 | CTTTTTTT others(4): Show |
C | 43 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(40): Show |
75 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-78-2214_-78-2204d others(13): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114614892 | ||||||
chr9:114614935 | C | T | 1 | a0001c0001t0027g0058 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-78-2183C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614935 | |||||||
chr9:114614936 | G | A | 19 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(16): Show |
27 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-78-2182G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114614936 | |||||||
chr9:114615058 | G | A | 1 | a0001c0001t0008g0052 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-78-2060G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615058 | |||||||
chr9:114615095 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA18994.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-78-2023C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615095 | |||||||
chr9:114615297 | T | C | 1 | a0001c0001t0016g0196 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-78-1821T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615297 | |||||||
chr9:114615485 | G | T | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1633G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615485 | |||||||
chr9:114615493 | A | G | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1625A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615493 | |||||||
chr9:114615495 | A | G | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1623A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615495 | |||||||
chr9:114615497 | T | A | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1621T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615497 | |||||||
chr9:114615525 | C | G | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1593C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615525 | |||||||
chr9:114615528 | T | A | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1590T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615528 | |||||||
chr9:114615539 | T | C | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1579T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615539 | |||||||
chr9:114615545 | T | C | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1573T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615545 | |||||||
chr9:114615546 | A | T | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1572A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615546 | |||||||
chr9:114615547 | A | G | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1571A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615547 | |||||||
chr9:114615550 | C | T | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1568C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615550 | |||||||
chr9:114615553 | T | A | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1565T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615553 | |||||||
chr9:114615563 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(199): Show |
311 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-78-1555G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615563 | |||||||
chr9:114615567 | C | CCTAGAAC others(20): Show |
2 | a0001c0001t0013g0204 a0001c0001t0013g0206 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-78-1548_-78-1522d others(29): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114615567 | ||||||
chr9:114615592 | A | C | 1 | a0001c0001t0004g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-78-1526A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615592 | |||||||
chr9:114615729 | T | A | 1 | a0001c0001t0034g0193 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-78-1389T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615729 | |||||||
chr9:114615810 | C | T | 1 | a0007c0011t0002g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-78-1308C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615810 | |||||||
chr9:114615818 | C | A | 2 | a0001c0001t0007g0217 a0001c0001t0007g0218 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-78-1300C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615818 | |||||||
chr9:114615827 | T | A | 1 | a0001c0001t0034g0193 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-78-1291T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615827 | |||||||
chr9:114615862 | T | C | 21 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(18): Show |
29 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-78-1256T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615862 | |||||||
chr9:114615870 | T | G | 2 | a0001c0001t0025g0113 a0001c0001t0045g0112 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-78-1248T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615870 | |||||||
chr9:114615872 | A | G | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-78-1246A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114615872 | |||||||
chr9:114616000 | TTTTTCTT others(5): Show |
T | 15 | a0001c0001t0012g0046 a0001c0001t0012g0047 a0001c0001t0012g0230 others(12): Show |
29 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.-78-1106_-78-1095d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616000 | ||||||
chr9:114616005 | CTTTTTTC others(6): Show |
C | 1 | a0001c0002t0005g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78-1106_-78-1094d others(15): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616005 | ||||||
chr9:114616017 | C | CT | 18 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0004g0073 others(15): Show |
22 | HG00738.hp2 HG01192.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-78-1085dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616017 | ||||||
chr9:114616017 | CT | C | 30 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0172 others(27): Show |
42 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-78-1085delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616017 | ||||||
chr9:114616200 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-78-918A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616200 | |||||||
chr9:114616205 | C | T | 1 | a0001c0001t0002g0017 | 3 | NA18972.hp1 NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-78-913C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616205 | |||||||
chr9:114616256 | G | C | 62 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(59): Show |
81 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.-78-862G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616256 | |||||||
chr9:114616267 | G | A | 1 | a0001c0002t0024g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-78-851G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616267 | |||||||
chr9:114616293 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0042g0121 others(1): Show |
4 | HG00639.hp1 HG01256.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-825G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616293 | |||||||
chr9:114616304 | C | T | 1 | a0001c0001t0004g0072 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-78-814C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616304 | |||||||
chr9:114616357 | GTTTGTT | G | 7 | a0001c0001t0006g0022 a0001c0001t0006g0198 a0001c0001t0006g0199 others(4): Show |
9 | HG01192.hp2 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-78-740_-78-735del others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616357 | ||||||
chr9:114616357 | GTTTGTTT others(5): Show |
G | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-78-746_-78-735del others(12): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616357 | ||||||
chr9:114616367 | GTTT | G | 43 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(40): Show |
75 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-78-748_-78-746del others(3): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 114616367 | ||||||
chr9:114616461 | G | T | 1 | a0001c0001t0034g0193 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-78-657G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616461 | |||||||
chr9:114616526 | C | A | 1 | a0001c0001t0051g0208 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-78-592C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616526 | |||||||
chr9:114616526 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-78-592C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616526 | |||||||
chr9:114616528 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-78-590G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616528 | |||||||
chr9:114616610 | C | T | 1 | a0001c0001t0024g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-78-508C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616610 | |||||||
chr9:114616646 | G | A | 1 | a0001c0001t0008g0053 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-78-472G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616646 | |||||||
chr9:114616739 | A | G | 1 | a0001c0001t0049g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-78-379A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616739 | |||||||
chr9:114616765 | T | G | 1 | a0001c0001t0002g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-78-353T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114616765 | |||||||
chr9:114617006 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(199): Show |
311 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-78-112G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617006 | |||||||
chr9:114617009 | C | T | 2 | a0003c0006t0021g0169 a0003c0006t0021g0221 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-78-109C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617009 | |||||||
chr9:114617010 | G | C | 9 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(6): Show |
13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78-108G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617010 | |||||||
chr9:114617107 | G | A | 1 | a0001c0001t0049g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-78-11G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 1/8 | chr9 | 114617107 | |||||||
chr9:114617309 | C | G | 14 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(11): Show |
18 | HG00738.hp2 HG01074.hp1 HG01192.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.106+8C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617309 | |||||||
chr9:114617469 | C | G | 2 | a0001c0001t0025g0113 a0001c0001t0045g0112 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.106+168C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617469 | |||||||
chr9:114617677 | C | T | 2 | a0003c0006t0021g0169 a0003c0006t0021g0221 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.106+376C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617677 | |||||||
chr9:114617813 | C | A | 19 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(16): Show |
27 | HG00609.hp1 HG00673.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.106+512C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617813 | |||||||
chr9:114617878 | TA | T | 7 | a0001c0001t0001g0167 a0001c0001t0003g0189 a0001c0001t0007g0217 others(4): Show |
