Item | Value |
---|---|
geneid | 50999 |
ensemblid | ENSG00000117500.13 |
hgncid | 24251 |
symbol | TMED5 |
name | transmembrane p24 trafficking protein 5 |
refseq_nuc | NM_016040.5 |
refseq_prot | NP_057124.3 |
ensembl_nuc | ENST00000370282.8 |
ensembl_prot | ENSP00000359305.3 |
mane_status | MANE Select |
chr | chr1 |
start | 93149742 |
end | 93180413 |
strand | - |
ver | v1.2 |
region | chr1:93149742-93180413 |
region5000 | chr1:93144742-93185413 |
regionname0 | TMED5_chr1_93149742_93180413 |
regionname5000 | TMED5_chr1_93144742_93185413 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 229 | 217 | 81 | 36 | 76 | 9 | 14 | 56 | TMED5_chr1_93144742_93185413 | TMED5 | MGDKI others(224): Show |
chr1 | 93144742 | 93185413 |
a0002 | 0/1 | 229 | 124 | 5 | 31 | 64 | 7 | 16 | 48 | TMED5_chr1_93144742_93185413 | TMED5 | MGDKI others(224): Show |
chr1 | 93144742 | 93185413 |
a0003 | 0/0 | 229 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | MGDKI others(224): Show |
chr1 | 93144742 | 93185413 |
a0004 | 0/0 | 229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | MGDKI others(224): Show |
chr1 | 93144742 | 93185413 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 687 | 217 | 81 | 36 | 76 | 9 | 14 | TMED5_chr1_93144742_93185413 | TMED5 | ATGGG others(682): Show |
chr1 | 93144742 | 93185413 | ||
a0002c0002 | 0/1 | 687 | 124 | 5 | 31 | 64 | 7 | 16 | TMED5_chr1_93144742_93185413 | TMED5 | ATGGG others(682): Show |
chr1 | 93144742 | 93185413 | ||
a0003c0003 | 0/0 | 687 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | ATGGG others(682): Show |
chr1 | 93144742 | 93185413 | ||
a0004c0004 | 0/0 | 687 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | ATGGG others(682): Show |
chr1 | 93144742 | 93185413 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5789 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0002 | 0/0 | 5789 | 79 | 3 | 16 | 52 | 2 | 6 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0003 | 1/0 | 5789 | 45 | 26 | 11 | 0 | 5 | 2 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0004 | 0/0 | 5789 | 32 | 12 | 6 | 9 | 0 | 5 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0005 | 0/0 | 5789 | 16 | 16 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0006 | 0/0 | 5789 | 8 | 8 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0007 | 0/0 | 5789 | 7 | 0 | 0 | 7 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0008 | 0/0 | 5789 | 6 | 6 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0009 | 0/0 | 5789 | 4 | 0 | 0 | 3 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0010 | 0/0 | 5791 | 4 | 3 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5786): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0011 | 0/0 | 5789 | 4 | 3 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0012 | 0/0 | 5789 | 2 | 0 | 0 | 0 | 2 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0013 | 0/0 | 5789 | 2 | 0 | 0 | 2 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0015 | 0/0 | 5789 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0016 | 0/0 | 5789 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0017 | 0/0 | 5789 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0019 | 0/0 | 5789 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0021 | 0/0 | 5789 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0024 | 0/0 | 5789 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0001c0001t0025 | 0/0 | 5789 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0002c0002t0001 | 0/1 | 5789 | 119 | 5 | 30 | 62 | 7 | 14 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0002c0002t0014 | 0/0 | 5789 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0002c0002t0018 | 0/0 | 5789 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0002c0002t0020 | 0/0 | 5789 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0002c0002t0022 | 0/0 | 5789 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0002c0002t0023 | 0/0 | 5789 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0003c0003t0004 | 0/0 | 5789 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
a0004c0004t0001 | 0/0 | 5789 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | GGAGA others(5784): Show |
chr1 | 93144742 | 93185413 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0001 | 0/0 | 11 | 1 | 7 | 1 | 2 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0006g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0007g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0009g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0009g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0010g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0010g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0011g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0012g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0013g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0013g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0017g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0019g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0021g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0024g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0001c0001t0025g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0003 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 4 | 1 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0005 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0014g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0018g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0020g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0022g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0002c0002t0023g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0003c0003t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0003c0003t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
a0004c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | GBR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0063 | EUR | GBR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0031 | EUR | FIN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0042 | EUR | FIN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0251 | EUR | FIN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0051 | EUR | FIN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0248 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00597 | hp2 | a0001 | c0001 | t0013 | g0269 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | CHS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG00741 | hp2 | a0004 | c0004 | t0001 | g0087 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0124 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01433 | hp2 | a0002 | c0002 | t0023 | g0091 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0027 | EUR | IBS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0198 | EUR | IBS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0099 | EUR | IBS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01516 | hp2 | a0001 | c0001 | t0012 | g0019 | EUR | IBS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01517 | hp1 | a0001 | c0001 | t0012 | g0019 | EUR | IBS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0203 | EUR | IBS | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01928 | hp1 | a0001 | c0001 | t0011 | g0238 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02015 | hp2 | a0001 | c0001 | t0013 | g0268 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02074 | hp1 | a0001 | c0001 | t0009 | g0247 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02145 | hp2 | a0003 | c0003 | t0004 | g0190 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | CDX | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0240 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02602 | hp2 | a0002 | c0002 | t0014 | g0110 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0245 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02723 | hp1 | a0003 | c0003 | t0004 | g0189 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02818 | hp2 | a0001 | c0001 | t0021 | g0112 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0241 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0226 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0230 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0244 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0266 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03139 | hp1 | a0001 | c0001 | t0017 | g0113 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0246 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03195 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03225 | hp1 | a0001 | c0001 | t0025 | g0271 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0114 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0243 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0174 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0026 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0125 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0204 | SAS | PJL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03834 | hp2 | a0001 | c0001 | t0009 | g0249 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0075 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG04184 | hp1 | a0002 | c0002 | t0022 | g0102 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | STU | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | STU | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0176 | SAS | STU | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | YRI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | YRI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18747 | hp1 | a0002 | c0002 | t0018 | g0077 | EAS | CHB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | CHB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | YRI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | YRI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18940 | hp2 | a0001 | c0001 | t0019 | g0141 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18942 | hp1 | a0002 | c0002 | t0020 | g0055 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18962 | hp2 | a0001 | c0001 | t0015 | g0156 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0264 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18968 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0232 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18981 | hp1 | a0001 | c0001 | t0024 | g0270 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | LWK | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | LWK | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19054 | hp2 | a0001 | c0001 | t0007 | g0233 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19055 | hp2 | a0001 | c0001 | t0009 | g0250 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | YRI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | YRI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20129 | hp1 | a0001 | c0001 | t0011 | g0239 | AFR | ASW | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ASW | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0090 | EUR | TSI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | GIH | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0070 | SAS | GIH | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | USA | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | USA | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | USA | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0097 | REF | REF | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0199 | REF | REF | TMED5_chr1_93144742_93185413 | TMED5 | chr1 | 93144742 | 93185413 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:93154761 | A | G | 1 | a0003 | 2 | HG02145.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.599T>C | p.Met200Thr | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 770/5789 | 599/690 | 200/229 | chr1 | 93154761 | |||
chr1:93154797 | T | C | 1 | a0004 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.563A>G | p.Gln188Arg | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 734/5789 | 563/690 | 188/229 | chr1 | 93154797 | |||
chr1:93154836 | G | A | 2 | a0002 a0004 |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
missense_variant | MODERATE | c.524C>T | p.Thr175Ile | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 695/5789 | 524/690 | 175/229 | chr1 | 93154836 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:93149990 | A | G | 1 | a0001c0001t0010 | 4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4680T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 4680 | chr1 | 93149990 | ||||||
chr1:93150292 | G | C | 1 | a0002c0002t0022 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4378C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 4378 | chr1 | 93150292 | ||||||
chr1:93150546 | C | T | 1 | a0001c0001t0008 | 6 | HG02451.hp2 HG02630.hp2 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4124G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 4124 | chr1 | 93150546 | ||||||
chr1:93150571 | C | T | 1 | a0001c0001t0019 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4099G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 4099 | chr1 | 93150571 | ||||||
chr1:93150645 | T | C | 13 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0012 others(10): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*4025A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 4025 | chr1 | 93150645 | ||||||
chr1:93150847 | C | G | 1 | a0001c0001t0021 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3823G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 3823 | chr1 | 93150847 | ||||||
chr1:93151625 | A | G | 1 | a0002c0002t0020 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3045T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 3045 | chr1 | 93151625 | ||||||
chr1:93151693 | T | C | 1 | a0002c0002t0023 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2977A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2977 | chr1 | 93151693 | ||||||
chr1:93151791 | A | AG | 1 | a0001c0001t0010 | 4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2878_*2879insC | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2878 | chr1 | 93151791 | ||||||
chr1:93151794 | A | T | 1 | a0001c0001t0010 | 4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2876T>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2876 | chr1 | 93151794 | ||||||
chr1:93151846 | T | G | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(14): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2824A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2824 | chr1 | 93151846 | ||||||
chr1:93151920 | A | G | 2 | a0001c0001t0007 a0001c0001t0012 |
9 | HG01516.hp2 HG01517.hp1 NA18952.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2750T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2750 | chr1 | 93151920 | ||||||
chr1:93151989 | T | C | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*2681A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2681 | chr1 | 93151989 | ||||||
chr1:93152199 | T | C | 1 | a0001c0001t0010 | 4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2471A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2471 | chr1 | 93152199 | ||||||
chr1:93152344 | A | G | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(2): Show |
31 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2326T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2326 | chr1 | 93152344 | ||||||
chr1:93152581 | A | C | 1 | a0001c0001t0011 | 4 | HG01928.hp1 HG02257.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2089T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 2089 | chr1 | 93152581 | ||||||
chr1:93153149 | C | T | 1 | a0001c0001t0010 | 4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1521G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 1521 | chr1 | 93153149 | ||||||
chr1:93153332 | A | AC | 1 | a0001c0001t0010 | 4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1337_*1338insG | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 1337 | chr1 | 93153332 | ||||||
chr1:93153537 | A | G | 1 | a0002c0002t0018 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1133T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 1133 | chr1 | 93153537 | ||||||
chr1:93153654 | T | G | 1 | a0001c0001t0006 | 8 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1016A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 1016 | chr1 | 93153654 | ||||||
chr1:93153681 | A | G | 1 | a0001c0001t0017 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*989T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 989 | chr1 | 93153681 | ||||||
chr1:93153739 | A | G | 4 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0024 others(1): Show |
36 | HG00423.hp2 HG01074.hp2 HG01081.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*931T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 931 | chr1 | 93153739 | ||||||
chr1:93153846 | A | G | 1 | a0001c0001t0015 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*824T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 824 | chr1 | 93153846 | ||||||
chr1:93153870 | C | G | 2 | a0001c0001t0006 a0001c0001t0009 |
12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*800G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 800 | chr1 | 93153870 | ||||||
chr1:93154220 | A | G | 1 | a0002c0002t0014 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 4/4 | 450 | chr1 | 93154220 | ||||||
chr1:93180333 | G | A | 1 | a0001c0001t0013 | 2 | HG00597.hp2 HG02015.hp2 |
5_prime_UTR_variant | MODIFIER | c.-91C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/4 | 91 | chr1 | 93180333 | ||||||
chr1:93180377 | G | A | 1 | a0001c0001t0024 | 1 | NA18981.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-135C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/4 | chr1 | 93180377 | |||||||
