Item | Value |
---|---|
geneid | 23243 |
ensemblid | ENSG00000206560.12 |
hgncid | 29024 |
symbol | ANKRD28 |
name | ankyrin repeat domain 28 |
refseq_nuc | NM_001349278.2 |
refseq_prot | NP_001336207.1 |
ensembl_nuc | ENST00000683139.1 |
ensembl_prot | ENSP00000508086.1 |
mane_status | MANE Select |
chr | chr3 |
start | 15667236 |
end | 15797979 |
strand | - |
ver | v1.2 |
region | chr3:15667236-15797979 |
region5000 | chr3:15662236-15802979 |
regionname0 | ANKRD28_chr3_15667236_15797979 |
regionname5000 | ANKRD28_chr3_15662236_15802979 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1083 | 329 | 91 | 55 | 139 | 10 | 32 | 105 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | MSRVC others(1078): Show |
chr3 | 15662236 | 15802979 |
a0002 | 0/0 | 1083 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | MSRVC others(1078): Show |
chr3 | 15662236 | 15802979 |
a0003 | 0/0 | 1083 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | MSRVC others(1078): Show |
chr3 | 15662236 | 15802979 |
a0004 | 0/0 | 1083 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | MSRVC others(1078): Show |
chr3 | 15662236 | 15802979 |
a0005 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | MSRVC others(1078): Show |
chr3 | 15662236 | 15802979 |
a0006 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | MSRVC others(1078): Show |
chr3 | 15662236 | 15802979 |
a0007 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | MSRVC others(1078): Show |
chr3 | 15662236 | 15802979 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3249 | 166 | 45 | 23 | 75 | 3 | 19 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0002 | 0/1 | 3249 | 124 | 12 | 30 | 61 | 7 | 13 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0003 | 0/0 | 3249 | 15 | 13 | 2 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0004 | 0/0 | 3249 | 9 | 9 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0005 | 0/0 | 3249 | 6 | 6 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0007 | 0/0 | 3249 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0009 | 0/0 | 3249 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0010 | 0/0 | 3249 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0014 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0001c0017 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0002c0006 | 0/0 | 3249 | 4 | 0 | 2 | 0 | 0 | 2 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0003c0013 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0003c0015 | 0/0 | 3249 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0004c0008 | 0/0 | 3249 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0005c0012 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0006c0016 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 | ||
a0007c0011 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | ATGAG others(3244): Show |
chr3 | 15662236 | 15802979 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0002 | 0/0 | 7742 | 85 | 15 | 8 | 56 | 0 | 6 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0003 | 1/0 | 7744 | 20 | 3 | 6 | 6 | 1 | 3 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0004 | 0/0 | 7745 | 14 | 8 | 2 | 0 | 0 | 4 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0006 | 0/0 | 7744 | 10 | 7 | 3 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0008 | 0/0 | 7744 | 8 | 5 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0010 | 0/0 | 7744 | 5 | 4 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0014 | 0/0 | 7741 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7736): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0015 | 0/0 | 7744 | 3 | 0 | 0 | 0 | 0 | 3 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0016 | 0/0 | 7744 | 3 | 0 | 2 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0023 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0024 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0028 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0029 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0030 | 0/0 | 7742 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0031 | 0/0 | 7742 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0032 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0037 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0044 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0046 | 0/0 | 7743 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7738): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0049 | 0/0 | 7743 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7738): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0055 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0057 | 0/0 | 7744 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0001t0058 | 0/0 | 7743 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7738): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0001 | 0/1 | 7745 | 94 | 11 | 21 | 44 | 7 | 10 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0007 | 0/0 | 7745 | 8 | 0 | 0 | 8 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0011 | 0/0 | 7746 | 3 | 0 | 2 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7741): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0013 | 0/0 | 7745 | 3 | 0 | 3 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0017 | 0/0 | 7743 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7738): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0022 | 0/0 | 7745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0027 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0033 | 0/0 | 7745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0034 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0035 | 0/0 | 7746 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7741): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0036 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0038 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0039 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0040 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0041 | 0/0 | 7744 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0042 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0045 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0048 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7741): Show |
chr3 | 15662236 | 15802979 |
a0001c0002t0054 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0003t0005 | 0/0 | 7744 | 10 | 8 | 2 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0003t0018 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0003t0019 | 0/0 | 7743 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7738): Show |
chr3 | 15662236 | 15802979 |