7 | HG01167.hp1 HG01515.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+578delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617878 | |||||||
chr9:114617879 | A | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(163): Show |
265 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.106+578A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617879 | |||||||
chr9:114617879 | AT | A | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.106+586delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114617879 | ||||||
chr9:114617881 | T | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | NA18948.hp2 NA18962.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.106+580T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617881 | |||||||
chr9:114617887 | T | A | 4 | a0001c0001t0009g0225 a0002c0004t0013g0222 a0002c0004t0013g0224 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+586T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617887 | |||||||
chr9:114617947 | G | A | 14 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(11): Show |
18 | HG00738.hp2 HG01074.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+646G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114617947 | |||||||
chr9:114618119 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.106+818C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618119 | |||||||
chr9:114618132 | C | G | 1 | a0001c0001t0003g0181 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.106+831C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618132 | |||||||
chr9:114618161 | G | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00673.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.106+860G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618161 | |||||||
chr9:114618202 | T | G | 16 | a0001c0001t0012g0046 a0001c0001t0012g0047 a0001c0001t0012g0230 others(13): Show |
30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+901T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618202 | |||||||
chr9:114618523 | T | A | 1 | a0001c0001t0011g0130 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.106+1222T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618523 | |||||||
chr9:114618567 | G | A | 1 | a0001c0001t0009g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.106+1266G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618567 | |||||||
chr9:114618604 | G | A | 16 | a0001c0001t0012g0046 a0001c0001t0012g0047 a0001c0001t0012g0230 others(13): Show |
30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+1303G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618604 | |||||||
chr9:114618662 | CA | C | 17 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(14): Show |
25 | HG00609.hp1 HG00673.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.106+1372delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114618662 | ||||||
chr9:114618673 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.106+1372A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618673 | |||||||
chr9:114618742 | G | T | 4 | a0001c0001t0009g0225 a0002c0004t0013g0222 a0002c0004t0013g0224 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1441G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618742 | |||||||
chr9:114618743 | GT | G | 4 | a0001c0001t0009g0225 a0002c0004t0013g0222 a0002c0004t0013g0224 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1443delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618743 | |||||||
chr9:114618784 | T | C | 1 | a0001c0001t0009g0100 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.106+1483T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618784 | |||||||
chr9:114618858 | G | A | 9 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(6): Show |
13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.106+1557G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618858 | |||||||
chr9:114618882 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(243): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.106+1581T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618882 | |||||||
chr9:114618946 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.106+1645A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114618946 | |||||||
chr9:114619073 | A | T | 2 | a0003c0006t0021g0169 a0003c0006t0021g0221 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.106+1772A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619073 | |||||||
chr9:114619276 | C | T | 1 | a0001c0001t0007g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.106+1975C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619276 | |||||||
chr9:114619282 | C | T | 3 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0203 |
3 | HG01884.hp2 HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.106+1981C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619282 | |||||||
chr9:114619288 | C | T | 14 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(11): Show |
18 | HG00738.hp2 HG01074.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+1987C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619288 | |||||||
chr9:114619291 | G | T | 4 | a0001c0001t0015g0043 a0001c0001t0015g0197 a0001c0001t0015g0202 others(1): Show |
5 | HG00738.hp2 HG01074.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+1990G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619291 | |||||||
chr9:114619293 | G | GCA | 47 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(44): Show |
80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.106+2019_106+2020d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | ||||||
chr9:114619293 | G | GCACA | 3 | a0001c0001t0002g0077 a0001c0001t0002g0079 a0001c0001t0028g0174 |
3 | HG01243.hp2 HG02027.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.106+2017_106+2020d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | ||||||
chr9:114619293 | GCA | G | 29 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0003g0195 others(26): Show |
38 | HG00609.hp1 HG00673.hp1 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.106+2019_106+2020d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | ||||||
chr9:114619293 | GCACA | G | 3 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0180 |
3 | HG00423.hp1 NA18948.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.106+2017_106+2020d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | ||||||
chr9:114619293 | GCACACAC others(1): Show |
G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(87): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.106+2013_106+2020d others(10): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | ||||||
chr9:114619293 | GCACACAC others(5): Show |
G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0170 a0001c0001t0001g0192 |
3 | NA18941.hp1 NA18955.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.106+2009_106+2020d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619293 | ||||||
chr9:114619483 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(242): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.106+2182G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619483 | |||||||
chr9:114619578 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0044g0038 |
2 | HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.106+2277C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619578 | |||||||
chr9:114619604 | C | T | 16 | a0001c0001t0012g0046 a0001c0001t0012g0047 a0001c0001t0012g0230 others(13): Show |
30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+2303C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619604 | |||||||
chr9:114619770 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.106+2469G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619770 | |||||||
chr9:114619864 | C | T | 28 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(25): Show |
40 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.106+2563C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619864 | |||||||
chr9:114619868 | CT | C | 9 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(6): Show |
13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.106+2576delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114619868 | ||||||
chr9:114619972 | G | A | 3 | a0001c0001t0017g0044 a0001c0001t0017g0215 a0001c0001t0017g0216 |
4 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2671G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114619972 | |||||||
chr9:114620071 | C | T | 4 | a0001c0001t0017g0044 a0001c0001t0017g0215 a0001c0001t0017g0216 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+2770C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620071 | |||||||
chr9:114620084 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
93 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.106+2783G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620084 | |||||||
chr9:114620108 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(88): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.106+2807G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620108 | |||||||
chr9:114620120 | CAGGAGAA others(21): Show |
C | 1 | a0001c0001t0004g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.106+2823_106+2850d others(30): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114620120 | ||||||
chr9:114620170 | G | A | 37 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(34): Show |
49 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.106+2869G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620170 | |||||||
chr9:114620243 | GTTAC | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(89): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.106+2950_106+2953d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114620243 | ||||||
chr9:114620253 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.106+2952T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620253 | |||||||
chr9:114620283 | T | G | 3 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 |
3 | HG02818.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.106+2982T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620283 | |||||||
chr9:114620305 | C | T | 2 | a0001c0001t0007g0217 a0001c0001t0007g0218 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.106+3004C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620305 | |||||||
chr9:114620306 | G | A | 1 | a0001c0001t0004g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.106+3005G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620306 | |||||||
chr9:114620322 | G | A | 1 | a0001c0001t0006g0201 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106+3021G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620322 | |||||||
chr9:114620370 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.106+3069G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620370 | |||||||
chr9:114620402 | G | A | 1 | a0001c0001t0004g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.106+3101G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620402 | |||||||
chr9:114620448 | C | T | 1 | a0001c0001t0010g0163 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.106+3147C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620448 | |||||||