chr1:93180386 | T | G | 1 | a0001c0001t0025 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/4 | 144 | chr1 | 93180386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:93154963 | T | C | 9 | a0001c0001t0006g0010 a0001c0001t0006g0021 a0001c0001t0006g0127 others(6): Show |
12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.472-75A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93154963 | |||||||
chr1:93155175 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.472-287T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155175 | |||||||
chr1:93155532 | G | GT | 9 | a0001c0001t0001g0267 a0001c0001t0003g0212 a0001c0001t0021g0112 others(6): Show |
9 | HG00642.hp2 HG00741.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-645dupA | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155532 | |||||||
chr1:93155532 | GT | G | 43 | a0001c0001t0002g0143 a0001c0001t0002g0146 a0001c0001t0004g0026 others(40): Show |
48 | HG00408.hp1 HG00423.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.472-645delA | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155532 | |||||||
chr1:93155532 | GTT | G | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.472-646_472-645del others(2): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155532 | |||||||
chr1:93155532 | GTTTTT | G | 31 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(28): Show |
33 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.472-649_472-645del others(5): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155532 | |||||||
chr1:93155581 | A | G | 3 | a0002c0002t0001g0066 a0002c0002t0001g0073 a0002c0002t0001g0104 |
3 | HG00544.hp1 HG02135.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.472-693T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155581 | |||||||
chr1:93155587 | G | T | 1 | a0001c0001t0003g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.472-699C>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155587 | |||||||
chr1:93155784 | T | A | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.471+516A>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155784 | |||||||
chr1:93155926 | A | G | 101 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0017g0113 others(98): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.471+374T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93155926 | |||||||
chr1:93156161 | A | G | 1 | a0001c0001t0004g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.471+139T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93156161 | |||||||
chr1:93156182 | A | C | 1 | a0001c0001t0012g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.471+118T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 3/3 | chr1 | 93156182 | |||||||
chr1:93156807 | CA | C | 189 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(186): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.288-325delT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93156807 | |||||||
chr1:93156807 | CAA | C | 36 | a0001c0001t0002g0138 a0001c0001t0002g0140 a0001c0001t0003g0259 others(33): Show |
37 | HG00323.hp2 HG01891.hp1 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.288-326_288-325del others(2): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93156807 | |||||||
chr1:93156952 | A | G | 1 | a0001c0001t0021g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.288-469T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93156952 | |||||||
chr1:93157094 | T | C | 3 | a0001c0001t0010g0020 a0001c0001t0010g0124 a0001c0001t0010g0125 |
4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.288-611A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93157094 | |||||||
chr1:93157232 | A | G | 234 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(231): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.288-749T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93157232 | |||||||
chr1:93157891 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.288-1408C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93157891 | |||||||
chr1:93157985 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.288-1502C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93157985 | |||||||
chr1:93157997 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.288-1514C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93157997 | |||||||
chr1:93157999 | C | T | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.288-1516G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93157999 | |||||||
chr1:93158058 | A | G | 1 | a0002c0002t0001g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.288-1575T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158058 | |||||||
chr1:93158122 | C | CA | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(93): Show |
123 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.288-1640dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158122 | |||||||
chr1:93158122 | C | CAA | 14 | a0001c0001t0002g0013 a0001c0001t0002g0022 a0001c0001t0002g0132 others(11): Show |
17 | HG01261.hp2 HG01928.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-1641_288-1640d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158122 | |||||||
chr1:93158122 | CA | C | 16 | a0001c0001t0001g0267 a0001c0001t0003g0206 a0001c0001t0004g0033 others(13): Show |
19 | HG01069.hp2 HG01168.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.288-1640delT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158122 | |||||||
chr1:93158577 | G | GT | 112 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(109): Show |
146 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.287+1551dupA | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158577 | |||||||
chr1:93158577 | G | GTT | 25 | a0001c0001t0002g0163 a0001c0001t0004g0171 a0001c0001t0004g0176 others(22): Show |
26 | HG01891.hp1 HG02055.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.287+1550_287+1551d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158577 | |||||||
chr1:93158582 | G | T | 234 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(231): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.287+1547C>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158582 | |||||||
chr1:93158662 | C | T | 2 | a0001c0001t0005g0223 a0001c0001t0005g0261 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.287+1467G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158662 | |||||||
chr1:93158817 | T | C | 136 | a0001c0001t0001g0267 a0001c0001t0005g0126 a0001c0001t0005g0223 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.287+1312A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93158817 | |||||||
chr1:93159172 | C | T | 1 | a0001c0001t0002g0166 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.287+957G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159172 | |||||||
chr1:93159251 | A | G | 1 | a0001c0001t0008g0246 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287+878T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159251 | |||||||
chr1:93159387 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.287+742A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159387 | |||||||
chr1:93159555 | T | C | 1 | a0001c0001t0012g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.287+574A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159555 | |||||||
chr1:93159677 | T | TA | 136 | a0001c0001t0001g0267 a0001c0001t0002g0155 a0001c0001t0005g0126 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.287+451dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159677 | |||||||
chr1:93159698 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0021g0112 |
2 | HG01168.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.287+431G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159698 | |||||||
chr1:93159713 | T | C | 3 | a0001c0001t0003g0198 a0001c0001t0003g0203 a0001c0001t0003g0204 |
3 | HG01515.hp2 HG01517.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.287+416A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159713 | |||||||
chr1:93159798 | T | C | 1 | a0001c0001t0005g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.287+331A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93159798 | |||||||
chr1:93160104 | A | G | 3 | a0002c0002t0001g0037 a0002c0002t0001g0048 a0002c0002t0001g0049 |
3 | NA18964.hp1 NA19007.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.287+25T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 2/3 | chr1 | 93160104 | |||||||
chr1:93160310 | G | C | 1 | a0001c0001t0004g0033 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.190-84C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160310 | |||||||
chr1:93160457 | T | C | 1 | a0001c0001t0008g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.190-231A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160457 | |||||||
chr1:93160528 | CAA | C | 3 | a0001c0001t0010g0020 a0001c0001t0010g0124 a0001c0001t0010g0125 |
4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-304_190-303del others(2): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160528 | |||||||
chr1:93160552 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190-326C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160552 | |||||||
