Item | Value |
---|---|
geneid | 272 |
ensemblid | ENSG00000133805.16 |
hgncid | 470 |
symbol | AMPD3 |
name | adenosine monophosphate deaminase 3 |
refseq_nuc | NM_001025389.2 |
refseq_prot | NP_001020560.1 |
ensembl_nuc | ENST00000396553.7 |
ensembl_prot | ENSP00000379801.2 |
mane_status | MANE Select |
chr | chr11 |
start | 10455264 |
end | 10507579 |
strand | + |
ver | v1.2 |
region | chr11:10455264-10507579 |
region5000 | chr11:10450264-10512579 |
regionname0 | AMPD3_chr11_10455264_10507579 |
regionname5000 | AMPD3_chr11_10450264_10512579 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 767 | 365 | 78 | 69 | 157 | 17 | 42 | 118 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0002 | 0/0 | 767 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0003 | 0/0 | 767 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0004 | 0/0 | 767 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0005 | 0/0 | 767 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0006 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0007 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0008 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0009 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
a0010 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | MPRQF others(762): Show |
chr11 | 10450264 | 10512579 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2301 | 188 | 50 | 39 | 66 | 10 | 22 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0001c0002 | 0/1 | 2301 | 127 | 3 | 23 | 80 | 4 | 16 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0001c0003 | 0/0 | 2301 | 32 | 23 | 5 | 0 | 2 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0001c0004 | 0/0 | 2301 | 6 | 0 | 0 | 6 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0001c0005 | 0/0 | 2301 | 5 | 0 | 0 | 5 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0001c0007 | 0/0 | 2301 | 3 | 0 | 1 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0001c0010 | 0/0 | 2301 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0001c0013 | 0/0 | 2301 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0002c0006 | 0/0 | 2301 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0002c0012 | 0/0 | 2301 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0002c0020 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0002c0024 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0003c0008 | 0/0 | 2301 | 3 | 0 | 1 | 0 | 1 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0003c0009 | 0/0 | 2301 | 3 | 0 | 2 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0004c0011 | 0/0 | 2301 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0004c0014 | 0/0 | 2301 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0004c0015 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0005c0016 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0005c0017 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0006c0021 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0007c0019 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0008c0018 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0009c0022 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 | ||
a0010c0023 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ATGCC others(2296): Show |
chr11 | 10450264 | 10512579 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4189 | 92 | 19 | 25 | 28 | 9 | 11 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0002 | 0/0 | 4189 | 32 | 1 | 8 | 19 | 0 | 4 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0003 | 0/0 | 4189 | 23 | 3 | 0 | 18 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0004 | 0/0 | 4191 | 18 | 11 | 5 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0005 | 0/0 | 4189 | 2 | 1 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0007 | 0/0 | 4189 | 4 | 4 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0008 | 0/0 | 4190 | 4 | 3 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0011 | 0/0 | 4191 | 3 | 1 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0013 | 0/0 | 4189 | 2 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0014 | 1/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0016 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0020 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0022 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0024 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0025 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0001t0027 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0001 | 0/1 | 4189 | 90 | 1 | 16 | 61 | 1 | 10 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0002 | 0/0 | 4189 | 10 | 0 | 1 | 9 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0003 | 0/0 | 4189 | 12 | 0 | 0 | 10 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0006 | 0/0 | 4189 | 11 | 1 | 5 | 0 | 2 | 3 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0008 | 0/0 | 4190 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0019 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0028 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0002t0029 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0002 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0003 | 0/0 | 4189 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0004 | 0/0 | 4191 | 7 | 6 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0005 | 0/0 | 4189 | 10 | 4 | 2 | 0 | 2 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0007 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0012 | 0/0 | 4190 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0014 | 0/0 | 4189 | 2 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0016 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0017 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0021 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0003t0023 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0001c0004t0001 | 0/0 | 4189 | 6 | 0 | 0 | 6 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0005t0001 | 0/0 | 4189 | 5 | 0 | 0 | 5 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0007t0001 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0007t0002 | 0/0 | 4189 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0010t0005 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0010t0009 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0001c0013t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0001c0013t0011 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4186): Show |
chr11 | 10450264 | 10512579 |
a0002c0006t0005 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0002c0006t0012 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0002c0012t0008 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0002c0012t0026 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0002c0020t0018 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0002c0024t0010 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4185): Show |
chr11 | 10450264 | 10512579 |
a0003c0008t0009 | 0/0 | 4189 | 2 | 0 | 1 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0003c0008t0019 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0003c0009t0005 | 0/0 | 4189 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0003c0009t0009 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0004c0011t0015 | 0/0 | 4189 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0004c0014t0015 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0004c0014t0018 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0004c0015t0007 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0005c0016t0005 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0005c0017t0001 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0006c0021t0001 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0007c0019t0013 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0008c0018t0001 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0009c0022t0001 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
a0010c0023t0001 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | ACTCT others(4184): Show |
chr11 | 10450264 | 10512579 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0014g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0020g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0022g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0024g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0025g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0001t0027g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0008g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0019g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0028g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0002t0029g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0014g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0017g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0021g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0003t0023g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0007t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0007t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0007t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0010t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0010t0009g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0013t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0001c0013t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0006t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0006t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0006t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0012t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0012t0026g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0020t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0002c0024t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0008t0009g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0008t0009g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0008t0019g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0009t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0009t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0003c0009t0009g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0011t0015g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0014t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0014t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0004c0015t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0005c0016t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0005c0017t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0006c0021t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0007c0019t0013g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0008c0018t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0009c0022t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
a0010c0023t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00099 | hp2 | a0001 | c0003 | t0005 | g0194 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00140 | hp1 | a0001 | c0002 | t0006 | g0065 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00280 | hp2 | a0001 | c0003 | t0005 | g0181 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0087 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00323 | hp2 | a0003 | c0008 | t0009 | g0198 | EUR | FIN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00639 | hp1 | a0001 | c0003 | t0004 | g0170 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00741 | hp1 | a0001 | c0003 | t0014 | g0007 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01069 | hp1 | a0003 | c0009 | t0005 | g0203 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01071 | hp1 | a0001 | c0002 | t0006 | g0005 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01071 | hp2 | a0003 | c0009 | t0005 | g0196 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0325 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01106 | hp2 | a0001 | c0007 | t0002 | g0034 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01109 | hp2 | a0001 | c0001 | t0013 | g0030 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01167 | hp1 | a0001 | c0002 | t0006 | g0053 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01168 | hp1 | a0001 | c0002 | t0006 | g0005 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01169 | hp2 | a0001 | c0002 | t0006 | g0005 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0350 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0091 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01255 | hp1 | a0001 | c0002 | t0028 | g0098 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01257 | hp2 | a0001 | c0010 | t0009 | g0180 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01361 | hp1 | a0001 | c0002 | t0006 | g0064 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01496 | hp1 | a0001 | c0003 | t0005 | g0355 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0333 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01516 | hp1 | a0001 | c0002 | t0006 | g0077 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0335 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | IBS | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01884 | hp1 | a0001 | c0003 | t0007 | g0172 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01891 | hp1 | a0005 | c0016 | t0005 | g0199 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01891 | hp2 | a0001 | c0001 | t0020 | g0204 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0296 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01943 | hp2 | a0001 | c0003 | t0005 | g0128 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02027 | hp1 | a0006 | c0021 | t0001 | g0004 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02055 | hp1 | a0002 | c0020 | t0018 | g0152 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CDX | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CDX | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02257 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02280 | hp1 | a0002 | c0012 | t0026 | g0040 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0336 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02451 | hp2 | a0001 | c0001 | t0022 | g0184 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0151 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02572 | hp1 | a0002 | c0012 | t0008 | g0131 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02572 | hp2 | a0001 | c0001 | t0016 | g0130 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02602 | hp2 | a0003 | c0009 | t0009 | g0191 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02615 | hp2 | a0005 | c0017 | t0001 | g0342 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02622 | hp1 | a0001 | c0003 | t0005 | g0185 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02630 | hp2 | a0004 | c0014 | t0015 | g0168 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0205 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0323 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02717 | hp1 | a0007 | c0019 | t0013 | g0337 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02717 | hp2 | a0004 | c0014 | t0018 | g0169 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02723 | hp1 | a0001 | c0003 | t0021 | g0200 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0041 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0147 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02735 | hp2 | a0001 | c0010 | t0005 | g0202 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02738 | hp2 | a0001 | c0007 | t0002 | g0126 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02809 | hp1 | a0002 | c0024 | t0010 | g0042 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02818 | hp1 | a0001 | c0003 | t0004 | g0003 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02818 | hp2 | a0002 | c0006 | t0005 | g0206 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02886 | hp1 | a0001 | c0003 | t0004 | g0003 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02895 | hp1 | a0004 | c0011 | t0015 | g0017 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02896 | hp1 | a0002 | c0006 | t0005 | g0207 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02896 | hp2 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02897 | hp2 | a0004 | c0011 | t0015 | g0017 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0353 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02965 | hp1 | a0001 | c0003 | t0005 | g0129 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0313 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02976 | hp1 | a0001 | c0003 | t0017 | g0188 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0156 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03041 | hp1 | a0001 | c0001 | t0025 | g0317 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0177 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03139 | hp1 | a0001 | c0013 | t0010 | g0175 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0348 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03195 | hp1 | a0001 | c0003 | t0010 | g0171 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03195 | hp2 | a0001 | c0013 | t0011 | g0178 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0352 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03225 | hp2 | a0001 | c0003 | t0014 | g0007 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03486 | hp2 | a0001 | c0003 | t0012 | g0187 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0157 | AFR | ESN | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03540 | hp1 | a0004 | c0015 | t0007 | g0174 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03540 | hp2 | a0008 | c0018 | t0001 | g0341 | AFR | GWD | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03579 | hp2 | a0001 | c0003 | t0017 | g0186 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0344 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03669 | hp1 | a0001 | c0001 | t0008 | g0138 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03688 | hp1 | a0001 | c0002 | t0008 | g0022 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0304 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0155 | SAS | PJL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03831 | hp2 | a0003 | c0008 | t0019 | g0167 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0286 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03942 | hp2 | a0001 | c0002 | t0006 | g0052 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0327 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0329 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04184 | hp1 | a0001 | c0002 | t0006 | g0075 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04184 | hp2 | a0001 | c0003 | t0005 | g0195 | SAS | BEB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04199 | hp1 | a0001 | c0001 | t0011 | g0162 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04199 | hp2 | a0001 | c0003 | t0005 | g0192 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG04204 | hp2 | a0001 | c0002 | t0006 | g0324 | SAS | STU | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0190 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18522 | hp2 | a0001 | c0002 | t0029 | g0118 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CHB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18906 | hp2 | a0001 | c0003 | t0012 | g0189 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18969 | hp2 | a0001 | c0004 | t0001 | g0288 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18974 | hp2 | a0001 | c0005 | t0001 | g0221 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18985 | hp1 | a0001 | c0005 | t0001 | g0253 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18991 | hp1 | a0001 | c0005 | t0001 | g0215 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18991 | hp2 | a0009 | c0022 | t0001 | g0247 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18994 | hp1 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18994 | hp2 | a0001 | c0004 | t0001 | g0213 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19000 | hp2 | a0001 | c0004 | t0001 | g0308 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19007 | hp1 | a0010 | c0023 | t0001 | g0228 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19011 | hp2 | a0001 | c0001 | t0027 | g0231 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19030 | hp1 | a0002 | c0006 | t0012 | g0208 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19055 | hp1 | a0001 | c0005 | t0001 | g0212 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19064 | hp2 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19077 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19079 | hp2 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19085 | hp1 | a0001 | c0005 | t0001 | g0223 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19085 | hp2 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA19240 | hp2 | a0001 | c0003 | t0016 | g0201 | AFR | YRI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20129 | hp1 | a0001 | c0003 | t0005 | g0193 | AFR | ASW | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ASW | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20752 | hp2 | a0001 | c0002 | t0019 | g0148 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0183 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20805 | hp2 | a0001 | c0007 | t0001 | g0334 | EUR | TSI | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | GIH | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01123 | hp1 | a0003 | c0008 | t0009 | g0197 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | CLM | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0038 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG02559 | hp2 | a0001 | c0002 | t0006 | g0306 | AFR | ACB | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03471 | hp1 | a0001 | c0003 | t0023 | g0003 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