chr9:114620457 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0161 a0001c0001t0001g0188 others(1): Show |
4 | HG00733.hp2 HG02004.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+3156C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620457 | |||||||
chr9:114620493 | C | T | 1 | a0001c0001t0009g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+3192C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620493 | |||||||
chr9:114620774 | C | T | 1 | a0001c0001t0049g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.106+3473C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620774 | |||||||
chr9:114620775 | G | A | 2 | a0001c0001t0007g0217 a0001c0001t0007g0218 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.106+3474G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114620775 | |||||||
chr9:114620926 | C | CA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(86): Show |
153 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.107-3415dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114620926 | ||||||
chr9:114621035 | A | C | 16 | a0001c0001t0012g0046 a0001c0001t0012g0047 a0001c0001t0012g0230 others(13): Show |
30 | HG00423.hp2 HG02027.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.107-3315A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621035 | |||||||
chr9:114621124 | G | C | 1 | a0001c0001t0003g0175 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.107-3226G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621124 | |||||||
chr9:114621245 | T | C | 34 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(31): Show |
48 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.107-3105T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621245 | |||||||
chr9:114621248 | C | T | 11 | a0001c0001t0003g0179 a0001c0001t0009g0225 a0001c0001t0009g0238 others(8): Show |
12 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.107-3102C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621248 | |||||||
chr9:114621310 | C | T | 1 | a0001c0001t0010g0158 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.107-3040C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621310 | |||||||
chr9:114621345 | C | CA | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.107-2991dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114621345 | ||||||
chr9:114621345 | C | CAA | 7 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0135 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-2992_107-2991d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114621345 | ||||||
chr9:114621366 | G | T | 42 | a0001c0001t0001g0126 a0001c0001t0001g0159 a0001c0001t0002g0002 others(39): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.107-2984G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621366 | |||||||
chr9:114621383 | A | G | 1 | a0001c0001t0013g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107-2967A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621383 | |||||||
chr9:114621542 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.107-2808T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621542 | |||||||
chr9:114621639 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(127): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.107-2711G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621639 | |||||||
chr9:114621675 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(173): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.107-2675A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621675 | |||||||
chr9:114621681 | A | G | 3 | a0001c0001t0013g0206 a0001c0001t0025g0113 a0001c0001t0045g0112 |
3 | HG02109.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.107-2669A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621681 | |||||||
chr9:114621795 | C | T | 7 | a0001c0001t0009g0225 a0001c0001t0009g0238 a0001c0001t0013g0104 others(4): Show |
7 | HG02615.hp2 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-2555C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621795 | |||||||
chr9:114621943 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(244): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.107-2407G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621943 | |||||||
chr9:114621959 | C | T | 14 | a0001c0001t0006g0220 a0001c0001t0008g0009 a0001c0001t0008g0052 others(11): Show |
20 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.107-2391C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114621959 | |||||||
chr9:114622404 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-1946C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622404 | |||||||
chr9:114622492 | T | C | 2 | a0001c0001t0016g0050 a0001c0001t0016g0051 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107-1858T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622492 | |||||||
chr9:114622718 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(196): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.107-1632G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622718 | |||||||
chr9:114622802 | G | A | 1 | a0001c0001t0022g0080 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107-1548G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622802 | |||||||
chr9:114622846 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(173): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.107-1504T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622846 | |||||||
chr9:114622850 | G | A | 1 | a0001c0001t0004g0064 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.107-1500G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622850 | |||||||
chr9:114622941 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(223): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.107-1409T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114622941 | |||||||
chr9:114623076 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.107-1274A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623076 | |||||||
chr9:114623094 | A | AAAC | 4 | a0001c0001t0002g0093 a0001c0001t0026g0137 a0001c0001t0026g0138 others(1): Show |
4 | HG01074.hp2 HG02257.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1229_107-1227d others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114623094 | ||||||
chr9:114623094 | A | C | 11 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(8): Show |
13 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-1256A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623094 | |||||||
chr9:114623094 | AAAC | A | 39 | a0001c0001t0002g0250 a0001c0001t0003g0004 a0001c0001t0003g0014 others(36): Show |
51 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.107-1229_107-1227d others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 114623094 | ||||||
chr9:114623097 | C | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0161 a0001c0001t0001g0188 others(1): Show |
4 | HG00733.hp2 HG02004.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-1253C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623097 | |||||||
chr9:114623111 | A | G | 31 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(28): Show |
43 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.107-1239A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623111 | |||||||
chr9:114623211 | C | T | 2 | a0003c0006t0021g0169 a0003c0006t0021g0221 |
2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.107-1139C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623211 | |||||||
chr9:114623295 | G | A | 1 | a0001c0001t0002g0028 | 2 | NA18962.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.107-1055G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623295 | |||||||
chr9:114623383 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(221): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.107-967C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623383 | |||||||
chr9:114623637 | C | T | 1 | a0001c0001t0017g0044 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.107-713C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623637 | |||||||
chr9:114623712 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(61): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.107-638G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623712 | |||||||
chr9:114623812 | C | G | 3 | a0002c0004t0013g0222 a0002c0004t0013g0224 a0002c0004t0029g0223 |
3 | HG02647.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.107-538C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114623812 | |||||||
chr9:114624068 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(138): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.107-282A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624068 | |||||||
chr9:114624114 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(243): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.107-236T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624114 | |||||||
chr9:114624136 | G | C | 1 | a0001c0001t0004g0024 | 2 | NA18961.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.107-214G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624136 | |||||||
chr9:114624285 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.107-65G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 2/8 | chr9 | 114624285 | |||||||
chr9:114624547 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.216+88T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624547 | |||||||
chr9:114624679 | A | T | 32 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(29): Show |
44 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.216+220A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624679 | |||||||
chr9:114624724 | A | G | 1 | a0001c0001t0049g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.216+265A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624724 | |||||||
chr9:114624754 | C | T | 1 | a0001c0001t0028g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.216+295C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624754 | |||||||
chr9:114624755 | G | A | 2 | a0001c0001t0013g0204 a0001c0001t0013g0206 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.216+296G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624755 | |||||||
chr9:114624885 | A | G | 4 | a0001c0001t0025g0113 a0001c0001t0045g0112 a0003c0006t0021g0169 others(1): Show |
4 | HG02109.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+426A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624885 | |||||||
chr9:114624977 | A | G | 13 | a0001c0001t0006g0220 a0001c0001t0007g0023 a0001c0001t0007g0209 others(10): Show |
15 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+518A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114624977 | |||||||
chr9:114625393 | T | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(219): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.216+934T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625393 | |||||||
chr9:114625427 | G | T | 1 | a0001c0001t0001g0033 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.216+968G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625427 | |||||||
chr9:114625443 | CT | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(166): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.216+1002delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 114625443 | ||||||