chr1:93160624 | G | A | 1 | a0001c0001t0004g0185 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.190-398C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160624 | |||||||
chr1:93160791 | A | G | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.190-565T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160791 | |||||||
chr1:93160798 | C | T | 1 | a0002c0002t0001g0017 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.190-572G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160798 | |||||||
chr1:93160808 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.190-582T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160808 | |||||||
chr1:93160821 | A | AC | 18 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0211 others(15): Show |
19 | HG00642.hp1 HG00673.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-596dupG | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160821 | |||||||
chr1:93160825 | C | CCG | 5 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0010g0124 others(2): Show |
5 | HG00423.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-600_190-599ins others(2): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160825 | |||||||
chr1:93160825 | C | T | 98 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(95): Show |
131 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.190-599G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160825 | |||||||
chr1:93160826 | G | C | 5 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0010g0124 others(2): Show |
5 | HG00423.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-600C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160826 | |||||||
chr1:93160826 | G | GC | 18 | a0001c0001t0003g0204 a0001c0001t0003g0256 a0001c0001t0005g0224 others(15): Show |
18 | HG00544.hp1 HG01123.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.190-601dupG | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160826 | |||||||
chr1:93160850 | C | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0013 others(20): Show |
36 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.190-624G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93160850 | |||||||
chr1:93161423 | T | G | 1 | a0001c0001t0004g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.190-1197A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93161423 | |||||||
chr1:93161427 | C | T | 98 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(95): Show |
131 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.190-1201G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93161427 | |||||||
chr1:93161477 | A | G | 1 | a0002c0002t0001g0063 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.190-1251T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93161477 | |||||||
chr1:93161684 | T | C | 9 | a0001c0001t0006g0010 a0001c0001t0006g0021 a0001c0001t0006g0127 others(6): Show |
12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-1458A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93161684 | |||||||
chr1:93161816 | G | C | 7 | a0001c0001t0004g0170 a0001c0001t0004g0178 a0001c0001t0004g0179 others(4): Show |
7 | HG01074.hp2 HG01106.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-1590C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93161816 | |||||||
chr1:93161972 | C | T | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.190-1746G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93161972 | |||||||
chr1:93162069 | A | C | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.190-1843T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162069 | |||||||
chr1:93162102 | G | GA | 14 | a0001c0001t0002g0145 a0001c0001t0002g0162 a0001c0001t0002g0165 others(11): Show |
15 | HG01123.hp2 HG02895.hp1 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-1877dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162102 | |||||||
chr1:93162170 | T | C | 136 | a0001c0001t0001g0267 a0001c0001t0005g0126 a0001c0001t0005g0223 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.190-1944A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162170 | |||||||
chr1:93162264 | T | C | 1 | a0002c0002t0001g0090 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.190-2038A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162264 | |||||||
chr1:93162456 | C | G | 136 | a0001c0001t0001g0267 a0001c0001t0005g0126 a0001c0001t0005g0223 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.190-2230G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162456 | |||||||
chr1:93162458 | A | G | 34 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0170 others(31): Show |
36 | HG00423.hp2 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.190-2232T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162458 | |||||||
chr1:93162505 | G | A | 101 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0017g0113 others(98): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.190-2279C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162505 | |||||||
chr1:93162582 | ATGAG | A | 4 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0009g0249 others(1): Show |
4 | HG00408.hp1 HG02074.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-2360_190-2357d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162582 | |||||||
chr1:93162706 | G | T | 3 | a0002c0002t0001g0094 a0002c0002t0001g0095 a0002c0002t0001g0108 |
3 | HG02056.hp2 NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.190-2480C>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162706 | |||||||
chr1:93162964 | G | T | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.190-2738C>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93162964 | |||||||
chr1:93163153 | TACTC | T | 101 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0017g0113 others(98): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.190-2931_190-2928d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163153 | |||||||
chr1:93163346 | C | CT | 40 | a0001c0001t0002g0142 a0001c0001t0003g0123 a0001c0001t0003g0208 others(37): Show |
42 | HG00423.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.190-3121dupA | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163346 | |||||||
chr1:93163361 | T | C | 1 | a0002c0002t0001g0040 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.190-3135A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163361 | |||||||
chr1:93163455 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.190-3229G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163455 | |||||||
chr1:93163458 | C | A | 6 | a0001c0001t0004g0033 a0001c0001t0004g0194 a0001c0001t0004g0196 others(3): Show |
7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-3232G>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163458 | |||||||
chr1:93163533 | G | A | 3 | a0001c0001t0010g0020 a0001c0001t0010g0124 a0001c0001t0010g0125 |
4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-3307C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163533 | |||||||
chr1:93163594 | C | G | 2 | a0002c0002t0001g0061 a0002c0002t0001g0069 |
2 | NA18950.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.190-3368G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163594 | |||||||
chr1:93163750 | T | C | 266 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(263): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.190-3524A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163750 | |||||||
chr1:93163981 | C | CA | 12 | a0001c0001t0003g0209 a0001c0001t0003g0218 a0001c0001t0004g0171 others(9): Show |
14 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.190-3756dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93163981 | |||||||
chr1:93164094 | A | G | 32 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(29): Show |
33 | HG01891.hp1 HG01928.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.190-3868T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164094 | |||||||
chr1:93164116 | G | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.190-3890C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164116 | |||||||
chr1:93164241 | T | C | 2 | a0001c0001t0004g0170 a0001c0001t0004g0179 |
2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.190-4015A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164241 | |||||||
chr1:93164389 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.190-4163C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164389 | |||||||
chr1:93164525 | T | C | 1 | a0001c0001t0012g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.190-4299A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164525 | |||||||
chr1:93164615 | G | A | 103 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0017g0113 others(100): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.190-4389C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164615 | |||||||