HG06807 | hp2 | a0001 | c0003 | t0005 | g0182 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20300 | hp1 | a0001 | c0003 | t0004 | g0173 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0137 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
NA21309 | hp2 | a0001 | c0001 | t0024 | g0302 | AFR | LWK | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0293 | REF | REF | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0135 | REF | REF | AMPD3_chr11_10450264_10512579 | AMPD3 | chr11 | 10450264 | 10512579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10482189 | C | T | 1 | a0003 | 6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
missense_variant | MODERATE | c.553C>T | p.Arg185Trp | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/15 | 743/4189 | 553/2304 | 185/767 | chr11 | 10482189 | |||
chr11:10493476 | G | A | 1 | a0005 | 2 | HG01891.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1067G>A | p.Arg356Gln | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1257/4189 | 1067/2304 | 356/767 | chr11 | 10493476 | |||
chr11:10493490 | G | A | 2 | a0004 a0008 |
6 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
missense_variant | MODERATE | c.1081G>A | p.Gly361Ser | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1271/4189 | 1081/2304 | 361/767 | chr11 | 10493490 | |||
chr11:10495666 | T | C | 3 | a0002 a0004 a0007 |
13 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
missense_variant | MODERATE | c.1363T>C | p.Tyr455His | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/15 | 1553/4189 | 1363/2304 | 455/767 | chr11 | 10495666 | |||
chr11:10501519 | G | A | 2 | a0006 a0007 |
2 | HG02027.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.1771G>A | p.Gly591Ser | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/15 | 1961/4189 | 1771/2304 | 591/767 | chr11 | 10501519 | |||
chr11:10504654 | C | T | 1 | a0009 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.2122C>T | p.His708Tyr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/15 | 2312/4189 | 2122/2304 | 708/767 | chr11 | 10504654 | |||
chr11:10505865 | T | C | 1 | a0010 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.2285T>C | p.Ile762Thr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 2475/4189 | 2285/2304 | 762/767 | chr11 | 10505865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10478727 | C | T | 1 | a0001c0005 | 5 | NA18974.hp2 NA18985.hp1 NA18991.hp1 others(2): Show |
synonymous_variant | LOW | c.423C>T | p.Ala141Ala | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/15 | 613/4189 | 423/2304 | 141/767 | chr11 | 10478727 | |||
chr11:10482209 | G | A | 8 | a0001c0003 a0001c0010 a0001c0013 others(5): Show |
45 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
synonymous_variant | LOW | c.573G>A | p.Pro191Pro | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/15 | 763/4189 | 573/2304 | 191/767 | chr11 | 10482209 | |||
chr11:10484899 | C | T | 5 | a0001c0013 a0002c0012 a0002c0024 others(2): Show |
8 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.669C>T | p.His223His | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/15 | 859/4189 | 669/2304 | 223/767 | chr11 | 10484899 | |||
chr11:10493369 | G | A | 1 | a0001c0004 | 6 | NA18969.hp2 NA18994.hp2 NA19000.hp2 others(3): Show |
synonymous_variant | LOW | c.960G>A | p.Ala320Ala | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1150/4189 | 960/2304 | 320/767 | chr11 | 10493369 | |||
chr11:10493540 | C | T | 3 | a0004c0011 a0004c0014 a0004c0015 |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.1131C>T | p.His377His | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/15 | 1321/4189 | 1131/2304 | 377/767 | chr11 | 10493540 | |||
chr11:10500202 | C | T | 1 | a0001c0007 | 3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.1674C>T | p.Tyr558Tyr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/15 | 1864/4189 | 1674/2304 | 558/767 | chr11 | 10500202 | |||
chr11:10500217 | T | C | 7 | a0001c0002 a0001c0004 a0001c0005 others(4): Show |
144 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
synonymous_variant | LOW | c.1689T>C | p.Tyr563Tyr | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/15 | 1879/4189 | 1689/2304 | 563/767 | chr11 | 10500217 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10455351 | T | C | 44 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(41): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
5_prime_UTR_variant | MODIFIER | c.-103T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/15 | 6169 | chr11 | 10455351 | ||||||
chr11:10455366 | G | T | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0028 others(3): Show |
47 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/15 | 6154 | chr11 | 10455366 | ||||||
chr11:10455372 | T | G | 17 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0020 others(14): Show |
32 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-82T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/15 | 6148 | chr11 | 10455372 | ||||||
chr11:10506221 | G | C | 1 | a0001c0003t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 337 | chr11 | 10506221 | ||||||
chr11:10506323 | G | C | 1 | a0001c0001t0020 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*439G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 439 | chr11 | 10506323 | ||||||
chr11:10506411 | C | T | 1 | a0001c0002t0029 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 527 | chr11 | 10506411 | ||||||
chr11:10506578 | A | G | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*694A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 694 | chr11 | 10506578 | ||||||
chr11:10506895 | T | TTG | 9 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0016 others(6): Show |
34 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1032dupGT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1033 | INFO_REALIGN_3_PRIME | chr11 | 10506895 | |||||
chr11:10506936 | A | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1052 | chr11 | 10506936 | ||||||
chr11:10506954 | A | G | 7 | a0001c0002t0006 a0001c0002t0019 a0001c0002t0028 others(4): Show |
18 | HG00140.hp1 HG00323.hp2 HG01071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1070A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1070 | chr11 | 10506954 | ||||||
chr11:10506974 | A | G | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(60): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*1090A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1090 | chr11 | 10506974 | ||||||
chr11:10507105 | T | C | 1 | a0002c0012t0026 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1221 | chr11 | 10507105 | ||||||
chr11:10507129 | G | A | 1 | a0001c0001t0025 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1245G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1245 | chr11 | 10507129 | ||||||
chr11:10507285 | T | TA | 9 | a0001c0001t0008 a0001c0001t0010 a0001c0002t0008 others(6): Show |
13 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1402dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1403 | INFO_REALIGN_3_PRIME | chr11 | 10507285 | |||||
chr11:10507442 | C | G | 1 | a0001c0001t0027 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1558C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1558 | chr11 | 10507442 | ||||||
chr11:10507469 | G | A | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(60): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*1585G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 15/15 | 1585 | chr11 | 10507469 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:10455493 | G | C | 1 | a0001c0001t0013g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6+45G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455493 | |||||||
chr11:10455580 | C | T | 185 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0209 others(182): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.-6+132C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455580 | |||||||
chr11:10455829 | G | T | 1 | a0001c0003t0005g0355 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-6+381G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455829 | |||||||
chr11:10455853 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-6+405G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10455853 | |||||||
chr11:10456177 | A | G | 1 | a0001c0002t0002g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-6+729A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456177 | |||||||
chr11:10456304 | C | G | 1 | a0001c0002t0001g0354 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-6+856C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456304 | |||||||
chr11:10456392 | G | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6+944G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456392 | |||||||
chr11:10456681 | C | T | 166 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(163): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-6+1233C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456681 | |||||||
chr11:10456722 | G | C | 3 | a0001c0003t0005g0181 a0001c0003t0005g0182 a0001c0010t0009g0180 |
3 | HG00280.hp2 HG01257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-6+1274G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456722 | |||||||
chr11:10456961 | T | A | 276 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(273): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.-6+1513T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10456961 | |||||||
chr11:10456977 | C | CT | 64 | a0001c0001t0001g0024 a0001c0001t0001g0124 a0001c0001t0001g0125 others(61): Show |
69 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.-6+1547dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10456977 | ||||||
chr11:10456977 | C | CTT | 10 | a0001c0001t0001g0347 a0001c0001t0001g0349 a0001c0001t0001g0351 others(7): Show |
10 | HG01192.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6+1546_-6+1547dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10456977 | ||||||
chr11:10456977 | CT | C | 8 | a0001c0001t0003g0127 a0001c0001t0004g0035 a0001c0002t0002g0033 others(5): Show |
9 | HG00741.hp1 HG01106.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+1547delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10456977 | ||||||
chr11:10457032 | C | T | 3 | a0001c0001t0008g0166 a0004c0014t0015g0168 a0004c0014t0018g0169 |
3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-6+1584C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457032 | |||||||
chr11:10457045 | A | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6+1597A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457045 | |||||||
chr11:10457241 | T | C | 32 | a0001c0001t0005g0190 a0001c0001t0016g0130 a0001c0001t0020g0204 others(29): Show |
32 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.-6+1793T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457241 | |||||||
chr11:10457698 | C | A | 65 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(62): Show |
74 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-6+2250C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457698 | |||||||
chr11:10457701 | C | T | 1 | a0001c0002t0001g0307 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-6+2253C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457701 | |||||||
chr11:10457723 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-6+2275C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457723 | |||||||
chr11:10457756 | A | G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(65): Show |
77 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-6+2308A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457756 | |||||||
chr11:10457788 | G | A | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-6+2340G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457788 | |||||||
chr11:10457827 | C | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(64): Show |
76 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.-6+2379C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457827 | |||||||
chr11:10457856 | C | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+2408C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457856 | |||||||
chr11:10457938 | GATCTGGC others(3): Show |
G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(65): Show |
77 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-6+2492_-6+2501del others(10): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10457938 | ||||||
chr11:10457941 | C | G | 1 | a0001c0002t0001g0336 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-6+2493C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10457941 | |||||||
chr11:10458002 | G | A | 3 | a0001c0001t0001g0347 a0001c0001t0001g0349 a0001c0001t0007g0348 |
3 | HG02451.hp1 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-6+2554G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458002 | |||||||
chr11:10458030 | C | G | 43 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0015 others(40): Show |
48 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-6+2582C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458030 | |||||||
chr11:10458175 | A | T | 3 | a0002c0006t0005g0206 a0002c0006t0005g0207 a0002c0006t0012g0208 |
3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-6+2727A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458175 | |||||||
chr11:10458254 | T | TA | 66 | a0001c0001t0001g0036 a0001c0001t0001g0331 a0001c0001t0001g0332 others(63): Show |
72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-6+2829dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | ||||||
chr11:10458254 | T | TAA | 36 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0294 others(33): Show |
40 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-6+2828_-6+2829dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | ||||||
chr11:10458254 | T | TAAA | 111 | a0001c0001t0001g0027 a0001c0001t0001g0176 a0001c0001t0001g0222 others(108): Show |
120 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-6+2827_-6+2829dup others(3): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | ||||||
chr11:10458254 | T | TAAAA | 35 | a0001c0001t0001g0214 a0001c0001t0005g0190 a0001c0001t0016g0130 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+2826_-6+2829dup others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458254 | ||||||
chr11:10458296 | GCTCC | G | 355 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(352): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-6+2863_-6+2866del others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10458296 | ||||||
chr11:10458305 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0004g0024 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-6+2857C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458305 | |||||||
chr11:10458308 | C | T | 4 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
5 | HG00140.hp2 HG00738.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2860C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458308 | |||||||
chr11:10458353 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-6+2905C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458353 | |||||||
chr11:10458502 | C | T | 2 | a0001c0003t0003g0032 a0001c0003t0014g0007 |
3 | HG00741.hp1 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-5-3013C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458502 | |||||||
chr11:10458777 | G | A | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5-2738G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458777 | |||||||
chr11:10458880 | A | G | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-5-2635A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458880 | |||||||
chr11:10458919 | C | T | 31 | a0001c0001t0005g0190 a0001c0001t0016g0130 a0001c0001t0022g0184 others(28): Show |
31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-5-2596C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458919 | |||||||
chr11:10458936 | T | G | 2 | a0001c0003t0003g0032 a0001c0003t0014g0007 |
3 | HG00741.hp1 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-5-2579T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458936 | |||||||
chr11:10458945 | G | T | 1 | a0001c0002t0001g0291 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-5-2570G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10458945 | |||||||
chr11:10459216 | G | A | 31 | a0001c0001t0005g0190 a0001c0001t0016g0130 a0001c0001t0020g0204 others(28): Show |
31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-5-2299G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459216 | |||||||
chr11:10459462 | T | G | 1 | a0001c0003t0021g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-5-2053T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459462 | |||||||
chr11:10459471 | G | A | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-5-2044G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459471 | |||||||
chr11:10459592 | A | G | 66 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(63): Show |
74 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-5-1923A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459592 | |||||||
chr11:10459632 | A | C | 1 | a0001c0002t0001g0290 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-5-1883A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459632 | |||||||
chr11:10459669 | A | G | 109 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(106): Show |
122 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-5-1846A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459669 | |||||||
chr11:10459727 | G | C | 14 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
15 | HG00639.hp2 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5-1788G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459727 | |||||||
chr11:10459749 | C | T | 43 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0015 others(40): Show |
48 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5-1766C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459749 | |||||||
chr11:10459796 | G | C | 1 | a0001c0001t0001g0049 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-5-1719G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459796 | |||||||
chr11:10459995 | T | G | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-1520T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10459995 | |||||||
chr11:10460040 | A | AAATATAT others(18): Show |
1 | a0001c0002t0001g0289 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-5-1474_-5-1450dup others(25): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460040 | ||||||
chr11:10460040 | AAATATAT others(9): Show |
A | 33 | a0001c0001t0005g0190 a0001c0001t0016g0130 a0001c0001t0020g0204 others(30): Show |
34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-1448_-5-1433del others(16): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460040 | ||||||
chr11:10460054 | T | C | 23 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0294 others(20): Show |
26 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-5-1461T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460054 | |||||||
chr11:10460066 | T | A | 156 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(153): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-5-1449T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460066 | |||||||
chr11:10460083 | T | TTA | 10 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0002g0014 others(7): Show |
11 | HG00558.hp1 HG02080.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-1416_-5-1415dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460083 | ||||||
chr11:10460083 | TTA | T | 3 | a0002c0012t0008g0131 a0004c0011t0015g0017 a0005c0016t0005g0199 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-1416_-5-1415del others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460083 | ||||||