chr9:114625443 | CTT | C | 48 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0110 others(45): Show |
62 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.216+1001_216+1002d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 114625443 | ||||||
chr9:114625655 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.216+1196C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625655 | |||||||
chr9:114625657 | G | C | 4 | a0001c0001t0015g0043 a0001c0001t0015g0197 a0001c0001t0015g0202 others(1): Show |
5 | HG00738.hp2 HG01074.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+1198G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625657 | |||||||
chr9:114625993 | A | G | 3 | a0001c0001t0011g0013 a0001c0001t0011g0130 a0001c0001t0011g0151 |
6 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-906A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114625993 | |||||||
chr9:114626071 | C | T | 1 | a0001c0001t0010g0163 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.217-828C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626071 | |||||||
chr9:114626201 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.217-698A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626201 | |||||||
chr9:114626238 | C | G | 3 | a0002c0004t0013g0222 a0002c0004t0013g0224 a0002c0004t0029g0223 |
3 | HG02647.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-661C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626238 | |||||||
chr9:114626280 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.217-619G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626280 | |||||||
chr9:114626333 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.217-566C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626333 | |||||||
chr9:114626650 | C | T | 8 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(5): Show |
11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.217-249C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626650 | |||||||
chr9:114626764 | C | G | 1 | a0001c0001t0009g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.217-135C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626764 | |||||||
chr9:114626770 | C | T | 3 | a0001c0001t0025g0113 a0001c0001t0025g0154 a0001c0001t0045g0112 |
3 | HG02109.hp1 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.217-129C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 3/8 | chr9 | 114626770 | |||||||
chr9:114627198 | C | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(223): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.324+192C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627198 | |||||||
chr9:114627311 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(129): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.324+305T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627311 | |||||||
chr9:114627428 | A | G | 5 | a0001c0002t0005g0003 a0001c0002t0005g0227 a0001c0002t0005g0233 others(2): Show |
15 | HG00423.hp2 NA18612.hp2 NA18982.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+422A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627428 | |||||||
chr9:114627701 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.325-400G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627701 | |||||||
chr9:114627838 | C | T | 5 | a0001c0002t0014g0048 a0001c0002t0014g0228 a0001c0002t0014g0231 others(2): Show |
6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-263C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627838 | |||||||
chr9:114627904 | G | C | 1 | a0001c0001t0036g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.325-197G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627904 | |||||||
chr9:114627918 | A | T | 17 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(14): Show |
24 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.325-183A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627918 | |||||||
chr9:114627923 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.325-178C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627923 | |||||||
chr9:114627936 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0239 |
2 | HG01099.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.325-165C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627936 | |||||||
chr9:114627944 | C | T | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.325-157C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114627944 | |||||||
chr9:114628020 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(127): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.325-81C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114628020 | |||||||
chr9:114628055 | C | T | 17 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(14): Show |
24 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.325-46C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114628055 | |||||||
chr9:114628081 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.325-20C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 4/8 | chr9 | 114628081 | |||||||
chr9:114628256 | A | C | 1 | a0002c0004t0013g0224 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.474+6A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628256 | |||||||
chr9:114628274 | C | A | 1 | a0001c0001t0049g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.474+24C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628274 | |||||||
chr9:114628280 | C | CT | 23 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(20): Show |
26 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+31dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114628280 | ||||||
chr9:114628293 | C | G | 13 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(10): Show |
19 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.474+43C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628293 | |||||||
chr9:114628293 | C | T | 1 | a0001c0001t0007g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.474+43C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628293 | |||||||
chr9:114628397 | C | A | 26 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(23): Show |
35 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.474+147C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628397 | |||||||
chr9:114628459 | G | A | 3 | a0001c0001t0017g0044 a0001c0001t0017g0215 a0001c0001t0017g0216 |
4 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+209G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628459 | |||||||
chr9:114628518 | G | A | 2 | a0001c0001t0016g0050 a0001c0001t0016g0051 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.474+268G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628518 | |||||||
chr9:114628861 | C | T | 27 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(24): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+611C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114628861 | |||||||
chr9:114629045 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(199): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.474+795A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629045 | |||||||
chr9:114629077 | A | T | 2 | a0001c0001t0025g0113 a0001c0001t0045g0112 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.474+827A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629077 | |||||||
chr9:114629309 | C | T | 27 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(24): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1059C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629309 | |||||||
chr9:114629417 | T | C | 1 | a0001c0001t0048g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474+1167T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629417 | |||||||
chr9:114629456 | C | T | 2 | a0001c0001t0018g0219 a0001c0001t0028g0174 |
2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.474+1206C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629456 | |||||||
chr9:114629755 | C | T | 2 | a0001c0001t0018g0219 a0001c0001t0028g0174 |
2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.474+1505C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629755 | |||||||
chr9:114629762 | T | C | 2 | a0001c0001t0016g0050 a0001c0001t0016g0051 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.474+1512T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629762 | |||||||
chr9:114629808 | G | A | 27 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(24): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1558G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629808 | |||||||
chr9:114629826 | C | T | 5 | a0001c0002t0014g0048 a0001c0002t0014g0228 a0001c0002t0014g0231 others(2): Show |
6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+1576C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629826 | |||||||
chr9:114629942 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.474+1692C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114629942 | |||||||
chr9:114630057 | C | T | 33 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(30): Show |
45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.474+1807C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630057 | |||||||
chr9:114630089 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.474+1839T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630089 | |||||||
chr9:114630161 | T | A | 1 | a0001c0001t0009g0100 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.474+1911T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630161 | |||||||
chr9:114630200 | C | T | 8 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(5): Show |
11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+1950C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630200 | |||||||
chr9:114630230 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(199): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.474+1980C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630230 | |||||||
chr9:114630275 | T | TATCCATC others(1): Show |
107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(104): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(10): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | ||||||
chr9:114630275 | T | TATCCATC others(5): Show |
24 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0131 others(21): Show |
27 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | ||||||
chr9:114630275 | T | TATCCATC others(9): Show |
8 | a0001c0001t0001g0192 a0001c0001t0015g0043 a0001c0001t0015g0197 others(5): Show |
10 | HG01074.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(18): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | ||||||
chr9:114630275 | T | TATCCATC others(13): Show |
4 | a0001c0001t0001g0148 a0001c0001t0043g0190 a0001c0001t0049g0205 others(1): Show |
4 | HG00642.hp2 HG00738.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+2028_474+2029i others(22): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | ||||||
chr9:114630275 | T | TATCCATC others(17): Show |
2 | a0001c0002t0024g0120 a0001c0002t0033g0232 |
2 | HG03017.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.474+2028_474+2029i others(26): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630275 | ||||||