chr1:93164663 | G | A | 1 | a0001c0001t0009g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.190-4437C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164663 | |||||||
chr1:93164733 | G | A | 4 | a0001c0001t0004g0182 a0001c0001t0004g0183 a0001c0001t0004g0184 others(1): Show |
4 | NA18977.hp2 NA18983.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-4507C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164733 | |||||||
chr1:93164953 | T | C | 136 | a0001c0001t0001g0267 a0001c0001t0005g0126 a0001c0001t0005g0223 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.190-4727A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93164953 | |||||||
chr1:93165062 | A | C | 1 | a0001c0001t0009g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.190-4836T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93165062 | |||||||
chr1:93165126 | A | G | 9 | a0001c0001t0006g0010 a0001c0001t0006g0021 a0001c0001t0006g0127 others(6): Show |
12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-4900T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93165126 | |||||||
chr1:93165654 | T | C | 2 | a0002c0002t0001g0060 a0002c0002t0001g0100 |
2 | HG01346.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.190-5428A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93165654 | |||||||
chr1:93165915 | A | G | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.190-5689T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93165915 | |||||||
chr1:93166030 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.190-5804G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93166030 | |||||||
chr1:93166177 | T | C | 1 | a0001c0001t0011g0241 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.190-5951A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93166177 | |||||||
chr1:93166275 | A | G | 2 | a0002c0002t0001g0082 a0002c0002t0001g0083 |
2 | NA18961.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.190-6049T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93166275 | |||||||
chr1:93166484 | C | T | 234 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(231): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.190-6258G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93166484 | |||||||
chr1:93166602 | AATTAG | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.190-6381_190-6377d others(7): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93166602 | |||||||
chr1:93166723 | G | A | 1 | a0001c0001t0004g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190-6497C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93166723 | |||||||
chr1:93166774 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.190-6548A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93166774 | |||||||
chr1:93167363 | A | G | 1 | a0001c0001t0012g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.190-7137T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167363 | |||||||
chr1:93167484 | G | A | 1 | a0002c0002t0001g0017 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.190-7258C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167484 | |||||||
chr1:93167564 | T | C | 1 | a0001c0001t0003g0032 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.190-7338A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167564 | |||||||
chr1:93167612 | C | A | 1 | a0001c0001t0012g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.190-7386G>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167612 | |||||||
chr1:93167687 | T | C | 1 | a0001c0001t0012g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.190-7461A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167687 | |||||||
chr1:93167696 | C | T | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | NA18947.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.190-7470G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167696 | |||||||
chr1:93167725 | C | T | 1 | a0001c0001t0021g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-7499G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167725 | |||||||
chr1:93167880 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.190-7654C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93167880 | |||||||
chr1:93168452 | G | A | 97 | a0001c0001t0017g0113 a0002c0002t0001g0003 a0002c0002t0001g0004 others(94): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.190-8226C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93168452 | |||||||
chr1:93168705 | C | T | 1 | a0002c0002t0001g0108 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.190-8479G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93168705 | |||||||
chr1:93168883 | A | G | 1 | a0001c0001t0025g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190-8657T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93168883 | |||||||
chr1:93168989 | T | G | 1 | a0002c0002t0001g0069 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.190-8763A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93168989 | |||||||
chr1:93169033 | C | A | 136 | a0001c0001t0001g0267 a0001c0001t0005g0126 a0001c0001t0005g0223 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.190-8807G>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169033 | |||||||
chr1:93169034 | A | G | 136 | a0001c0001t0001g0267 a0001c0001t0005g0126 a0001c0001t0005g0223 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.190-8808T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169034 | |||||||
chr1:93169067 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.190-8841A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169067 | |||||||
chr1:93169591 | G | C | 234 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(231): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.190-9365C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169591 | |||||||
chr1:93169594 | G | GA | 223 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(220): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.190-9369dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169594 | |||||||
chr1:93169594 | G | GAA | 37 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(34): Show |
39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.190-9370_190-9369d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169594 | |||||||
chr1:93169774 | G | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.190-9548C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169774 | |||||||
chr1:93169882 | T | TAC | 34 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0003g0027 others(31): Show |
40 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.190-9658_190-9657d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACAC | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(67): Show |
101 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.190-9660_190-9657d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACACAC | 31 | a0001c0001t0001g0267 a0001c0001t0002g0025 a0001c0001t0002g0135 others(28): Show |
35 | HG00408.hp1 HG00733.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.190-9662_190-9657d others(8): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACACACA others(1): Show |
20 | a0001c0001t0002g0148 a0001c0001t0003g0216 a0001c0001t0004g0193 others(17): Show |
28 | HG01069.hp2 HG01070.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.190-9664_190-9657d others(10): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACACACA others(3): Show |
49 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0003g0029 others(46): Show |
57 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-9666_190-9657d others(12): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACACACA others(5): Show |
26 | a0001c0001t0002g0149 a0001c0001t0004g0170 a0001c0001t0004g0186 others(23): Show |
31 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.190-9668_190-9657d others(14): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACACACA others(7): Show |
16 | a0001c0001t0004g0033 a0001c0001t0004g0180 a0001c0001t0004g0185 others(13): Show |
21 | HG00558.hp1 HG01943.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.190-9670_190-9657d others(16): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACACACA others(9): Show |
3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0098 |
3 | HG00423.hp1 NA18959.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.190-9672_190-9657d others(18): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | T | TACACACA others(11): Show |
3 | a0002c0002t0001g0034 a0002c0002t0001g0082 a0002c0002t0001g0083 |
3 | NA18943.hp2 NA18961.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.190-9674_190-9657d others(20): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | TACACACA others(5): Show |
T | 1 | a0001c0001t0004g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190-9668_190-9657d others(14): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169882 | TACACACA others(7): Show |
T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0136 a0001c0001t0002g0163 |
5 | NA18941.hp1 NA18954.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-9670_190-9657d others(16): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169882 | |||||||