a0001c0003t0051 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0004t0009 | 0/0 | 7742 | 7 | 7 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0004t0025 | 0/0 | 7742 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0004t0053 | 0/0 | 7743 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7738): Show |
chr3 | 15662236 | 15802979 |
a0001c0005t0012 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0005t0020 | 0/0 | 7743 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7738): Show |
chr3 | 15662236 | 15802979 |
a0001c0005t0052 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0005t0056 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0007t0021 | 0/0 | 7744 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0007t0043 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0001c0009t0005 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0010t0012 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0001c0014t0026 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0001c0017t0004 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0002c0006t0001 | 0/0 | 7745 | 4 | 0 | 2 | 0 | 0 | 2 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0003c0013t0050 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7740): Show |
chr3 | 15662236 | 15802979 |
a0003c0015t0011 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7741): Show |
chr3 | 15662236 | 15802979 |
a0004c0008t0002 | 0/0 | 7742 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7737): Show |
chr3 | 15662236 | 15802979 |
a0005c0012t0006 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
a0006c0016t0047 | 0/0 | 7746 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7741): Show |
chr3 | 15662236 | 15802979 |
a0007c0011t0003 | 0/0 | 7744 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | AGATC others(7739): Show |
chr3 | 15662236 | 15802979 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0008g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0010g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0010g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0014g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0014g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0015g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0015g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0015g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0016g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0016g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0016g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0023g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0024g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0028g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0029g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0030g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0031g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0032g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0037g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0044g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0046g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0049g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0055g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0057g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0001t0058g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0011g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0011g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0011g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0013g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0013g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0013g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0017g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0017g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0022g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0027g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0033g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0034g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0035g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0036g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0038g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0039g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0040g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0041g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0042g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0045g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0048g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0002t0054g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0018g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0018g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0019g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0019g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0003t0051g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0025g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0004t0053g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0005t0012g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0005t0012g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0005t0020g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0005t0020g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0005t0052g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0005t0056g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0007t0021g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0007t0021g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0007t0043g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0009t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0009t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0010t0012g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0010t0012g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0014t0026g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0001c0017t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0002c0006t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0002c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0002c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0002c0006t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0003c0013t0050g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0003c0015t0011g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0004c0008t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0004c0008t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0005c0012t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0006c0016t0047g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