chr11:10460091 | A | G | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-1424A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460091 | |||||||
chr11:10460099 | A | T | 1 | a0001c0001t0001g0346 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-5-1416A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460099 | |||||||
chr11:10460101 | T | A | 3 | a0001c0001t0008g0166 a0004c0014t0015g0168 a0004c0014t0018g0169 |
3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-5-1414T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460101 | |||||||
chr11:10460120 | C | T | 155 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(152): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-5-1395C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460120 | |||||||
chr11:10460155 | T | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0088 a0001c0001t0002g0092 others(1): Show |
5 | HG00558.hp1 HG02132.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-1360T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460155 | |||||||
chr11:10460260 | G | A | 1 | a0001c0002t0028g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-5-1255G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460260 | |||||||
chr11:10460395 | G | A | 12 | a0001c0001t0001g0176 a0001c0003t0004g0003 a0001c0003t0004g0023 others(9): Show |
14 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5-1120G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460395 | |||||||
chr11:10460409 | CT | C | 201 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(198): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-5-1091delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 10460409 | ||||||
chr11:10460456 | G | T | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-5-1059G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460456 | |||||||
chr11:10460635 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-880C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460635 | |||||||
chr11:10460639 | C | T | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-5-876C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460639 | |||||||
chr11:10460648 | A | G | 55 | a0001c0001t0001g0176 a0001c0001t0001g0209 a0001c0001t0001g0210 others(52): Show |
61 | HG00423.hp2 HG00639.hp1 HG01884.hp1 others(58): Show |
intron_variant | MODIFIER | c.-5-867A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460648 | |||||||
chr11:10460700 | C | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5-815C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460700 | |||||||
chr11:10460789 | A | G | 1 | a0001c0001t0011g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-5-726A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460789 | |||||||
chr11:10460878 | T | G | 33 | a0001c0001t0005g0190 a0001c0001t0016g0130 a0001c0001t0020g0204 others(30): Show |
34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-637T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460878 | |||||||
chr11:10460981 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-5-534A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10460981 | |||||||
chr11:10461129 | A | G | 1 | a0001c0002t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-5-386A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461129 | |||||||
chr11:10461187 | C | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5-328C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461187 | |||||||
chr11:10461254 | A | G | 1 | a0001c0002t0029g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-5-261A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461254 | |||||||
chr11:10461374 | C | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5-141C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461374 | |||||||
chr11:10461428 | G | C | 2 | a0001c0001t0001g0222 a0001c0005t0001g0223 |
2 | NA18997.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-5-87G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461428 | |||||||
chr11:10461429 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0123 |
2 | HG00733.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-5-86G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461429 | |||||||
chr11:10461447 | T | C | 1 | a0001c0002t0001g0224 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-5-68T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 1/14 | chr11 | 10461447 | |||||||
chr11:10461765 | G | A | 2 | a0001c0001t0001g0225 a0001c0002t0001g0226 |
2 | NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.221+25G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10461765 | |||||||
chr11:10461912 | G | A | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.221+172G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10461912 | |||||||
chr11:10461993 | C | T | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.221+253C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10461993 | |||||||
chr11:10462080 | T | A | 1 | a0001c0001t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.221+340T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462080 | |||||||
chr11:10462203 | C | T | 3 | a0002c0012t0008g0131 a0004c0011t0015g0017 a0005c0016t0005g0199 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+463C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462203 | |||||||
chr11:10462241 | A | G | 45 | a0001c0001t0001g0083 a0001c0001t0003g0018 a0001c0001t0003g0019 others(42): Show |
51 | HG00423.hp2 HG00609.hp2 HG02040.hp1 others(48): Show |
intron_variant | MODIFIER | c.221+501A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462241 | |||||||
chr11:10462338 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.221+598G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462338 | |||||||
chr11:10462524 | T | G | 45 | a0001c0001t0001g0083 a0001c0001t0003g0018 a0001c0001t0003g0019 others(42): Show |
51 | HG00423.hp2 HG00609.hp2 HG02040.hp1 others(48): Show |
intron_variant | MODIFIER | c.221+784T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462524 | |||||||
chr11:10462706 | G | A | 3 | a0002c0012t0008g0131 a0004c0011t0015g0017 a0005c0016t0005g0199 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+966G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462706 | |||||||
chr11:10462725 | G | GAGAGAAA others(19): Show |
1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221+987_221+1012du others(27): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10462725 | ||||||
chr11:10462817 | C | A | 4 | a0001c0002t0001g0229 a0001c0002t0001g0289 a0001c0002t0001g0307 others(1): Show |
4 | HG02155.hp1 NA18941.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1077C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462817 | |||||||
chr11:10462824 | G | A | 9 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(6): Show |
11 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+1084G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462824 | |||||||
chr11:10462903 | C | T | 2 | a0001c0004t0001g0285 a0001c0004t0001g0288 |
2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.221+1163C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10462903 | |||||||
chr11:10463008 | A | T | 1 | a0003c0008t0009g0198 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.221+1268A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463008 | |||||||
chr11:10463015 | T | C | 6 | a0001c0001t0022g0184 a0001c0003t0005g0128 a0001c0003t0005g0129 others(3): Show |
6 | HG01943.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+1275T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463015 | |||||||
chr11:10463096 | C | T | 1 | a0001c0002t0002g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.221+1356C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463096 | |||||||
chr11:10463299 | G | T | 3 | a0002c0012t0008g0131 a0004c0011t0015g0017 a0005c0016t0005g0199 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1559G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463299 | |||||||
chr11:10463451 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+1711G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463451 | |||||||
chr11:10463498 | G | A | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG01928.hp2 NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.221+1758G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463498 | |||||||
chr11:10463640 | A | G | 43 | a0001c0001t0001g0083 a0001c0001t0003g0018 a0001c0001t0003g0019 others(40): Show |
49 | HG00423.hp2 HG00609.hp2 HG02040.hp1 others(46): Show |
intron_variant | MODIFIER | c.221+1900A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463640 | |||||||
chr11:10463837 | C | T | 1 | a0001c0001t0002g0117 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.221+2097C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463837 | |||||||
chr11:10463886 | G | A | 42 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(39): Show |
47 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.221+2146G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10463886 | |||||||
chr11:10464243 | A | G | 3 | a0002c0006t0005g0206 a0002c0006t0005g0207 a0002c0006t0012g0208 |
3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.221+2503A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464243 | |||||||
chr11:10464571 | G | A | 1 | a0001c0001t0020g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.221+2831G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464571 | |||||||
chr11:10464603 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.221+2863C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464603 | |||||||
chr11:10464626 | T | C | 296 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(293): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.221+2886T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464626 | |||||||
chr11:10464640 | G | A | 212 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(209): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.221+2900G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464640 | |||||||
chr11:10464707 | C | T | 128 | a0001c0001t0001g0027 a0001c0001t0001g0214 a0001c0001t0001g0222 others(125): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.221+2967C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10464707 | |||||||
chr11:10465271 | A | T | 30 | a0001c0001t0022g0184 a0001c0003t0003g0032 a0001c0003t0003g0205 others(27): Show |
31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.221+3531A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465271 | |||||||
chr11:10465284 | A | G | 3 | a0001c0001t0008g0166 a0004c0014t0015g0168 a0004c0014t0018g0169 |
3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.221+3544A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465284 | |||||||
chr11:10465307 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.221+3567T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465307 | |||||||
chr11:10465351 | G | A | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.221+3611G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465351 | |||||||
chr11:10465397 | TA | T | 30 | a0001c0001t0022g0184 a0001c0003t0003g0032 a0001c0003t0003g0205 others(27): Show |
31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.221+3663delA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10465397 | ||||||
chr11:10465410 | T | C | 10 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(7): Show |
12 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+3670T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465410 | |||||||
chr11:10465474 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+3734G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465474 | |||||||
chr11:10465545 | C | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0002t0029g0118 others(2): Show |
5 | HG01243.hp1 HG02258.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+3805C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465545 | |||||||
chr11:10465558 | A | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+3818A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465558 | |||||||
chr11:10465784 | C | T | 1 | a0001c0003t0012g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.221+4044C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465784 | |||||||
chr11:10465793 | A | G | 10 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0330 others(7): Show |
11 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+4053A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465793 | |||||||
chr11:10465819 | G | GT | 62 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0278 others(59): Show |
62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.221+4100dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10465819 | ||||||
chr11:10465819 | GT | G | 13 | a0001c0001t0001g0209 a0001c0001t0001g0330 a0001c0001t0001g0347 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.221+4100delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10465819 | ||||||
chr11:10465988 | G | A | 1 | a0001c0003t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.221+4248G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10465988 | |||||||
chr11:10466122 | C | T | 10 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(7): Show |
12 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+4382C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466122 | |||||||
chr11:10466123 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.221+4383G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466123 | |||||||
chr11:10466450 | C | T | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.221+4710C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466450 | |||||||
chr11:10466466 | T | C | 354 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(351): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.221+4726T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466466 | |||||||
chr11:10466552 | T | C | 46 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(43): Show |
51 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.221+4812T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466552 | |||||||
chr11:10466604 | G | C | 1 | a0001c0001t0003g0139 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.221+4864G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466604 | |||||||
chr11:10466625 | A | C | 13 | a0001c0001t0008g0166 a0001c0003t0004g0003 a0001c0003t0004g0023 others(10): Show |
15 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.221+4885A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466625 | |||||||
chr11:10466761 | T | C | 46 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(43): Show |
51 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.221+5021T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466761 | |||||||
chr11:10466865 | G | C | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+5125G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466865 | |||||||
chr11:10466932 | C | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+5192C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466932 | |||||||
chr11:10466955 | G | A | 1 | a0001c0003t0016g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.221+5215G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10466955 | |||||||
chr11:10467132 | G | T | 3 | a0001c0001t0008g0166 a0004c0014t0015g0168 a0004c0014t0018g0169 |
3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.221+5392G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467132 | |||||||
chr11:10467148 | A | C | 1 | a0001c0001t0001g0275 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.221+5408A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467148 | |||||||
chr11:10467172 | C | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+5432C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467172 | |||||||
chr11:10467220 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+5480G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467220 | |||||||
chr11:10467309 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.221+5569A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467309 | |||||||
chr11:10467328 | C | T | 42 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0330 others(39): Show |
43 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.221+5588C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467328 | |||||||
chr11:10467353 | G | A | 3 | a0001c0001t0027g0231 a0001c0002t0001g0232 a0001c0013t0011g0178 |
3 | HG03195.hp2 NA19002.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.221+5613G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467353 | |||||||
chr11:10467395 | A | G | 10 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(7): Show |
12 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+5655A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467395 | |||||||
chr11:10467535 | C | T | 1 | a0001c0013t0010g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.221+5795C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467535 | |||||||
chr11:10467685 | C | T | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.221+5945C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467685 | |||||||
chr11:10467771 | G | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.221+6031G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467771 | |||||||
chr11:10467881 | G | T | 1 | a0003c0008t0019g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.221+6141G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10467881 | |||||||
chr11:10468084 | C | G | 44 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(41): Show |
49 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.221+6344C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468084 | |||||||
chr11:10468252 | T | C | 1 | a0001c0003t0003g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.221+6512T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468252 | |||||||
chr11:10468279 | A | C | 86 | a0001c0001t0001g0294 a0001c0001t0001g0330 a0001c0001t0001g0347 others(83): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.221+6539A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468279 | |||||||
chr11:10468280 | G | T | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+6540G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468280 | |||||||
chr11:10468311 | G | A | 38 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0127 others(35): Show |
42 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.221+6571G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468311 | |||||||
chr11:10468334 | A | T | 3 | a0001c0003t0004g0023 a0001c0003t0004g0173 a0004c0015t0007g0174 |
4 | HG02896.hp2 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+6594A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468334 | |||||||
chr11:10468343 | G | GA | 158 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(155): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.221+6615dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10468343 | ||||||
chr11:10468361 | A | T | 2 | a0001c0002t0001g0220 a0001c0002t0001g0274 |
2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.221+6621A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468361 | |||||||
chr11:10468597 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.221+6857A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468597 | |||||||
chr11:10468681 | G | A | 1 | a0001c0001t0025g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.221+6941G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468681 | |||||||
chr11:10468724 | T | C | 35 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0235 others(32): Show |
37 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.221+6984T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468724 | |||||||
chr11:10468868 | T | C | 155 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(152): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.221+7128T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10468868 | |||||||
chr11:10469164 | G | C | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+7424G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469164 | |||||||
chr11:10469343 | T | C | 45 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(42): Show |
50 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.221+7603T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469343 | |||||||
chr11:10469349 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.221+7609C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469349 | |||||||
chr11:10469375 | C | A | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221+7635C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469375 | |||||||
chr11:10469376 | A | C | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.221+7636A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469376 | |||||||