chr1:93169919 | A | ACACACAC others(4): Show |
1 | a0002c0002t0001g0090 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.190-9694_190-9693i others(13): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169919 | |||||||
chr1:93169919 | A | ACACACAC others(6): Show |
2 | a0002c0002t0001g0046 a0002c0002t0023g0091 |
2 | HG01433.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.190-9694_190-9693i others(15): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93169919 | |||||||
chr1:93170023 | G | C | 1 | a0001c0001t0008g0246 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.190-9797C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170023 | |||||||
chr1:93170137 | G | A | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.190-9911C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170137 | |||||||
chr1:93170343 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.189+9711G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170343 | |||||||
chr1:93170359 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.189+9695C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170359 | |||||||
chr1:93170406 | C | G | 1 | a0001c0001t0024g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.189+9648G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170406 | |||||||
chr1:93170533 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.189+9521C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170533 | |||||||
chr1:93170547 | C | T | 1 | a0002c0002t0001g0044 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.189+9507G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170547 | |||||||
chr1:93170555 | G | A | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+9499C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170555 | |||||||
chr1:93170745 | A | G | 234 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(231): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.189+9309T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170745 | |||||||
chr1:93170804 | T | C | 10 | a0001c0001t0008g0242 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
10 | HG01928.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.189+9250A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170804 | |||||||
chr1:93170878 | CAAAACAG others(17): Show |
C | 1 | a0001c0001t0002g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.189+9152_189+9175d others(26): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170878 | |||||||
chr1:93170966 | A | G | 3 | a0001c0001t0010g0020 a0001c0001t0010g0124 a0001c0001t0010g0125 |
4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+9088T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93170966 | |||||||
chr1:93171117 | C | T | 1 | a0002c0002t0001g0045 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.189+8937G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93171117 | |||||||
chr1:93171152 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.189+8902C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93171152 | |||||||
chr1:93171286 | G | A | 2 | a0003c0003t0004g0189 a0003c0003t0004g0190 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.189+8768C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93171286 | |||||||
chr1:93171899 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.189+8155T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93171899 | |||||||
chr1:93171938 | A | T | 1 | a0001c0001t0005g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+8116T>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93171938 | |||||||
chr1:93172063 | T | G | 1 | a0002c0002t0022g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.189+7991A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172063 | |||||||
chr1:93172220 | T | C | 34 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0170 others(31): Show |
36 | HG00423.hp2 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.189+7834A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172220 | |||||||
chr1:93172286 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.189+7768T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172286 | |||||||
chr1:93172314 | C | CA | 7 | a0001c0001t0002g0153 a0001c0001t0002g0167 a0001c0001t0003g0210 others(4): Show |
7 | HG02074.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+7739dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172314 | |||||||
chr1:93172469 | A | G | 4 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(1): Show |
4 | NA18947.hp1 NA18964.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+7585T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172469 | |||||||
chr1:93172571 | CTGAGCCC others(7): Show |
C | 1 | a0001c0001t0005g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+7469_189+7482d others(16): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172571 | |||||||
chr1:93172586 | T | C | 1 | a0001c0001t0005g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+7468A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172586 | |||||||
chr1:93172674 | G | A | 1 | a0001c0001t0004g0186 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.189+7380C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172674 | |||||||
chr1:93172737 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.189+7317C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172737 | |||||||
chr1:93172739 | A | G | 1 | a0002c0002t0001g0044 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.189+7315T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172739 | |||||||
chr1:93172752 | G | A | 2 | a0002c0002t0001g0085 a0002c0002t0001g0086 |
2 | NA18747.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.189+7302C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172752 | |||||||
chr1:93172821 | T | TA | 3 | a0001c0001t0005g0229 a0001c0001t0005g0230 a0001c0001t0005g0231 |
3 | HG02258.hp1 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.189+7232dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172821 | |||||||
chr1:93172843 | G | A | 97 | a0001c0001t0017g0113 a0002c0002t0001g0003 a0002c0002t0001g0004 others(94): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.189+7211C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172843 | |||||||
chr1:93172938 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0021g0112 a0001c0001t0025g0271 |
3 | HG01168.hp2 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.189+7116G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93172938 | |||||||
chr1:93173113 | CAGAA | C | 6 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0042 others(3): Show |
6 | HG00280.hp2 HG00639.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+6937_189+6940d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173113 | |||||||
chr1:93173152 | G | A | 34 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0170 others(31): Show |
36 | HG00423.hp2 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.189+6902C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173152 | |||||||
chr1:93173193 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189+6861G>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173193 | |||||||
chr1:93173286 | CAT | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(86): Show |
119 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.189+6766_189+6767d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173286 | |||||||
chr1:93173299 | C | T | 1 | a0002c0002t0001g0089 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189+6755G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173299 | |||||||
chr1:93173325 | G | C | 3 | a0002c0002t0001g0096 a0002c0002t0001g0109 a0002c0002t0014g0110 |
3 | HG02258.hp2 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.189+6729C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173325 | |||||||
chr1:93173378 | T | TAGAGCTG others(9): Show |
1 | a0001c0001t0003g0123 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.189+6660_189+6675d others(18): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173378 | |||||||
chr1:93173399 | T | C | 1 | a0004c0004t0001g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.189+6655A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173399 | |||||||
chr1:93173527 | A | G | 1 | a0002c0002t0022g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.189+6527T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173527 | |||||||
chr1:93173544 | T | G | 101 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0017g0113 others(98): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.189+6510A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173544 | |||||||
chr1:93173661 | A | C | 1 | a0001c0001t0002g0161 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189+6393T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173661 | |||||||
chr1:93173730 | A | T | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+6324T>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173730 | |||||||