a0007c0011t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0267 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0105 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00140 | hp1 | a0001 | c0001 | t0016 | g0326 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0126 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00597 | hp1 | a0001 | c0002 | t0017 | g0132 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00639 | hp2 | a0001 | c0002 | t0022 | g0003 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00642 | hp1 | a0002 | c0006 | t0001 | g0042 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00738 | hp2 | a0001 | c0002 | t0013 | g0016 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01099 | hp2 | a0001 | c0002 | t0048 | g0275 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01109 | hp1 | a0002 | c0006 | t0001 | g0113 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01109 | hp2 | a0001 | c0003 | t0005 | g0279 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0310 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01168 | hp2 | a0001 | c0003 | t0005 | g0283 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0309 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01192 | hp1 | a0001 | c0002 | t0013 | g0017 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0307 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01255 | hp1 | a0001 | c0002 | t0011 | g0232 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01255 | hp2 | a0001 | c0002 | t0033 | g0014 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01261 | hp2 | a0001 | c0001 | t0016 | g0327 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01433 | hp1 | a0001 | c0001 | t0016 | g0329 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01433 | hp2 | a0001 | c0001 | t0031 | g0012 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01515 | hp2 | a0001 | c0001 | t0057 | g0328 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0043 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0303 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01884 | hp2 | a0003 | c0013 | t0050 | g0290 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01934 | hp2 | a0001 | c0001 | t0010 | g0263 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01981 | hp1 | a0001 | c0002 | t0013 | g0015 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01993 | hp2 | a0003 | c0015 | t0011 | g0229 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02004 | hp2 | a0001 | c0002 | t0011 | g0231 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02055 | hp1 | a0001 | c0003 | t0005 | g0286 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0264 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02071 | hp1 | a0001 | c0001 | t0008 | g0337 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02083 | hp1 | a0001 | c0002 | t0027 | g0008 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02145 | hp2 | a0001 | c0005 | t0020 | g0298 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02257 | hp1 | a0001 | c0004 | t0009 | g0293 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02258 | hp1 | a0001 | c0004 | t0009 | g0291 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0302 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02280 | hp2 | a0001 | c0003 | t0005 | g0288 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02300 | hp1 | a0001 | c0002 | t0041 | g0130 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02602 | hp1 | a0001 | c0002 | t0035 | g0039 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02615 | hp1 | a0001 | c0004 | t0009 | g0292 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02622 | hp1 | a0001 | c0010 | t0012 | g0315 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02630 | hp1 | a0001 | c0001 | t0028 | g0009 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02647 | hp1 | a0001 | c0003 | t0005 | g0284 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02647 | hp2 | a0001 | c0005 | t0052 | g0314 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02683 | hp2 | a0001 | c0001 | t0015 | g0325 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02717 | hp1 | a0001 | c0003 | t0005 | g0278 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0304 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0306 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02723 | hp2 | a0001 | c0004 | t0025 | g0006 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02809 | hp2 | a0001 | c0003 | t0005 | g0285 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02895 | hp1 | a0001 | c0001 | t0030 | g0011 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02896 | hp1 | a0001 | c0009 | t0005 | g0281 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0335 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02897 | hp2 | a0001 | c0009 | t0005 | g0280 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02922 | hp1 | a0001 | c0003 | t0005 | g0282 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0305 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02965 | hp1 | a0001 | c0014 | t0026 | g0007 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0273 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0274 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03041 | hp1 | a0001 | c0004 | t0053 | g0319 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03041 | hp2 | a0001 | c0003 | t0005 | g0289 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03098 | hp1 | a0001 | c0004 | t0009 | g0297 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03098 | hp2 | a0001 | c0005 | t0020 | g0299 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0336 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03130 | hp2 | a0001 | c0003 | t0018 | g0227 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03139 | hp2 | a0001 | c0004 | t0009 | g0296 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03195 | hp2 | a0001 | c0003 | t0018 | g0228 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03209 | hp1 | a0001 | c0005 | t0012 | g0317 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03209 | hp2 | a0001 | c0003 | t0019 | g0225 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03225 | hp1 | a0001 | c0005 | t0056 | g0322 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03486 | hp1 | a0001 | c0001 | t0055 | g0321 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03486 | hp2 | a0006 | c0016 | t0047 | g0276 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03516 | hp2 | a0001 | c0003 | t0051 | g0311 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03831 | hp2 | a0001 | c0001 | t0058 | g0332 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0234 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03927 | hp1 | a0001 | c0002 | t0039 | g0062 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0241 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03942 | hp2 | a0001 | c0001 | t0015 | g0323 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0257 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04115 | hp2 | a0002 | c0006 | t0001 | g0108 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04184 | hp2 | a0001 | c0001 | t0015 | g0324 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04204 | hp1 | a0001 | c0002 | t0038 | g0059 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04228 | hp1 | a0002 | c0006 | t0001 | g0109 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18522 | hp1 | a0001 | c0003 | t0019 | g0226 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0312 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18747 | hp2 | a0001 | c0002 | t0045 | g0224 | EAS | CHB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0334 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18944 | hp2 | a0001 | c0002 | t0007 | g0087 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18945 | hp1 | a0001 | c0001 | t0014 | g0002 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18950 | hp1 | a0001 | c0002 | t0007 | g0083 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18954 | hp2 | a0001 | c0001 | t0032 | g0013 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18956 | hp1 | a0001 | c0002 | t0017 | g0133 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18956 | hp2 | a0001 | c0001 | t0008 | g0338 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18957 | hp1 | a0001 | c0007 | t0043 | g0172 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18961 | hp2 | a0007 | c0011 | t0003 | g0251 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18967 | hp1 | a0001 | c0002 | t0011 | g0230 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18967 | hp2 | a0001 | c0001 | t0029 | g0010 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18969 | hp1 | a0001 | c0001 | t0023 | g0004 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18970 | hp2 | a0001 | c0002 | t0054 | g0320 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0333 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18977 | hp2 | a0001 | c0001 | t0014 | g0150 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18980 | hp1 | a0001 | c0001 | t0046 | g0233 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18983 | hp1 | a0001 | c0002 | t0007 | g0090 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18985 | hp1 | a0001 | c0002 | t0007 | g0095 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18991 | hp1 | a0001 | c0002 | t0034 | g0075 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19003 | hp2 | a0001 | c0002 | t0007 | g0082 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19007 | hp1 | a0001 | c0001 | t0014 | g0002 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19011 | hp1 | a0001 | c0002 | t0007 | g0084 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0330 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19043 | hp2 | a0001 | c0005 | t0012 | g0318 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19054 | hp2 | a0001 | c0001 | t0044 | g0188 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19057 | hp2 | a0001 | c0002 | t0040 | g0097 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19058 | hp2 | a0001 | c0002 | t0007 | g0085 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19060 | hp2 | a0001 | c0002 | t0007 | g0092 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19068 | hp1 | a0001 | c0002 | t0036 | g0028 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19077 | hp1 | a0004 | c0008 | t0002 | g0166 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19077 | hp2 | a0004 | c0008 | t0002 | g0211 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19087 | hp1 | a0001 | c0007 | t0021 | g0300 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19089 | hp1 | a0001 | c0001 | t0049 | g0277 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19090 | hp1 | a0001 | c0007 | t0021 | g0301 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19091 | hp2 | a0001 | c0001 | t0024 | g0005 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA19240 | hp2 | a0001 | c0001 | t0010 | g0272 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ASW | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ASW | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0116 | EUR | TSI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0123 | EUR | TSI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20905 | hp2 | a0001 | c0001 | t0037 | g0086 | SAS | GIH | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02109 | hp1 | a0005 | c0012 | t0006 | g0308 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02486 | hp1 | a0001 | c0017 | t0004 | g0246 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02559 | hp1 | a0001 | c0004 | t0009 | g0294 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0313 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03471 | hp1 | a0001 | c0010 | t0012 | g0316 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG03471 | hp2 | a0001 | c0003 | t0005 | g0287 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG06807 | hp1 | a0001 | c0004 | t0009 | g0295 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
NA21309 | hp2 | a0001 | c0002 | t0042 | g0131 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0118 | REF | REF | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0265 | REF | REF | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15677542 | T | C | 1 | a0002 | 4 | HG00642.hp1 HG01109.hp1 HG04115.hp2 others(1): Show |
missense_variant | MODERATE | c.2728A>G | p.Ser910Gly | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 25/28 | 4186/7744 | 2728/3252 | 910/1083 | chr3 | 15677542 | |||
chr3:15679512 | G | A | 1 | a0003 | 2 | HG01884.hp2 HG01993.hp2 |
missense_variant | MODERATE | c.2441C>T | p.Thr814Met | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/28 | 3899/7744 | 2441/3252 | 814/1083 | chr3 | 15679512 | |||
chr3:15707993 | C | G | 1 | a0005 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1478G>C | p.Ser493Thr | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/28 | 2936/7744 | 1478/3252 | 493/1083 | chr3 | 15707993 | |||
chr3:15713537 | C | T | 1 | a0004 | 2 | NA19077.hp1 NA19077.hp2 |
missense_variant | MODERATE | c.1180G>A | p.Asp394Asn | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/28 | 2638/7744 | 1180/3252 | 394/1083 | chr3 | 15713537 | |||