chr11:10469388 | A | C | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+7648A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469388 | |||||||
chr11:10469401 | T | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+7661T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469401 | |||||||
chr11:10469412 | C | T | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+7672C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469412 | |||||||
chr11:10469418 | T | C | 295 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(292): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.221+7678T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469418 | |||||||
chr11:10469419 | G | A | 1 | a0001c0001t0020g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.221+7679G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469419 | |||||||
chr11:10469551 | A | G | 1 | a0001c0002t0003g0156 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.221+7811A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469551 | |||||||
chr11:10469552 | A | C | 45 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(42): Show |
50 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.221+7812A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469552 | |||||||
chr11:10469698 | A | G | 1 | a0005c0017t0001g0342 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221+7958A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469698 | |||||||
chr11:10469758 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8018G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469758 | |||||||
chr11:10469762 | G | A | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.221+8022G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469762 | |||||||
chr11:10469766 | G | A | 1 | a0001c0003t0017g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221+8026G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469766 | |||||||
chr11:10469767 | C | T | 9 | a0001c0001t0022g0184 a0001c0003t0003g0032 a0001c0003t0003g0205 others(6): Show |
10 | HG00741.hp1 HG01943.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+8027C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469767 | |||||||
chr11:10469810 | C | T | 131 | a0001c0001t0001g0027 a0001c0001t0001g0222 a0001c0001t0001g0225 others(128): Show |
138 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.221+8070C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469810 | |||||||
chr11:10469815 | A | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8075A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469815 | |||||||
chr11:10469857 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8117G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469857 | |||||||
chr11:10469897 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.221+8157G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469897 | |||||||
chr11:10469902 | TAGTGGCG others(5): Show |
T | 9 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(6): Show |
11 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.221+8163_221+8174d others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469902 | |||||||
chr11:10469909 | G | A | 1 | a0001c0001t0016g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.221+8169G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469909 | |||||||
chr11:10469957 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.221+8217G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469957 | |||||||
chr11:10469964 | C | T | 1 | a0001c0002t0003g0156 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.221+8224C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469964 | |||||||
chr11:10469996 | C | T | 4 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
5 | HG00140.hp2 HG00738.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+8256C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469996 | |||||||
chr11:10469997 | G | A | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+8257G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10469997 | |||||||
chr11:10470026 | C | T | 3 | a0001c0001t0001g0347 a0001c0001t0001g0349 a0001c0001t0007g0348 |
3 | HG02451.hp1 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.221+8286C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470026 | |||||||
chr11:10470039 | C | CA | 7 | a0001c0001t0002g0114 a0001c0001t0004g0122 a0001c0002t0029g0118 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+8317dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10470039 | ||||||
chr11:10470039 | CA | C | 162 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0214 others(159): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.221+8317delA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10470039 | ||||||
chr11:10470039 | CAA | C | 6 | a0001c0001t0001g0303 a0001c0002t0001g0273 a0001c0002t0001g0279 others(3): Show |
6 | HG02602.hp1 HG03710.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+8316_221+8317d others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10470039 | ||||||
chr11:10470187 | C | A | 1 | a0001c0001t0001g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.222-8339C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470187 | |||||||
chr11:10470194 | A | T | 165 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0214 others(162): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.222-8332A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470194 | |||||||
chr11:10470272 | T | C | 1 | a0001c0002t0001g0233 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.222-8254T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470272 | |||||||
chr11:10470398 | C | T | 20 | a0001c0003t0005g0181 a0001c0003t0005g0182 a0001c0003t0005g0192 others(17): Show |
20 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-8128C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470398 | |||||||
chr11:10470399 | T | C | 14 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0002t0001g0026 others(11): Show |
15 | HG02155.hp1 NA18941.hp1 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.222-8127T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470399 | |||||||
chr11:10470403 | G | A | 75 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(72): Show |
82 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.222-8123G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470403 | |||||||
chr11:10470425 | C | T | 3 | a0002c0006t0005g0206 a0002c0006t0005g0207 a0002c0006t0012g0208 |
3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-8101C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470425 | |||||||
chr11:10470445 | G | T | 61 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(58): Show |
67 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.222-8081G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470445 | |||||||
chr11:10470568 | A | T | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.222-7958A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470568 | |||||||
chr11:10470751 | CAAGGGAT others(5): Show |
C | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.222-7774_222-7763d others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470751 | |||||||
chr11:10470773 | C | G | 23 | a0001c0001t0001g0028 a0001c0001t0001g0300 a0001c0001t0001g0301 others(20): Show |
26 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.222-7753C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470773 | |||||||
chr11:10470842 | C | T | 1 | a0001c0003t0021g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.222-7684C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470842 | |||||||
chr11:10470849 | A | G | 1 | a0001c0001t0011g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.222-7677A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10470849 | |||||||
chr11:10471024 | A | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-7502A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471024 | |||||||
chr11:10471062 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0326 a0001c0001t0024g0302 |
4 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-7464A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471062 | |||||||
chr11:10471082 | A | C | 51 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(48): Show |
57 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.222-7444A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471082 | |||||||
chr11:10471164 | C | T | 20 | a0001c0003t0005g0181 a0001c0003t0005g0182 a0001c0003t0005g0192 others(17): Show |
20 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-7362C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471164 | |||||||
chr11:10471174 | C | G | 1 | a0001c0004t0001g0213 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.222-7352C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471174 | |||||||
chr11:10471281 | C | CTCCT | 46 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(43): Show |
51 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.222-7243_222-7240d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10471281 | ||||||
chr11:10471318 | T | A | 65 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0043 others(62): Show |
73 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.222-7208T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471318 | |||||||
chr11:10471448 | G | C | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-7078G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471448 | |||||||
chr11:10471462 | T | C | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-7064T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471462 | |||||||
chr11:10471532 | G | A | 3 | a0002c0012t0008g0131 a0004c0011t0015g0017 a0005c0016t0005g0199 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-6994G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471532 | |||||||
chr11:10471628 | T | G | 1 | a0001c0002t0001g0296 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.222-6898T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471628 | |||||||
chr11:10471709 | C | T | 42 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0015 others(39): Show |
47 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.222-6817C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471709 | |||||||
chr11:10471774 | G | T | 32 | a0001c0001t0020g0204 a0001c0001t0022g0184 a0001c0003t0003g0032 others(29): Show |
33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.222-6752G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471774 | |||||||
chr11:10471806 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-6720G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471806 | |||||||
chr11:10471852 | G | A | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-6674G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471852 | |||||||
chr11:10471853 | T | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-6673T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471853 | |||||||
chr11:10471958 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.222-6568A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10471958 | |||||||
chr11:10472022 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.222-6504T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472022 | |||||||
chr11:10472160 | A | G | 20 | a0001c0003t0005g0181 a0001c0003t0005g0182 a0001c0003t0005g0192 others(17): Show |
20 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.222-6366A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472160 | |||||||
chr11:10472224 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.222-6302A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472224 | |||||||
chr11:10472308 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-6218G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472308 | |||||||
chr11:10472401 | C | T | 1 | a0001c0002t0001g0325 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.222-6125C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472401 | |||||||
chr11:10472462 | G | A | 1 | a0001c0003t0016g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.222-6064G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472462 | |||||||
chr11:10472544 | G | C | 1 | a0004c0014t0015g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.222-5982G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472544 | |||||||
chr11:10472585 | A | G | 25 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0300 others(22): Show |
28 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.222-5941A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472585 | |||||||
chr11:10472626 | T | C | 3 | a0001c0001t0008g0166 a0004c0014t0015g0168 a0004c0014t0018g0169 |
3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.222-5900T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472626 | |||||||
chr11:10472628 | A | G | 1 | a0009c0022t0001g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.222-5898A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472628 | |||||||
chr11:10472707 | G | C | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.222-5819G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472707 | |||||||
chr11:10472940 | G | C | 47 | a0001c0001t0001g0294 a0001c0001t0001g0343 a0001c0001t0002g0002 others(44): Show |
52 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.222-5586G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472940 | |||||||
chr11:10472950 | G | A | 2 | a0001c0001t0001g0305 a0001c0002t0001g0298 |
2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.222-5576G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472950 | |||||||
chr11:10472960 | C | A | 39 | a0001c0001t0001g0214 a0001c0001t0003g0018 a0001c0001t0003g0019 others(36): Show |
43 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.222-5566C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10472960 | |||||||
chr11:10473077 | C | G | 3 | a0002c0012t0008g0131 a0004c0011t0015g0017 a0005c0016t0005g0199 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-5449C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473077 | |||||||
chr11:10473131 | A | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-5395A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473131 | |||||||
chr11:10473275 | A | C | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222-5251A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473275 | |||||||
chr11:10473402 | G | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0176 others(8): Show |
13 | HG01891.hp1 HG02080.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.222-5124G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473402 | |||||||
chr11:10473438 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.222-5088G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473438 | |||||||
chr11:10473621 | C | T | 3 | a0002c0012t0008g0131 a0004c0011t0015g0017 a0005c0016t0005g0199 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-4905C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473621 | |||||||
chr11:10473678 | C | T | 41 | a0001c0001t0001g0214 a0001c0001t0001g0343 a0001c0001t0002g0113 others(38): Show |
45 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.222-4848C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473678 | |||||||
chr11:10473788 | G | A | 2 | a0001c0001t0001g0318 a0001c0001t0004g0029 |
3 | HG00140.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.222-4738G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473788 | |||||||
chr11:10473870 | A | G | 2 | a0001c0001t0001g0343 a0001c0001t0011g0031 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.222-4656A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473870 | |||||||
chr11:10473932 | C | T | 3 | a0001c0001t0008g0166 a0004c0014t0015g0168 a0004c0014t0018g0169 |
3 | HG01884.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.222-4594C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473932 | |||||||
chr11:10473933 | G | A | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.222-4593G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10473933 | |||||||
chr11:10474172 | C | T | 42 | a0001c0001t0001g0214 a0001c0001t0002g0113 a0001c0001t0003g0018 others(39): Show |
47 | HG00423.hp2 HG02040.hp1 HG02055.hp1 others(44): Show |
intron_variant | MODIFIER | c.222-4354C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474172 | |||||||
chr11:10474261 | G | A | 1 | a0001c0004t0001g0234 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.222-4265G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474261 | |||||||
chr11:10474448 | A | C | 1 | a0001c0002t0003g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.222-4078A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474448 | |||||||
chr11:10474582 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.222-3944C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474582 | |||||||
chr11:10474620 | G | A | 32 | a0001c0001t0020g0204 a0001c0001t0022g0184 a0001c0003t0003g0032 others(29): Show |
33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.222-3906G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474620 | |||||||
chr11:10474664 | T | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222-3862T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474664 | |||||||
chr11:10474674 | C | G | 10 | a0001c0001t0020g0204 a0001c0001t0022g0184 a0001c0003t0003g0032 others(7): Show |
11 | HG00741.hp1 HG01891.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.222-3852C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474674 | |||||||
chr11:10474675 | G | A | 3 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0004g0029 |
4 | HG00140.hp2 HG02886.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-3851G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474675 | |||||||
chr11:10474782 | C | T | 1 | a0001c0005t0001g0221 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.222-3744C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10474782 | |||||||
chr11:10475119 | T | C | 1 | a0001c0003t0003g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.222-3407T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475119 | |||||||
chr11:10475634 | T | A | 4 | a0001c0001t0001g0321 a0001c0002t0001g0322 a0001c0002t0001g0323 others(1): Show |
4 | HG00642.hp1 HG01192.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-2892T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475634 | |||||||
chr11:10475706 | G | C | 1 | a0001c0001t0003g0139 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.222-2820G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475706 | |||||||
chr11:10475844 | A | G | 1 | a0001c0002t0001g0054 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.222-2682A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475844 | |||||||
chr11:10475920 | C | A | 121 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0001c0001t0001g0222 others(118): Show |
127 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.222-2606C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10475920 | |||||||
chr11:10476053 | G | A | 98 | a0001c0001t0001g0027 a0001c0001t0001g0222 a0001c0001t0001g0225 others(95): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.222-2473G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476053 | |||||||
chr11:10476092 | A | G | 1 | a0001c0001t0001g0351 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.222-2434A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476092 | |||||||
chr11:10476098 | A | G | 1 | a0001c0001t0008g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.222-2428A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476098 | |||||||
chr11:10476112 | G | C | 28 | a0001c0001t0007g0352 a0001c0001t0020g0204 a0001c0001t0022g0184 others(25): Show |
29 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.222-2414G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476112 | |||||||
chr11:10476254 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.222-2272G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476254 | |||||||
chr11:10476304 | C | A | 1 | a0001c0002t0001g0281 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.222-2222C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476304 | |||||||
chr11:10476420 | G | C | 49 | a0001c0001t0002g0015 a0001c0001t0002g0100 a0001c0001t0002g0101 others(46): Show |
55 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.222-2106G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476420 | |||||||
chr11:10476442 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.222-2084C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476442 | |||||||
chr11:10476465 | G | GT | 138 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0055 others(135): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.222-2050dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10476465 | ||||||