chr1:93173778 | G | A | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+6276C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173778 | |||||||
chr1:93173912 | A | C | 1 | a0002c0002t0001g0088 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.189+6142T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173912 | |||||||
chr1:93173966 | T | G | 1 | a0001c0001t0002g0155 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.189+6088A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93173966 | |||||||
chr1:93174039 | T | C | 136 | a0001c0001t0001g0267 a0001c0001t0005g0126 a0001c0001t0005g0223 others(133): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.189+6015A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93174039 | |||||||
chr1:93174068 | C | G | 2 | a0002c0002t0001g0040 a0002c0002t0001g0041 |
2 | HG00673.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.189+5986G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93174068 | |||||||
chr1:93174070 | G | T | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+5984C>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93174070 | |||||||
chr1:93174215 | C | G | 1 | a0001c0001t0002g0011 | 3 | HG00544.hp2 NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.189+5839G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93174215 | |||||||
chr1:93174266 | A | G | 234 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(231): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.189+5788T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93174266 | |||||||
chr1:93174295 | G | C | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+5759C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93174295 | |||||||
chr1:93174386 | A | T | 34 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(31): Show |
36 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.189+5668T>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93174386 | |||||||
chr1:93175036 | TA | T | 7 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0003g0198 others(4): Show |
7 | HG01515.hp2 HG01928.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+5017delT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175036 | |||||||
chr1:93175175 | T | TTA | 13 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0123 others(10): Show |
21 | HG00280.hp1 HG00323.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.189+4877_189+4878d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATA | 3 | a0001c0001t0003g0211 a0001c0001t0011g0238 a0001c0001t0016g0114 |
3 | HG01928.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.189+4875_189+4878d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(1): Show |
3 | a0001c0001t0011g0239 a0001c0001t0011g0240 a0001c0001t0011g0241 |
3 | HG02257.hp1 HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.189+4871_189+4878d others(10): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(3): Show |
17 | a0001c0001t0004g0026 a0001c0001t0004g0170 a0001c0001t0004g0171 others(14): Show |
18 | HG01074.hp2 HG01081.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+4869_189+4878d others(12): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(5): Show |
7 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0004g0183 others(4): Show |
7 | HG00423.hp2 HG02293.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+4867_189+4878d others(14): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(7): Show |
6 | a0001c0001t0005g0223 a0001c0001t0005g0225 a0001c0001t0005g0226 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+4865_189+4878d others(16): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(9): Show |
6 | a0001c0001t0005g0227 a0001c0001t0005g0228 a0001c0001t0007g0030 others(3): Show |
7 | HG02647.hp2 HG02723.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+4863_189+4878d others(18): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(11): Show |
7 | a0001c0001t0004g0191 a0001c0001t0004g0192 a0001c0001t0007g0233 others(4): Show |
8 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4861_189+4878d others(20): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(13): Show |
6 | a0001c0001t0004g0193 a0001c0001t0005g0229 a0001c0001t0007g0263 others(3): Show |
6 | HG02258.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+4859_189+4878d others(22): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(15): Show |
5 | a0001c0001t0004g0194 a0001c0001t0005g0230 a0001c0001t0005g0231 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4857_189+4878d others(24): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(17): Show |
7 | a0001c0001t0004g0033 a0001c0001t0004g0195 a0001c0001t0004g0257 others(4): Show |
8 | HG02559.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4855_189+4878d others(26): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(21): Show |
1 | a0001c0001t0004g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.189+4878_189+4879i others(30): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | T | TTATATAT others(23): Show |
1 | a0001c0001t0004g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189+4878_189+4879i others(32): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175175 | TTA | T | 141 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(138): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.189+4877_189+4878d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175175 | |||||||
chr1:93175208 | C | A | 5 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0220 others(2): Show |
5 | HG00642.hp2 HG00741.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+4846G>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175208 | |||||||
chr1:93175243 | C | T | 1 | a0001c0001t0004g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189+4811G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175243 | |||||||
chr1:93175299 | C | CTA | 5 | a0001c0001t0002g0159 a0001c0001t0002g0169 a0002c0002t0001g0096 others(2): Show |
5 | HG00673.hp1 HG02258.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4753_189+4754d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175299 | |||||||
chr1:93175314 | T | C | 1 | a0001c0001t0025g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+4740A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175314 | |||||||
chr1:93175314 | TATAC | T | 32 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0170 others(29): Show |
34 | HG00423.hp2 HG01074.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.189+4736_189+4739d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175314 | |||||||
chr1:93175316 | T | C | 14 | a0001c0001t0003g0032 a0001c0001t0008g0242 a0001c0001t0008g0243 others(11): Show |
16 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.189+4738A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175316 | |||||||
chr1:93175316 | T | TAC | 104 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(101): Show |
130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.189+4736_189+4737d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175316 | |||||||
chr1:93175316 | T | TACAC | 13 | a0001c0001t0021g0112 a0002c0002t0001g0004 a0002c0002t0001g0006 others(10): Show |
13 | HG00140.hp2 HG00280.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.189+4734_189+4737d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175316 | |||||||
chr1:93175316 | TAC | T | 9 | a0001c0001t0006g0010 a0001c0001t0006g0021 a0001c0001t0006g0127 others(6): Show |
11 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+4736_189+4737d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175316 | |||||||
chr1:93175455 | AATAG | A | 3 | a0001c0001t0010g0020 a0001c0001t0010g0124 a0001c0001t0010g0125 |
4 | HG01109.hp2 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+4595_189+4598d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175455 | |||||||
chr1:93175567 | C | T | 101 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0017g0113 others(98): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.189+4487G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175567 | |||||||
chr1:93175675 | T | G | 1 | a0002c0002t0001g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.189+4379A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175675 | |||||||
chr1:93175781 | T | C | 2 | a0002c0002t0001g0099 a0002c0002t0001g0111 |
2 | HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.189+4273A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175781 | |||||||
chr1:93175800 | T | C | 10 | a0001c0001t0005g0224 a0001c0001t0005g0225 a0001c0001t0005g0226 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.189+4254A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175800 | |||||||
chr1:93175925 | T | G | 9 | a0001c0001t0006g0010 a0001c0001t0006g0021 a0001c0001t0006g0127 others(6): Show |
12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+4129A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175925 | |||||||