chr9:114630279 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.474+2029T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630279 | |||||||
chr9:114630279 | T | TATCCATC others(1): Show |
6 | a0001c0001t0006g0042 a0001c0001t0006g0199 a0001c0001t0006g0200 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+2059_474+2066d others(10): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | ||||||
chr9:114630279 | T | TATCCATC others(5): Show |
2 | a0001c0001t0006g0022 a0001c0001t0006g0198 |
4 | HG01192.hp2 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+2055_474+2066d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | ||||||
chr9:114630279 | TATCC | T | 71 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(68): Show |
108 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.474+2063_474+2066d others(6): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | ||||||
chr9:114630279 | TATCCATC others(9): Show |
T | 1 | a0001c0001t0032g0234 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.474+2051_474+2066d others(18): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630279 | ||||||
chr9:114630357 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(128): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.474+2107T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630357 | |||||||
chr9:114630359 | C | T | 1 | a0001c0001t0017g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.474+2109C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630359 | |||||||
chr9:114630486 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.474+2236A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630486 | |||||||
chr9:114630531 | A | G | 1 | a0001c0001t0006g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.474+2281A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630531 | |||||||
chr9:114630548 | C | T | 33 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(30): Show |
45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.474+2298C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630548 | |||||||
chr9:114630605 | A | C | 8 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(5): Show |
11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+2355A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630605 | |||||||
chr9:114630609 | T | G | 7 | a0001c0001t0001g0031 a0001c0001t0002g0015 a0001c0001t0002g0240 others(4): Show |
11 | HG02015.hp1 HG02074.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.474+2359T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630609 | |||||||
chr9:114630805 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.474+2555C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114630805 | |||||||
chr9:114630933 | C | CTG | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.474+2685_474+2686d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114630933 | ||||||
chr9:114631167 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(128): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.475-2601G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631167 | |||||||
chr9:114631170 | G | A | 12 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(9): Show |
18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.475-2598G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631170 | |||||||
chr9:114631172 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.475-2596G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631172 | |||||||
chr9:114631177 | G | C | 1 | a0001c0015t0001g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.475-2591G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631177 | |||||||
chr9:114631187 | C | T | 2 | a0001c0001t0003g0115 a0001c0001t0003g0184 |
2 | HG01167.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.475-2581C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631187 | |||||||
chr9:114631246 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.475-2522T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631246 | |||||||
chr9:114631252 | C | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-2516C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631252 | |||||||
chr9:114631282 | C | CA | 26 | a0001c0001t0003g0117 a0001c0001t0003g0180 a0001c0001t0004g0006 others(23): Show |
44 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.475-2462dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | ||||||
chr9:114631282 | C | CAA | 38 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(35): Show |
53 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.475-2463_475-2462d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | ||||||
chr9:114631282 | C | CAAA | 15 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0189 others(12): Show |
20 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.475-2464_475-2462d others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | ||||||
chr9:114631282 | CAAAAAAA others(4): Show |
C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(121): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.475-2472_475-2462d others(13): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | ||||||
chr9:114631282 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0146 |
2 | NA18990.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.475-2473_475-2462d others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631282 | ||||||
chr9:114631290 | A | AAAAAAAA others(7): Show |
3 | a0001c0001t0015g0043 a0001c0001t0015g0202 a0001c0001t0043g0190 |
3 | HG00738.hp2 HG01257.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.475-2465_475-2464i others(16): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631290 | ||||||
chr9:114631290 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0015g0043 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.475-2466_475-2465i others(15): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631290 | ||||||
chr9:114631291 | A | AAAAAAAA others(9): Show |
5 | a0001c0001t0013g0104 a0001c0001t0024g0226 a0002c0004t0013g0222 others(2): Show |
5 | HG02647.hp2 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-2475_475-2460d others(18): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | ||||||
chr9:114631291 | A | AAAAAAAA others(8): Show |
2 | a0001c0001t0013g0204 a0001c0001t0013g0206 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.475-2463_475-2462i others(17): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | ||||||
chr9:114631291 | A | AAAAAAAA others(6): Show |
9 | a0001c0001t0015g0197 a0001c0001t0016g0050 a0001c0001t0016g0051 others(6): Show |
9 | HG01074.hp1 HG02027.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-2465_475-2464i others(15): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | ||||||
chr9:114631291 | A | AAAAAAAA others(5): Show |
1 | a0001c0002t0014g0048 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.475-2466_475-2465i others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631291 | ||||||
chr9:114631292 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0002g0093 a0001c0001t0048g0249 |
2 | HG01074.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.475-2465_475-2464i others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114631292 | ||||||
chr9:114631364 | G | A | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0065 others(1): Show |
6 | NA18953.hp2 NA18961.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-2404G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631364 | |||||||
chr9:114631378 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-2390C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631378 | |||||||
chr9:114631388 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-2380C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631388 | |||||||
chr9:114631454 | A | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-2314A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631454 | |||||||
chr9:114631456 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-2312C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631456 | |||||||
chr9:114631605 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0110 others(6): Show |
16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.475-2163G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631605 | |||||||
chr9:114631625 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-2143G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631625 | |||||||
chr9:114631628 | C | T | 1 | a0001c0001t0025g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-2140C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631628 | |||||||
chr9:114631654 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-2114C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631654 | |||||||
chr9:114631658 | T | A | 2 | a0001c0001t0016g0050 a0001c0001t0016g0051 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.475-2110T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631658 | |||||||
chr9:114631748 | C | T | 33 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(30): Show |
45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.475-2020C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631748 | |||||||
chr9:114631779 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-1989T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631779 | |||||||
chr9:114631812 | G | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-1956G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631812 | |||||||
chr9:114631826 | C | T | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.475-1942C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631826 | |||||||
chr9:114631830 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(243): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.475-1938A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114631830 | |||||||
chr9:114632006 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.475-1762T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632006 | |||||||
chr9:114632085 | G | A | 27 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(24): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-1683G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632085 | |||||||
chr9:114632098 | C | CA | 77 | a0001c0001t0001g0019 a0001c0001t0001g0110 a0001c0001t0001g0147 others(74): Show |
112 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.475-1651dupA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632098 | ||||||
chr9:114632098 | C | CAA | 7 | a0001c0001t0003g0160 a0001c0001t0003g0184 a0001c0001t0004g0063 others(4): Show |
7 | HG02738.hp2 HG03098.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-1652_475-1651d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632098 | ||||||
chr9:114632098 | CA | C | 7 | a0001c0001t0009g0225 a0001c0001t0012g0230 a0001c0001t0016g0050 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.475-1651delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632098 | ||||||
chr9:114632135 | G | A | 29 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(26): Show |
41 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.475-1633G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632135 | |||||||