chr11:10476465 | G | GTT | 6 | a0001c0001t0001g0222 a0003c0008t0009g0197 a0003c0008t0009g0198 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-2051_222-2050d others(4): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10476465 | ||||||
chr11:10476471 | T | G | 8 | a0001c0001t0002g0014 a0001c0001t0002g0088 a0001c0001t0002g0092 others(5): Show |
9 | HG00558.hp1 HG02083.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-2055T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476471 | |||||||
chr11:10476473 | T | G | 32 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0016 others(29): Show |
36 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.222-2053T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476473 | |||||||
chr11:10476473 | T | TG | 4 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0007g0037 others(1): Show |
5 | HG02109.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-2053_222-2052i others(3): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476473 | |||||||
chr11:10476475 | T | G | 112 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0294 others(109): Show |
127 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.222-2051T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476475 | |||||||
chr11:10476475 | T | TG | 67 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0036 others(64): Show |
73 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.222-2051_222-2050i others(3): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476475 | |||||||
chr11:10476477 | G | T | 2 | a0001c0002t0001g0286 a0001c0003t0003g0032 |
2 | HG02257.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.222-2049G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476477 | |||||||
chr11:10476668 | G | A | 2 | a0001c0001t0011g0031 a0005c0017t0001g0342 |
2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.222-1858G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476668 | |||||||
chr11:10476841 | A | G | 1 | a0001c0002t0001g0245 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.222-1685A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476841 | |||||||
chr11:10476923 | T | TAGCA | 210 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(207): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.222-1602_222-1599d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 10476923 | ||||||
chr11:10476973 | C | G | 4 | a0002c0012t0008g0131 a0002c0012t0026g0040 a0004c0011t0015g0017 others(1): Show |
5 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-1553C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10476973 | |||||||
chr11:10477490 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.222-1036A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477490 | |||||||
chr11:10477556 | A | G | 210 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(207): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.222-970A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477556 | |||||||
chr11:10477787 | G | T | 318 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(315): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.222-739G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477787 | |||||||
chr11:10477889 | A | G | 1 | a0001c0002t0001g0219 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.222-637A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477889 | |||||||
chr11:10477925 | C | T | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-601C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10477925 | |||||||
chr11:10478157 | G | A | 2 | a0001c0001t0003g0153 a0001c0001t0003g0165 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.222-369G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478157 | |||||||
chr11:10478209 | G | A | 26 | a0001c0001t0022g0184 a0001c0003t0002g0091 a0001c0003t0003g0032 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.222-317G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478209 | |||||||
chr11:10478340 | G | A | 2 | a0001c0001t0001g0318 a0001c0001t0004g0029 |
3 | HG00140.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.222-186G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478340 | |||||||
chr11:10478448 | G | A | 52 | a0001c0001t0002g0015 a0001c0001t0002g0100 a0001c0001t0002g0101 others(49): Show |
58 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.222-78G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478448 | |||||||
chr11:10478509 | T | C | 39 | a0001c0001t0001g0056 a0001c0001t0001g0176 a0001c0001t0001g0345 others(36): Show |
42 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.222-17T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 2/14 | chr11 | 10478509 | |||||||
chr11:10478738 | G | A | 3 | a0002c0006t0005g0206 a0002c0006t0005g0207 a0002c0006t0012g0208 |
3 | HG02818.hp2 HG02896.hp1 NA19030.hp1 |
splice_region_variant&intron_variant | LOW | c.426+8G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478738 | |||||||
chr11:10478746 | G | C | 9 | a0001c0001t0022g0184 a0001c0003t0003g0137 a0001c0003t0003g0205 others(6): Show |
10 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.426+16G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478746 | |||||||
chr11:10478787 | T | C | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.426+57T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478787 | |||||||
chr11:10478882 | A | C | 2 | a0001c0003t0005g0128 a0001c0003t0005g0129 |
2 | HG01943.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.426+152A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10478882 | |||||||
chr11:10479100 | A | G | 4 | a0001c0001t0001g0340 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01123.hp2 HG01258.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.426+370A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479100 | |||||||
chr11:10479114 | G | A | 51 | a0001c0001t0002g0015 a0001c0001t0002g0100 a0001c0001t0002g0101 others(48): Show |
57 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.426+384G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479114 | |||||||
chr11:10479214 | G | C | 1 | a0001c0002t0003g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.426+484G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479214 | |||||||
chr11:10479242 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.426+512T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479242 | |||||||
chr11:10479279 | C | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.426+549C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479279 | |||||||
chr11:10479481 | A | G | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.426+751A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479481 | |||||||
chr11:10479619 | G | A | 10 | a0001c0001t0002g0113 a0001c0001t0003g0018 a0001c0001t0003g0019 others(7): Show |
12 | HG00408.hp1 NA18953.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.426+889G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479619 | |||||||
chr11:10479664 | C | T | 7 | a0001c0001t0001g0248 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG01255.hp2 HG01496.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.426+934C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479664 | |||||||
chr11:10479757 | C | G | 227 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(224): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.426+1027C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10479757 | |||||||
chr11:10480230 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.426+1500C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480230 | |||||||
chr11:10480389 | A | T | 1 | a0009c0022t0001g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.426+1659A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480389 | |||||||
chr11:10480396 | C | G | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.426+1666C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480396 | |||||||
chr11:10480402 | G | A | 3 | a0001c0001t0001g0315 a0001c0001t0004g0006 a0001c0001t0004g0313 |
5 | HG02109.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1661G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480402 | |||||||
chr11:10480511 | T | TGTATTTA others(27): Show |
7 | a0001c0002t0001g0309 a0003c0008t0009g0197 a0003c0008t0009g0198 others(4): Show |
7 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.427-1541_427-1508d others(36): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 10480511 | ||||||
chr11:10480651 | G | T | 4 | a0001c0001t0001g0340 a0001c0002t0001g0328 a0001c0002t0001g0329 others(1): Show |
4 | HG01123.hp2 HG01258.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-1412G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480651 | |||||||
chr11:10480668 | C | G | 53 | a0001c0001t0001g0305 a0001c0001t0002g0015 a0001c0001t0002g0100 others(50): Show |
59 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.427-1395C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480668 | |||||||
chr11:10480740 | G | A | 2 | a0001c0004t0001g0285 a0001c0004t0001g0288 |
2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.427-1323G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480740 | |||||||
chr11:10480850 | G | A | 1 | a0001c0001t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.427-1213G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480850 | |||||||
chr11:10480875 | A | G | 115 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0028 others(112): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.427-1188A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480875 | |||||||
chr11:10480962 | C | T | 2 | a0001c0001t0001g0305 a0001c0002t0001g0298 |
2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.427-1101C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480962 | |||||||
chr11:10480976 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.427-1087G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10480976 | |||||||
chr11:10481422 | C | T | 1 | a0005c0017t0001g0342 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427-641C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481422 | |||||||
chr11:10481427 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.427-636T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481427 | |||||||
chr11:10481444 | C | T | 40 | a0001c0003t0002g0091 a0001c0003t0003g0032 a0001c0003t0003g0137 others(37): Show |
44 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.427-619C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481444 | |||||||
chr11:10481666 | G | A | 2 | a0001c0001t0004g0035 a0001c0001t0004g0122 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.427-397G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481666 | |||||||
chr11:10481864 | G | A | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.427-199G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481864 | |||||||
chr11:10481893 | G | A | 40 | a0001c0003t0002g0091 a0001c0003t0003g0032 a0001c0003t0003g0137 others(37): Show |
44 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.427-170G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481893 | |||||||
chr11:10481904 | G | A | 29 | a0001c0003t0002g0091 a0001c0003t0003g0032 a0001c0003t0003g0137 others(26): Show |
31 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.427-159G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 3/14 | chr11 | 10481904 | |||||||
chr11:10482461 | G | T | 248 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(245): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.589+236G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482461 | |||||||
chr11:10482520 | T | C | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+295T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482520 | |||||||
chr11:10482521 | C | T | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+296C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482521 | |||||||
chr11:10482590 | C | T | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.589+365C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482590 | |||||||
chr11:10482687 | ATATATAT | A | 248 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(245): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.589+466_589+472del others(7): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 10482687 | ||||||
chr11:10482940 | C | T | 2 | a0001c0001t0001g0235 a0001c0002t0001g0244 |
2 | NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.589+715C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10482940 | |||||||
chr11:10483086 | A | T | 9 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(6): Show |
11 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+861A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483086 | |||||||
chr11:10483093 | A | C | 217 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(214): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.589+868A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483093 | |||||||
chr11:10483204 | A | G | 251 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(248): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.589+979A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483204 | |||||||
chr11:10483477 | A | G | 1 | a0001c0001t0003g0160 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.589+1252A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483477 | |||||||
chr11:10483609 | G | C | 1 | a0001c0001t0002g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.590-1211G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483609 | |||||||
chr11:10483627 | C | T | 248 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(245): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.590-1193C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483627 | |||||||
chr11:10483646 | A | C | 41 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0294 others(38): Show |
45 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.590-1174A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483646 | |||||||
chr11:10483662 | C | G | 248 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(245): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.590-1158C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483662 | |||||||
chr11:10483790 | G | A | 52 | a0001c0001t0001g0214 a0001c0001t0002g0015 a0001c0001t0002g0100 others(49): Show |
58 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.590-1030G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483790 | |||||||
chr11:10483842 | A | T | 1 | a0001c0003t0017g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.590-978A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483842 | |||||||
chr11:10483854 | A | C | 248 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(245): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.590-966A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483854 | |||||||
chr11:10483888 | C | T | 1 | a0001c0002t0006g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.590-932C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483888 | |||||||
chr11:10483911 | A | G | 248 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(245): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.590-909A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10483911 | |||||||
chr11:10484013 | A | G | 1 | a0001c0001t0013g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.590-807A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484013 | |||||||
chr11:10484047 | G | T | 69 | a0001c0001t0001g0083 a0001c0001t0001g0209 a0001c0001t0001g0210 others(66): Show |
77 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.590-773G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484047 | |||||||
chr11:10484149 | A | G | 10 | a0001c0001t0002g0002 a0001c0001t0002g0110 a0001c0001t0002g0111 others(7): Show |
12 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.590-671A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484149 | |||||||
chr11:10484171 | A | C | 26 | a0001c0003t0002g0091 a0001c0003t0003g0032 a0001c0003t0003g0137 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.590-649A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484171 | |||||||
chr11:10484379 | C | T | 2 | a0001c0001t0001g0305 a0001c0002t0001g0298 |
2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.590-441C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484379 | |||||||
chr11:10484395 | G | A | 52 | a0001c0001t0001g0214 a0001c0001t0002g0015 a0001c0001t0002g0100 others(49): Show |
58 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.590-425G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484395 | |||||||
chr11:10484410 | T | C | 1 | a0001c0002t0001g0026 | 2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.590-410T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484410 | |||||||
chr11:10484467 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.590-353G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484467 | |||||||
chr11:10484488 | A | G | 341 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(338): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.590-332A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484488 | |||||||
chr11:10484647 | A | G | 5 | a0001c0001t0001g0268 a0001c0001t0003g0019 a0001c0001t0003g0136 others(2): Show |
6 | NA18967.hp1 NA18969.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-173A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484647 | |||||||
chr11:10484708 | G | T | 211 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(208): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.590-112G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484708 | |||||||
chr11:10484712 | A | G | 341 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(338): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.590-108A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484712 | |||||||
chr11:10484741 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.590-79G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484741 | |||||||
chr11:10484750 | C | T | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-70C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 4/14 | chr11 | 10484750 | |||||||
chr11:10485072 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.809+33G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485072 | |||||||
chr11:10485127 | G | C | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+88G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485127 | |||||||
chr11:10485137 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0097 |
2 | NA19063.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.809+98T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485137 | |||||||
chr11:10485160 | C | T | 248 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(245): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.809+121C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485160 | |||||||
chr11:10485162 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.809+123C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485162 | |||||||
chr11:10485253 | T | C | 341 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(338): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.809+214T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485253 | |||||||
chr11:10485309 | C | A | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+270C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485309 | |||||||
chr11:10485332 | T | C | 3 | a0001c0001t0002g0014 a0001c0001t0002g0088 a0001c0001t0002g0093 |
4 | HG00558.hp1 NA18974.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+293T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485332 | |||||||
chr11:10485393 | C | T | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+354C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485393 | |||||||
chr11:10485405 | G | C | 59 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0214 others(56): Show |
65 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.809+366G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485405 | |||||||
chr11:10485432 | C | T | 2 | a0001c0013t0010g0175 a0001c0013t0011g0178 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.809+393C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485432 | |||||||
chr11:10485557 | C | T | 1 | a0001c0003t0007g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.809+518C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485557 | |||||||
chr11:10485706 | C | T | 32 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0014 others(29): Show |
36 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.809+667C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485706 | |||||||
chr11:10485765 | T | TTGCTCAT others(18): Show |