chr1:93175970 | G | C | 1 | a0001c0001t0006g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.189+4084C>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93175970 | |||||||
chr1:93176030 | C | T | 1 | a0001c0001t0025g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+4024G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176030 | |||||||
chr1:93176265 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189+3789C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176265 | |||||||
chr1:93176303 | CATTATGC others(18): Show |
C | 1 | a0002c0002t0001g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.189+3726_189+3750d others(27): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176303 | |||||||
chr1:93176489 | T | G | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.189+3565A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176489 | |||||||
chr1:93176508 | T | TAC | 106 | a0001c0001t0001g0267 a0001c0001t0003g0007 a0001c0001t0003g0032 others(103): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.189+3544_189+3545d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176508 | |||||||
chr1:93176508 | T | TACAC | 25 | a0001c0001t0005g0224 a0001c0001t0005g0225 a0001c0001t0005g0226 others(22): Show |
26 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.189+3542_189+3545d others(6): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176508 | |||||||
chr1:93176508 | T | TACACAC | 12 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0235 others(9): Show |
13 | HG01891.hp1 HG02895.hp1 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.189+3540_189+3545d others(8): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176508 | |||||||
chr1:93176543 | A | T | 12 | a0001c0001t0001g0267 a0001c0001t0008g0242 a0001c0001t0008g0243 others(9): Show |
12 | HG01168.hp2 HG01928.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+3511T>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176543 | |||||||
chr1:93176766 | A | C | 9 | a0001c0001t0006g0010 a0001c0001t0006g0021 a0001c0001t0006g0127 others(6): Show |
12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+3288T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176766 | |||||||
chr1:93176869 | T | G | 10 | a0001c0001t0008g0242 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
10 | HG01928.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.189+3185A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176869 | |||||||
chr1:93176989 | G | T | 1 | a0001c0001t0025g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+3065C>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93176989 | |||||||
chr1:93177584 | C | CA | 51 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(48): Show |
55 | HG00597.hp1 HG00673.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.189+2469dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93177584 | |||||||
chr1:93177584 | C | CAA | 10 | a0001c0001t0001g0267 a0001c0001t0003g0222 a0001c0001t0004g0188 others(7): Show |
13 | HG01106.hp1 HG01168.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.189+2468_189+2469d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93177584 | |||||||
chr1:93177584 | CA | C | 86 | a0001c0001t0002g0130 a0001c0001t0002g0135 a0001c0001t0003g0123 others(83): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.189+2469delT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93177584 | |||||||
chr1:93177584 | CAA | C | 7 | a0001c0001t0010g0020 a0001c0001t0010g0124 a0001c0001t0010g0125 others(4): Show |
8 | HG01109.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+2468_189+2469d others(4): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93177584 | |||||||
chr1:93177612 | GGAACAGT others(27): Show |
G | 2 | a0003c0003t0004g0189 a0003c0003t0004g0190 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.189+2408_189+2441d others(36): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93177612 | |||||||
chr1:93177715 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.189+2339T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93177715 | |||||||
chr1:93178120 | T | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.189+1934A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93178120 | |||||||
chr1:93178318 | T | C | 35 | a0001c0001t0005g0126 a0001c0001t0005g0223 a0001c0001t0005g0224 others(32): Show |
37 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+1736A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93178318 | |||||||
chr1:93178425 | G | A | 9 | a0001c0001t0006g0010 a0001c0001t0006g0021 a0001c0001t0006g0127 others(6): Show |
12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+1629C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93178425 | |||||||
chr1:93178437 | T | C | 1 | a0001c0001t0005g0265 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+1617A>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93178437 | |||||||
chr1:93178582 | T | G | 1 | a0001c0001t0003g0251 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.189+1472A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93178582 | |||||||
chr1:93178845 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0021g0112 |
2 | HG01168.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.189+1209T>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93178845 | |||||||
chr1:93178853 | C | T | 102 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0016g0114 others(99): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.189+1201G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93178853 | |||||||
chr1:93179052 | A | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG00558.hp2 HG00597.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+1002T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179052 | |||||||
chr1:93179181 | G | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.189+873C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179181 | |||||||
chr1:93179286 | C | G | 96 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(93): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.189+768G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179286 | |||||||
chr1:93179292 | G | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0011 others(52): Show |
83 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.189+762C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179292 | |||||||
chr1:93179336 | C | G | 21 | a0001c0001t0004g0026 a0001c0001t0004g0170 a0001c0001t0004g0171 others(18): Show |
22 | HG00423.hp2 HG01074.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.189+718G>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179336 | |||||||
chr1:93179367 | C | CA | 12 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0256 others(9): Show |
14 | HG00280.hp1 HG01069.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.189+686dupT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179367 | |||||||
chr1:93179367 | CA | C | 153 | a0001c0001t0001g0267 a0001c0001t0002g0001 a0001c0001t0002g0002 others(150): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.189+686delT | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179367 | |||||||
chr1:93179368 | A | ACAAACAA others(21): Show |
1 | a0002c0002t0001g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.189+685_189+686ins others(28): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179368 | |||||||
chr1:93179383 | A | C | 1 | a0002c0002t0001g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.189+671T>G | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179383 | |||||||
chr1:93179457 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0035 |
2 | HG02080.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.189+597G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179457 | |||||||
chr1:93179545 | AATCGGGC others(54): Show |
A | 1 | a0002c0002t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.189+448_189+508del others(61): Show |
TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179545 | |||||||
chr1:93179559 | C | A | 2 | a0001c0001t0003g0123 a0001c0001t0003g0208 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.189+495G>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179559 | |||||||
chr1:93179625 | C | T | 102 | a0001c0001t0001g0267 a0001c0001t0012g0019 a0001c0001t0016g0114 others(99): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.189+429G>A | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179625 | |||||||
chr1:93179799 | T | G | 1 | a0001c0001t0008g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.189+255A>C | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179799 | |||||||
chr1:93179939 | G | A | 1 | a0001c0001t0004g0033 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.189+115C>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179939 | |||||||
chr1:93179951 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.189+103A>T | TMED5 | ENSG00000117500.13 | transcript | ENST00000370282.8 | protein_coding | 1/3 | chr1 | 93179951 |