chr9:114632142 | G | A | 4 | a0001c0001t0016g0050 a0001c0001t0016g0051 a0001c0001t0048g0249 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1626G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632142 | |||||||
chr9:114632177 | AT | A | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1582delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114632177 | ||||||
chr9:114632315 | A | G | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1453A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632315 | |||||||
chr9:114632474 | T | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1294T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632474 | |||||||
chr9:114632543 | C | T | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1225C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632543 | |||||||
chr9:114632557 | C | T | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-1211C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632557 | |||||||
chr9:114632605 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.475-1163G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632605 | |||||||
chr9:114632923 | G | A | 53 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(50): Show |
77 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.475-845G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632923 | |||||||
chr9:114632942 | C | A | 2 | a0001c0001t0048g0249 a0001c0001t0049g0205 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.475-826C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632942 | |||||||
chr9:114632947 | T | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-821T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114632947 | |||||||
chr9:114633143 | A | T | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-625A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633143 | |||||||
chr9:114633159 | T | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-609T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633159 | |||||||
chr9:114633162 | AT | A | 100 | a0001c0001t0001g0127 a0001c0001t0002g0081 a0001c0001t0003g0004 others(97): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.475-589delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114633162 | ||||||
chr9:114633171 | T | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
11 | HG00639.hp1 HG01081.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.475-597T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633171 | |||||||
chr9:114633185 | A | G | 104 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(101): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.475-583A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633185 | |||||||
chr9:114633222 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.475-546C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633222 | |||||||
chr9:114633247 | T | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-521T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633247 | |||||||
chr9:114633256 | G | A | 12 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(9): Show |
18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.475-512G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633256 | |||||||
chr9:114633305 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.475-463G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633305 | |||||||
chr9:114633306 | T | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-462T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633306 | |||||||
chr9:114633319 | G | A | 5 | a0001c0002t0014g0048 a0001c0002t0014g0228 a0001c0002t0014g0231 others(2): Show |
6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-449G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633319 | |||||||
chr9:114633381 | C | T | 64 | a0001c0001t0003g0194 a0001c0001t0004g0006 a0001c0001t0004g0024 others(61): Show |
90 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.475-387C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633381 | |||||||
chr9:114633404 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.475-364C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633404 | |||||||
chr9:114633412 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.475-356G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633412 | |||||||
chr9:114633464 | G | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-304G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633464 | |||||||
chr9:114633522 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0110 others(6): Show |
16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.475-246G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633522 | |||||||
chr9:114633601 | A | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.475-167A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633601 | |||||||
chr9:114633610 | A | AC | 12 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(9): Show |
18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.475-153dupC | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 114633610 | ||||||
chr9:114633615 | C | T | 1 | a0001c0001t0041g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.475-153C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633615 | |||||||
chr9:114633710 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.475-58C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633710 | |||||||
chr9:114633755 | G | A | 1 | a0001c0012t0001g0122 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.475-13G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 5/8 | chr9 | 114633755 | |||||||
chr9:114633899 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.585+21C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114633899 | |||||||
chr9:114633957 | C | T | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+79C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114633957 | |||||||
chr9:114634044 | C | A | 1 | a0001c0001t0002g0029 | 2 | NA18973.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.585+166C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634044 | |||||||
chr9:114634248 | C | G | 2 | a0001c0001t0018g0219 a0001c0001t0028g0174 |
2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.585+370C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634248 | |||||||
chr9:114634267 | C | T | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+389C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634267 | |||||||
chr9:114634294 | C | G | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.585+416C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634294 | |||||||
chr9:114634377 | T | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+499T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634377 | |||||||
chr9:114634394 | G | A | 2 | a0001c0001t0016g0050 a0001c0001t0016g0051 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.585+516G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634394 | |||||||
chr9:114634397 | G | A | 33 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(30): Show |
45 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.585+519G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634397 | |||||||
chr9:114634417 | C | T | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+539C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634417 | |||||||
chr9:114634467 | C | T | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+589C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634467 | |||||||
chr9:114634474 | G | T | 43 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(40): Show |
61 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.585+596G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634474 | |||||||
chr9:114634537 | C | T | 1 | a0001c0001t0017g0044 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.585+659C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634537 | |||||||
chr9:114634577 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.585+699C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634577 | |||||||
chr9:114634594 | A | G | 7 | a0001c0001t0013g0104 a0001c0001t0013g0204 a0001c0001t0013g0206 others(4): Show |
7 | HG02647.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+716A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634594 | |||||||
chr9:114634683 | C | T | 10 | a0001c0001t0013g0104 a0001c0001t0013g0204 a0001c0001t0013g0206 others(7): Show |
10 | HG02257.hp2 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+805C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634683 | |||||||
chr9:114634724 | T | G | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+846T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634724 | |||||||
chr9:114634732 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+854G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634732 | |||||||
chr9:114634775 | G | A | 2 | a0001c0001t0018g0134 a0001c0001t0018g0178 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.585+897G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634775 | |||||||
chr9:114634798 | AC | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.585+921delC | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634798 | |||||||
chr9:114634800 | A | G | 1 | a0001c0002t0014g0231 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.585+922A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634800 | |||||||
chr9:114634864 | C | G | 53 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(50): Show |
77 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.585+986C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634864 | |||||||
chr9:114634903 | C | T | 2 | a0001c0001t0016g0050 a0001c0001t0016g0051 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.585+1025C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114634903 | |||||||
chr9:114635016 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0135 others(3): Show |
12 | HG01496.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+1138A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635016 | |||||||
chr9:114635026 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.585+1148T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635026 | |||||||
chr9:114635066 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.585+1188C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635066 | |||||||
chr9:114635078 | C | T | 11 | a0001c0001t0004g0073 a0001c0001t0007g0023 a0001c0001t0007g0209 others(8): Show |
13 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+1200C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635078 | |||||||
chr9:114635079 | A | G | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.585+1201A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635079 | |||||||
chr9:114635091 | A | G | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+1213A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635091 | |||||||
chr9:114635195 | T | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.585+1317T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635195 | |||||||
chr9:114635333 | G | T | 1 | a0001c0015t0001g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.585+1455G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635333 | |||||||