6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+732_809+756dup others(25): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 10485765 | ||||||
chr11:10485780 | G | A | 341 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(338): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.809+741G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485780 | |||||||
chr11:10485796 | G | A | 16 | a0001c0001t0001g0056 a0001c0001t0001g0176 a0001c0001t0001g0345 others(13): Show |
17 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.809+757G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10485796 | |||||||
chr11:10486001 | G | GTC | 93 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0214 others(90): Show |
103 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.809+965_809+966dup others(2): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 10486001 | ||||||
chr11:10486006 | G | C | 340 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(337): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.809+967G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486006 | |||||||
chr11:10486099 | C | T | 118 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0076 others(115): Show |
131 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.809+1060C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486099 | |||||||
chr11:10486208 | C | T | 3 | a0001c0001t0001g0315 a0001c0001t0004g0006 a0001c0001t0004g0313 |
5 | HG02109.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.810-1027C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486208 | |||||||
chr11:10486251 | G | A | 9 | a0001c0001t0001g0056 a0001c0001t0001g0345 a0001c0001t0004g0035 others(6): Show |
10 | HG02080.hp2 HG02145.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.810-984G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486251 | |||||||
chr11:10486434 | A | G | 99 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0214 others(96): Show |
109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.810-801A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486434 | |||||||
chr11:10486541 | G | C | 1 | a0001c0002t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.810-694G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486541 | |||||||
chr11:10486632 | C | T | 1 | a0001c0003t0003g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.810-603C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486632 | |||||||
chr11:10486665 | G | A | 1 | a0001c0002t0001g0009 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.810-570G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486665 | |||||||
chr11:10486797 | A | C | 2 | a0001c0003t0003g0205 a0001c0003t0021g0200 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.810-438A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486797 | |||||||
chr11:10486820 | T | A | 54 | a0001c0001t0001g0214 a0001c0001t0002g0015 a0001c0001t0002g0100 others(51): Show |
60 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.810-415T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486820 | |||||||
chr11:10486848 | C | T | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-387C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486848 | |||||||
chr11:10486861 | C | G | 306 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(303): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.810-374C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10486861 | |||||||
chr11:10487017 | T | C | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-218T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10487017 | |||||||
chr11:10487119 | G | A | 1 | a0001c0001t0008g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.810-116G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 5/14 | chr11 | 10487119 | |||||||
chr11:10487391 | T | C | 97 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0214 others(94): Show |
107 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.939+27T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487391 | |||||||
chr11:10487468 | G | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0287 |
2 | HG02074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.939+104G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487468 | |||||||
chr11:10487491 | G | A | 1 | a0001c0003t0005g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.939+127G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487491 | |||||||
chr11:10487646 | G | C | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+282G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487646 | |||||||
chr11:10487797 | G | A | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.939+433G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487797 | |||||||
chr11:10487853 | G | C | 234 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(231): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.939+489G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10487853 | |||||||
chr11:10488010 | GA | G | 10 | a0001c0001t0001g0056 a0001c0001t0001g0176 a0001c0001t0001g0345 others(7): Show |
11 | HG02080.hp2 HG02145.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.939+658delA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 10488010 | ||||||
chr11:10488125 | C | T | 13 | a0001c0001t0001g0036 a0001c0001t0004g0047 a0001c0003t0003g0032 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+761C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488125 | |||||||
chr11:10488219 | T | G | 9 | a0001c0001t0002g0015 a0001c0001t0002g0100 a0001c0001t0002g0101 others(6): Show |
10 | HG00558.hp2 NA18942.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.939+855T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488219 | |||||||
chr11:10488349 | T | C | 1 | a0002c0006t0005g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.939+985T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488349 | |||||||
chr11:10488371 | G | A | 1 | a0001c0002t0006g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.939+1007G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488371 | |||||||
chr11:10488466 | TGAGAGAG others(2): Show |
T | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(160): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.939+1112_939+1120d others(11): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 10488466 | ||||||
chr11:10488499 | A | G | 160 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(157): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.939+1135A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488499 | |||||||
chr11:10488501 | A | G | 307 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(304): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.939+1137A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488501 | |||||||
chr11:10488517 | T | C | 295 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(292): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.939+1153T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488517 | |||||||
chr11:10488605 | A | C | 198 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(195): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.939+1241A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488605 | |||||||
chr11:10488612 | G | T | 132 | a0001c0001t0001g0078 a0001c0001t0001g0214 a0001c0001t0001g0222 others(129): Show |
140 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.939+1248G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488612 | |||||||
chr11:10488634 | G | T | 4 | a0001c0001t0001g0076 a0001c0002t0001g0295 a0001c0002t0001g0296 others(1): Show |
4 | HG01928.hp2 HG01975.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+1270G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488634 | |||||||
chr11:10488693 | C | T | 1 | a0001c0003t0014g0007 | 2 | HG00741.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.939+1329C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488693 | |||||||
chr11:10488725 | T | C | 236 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0043 others(233): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.939+1361T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10488725 | |||||||
chr11:10489276 | C | T | 1 | a0001c0001t0016g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+1912C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489276 | |||||||
chr11:10489341 | G | C | 1 | a0001c0002t0001g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.939+1977G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489341 | |||||||
chr11:10489470 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0338 a0001c0001t0001g0351 |
3 | HG02615.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.939+2106G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489470 | |||||||
chr11:10489595 | C | T | 49 | a0001c0001t0001g0210 a0001c0001t0001g0294 a0001c0001t0001g0318 others(46): Show |
55 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.939+2231C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489595 | |||||||
chr11:10489685 | C | CT | 26 | a0001c0001t0001g0210 a0001c0001t0001g0330 a0001c0001t0001g0343 others(23): Show |
26 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.939+2333dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr11 | 10489685 | ||||||
chr11:10489771 | C | T | 1 | a0001c0001t0011g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.939+2407C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489771 | |||||||
chr11:10489805 | C | T | 59 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0086 others(56): Show |
64 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.939+2441C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10489805 | |||||||
chr11:10490034 | C | A | 1 | a0001c0003t0016g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.939+2670C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490034 | |||||||
chr11:10490060 | G | A | 1 | a0001c0002t0001g0283 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.939+2696G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490060 | |||||||
chr11:10490125 | C | T | 1 | a0001c0001t0003g0149 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.939+2761C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490125 | |||||||
chr11:10490152 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.939+2788G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490152 | |||||||
chr11:10490204 | C | T | 2 | a0001c0001t0001g0351 a0001c0003t0014g0007 |
3 | HG00741.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.939+2840C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490204 | |||||||
chr11:10490426 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.940-2923C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490426 | |||||||
chr11:10490611 | C | A | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-2738C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490611 | |||||||
chr11:10490761 | C | T | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-2588C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490761 | |||||||
chr11:10490817 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.940-2532C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490817 | |||||||
chr11:10490840 | C | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0319 a0001c0001t0001g0321 others(17): Show |
21 | HG00642.hp1 HG01081.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.940-2509C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10490840 | |||||||
chr11:10491072 | C | T | 2 | a0001c0001t0001g0264 a0001c0002t0001g0263 |
2 | HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.940-2277C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491072 | |||||||
chr11:10491081 | G | A | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-2268G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491081 | |||||||
chr11:10491098 | C | A | 2 | a0001c0003t0002g0091 a0001c0003t0017g0186 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.940-2251C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491098 | |||||||
chr11:10491129 | C | T | 1 | a0001c0002t0001g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.940-2220C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491129 | |||||||
chr11:10491130 | G | A | 1 | a0001c0001t0002g0014 | 2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.940-2219G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491130 | |||||||
chr11:10491135 | G | A | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-2214G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491135 | |||||||
chr11:10491147 | G | T | 1 | a0001c0007t0002g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.940-2202G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491147 | |||||||
chr11:10491152 | C | T | 1 | a0001c0002t0001g0350 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.940-2197C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491152 | |||||||
chr11:10491222 | C | T | 1 | a0001c0003t0017g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.940-2127C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491222 | |||||||
chr11:10491473 | G | A | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-1876G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491473 | |||||||
chr11:10491563 | A | G | 1 | a0001c0002t0006g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.940-1786A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491563 | |||||||
chr11:10491770 | A | C | 283 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0043 others(280): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.940-1579A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491770 | |||||||
chr11:10491959 | G | A | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-1390G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10491959 | |||||||
chr11:10492002 | C | T | 7 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(4): Show |
9 | HG00639.hp1 HG01884.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.940-1347C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492002 | |||||||
chr11:10492008 | C | T | 2 | a0001c0001t0016g0130 a0001c0013t0011g0178 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.940-1341C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492008 | |||||||
chr11:10492195 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1154T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492195 | |||||||
chr11:10492209 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1140G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492209 | |||||||
chr11:10492216 | C | A | 2 | a0001c0003t0003g0205 a0001c0003t0021g0200 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.940-1133C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492216 | |||||||
chr11:10492216 | C | T | 2 | a0001c0001t0016g0130 a0001c0013t0011g0178 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.940-1133C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492216 | |||||||
chr11:10492218 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1131T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492218 | |||||||
chr11:10492219 | G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1130G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492219 | |||||||
chr11:10492222 | A | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1127A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492222 | |||||||
chr11:10492223 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1126T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492223 | |||||||
chr11:10492224 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1125G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492224 | |||||||
chr11:10492226 | G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1123G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492226 | |||||||
chr11:10492228 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1121G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492228 | |||||||
chr11:10492236 | C | CAACACTG others(5): Show |
1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1113_940-1112i others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492236 | |||||||
chr11:10492237 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1112T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492237 | |||||||
chr11:10492247 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1102G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492247 | |||||||
chr11:10492248 | T | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1101T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492248 | |||||||
chr11:10492255 | C | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1094C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492255 | |||||||
chr11:10492256 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1093T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492256 | |||||||
chr11:10492257 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1092G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492257 | |||||||
chr11:10492259 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1090T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492259 | |||||||
chr11:10492275 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1074T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492275 | |||||||
chr11:10492278 | G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1071G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492278 | |||||||
chr11:10492280 | T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1069T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492280 | |||||||
chr11:10492337 | G | A | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-1012G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492337 | |||||||
chr11:10492340 | T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-1009T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492340 | |||||||
chr11:10492385 | T | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-964T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492385 | |||||||
chr11:10492449 | T | C | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-900T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492449 | |||||||
chr11:10492483 | A | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-866A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492483 | |||||||
chr11:10492485 | G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-864G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492485 | |||||||
chr11:10492487 | T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-862T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492487 | |||||||
chr11:10492491 | A | G | 1 | a0002c0024t0010g0042 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.940-858A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492491 | |||||||
chr11:10492492 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-857G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492492 | |||||||
chr11:10492493 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-856G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492493 | |||||||
chr11:10492494 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-855G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492494 | |||||||
chr11:10492495 | T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-854T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492495 | |||||||
chr11:10492497 | C | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-852C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492497 | |||||||
chr11:10492499 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-850G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492499 | |||||||
chr11:10492501 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-848G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492501 | |||||||
chr11:10492503 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-846G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492503 | |||||||
chr11:10492504 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-845G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492504 | |||||||
chr11:10492505 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-844G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492505 | |||||||
chr11:10492506 | A | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-843A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492506 | |||||||
chr11:10492507 | T | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-842T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492507 | |||||||
chr11:10492510 | A | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-839A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492510 | |||||||
chr11:10492512 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-837G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492512 | |||||||