chr9:114635349 | CA | C | 17 | a0001c0001t0001g0037 a0001c0001t0007g0209 a0001c0001t0013g0104 others(14): Show |
19 | HG00642.hp1 HG02027.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+1483delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114635349 | ||||||
chr9:114635349 | CAA | C | 106 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(103): Show |
150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.585+1482_585+1483d others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114635349 | ||||||
chr9:114635488 | T | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.586-1502T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635488 | |||||||
chr9:114635548 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-1442G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635548 | |||||||
chr9:114635603 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.586-1387C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635603 | |||||||
chr9:114635604 | G | A | 3 | a0001c0001t0025g0113 a0001c0001t0025g0154 a0001c0001t0045g0112 |
3 | HG02109.hp1 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.586-1386G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635604 | |||||||
chr9:114635663 | A | C | 9 | a0001c0001t0009g0018 a0001c0001t0009g0088 a0001c0001t0009g0098 others(6): Show |
10 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.586-1327A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635663 | |||||||
chr9:114635920 | A | T | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.586-1070A>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635920 | |||||||
chr9:114635925 | A | G | 1 | a0001c0001t0042g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.586-1065A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114635925 | |||||||
chr9:114636006 | A | G | 12 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(9): Show |
18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.586-984A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636006 | |||||||
chr9:114636211 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-779G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636211 | |||||||
chr9:114636281 | A | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.586-709A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636281 | |||||||
chr9:114636363 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.586-627G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636363 | |||||||
chr9:114636426 | C | T | 29 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(26): Show |
41 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.586-564C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636426 | |||||||
chr9:114636484 | C | CTTTT | 28 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0041 others(25): Show |
39 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.586-504_586-501dup others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636484 | ||||||
chr9:114636485 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0008g0055 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.586-501_586-500ins others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | ||||||
chr9:114636485 | T | TTTTTTTT others(17): Show |
8 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0056 others(5): Show |
14 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-501_586-500ins others(24): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | ||||||
chr9:114636485 | T | TTTTTTTT others(22): Show |
2 | a0001c0001t0008g0053 a0001c0001t0027g0058 |
2 | HG01928.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.586-501_586-500ins others(29): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | ||||||
chr9:114636485 | T | TTTTTTTT others(32): Show |
1 | a0001c0001t0027g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.586-501_586-500ins others(39): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636485 | ||||||
chr9:114636489 | TC | T | 4 | a0001c0001t0003g0040 a0001c0001t0003g0175 a0001c0001t0003g0176 others(1): Show |
5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-500delC | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636489 | |||||||
chr9:114636491 | TTTTCTTT others(7): Show |
T | 7 | a0001c0001t0013g0104 a0001c0001t0013g0204 a0001c0001t0013g0206 others(4): Show |
7 | HG02647.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-484_586-471del others(14): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636491 | ||||||
chr9:114636501 | TTTTC | T | 4 | a0001c0001t0003g0040 a0001c0001t0003g0175 a0001c0001t0003g0176 others(1): Show |
5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-481_586-478del others(4): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636501 | ||||||
chr9:114636505 | C | CT | 41 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0041 others(38): Show |
58 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.586-482dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 114636505 | ||||||
chr9:114636690 | T | C | 38 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(35): Show |
51 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.586-300T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636690 | |||||||
chr9:114636823 | G | T | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-167G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636823 | |||||||
chr9:114636865 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.586-125A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636865 | |||||||
chr9:114636962 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.586-28C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636962 | |||||||
chr9:114636983 | C | T | 10 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(7): Show |
12 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.586-7C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 6/8 | chr9 | 114636983 | |||||||
chr9:114637117 | G | A | 3 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 |
3 | HG02818.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.666+47G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637117 | |||||||
chr9:114637288 | CT | C | 37 | a0001c0001t0001g0036 a0001c0001t0001g0109 a0001c0001t0002g0007 others(34): Show |
63 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.666+237delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 114637288 | ||||||
chr9:114637288 | CTT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(145): Show |
227 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.666+236_666+237del others(2): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 114637288 | ||||||
chr9:114637288 | CTTTTT | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(41): Show |
62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.666+233_666+237del others(5): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 114637288 | ||||||
chr9:114637292 | T | C | 1 | a0001c0001t0004g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.666+222T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637292 | |||||||
chr9:114637293 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.666+223T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637293 | |||||||
chr9:114637338 | A | G | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.666+268A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637338 | |||||||
chr9:114637378 | C | T | 4 | a0001c0001t0003g0040 a0001c0001t0003g0175 a0001c0001t0003g0176 others(1): Show |
5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+308C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637378 | |||||||
chr9:114637417 | G | T | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.666+347G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637417 | |||||||
chr9:114637424 | C | T | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.666+354C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637424 | |||||||
chr9:114637463 | G | C | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.666+393G>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637463 | |||||||
chr9:114637493 | C | T | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.666+423C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637493 | |||||||
chr9:114637508 | A | G | 108 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(105): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.666+438A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637508 | |||||||
chr9:114637533 | A | G | 27 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(24): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.666+463A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637533 | |||||||
chr9:114637542 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0035 |
4 | HG00735.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+472C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637542 | |||||||
chr9:114637590 | G | A | 5 | a0001c0002t0014g0048 a0001c0002t0014g0228 a0001c0002t0014g0231 others(2): Show |
6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+520G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637590 | |||||||
chr9:114637690 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0110 others(6): Show |
16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.666+620C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637690 | |||||||
chr9:114637734 | G | A | 7 | a0001c0001t0013g0104 a0001c0001t0013g0204 a0001c0001t0013g0206 others(4): Show |
7 | HG02647.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+664G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637734 | |||||||
chr9:114637765 | C | T | 1 | a0001c0001t0010g0145 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.666+695C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114637765 | |||||||
chr9:114638227 | T | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(42): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.667-317T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638227 | |||||||
chr9:114638272 | T | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(41): Show |
62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.667-272T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638272 | |||||||
chr9:114638326 | G | A | 5 | a0001c0002t0014g0048 a0001c0002t0014g0228 a0001c0002t0014g0231 others(2): Show |
6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-218G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638326 | |||||||
chr9:114638366 | A | G | 1 | a0001c0001t0048g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.667-178A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 7/8 | chr9 | 114638366 | |||||||
chr9:114638736 | A | C | 19 | a0001c0001t0009g0018 a0001c0001t0009g0088 a0001c0001t0009g0098 others(16): Show |
20 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.849+10A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638736 | |||||||
chr9:114638751 | G | A | 11 | a0001c0001t0009g0018 a0001c0001t0009g0088 a0001c0001t0009g0098 others(8): Show |
12 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+25G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638751 | |||||||
chr9:114638802 | C | G | 9 | a0001c0001t0009g0018 a0001c0001t0009g0088 a0001c0001t0009g0098 others(6): Show |