chr11:10492513 | G | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-836G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492513 | |||||||
chr11:10492514 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-835G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492514 | |||||||
chr11:10492515 | A | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-834A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492515 | |||||||
chr11:10492579 | A | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-770A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492579 | |||||||
chr11:10492583 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-766T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492583 | |||||||
chr11:10492584 | G | A | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-765G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492584 | |||||||
chr11:10492713 | G | A | 41 | a0001c0001t0001g0210 a0001c0001t0001g0284 a0001c0001t0001g0294 others(38): Show |
47 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.940-636G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10492713 | |||||||
chr11:10493053 | C | G | 3 | a0001c0001t0001g0209 a0001c0003t0005g0128 a0001c0003t0005g0129 |
3 | HG01943.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.940-296C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493053 | |||||||
chr11:10493104 | C | G | 3 | a0001c0001t0020g0204 a0001c0003t0003g0205 a0001c0003t0021g0200 |
3 | HG01891.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.940-245C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493104 | |||||||
chr11:10493160 | A | G | 24 | a0001c0001t0001g0284 a0001c0001t0001g0294 a0001c0001t0001g0318 others(21): Show |
29 | HG00140.hp2 HG00639.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.940-189A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493160 | |||||||
chr11:10493179 | C | G | 6 | a0001c0001t0001g0209 a0001c0003t0005g0128 a0001c0003t0005g0129 others(3): Show |
6 | HG01943.hp2 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-170C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493179 | |||||||
chr11:10493221 | A | G | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-128A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493221 | |||||||
chr11:10493269 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.940-80C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 6/14 | chr11 | 10493269 | |||||||
chr11:10493756 | G | A | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+213G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493756 | |||||||
chr11:10493815 | A | G | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+272A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493815 | |||||||
chr11:10493938 | A | G | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+395A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493938 | |||||||
chr11:10493944 | G | A | 1 | a0001c0002t0001g0224 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1134+401G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10493944 | |||||||
chr11:10494115 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1134+572G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494115 | |||||||
chr11:10494124 | C | G | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+581C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494124 | |||||||
chr11:10494154 | A | G | 11 | a0001c0001t0001g0210 a0001c0001t0005g0190 a0001c0001t0013g0041 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1134+611A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494154 | |||||||
chr11:10494162 | A | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0278 |
2 | HG02135.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1134+619A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494162 | |||||||
chr11:10494216 | C | T | 4 | a0004c0011t0015g0017 a0004c0014t0015g0168 a0004c0014t0018g0169 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+673C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494216 | |||||||
chr11:10494217 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0123 |
2 | HG00733.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1134+674G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494217 | |||||||
chr11:10494246 | A | G | 49 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0043 others(46): Show |
52 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1135-653A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494246 | |||||||
chr11:10494397 | A | G | 1 | a0001c0002t0001g0256 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1135-502A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494397 | |||||||
chr11:10494509 | C | CA | 258 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0043 others(255): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1135-382dupA | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 10494509 | ||||||
chr11:10494597 | A | G | 1 | a0001c0001t0025g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-302A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494597 | |||||||
chr11:10494656 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1135-243G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494656 | |||||||
chr11:10494672 | G | A | 14 | a0001c0003t0003g0137 a0001c0003t0012g0187 a0001c0003t0017g0188 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1135-227G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494672 | |||||||
chr11:10494799 | G | A | 11 | a0001c0003t0003g0137 a0002c0006t0005g0206 a0002c0006t0005g0207 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135-100G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494799 | |||||||
chr11:10494829 | A | G | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1135-70A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494829 | |||||||
chr11:10494831 | G | T | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1135-68G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494831 | |||||||
chr11:10494832 | T | C | 1 | a0001c0002t0001g0312 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1135-67T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494832 | |||||||
chr11:10494867 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1135-32G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494867 | |||||||
chr11:10494872 | G | A | 9 | a0001c0001t0001g0209 a0001c0001t0004g0035 a0001c0003t0005g0128 others(6): Show |
9 | HG01891.hp1 HG01943.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1135-27G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 7/14 | chr11 | 10494872 | |||||||
chr11:10495135 | G | C | 4 | a0002c0006t0005g0206 a0002c0006t0005g0207 a0002c0006t0012g0208 others(1): Show |
4 | HG02055.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+105G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495135 | |||||||
chr11:10495199 | C | T | 8 | a0002c0006t0005g0206 a0002c0006t0005g0207 a0002c0006t0012g0208 others(5): Show |
8 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+169C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495199 | |||||||
chr11:10495287 | T | A | 21 | a0001c0001t0001g0055 a0001c0001t0001g0331 a0001c0001t0001g0332 others(18): Show |
21 | HG01109.hp2 HG01123.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1266+257T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495287 | |||||||
chr11:10495447 | G | C | 27 | a0001c0001t0001g0209 a0001c0001t0016g0130 a0001c0003t0005g0128 others(24): Show |
28 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1267-123G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495447 | |||||||
chr11:10495492 | C | T | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267-78C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 8/14 | chr11 | 10495492 | |||||||
chr11:10495902 | A | G | 1 | a0003c0008t0009g0198 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1430+169A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10495902 | |||||||
chr11:10495916 | C | CT | 50 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0043 others(47): Show |
53 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1430+201dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 10495916 | ||||||
chr11:10495916 | CT | C | 25 | a0001c0001t0001g0078 a0001c0001t0001g0260 a0001c0001t0001g0333 others(22): Show |
26 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.1430+201delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 10495916 | ||||||
chr11:10495935 | G | T | 51 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0043 others(48): Show |
54 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1430+202G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10495935 | |||||||
chr11:10496105 | T | A | 2 | a0001c0001t0001g0264 a0001c0002t0001g0263 |
2 | HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1430+372T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496105 | |||||||
chr11:10496114 | A | G | 6 | a0003c0008t0009g0197 a0003c0008t0009g0198 a0003c0008t0019g0167 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1430+381A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496114 | |||||||
chr11:10496151 | G | A | 2 | a0001c0002t0001g0013 a0001c0002t0001g0309 |
3 | HG02080.hp2 HG02155.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1430+418G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496151 | |||||||
chr11:10496329 | C | T | 1 | a0001c0003t0005g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1431-483C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496329 | |||||||
chr11:10496411 | C | T | 1 | a0001c0001t0016g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1431-401C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496411 | |||||||
chr11:10496555 | C | T | 13 | a0001c0001t0001g0044 a0001c0001t0001g0176 a0001c0001t0001g0330 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1431-257C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496555 | |||||||
chr11:10496704 | G | C | 44 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0043 others(41): Show |
47 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1431-108G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496704 | |||||||
chr11:10496742 | T | C | 262 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(259): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1431-70T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496742 | |||||||
chr11:10496791 | C | T | 2 | a0005c0016t0005g0199 a0005c0017t0001g0342 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1431-21C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 9/14 | chr11 | 10496791 | |||||||
chr11:10496974 | C | T | 195 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0081 others(192): Show |
214 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.1557+36C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10496974 | |||||||
chr11:10496995 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1557+57C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10496995 | |||||||
chr11:10497038 | A | G | 103 | a0001c0001t0001g0072 a0001c0001t0001g0225 a0001c0001t0001g0230 others(100): Show |
112 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1557+100A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497038 | |||||||
chr11:10497068 | G | A | 13 | a0001c0001t0001g0260 a0001c0001t0001g0347 a0001c0001t0007g0352 others(10): Show |
13 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+130G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497068 | |||||||
chr11:10497292 | G | GT | 163 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0036 others(160): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1557+363dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10497292 | ||||||
chr11:10497311 | A | G | 16 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0326 others(13): Show |
17 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1557+373A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497311 | |||||||
chr11:10497313 | A | G | 99 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0056 others(96): Show |
106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1557+375A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497313 | |||||||
chr11:10497338 | C | A | 5 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(2): Show |
7 | HG00639.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1557+400C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497338 | |||||||
chr11:10497349 | C | T | 319 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(316): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1557+411C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497349 | |||||||
chr11:10497355 | C | A | 129 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0056 others(126): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1557+417C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497355 | |||||||
chr11:10497370 | A | G | 353 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(350): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.1557+432A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497370 | |||||||
chr11:10497430 | A | G | 239 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(236): Show |
255 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1557+492A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497430 | |||||||
chr11:10497440 | A | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0210 a0001c0001t0003g0153 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+502A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497440 | |||||||
chr11:10497468 | G | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0315 a0001c0001t0001g0343 others(12): Show |
15 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+530G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497468 | |||||||
chr11:10497470 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1557+532C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497470 | |||||||
chr11:10497483 | C | T | 1 | a0001c0010t0009g0180 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1557+545C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497483 | |||||||
chr11:10497491 | G | A | 1 | a0001c0002t0001g0232 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1557+553G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497491 | |||||||
chr11:10497504 | C | T | 1 | a0001c0002t0006g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1557+566C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497504 | |||||||
chr11:10497505 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1557+567G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497505 | |||||||
chr11:10497530 | G | A | 44 | a0001c0001t0001g0056 a0001c0001t0001g0287 a0001c0001t0001g0303 others(41): Show |
45 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1557+592G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497530 | |||||||
chr11:10497533 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0210 a0001c0001t0004g0024 |
3 | HG02809.hp2 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1557+595A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497533 | |||||||
chr11:10497541 | G | C | 57 | a0001c0001t0001g0028 a0001c0001t0001g0043 a0001c0001t0001g0046 others(54): Show |
62 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1557+603G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497541 | |||||||
chr11:10497602 | A | G | 4 | a0001c0002t0006g0052 a0001c0002t0006g0053 a0003c0008t0009g0197 others(1): Show |
4 | HG01123.hp1 HG01167.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+664A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497602 | |||||||
chr11:10497604 | A | G | 4 | a0001c0002t0006g0052 a0001c0002t0006g0053 a0003c0008t0009g0197 others(1): Show |
4 | HG01123.hp1 HG01167.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+666A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497604 | |||||||
chr11:10497700 | T | A | 63 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0044 others(60): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1557+762T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497700 | |||||||
chr11:10497769 | A | G | 175 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0043 others(172): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1557+831A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497769 | |||||||
chr11:10497772 | G | A | 1 | a0001c0001t0004g0029 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1557+834G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497772 | |||||||
chr11:10497808 | G | A | 1 | a0001c0003t0014g0007 | 2 | HG00741.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1557+870G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497808 | |||||||
chr11:10497833 | G | A | 1 | a0001c0003t0012g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1557+895G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497833 | |||||||
chr11:10497871 | G | A | 11 | a0001c0001t0001g0036 a0001c0001t0001g0176 a0001c0001t0001g0349 others(8): Show |
12 | HG00639.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557+933G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497871 | |||||||
chr11:10497926 | G | A | 12 | a0001c0001t0007g0037 a0001c0001t0010g0038 a0001c0003t0007g0172 others(9): Show |
13 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+988G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497926 | |||||||
chr11:10497926 | G | C | 2 | a0001c0001t0001g0078 a0001c0001t0002g0102 |
2 | NA19054.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1557+988G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10497926 | |||||||
chr11:10498006 | A | G | 1 | a0001c0001t0007g0352 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1557+1068A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498006 | |||||||
chr11:10498077 | G | A | 1 | a0001c0003t0005g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1557+1139G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498077 | |||||||
chr11:10498091 | T | C | 2 | a0001c0001t0004g0029 a0001c0003t0002g0091 |
3 | HG01243.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1557+1153T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498091 | |||||||
chr11:10498135 | G | A | 2 | a0001c0001t0001g0067 a0001c0002t0001g0336 |
2 | HG01168.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1557+1197G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498135 | |||||||
chr11:10498269 | G | T | 9 | a0001c0001t0008g0157 a0001c0001t0010g0038 a0001c0003t0005g0193 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+1331G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498269 | |||||||
chr11:10498323 | G | A | 14 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0010 others(11): Show |
18 | HG00639.hp2 HG01106.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1557+1385G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498323 | |||||||
chr11:10498349 | A | G | 8 | a0001c0001t0008g0157 a0001c0001t0010g0038 a0001c0003t0012g0189 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1557+1411A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498349 | |||||||
chr11:10498395 | G | T | 8 | a0001c0001t0007g0348 a0001c0001t0007g0353 a0001c0003t0012g0187 others(5): Show |
8 | HG02055.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1557+1457G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498395 | |||||||
chr11:10498402 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0004g0024 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1557+1464C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498402 | |||||||
chr11:10498489 | G | C | 48 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0070 others(45): Show |
51 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1557+1551G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498489 | |||||||
chr11:10498651 | T | C | 1 | a0001c0002t0001g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1558-1435T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498651 | |||||||
chr11:10498729 | T | C | 347 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(344): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1558-1357T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498729 | |||||||
chr11:10498824 | A | G | 3 | a0001c0001t0001g0303 a0001c0001t0002g0110 a0001c0002t0006g0064 |
3 | HG01358.hp2 HG01361.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1558-1262A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498824 | |||||||
chr11:10498857 | C | G | 6 | a0001c0003t0004g0003 a0001c0003t0004g0023 a0001c0003t0004g0170 others(3): Show |
8 | HG00639.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-1229C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498857 | |||||||
chr11:10498888 | T | C | 3 | a0001c0002t0001g0048 a0001c0003t0004g0177 a0001c0013t0011g0178 |
3 | HG03130.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1558-1198T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498888 | |||||||
chr11:10498980 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0002g0100 |
2 | NA18966.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1558-1106G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10498980 | |||||||
chr11:10499025 | AGAGG | A | 45 | a0001c0001t0001g0036 a0001c0001t0001g0222 a0001c0001t0001g0225 others(42): Show |
47 | HG00140.hp2 HG00558.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.1558-1059_1558-105 others(8): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10499025 | ||||||
chr11:10499028 | G | C | 52 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0070 others(49): Show |
55 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1558-1058G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499028 | |||||||
chr11:10499089 | GCAAGGAC others(3): Show |
G | 9 | a0001c0001t0007g0037 a0001c0001t0007g0348 a0001c0001t0007g0352 others(6): Show |
10 | HG01884.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-995_1558-986d others(12): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10499089 | ||||||
chr11:10499109 | C | G | 1 | a0001c0013t0011g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1558-977C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499109 | |||||||
chr11:10499124 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0004g0024 a0001c0001t0016g0130 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-962C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499124 | |||||||
chr11:10499143 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0004g0024 a0001c0001t0016g0130 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-943C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499143 | |||||||
chr11:10499175 | C | T | 1 | a0001c0001t0005g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1558-911C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499175 | |||||||
chr11:10499234 | G | GT | 12 | a0001c0001t0008g0022 a0001c0001t0008g0138 a0001c0001t0008g0157 others(9): Show |
12 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1558-844dupT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 10499234 | ||||||
chr11:10499236 | T | A | 4 | a0001c0001t0001g0024 a0001c0001t0004g0024 a0001c0001t0016g0130 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-850T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499236 | |||||||
chr11:10499251 | T | C | 1 | a0001c0001t0010g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1558-835T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499251 | |||||||
chr11:10499276 | C | A | 52 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0070 others(49): Show |
55 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1558-810C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499276 | |||||||
chr11:10499280 | C | A | 3 | a0001c0002t0001g0048 a0001c0003t0004g0177 a0001c0013t0011g0178 |
3 | HG03130.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1558-806C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499280 | |||||||
chr11:10499305 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0176 a0001c0001t0003g0153 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-781C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499305 | |||||||
chr11:10499362 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1558-724C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499362 | |||||||
chr11:10499517 | A | T | 1 | a0001c0002t0002g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1558-569A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499517 | |||||||
chr11:10499528 | T | G | 1 | a0001c0003t0005g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1558-558T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499528 | |||||||
chr11:10499700 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1558-386G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499700 | |||||||
chr11:10499884 | G | A | 1 | a0005c0016t0005g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1558-202G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10499884 | |||||||
chr11:10500025 | C | T | 20 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0010 others(17): Show |
26 | HG00639.hp2 HG01106.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1558-61C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10500025 | |||||||
chr11:10500032 | G | A | 2 | a0001c0001t0007g0348 a0001c0001t0007g0353 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1558-54G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 10/14 | chr11 | 10500032 | |||||||
chr11:10500268 | C | T | 1 | a0001c0001t0020g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1721+19C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500268 | |||||||
chr11:10500296 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1721+47C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500296 | |||||||
chr11:10500303 | G | A | 166 | a0001c0001t0001g0043 a0001c0001t0001g0176 a0001c0001t0001g0349 others(163): Show |
185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1721+54G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500303 | |||||||
chr11:10500373 | T | C | 1 | a0001c0003t0005g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1721+124T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500373 | |||||||
chr11:10500401 | C | T | 171 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0176 others(168): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1721+152C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500401 | |||||||
chr11:10500450 | C | T | 184 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0176 others(181): Show |
203 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1721+201C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500450 | |||||||
chr11:10500453 | G | C | 9 | a0001c0001t0004g0029 a0001c0001t0013g0030 a0001c0001t0013g0041 others(6): Show |
10 | HG01109.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1721+204G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500453 | |||||||
chr11:10500554 | C | T | 1 | a0001c0003t0003g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1721+305C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500554 | |||||||
chr11:10500573 | C | T | 169 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0176 others(166): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1721+324C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500573 | |||||||
chr11:10500737 | G | A | 9 | a0001c0002t0001g0001 a0001c0002t0001g0240 a0001c0002t0001g0241 others(6): Show |
11 | NA18747.hp1 NA18959.hp1 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.1721+488G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500737 | |||||||
chr11:10500779 | G | A | 9 | a0001c0001t0007g0037 a0001c0001t0007g0348 a0001c0001t0007g0352 others(6): Show |
10 | HG01884.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1721+530G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500779 | |||||||
chr11:10500796 | G | A | 137 | a0001c0001t0001g0043 a0001c0001t0001g0176 a0001c0001t0001g0349 others(134): Show |
149 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1721+547G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500796 | |||||||
chr11:10500801 | C | G | 4 | a0001c0001t0001g0024 a0001c0001t0004g0024 a0001c0001t0016g0130 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721+552C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500801 | |||||||
chr11:10500814 | C | T | 11 | a0001c0001t0001g0248 a0001c0001t0001g0270 a0001c0001t0001g0271 others(8): Show |
13 | HG01255.hp2 HG01496.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1721+565C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500814 | |||||||
chr11:10500832 | G | A | 4 | a0001c0003t0017g0188 a0002c0020t0018g0152 a0004c0014t0018g0169 others(1): Show |
4 | HG02055.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721+583G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500832 | |||||||
chr11:10500958 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1722-512C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10500958 | |||||||
chr11:10501166 | G | A | 3 | a0001c0007t0001g0334 a0001c0007t0002g0034 a0001c0007t0002g0126 |
3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1722-304G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501166 | |||||||
chr11:10501209 | G | A | 45 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0230 others(42): Show |
47 | HG00140.hp2 HG00558.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.1722-261G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501209 | |||||||
chr11:10501247 | G | A | 1 | a0001c0002t0029g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1722-223G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501247 | |||||||
chr11:10501295 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1722-175C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501295 | |||||||
chr11:10501299 | A | G | 355 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(352): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1722-171A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501299 | |||||||
chr11:10501322 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1722-148G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501322 | |||||||
chr11:10501383 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1722-87C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501383 | |||||||
chr11:10501413 | C | T | 9 | a0001c0001t0007g0037 a0001c0001t0007g0348 a0001c0001t0007g0352 others(6): Show |
10 | HG01884.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1722-57C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501413 | |||||||
chr11:10501430 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1722-40G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501430 | |||||||
chr11:10501431 | G | T | 89 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0044 others(86): Show |
95 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1722-39G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501431 | |||||||
chr11:10501436 | G | T | 171 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0058 others(168): Show |
186 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1722-34G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 11/14 | chr11 | 10501436 | |||||||
chr11:10501607 | C | T | 1 | a0001c0001t0003g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1842+17C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501607 | |||||||
chr11:10501612 | G | A | 1 | a0001c0003t0014g0007 | 2 | HG00741.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1842+22G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501612 | |||||||
chr11:10501677 | G | A | 28 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0010 others(25): Show |
35 | HG00639.hp2 HG01106.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1842+87G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501677 | |||||||
chr11:10501926 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1842+336C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501926 | |||||||
chr11:10501929 | C | T | 286 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(283): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1842+339C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501929 | |||||||
chr11:10501954 | A | G | 52 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0222 others(49): Show |
54 | HG00140.hp2 HG00558.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.1842+364A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501954 | |||||||
chr11:10501972 | G | A | 146 | a0001c0001t0001g0043 a0001c0001t0001g0176 a0001c0001t0001g0349 others(143): Show |
159 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1842+382G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501972 | |||||||
chr11:10501975 | A | G | 3 | a0001c0001t0008g0157 a0001c0001t0010g0038 a0001c0013t0010g0175 |
3 | HG02109.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1842+385A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10501975 | |||||||
chr11:10502125 | C | T | 3 | a0001c0002t0001g0229 a0001c0004t0001g0234 a0001c0005t0001g0221 |
3 | HG02155.hp1 NA18974.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1842+535C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502125 | |||||||
chr11:10502261 | G | A | 1 | a0001c0002t0003g0156 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1843-460G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502261 | |||||||
chr11:10502398 | A | G | 2 | a0005c0016t0005g0199 a0005c0017t0001g0342 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1843-323A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502398 | |||||||
chr11:10502427 | T | C | 1 | a0001c0002t0001g0327 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1843-294T>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502427 | |||||||
chr11:10502442 | G | A | 1 | a0001c0001t0025g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1843-279G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502442 | |||||||
chr11:10502532 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1843-189T>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502532 | |||||||
chr11:10502627 | C | G | 1 | a0001c0002t0001g0236 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1843-94C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 12/14 | chr11 | 10502627 | |||||||
chr11:10502964 | G | T | 1 | a0002c0012t0026g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2016+70G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10502964 | |||||||
chr11:10503059 | C | G | 130 | a0001c0001t0003g0140 a0001c0002t0001g0001 a0001c0002t0001g0004 others(127): Show |
142 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.2016+165C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503059 | |||||||
chr11:10503125 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2016+231A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503125 | |||||||
chr11:10503274 | C | T | 3 | a0001c0001t0001g0209 a0001c0003t0005g0128 a0001c0003t0005g0129 |
3 | HG01943.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2016+380C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503274 | |||||||
chr11:10503440 | A | T | 4 | a0001c0001t0001g0225 a0001c0001t0003g0149 a0001c0001t0003g0163 others(1): Show |
4 | NA18940.hp2 NA18952.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2016+546A>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503440 | |||||||
chr11:10503554 | C | A | 1 | a0001c0002t0006g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2016+660C>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503554 | |||||||
chr11:10503566 | G | A | 1 | a0001c0002t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2016+672G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503566 | |||||||
chr11:10503832 | A | G | 51 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0070 others(48): Show |
54 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2017-717A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10503832 | |||||||
chr11:10504115 | C | CATCT | 13 | a0001c0001t0001g0055 a0001c0001t0001g0225 a0001c0001t0001g0294 others(10): Show |
14 | HG00558.hp1 HG01515.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017-403_2017-400d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | ||||||
chr11:10504115 | CATCT | C | 7 | a0001c0001t0013g0030 a0001c0003t0017g0186 a0001c0003t0017g0188 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-403_2017-400d others(6): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | ||||||
chr11:10504115 | CATCTATC others(1): Show |
C | 110 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(107): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.2017-407_2017-400d others(10): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | ||||||
chr11:10504115 | CATCTATC others(5): Show |
C | 170 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0059 others(167): Show |
185 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.2017-411_2017-400d others(14): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | ||||||
chr11:10504115 | CATCTATC others(9): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2017-415_2017-400d others(18): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 10504115 | ||||||
chr11:10504160 | A | G | 51 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0070 others(48): Show |
54 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2017-389A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504160 | |||||||
chr11:10504244 | A | C | 13 | a0001c0001t0008g0022 a0001c0001t0008g0138 a0001c0001t0008g0157 others(10): Show |
13 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2017-305A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504244 | |||||||
chr11:10504248 | G | T | 34 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0049 others(31): Show |
37 | HG00280.hp1 HG00733.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2017-301G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504248 | |||||||
chr11:10504372 | A | G | 98 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0044 others(95): Show |
108 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.2017-177A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504372 | |||||||
chr11:10504513 | C | T | 287 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(284): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2017-36C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 13/14 | chr11 | 10504513 | |||||||
chr11:10504729 | A | G | 1 | a0001c0003t0004g0023 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2127+70A>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504729 | |||||||
chr11:10504889 | A | C | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2127+230A>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504889 | |||||||
chr11:10504903 | C | G | 1 | a0001c0002t0001g0297 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2127+244C>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504903 | |||||||
chr11:10504908 | T | G | 2 | a0001c0001t0001g0349 a0001c0001t0020g0204 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2127+249T>G | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10504908 | |||||||
chr11:10505074 | C | T | 1 | a0001c0002t0001g0350 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2127+415C>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505074 | |||||||
chr11:10505075 | G | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
24 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2127+416G>T | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505075 | |||||||
chr11:10505178 | G | C | 1 | a0001c0002t0001g0246 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2127+519G>C | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505178 | |||||||
chr11:10505279 | TG | T | 33 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0049 others(30): Show |
36 | HG00280.hp1 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2128-428delG | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505279 | |||||||
chr11:10505375 | C | CAGG | 347 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(344): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.2128-332_2128-330d others(5): Show |
AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 10505375 | ||||||
chr11:10505380 | G | A | 347 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0027 others(344): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.2128-328G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505380 | |||||||
chr11:10505406 | TC | T | 27 | a0001c0001t0001g0024 a0001c0001t0001g0068 a0001c0001t0004g0006 others(24): Show |
34 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2128-298delC | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 10505406 | ||||||
chr11:10505410 | CT | C | 320 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(317): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2128-295delT | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr11 | 10505410 | ||||||
chr11:10505505 | AC | A | 138 | a0001c0001t0001g0043 a0001c0001t0001g0176 a0001c0001t0001g0349 others(135): Show |
150 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2128-202delC | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505505 | |||||||
chr11:10505597 | G | A | 1 | a0001c0001t0004g0029 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2128-111G>A | AMPD3 | ENSG00000133805.16 | transcript | ENST00000396553.7 | protein_coding | 14/14 | chr11 | 10505597 |