10 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.849+76C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638802 | |||||||
chr9:114638869 | A | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0110 others(6): Show |
16 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.849+143A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638869 | |||||||
chr9:114638913 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(76): Show |
141 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.849+187G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114638913 | |||||||
chr9:114639039 | C | T | 125 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(122): Show |
170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.849+313C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639039 | |||||||
chr9:114639079 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.849+353A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639079 | |||||||
chr9:114639516 | G | A | 48 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(45): Show |
74 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.849+790G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639516 | |||||||
chr9:114639568 | G | A | 27 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(24): Show |
31 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.849+842G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639568 | |||||||
chr9:114639578 | G | A | 2 | a0001c0001t0013g0204 a0001c0001t0013g0206 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849+852G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639578 | |||||||
chr9:114639860 | C | T | 2 | a0001c0001t0013g0204 a0001c0001t0013g0206 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.849+1134C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639860 | |||||||
chr9:114639987 | C | T | 27 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(24): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.849+1261C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114639987 | |||||||
chr9:114640005 | C | T | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.849+1279C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640005 | |||||||
chr9:114640056 | TA | T | 8 | a0001c0001t0001g0143 a0001c0001t0001g0172 a0001c0001t0002g0084 others(5): Show |
9 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+1342delA | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114640056 | ||||||
chr9:114640067 | A | G | 14 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(11): Show |
20 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.849+1341A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640067 | |||||||
chr9:114640083 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.849+1357C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640083 | |||||||
chr9:114640114 | CT | C | 29 | a0001c0001t0001g0020 a0001c0001t0002g0082 a0001c0001t0004g0006 others(26): Show |
50 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.849+1401delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114640114 | ||||||
chr9:114640233 | T | G | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849+1507T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640233 | |||||||
chr9:114640392 | C | T | 5 | a0001c0002t0014g0048 a0001c0002t0014g0228 a0001c0002t0014g0231 others(2): Show |
6 | HG02027.hp2 HG02155.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+1666C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640392 | |||||||
chr9:114640632 | T | A | 4 | a0001c0001t0003g0040 a0001c0001t0003g0175 a0001c0001t0003g0176 others(1): Show |
5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+1906T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640632 | |||||||
chr9:114640634 | C | A | 4 | a0001c0001t0003g0040 a0001c0001t0003g0175 a0001c0001t0003g0176 others(1): Show |
5 | HG02602.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+1908C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640634 | |||||||
chr9:114640639 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.849+1913C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640639 | |||||||
chr9:114640881 | C | CT | 8 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(5): Show |
11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+2166dupT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114640881 | ||||||
chr9:114640894 | G | A | 4 | a0001c0001t0006g0220 a0001c0001t0017g0044 a0001c0001t0017g0215 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+2168G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640894 | |||||||
chr9:114640902 | G | A | 1 | a0001c0001t0011g0151 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.849+2176G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640902 | |||||||
chr9:114640908 | C | T | 34 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(31): Show |
46 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.849+2182C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640908 | |||||||
chr9:114640922 | C | G | 3 | a0001c0001t0017g0044 a0001c0001t0017g0215 a0001c0001t0017g0216 |
4 | HG01891.hp1 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+2196C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114640922 | |||||||
chr9:114641170 | C | T | 11 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(8): Show |
17 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.850-1964C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641170 | |||||||
chr9:114641171 | C | T | 1 | a0001c0001t0009g0225 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-1963C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641171 | |||||||
chr9:114641209 | G | A | 1 | a0001c0001t0010g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.850-1925G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641209 | |||||||
chr9:114641229 | T | G | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1905T>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641229 | |||||||
chr9:114641240 | A | G | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1894A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641240 | |||||||
chr9:114641362 | C | T | 9 | a0001c0001t0009g0018 a0001c0001t0009g0088 a0001c0001t0009g0098 others(6): Show |
10 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-1772C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641362 | |||||||
chr9:114641399 | C | A | 1 | a0001c0001t0037g0244 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-1735C>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641399 | |||||||
chr9:114641596 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-1538G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641596 | |||||||
chr9:114641637 | A | C | 125 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(122): Show |
170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.850-1497A>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641637 | |||||||
chr9:114641658 | C | T | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1476C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641658 | |||||||
chr9:114641728 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.850-1406C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641728 | |||||||
chr9:114641793 | A | G | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-1341A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114641793 | |||||||
chr9:114642012 | G | T | 129 | a0001c0001t0003g0004 a0001c0001t0003g0014 a0001c0001t0003g0040 others(126): Show |
175 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.850-1122G>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642012 | |||||||
chr9:114642017 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.850-1117A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642017 | |||||||
chr9:114642019 | T | C | 20 | a0001c0001t0007g0023 a0001c0001t0007g0209 a0001c0001t0007g0210 others(17): Show |
23 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.850-1115T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642019 | |||||||
chr9:114642101 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-1033G>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642101 | |||||||
chr9:114642111 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.850-1023C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642111 | |||||||
chr9:114642112 | A | G | 27 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(24): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.850-1022A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642112 | |||||||
chr9:114642240 | C | T | 12 | a0001c0001t0008g0009 a0001c0001t0008g0052 a0001c0001t0008g0053 others(9): Show |
18 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.850-894C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642240 | |||||||
chr9:114642256 | T | A | 8 | a0001c0001t0006g0022 a0001c0001t0006g0042 a0001c0001t0006g0198 others(5): Show |
11 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-878T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642256 | |||||||
chr9:114642271 | C | G | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-863C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642271 | |||||||
chr9:114642340 | C | T | 1 | a0001c0001t0037g0244 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-794C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642340 | |||||||
chr9:114642343 | T | C | 1 | a0001c0001t0037g0244 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-791T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642343 | |||||||
chr9:114642361 | CT | C | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-764delT | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114642361 | ||||||
chr9:114642462 | T | A | 1 | a0001c0001t0037g0244 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.850-672T>A | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642462 | |||||||
chr9:114642499 | A | G | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-635A>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642499 | |||||||
chr9:114642545 | C | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0143 |
2 | NA18977.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.850-589C>G | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642545 | |||||||
chr9:114642624 | T | C | 1 | a0001c0001t0002g0030 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.850-510T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642624 | |||||||
chr9:114642909 | T | C | 59 | a0001c0001t0004g0006 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
87 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-225T>C | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114642909 | |||||||
chr9:114643061 | CCCCTGGT others(7): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.850-68_850-55delGG others(12): Show |
TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 114643061 | ||||||
chr9:114643119 | C | T | 1 | a0001c0001t0001g0021 | 3 | NA18972.hp2 NA18986.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.850-15C>T | TMEM268 | ENSG00000157693.15 | transcript | ENST00000288502.9 | protein_coding | 8/8 | chr9 | 114643119 |