chr3:15721027 | A | G | 1 | a0007 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.884T>C | p.Val295Ala | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/28 | 2342/7744 | 884/3252 | 295/1083 | chr3 | 15721027 | |||
chr3:15737037 | C | A | 1 | a0006 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.548G>T | p.Gly183Val | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/28 | 2006/7744 | 548/3252 | 183/1083 | chr3 | 15737037 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15675914 | A | C | 1 | a0001c0007 | 3 | NA18957.hp1 NA19087.hp1 NA19090.hp1 |
synonymous_variant | LOW | c.2949T>G | p.Leu983Leu | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/28 | 4407/7744 | 2949/3252 | 983/1083 | chr3 | 15675914 | |||
chr3:15678311 | A | G | 1 | a0001c0014 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2605T>C | p.Leu869Leu | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/28 | 4063/7744 | 2605/3252 | 869/1083 | chr3 | 15678311 | |||
chr3:15679478 | G | A | 1 | a0001c0009 | 2 | HG02896.hp1 HG02897.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2475C>T | p.Ala825Ala | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/28 | 3933/7744 | 2475/3252 | 825/1083 | chr3 | 15679478 | |||
chr3:15686293 | T | C | 1 | a0001c0010 | 2 | HG02622.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.1980A>G | p.Ser660Ser | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/28 | 3438/7744 | 1980/3252 | 660/1083 | chr3 | 15686293 | |||
chr3:15690029 | A | T | 3 | a0001c0003 a0001c0004 a0001c0009 |
26 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(23): Show |
synonymous_variant | LOW | c.1953T>A | p.Ile651Ile | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/28 | 3411/7744 | 1953/3252 | 651/1083 | chr3 | 15690029 | |||
chr3:15696182 | G | A | 9 | a0001c0002 a0001c0003 a0001c0005 others(6): Show |
155 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(152): Show |
synonymous_variant | LOW | c.1611C>T | p.Asn537Asn | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/28 | 3069/7744 | 1611/3252 | 537/1083 | chr3 | 15696182 | |||
chr3:15696191 | T | C | 6 | a0001c0002 a0001c0004 a0001c0014 others(3): Show |
139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
synonymous_variant | LOW | c.1602A>G | p.Gln534Gln | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/28 | 3060/7744 | 1602/3252 | 534/1083 | chr3 | 15696191 | |||
chr3:15766256 | G | A | 1 | a0001c0017 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.258C>T | p.Ile86Ile | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/28 | 1716/7744 | 258/3252 | 86/1083 | chr3 | 15766256 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15667296 | A | G | 2 | a0001c0007t0021 a0001c0007t0043 |
3 | NA18957.hp1 NA19087.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2974T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2974 | chr3 | 15667296 | ||||||
chr3:15667359 | G | C | 2 | a0001c0003t0005 a0001c0009t0005 |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2911C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2911 | chr3 | 15667359 | ||||||
chr3:15667633 | G | A | 2 | a0001c0002t0013 a0001c0002t0048 |
4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2637C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2637 | chr3 | 15667633 | ||||||
chr3:15667807 | A | T | 1 | a0001c0002t0036 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2463 | chr3 | 15667807 | ||||||
chr3:15667919 | T | C | 2 | a0001c0001t0006 a0005c0012t0006 |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2351A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2351 | chr3 | 15667919 | ||||||
chr3:15667942 | G | A | 1 | a0001c0001t0044 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2328 | chr3 | 15667942 | ||||||
chr3:15668031 | T | C | 2 | a0001c0002t0042 a0001c0014t0026 |
2 | HG02965.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2239A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2239 | chr3 | 15668031 | ||||||
chr3:15668355 | A | AT | 5 | a0001c0002t0035 a0001c0003t0018 a0001c0003t0019 others(2): Show |
7 | HG01884.hp2 HG02602.hp1 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1914dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1914 | chr3 | 15668355 | ||||||
chr3:15668355 | AT | A | 5 | a0001c0001t0014 a0001c0001t0058 a0001c0004t0009 others(2): Show |
13 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1914delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1914 | chr3 | 15668355 | ||||||
chr3:15668504 | T | C | 26 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0014 others(23): Show |
142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1766A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1766 | chr3 | 15668504 | ||||||
chr3:15668766 | A | T | 2 | a0001c0002t0007 a0001c0002t0040 |
9 | NA18944.hp2 NA18950.hp1 NA18983.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1504T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1504 | chr3 | 15668766 | ||||||
chr3:15669006 | T | A | 1 | a0001c0005t0020 | 2 | HG02145.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1264A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1264 | chr3 | 15669006 | ||||||
chr3:15669163 | C | T | 2 | a0001c0003t0005 a0001c0009t0005 |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1107G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1107 | chr3 | 15669163 | ||||||
chr3:15669259 | A | G | 1 | a0001c0002t0034 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1011 | chr3 | 15669259 | ||||||
chr3:15669286 | G | C | 1 | a0001c0001t0057 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*984C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 984 | chr3 | 15669286 | ||||||
chr3:15669716 | C | T | 2 | a0001c0001t0010 a0001c0001t0055 |
6 | HG01934.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*554G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 554 | chr3 | 15669716 | ||||||
chr3:15669853 | C | A | 1 | a0001c0002t0038 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 417 | chr3 | 15669853 | ||||||
chr3:15669884 | CT | C | 2 | a0001c0003t0019 a0001c0003t0051 |
3 | HG03209.hp2 HG03516.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 385 | chr3 | 15669884 | ||||||
chr3:15669937 | T | C | 1 | a0001c0002t0039 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 333 | chr3 | 15669937 | ||||||
chr3:15670198 | T | A | 1 | a0001c0002t0040 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 72 | chr3 | 15670198 | ||||||
chr3:15796643 | G | GT | 5 | a0001c0001t0004 a0001c0002t0041 a0001c0002t0042 others(2): Show |
18 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-123dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 123 | chr3 | 15796643 | ||||||
chr3:15796643 | G | GTT | 21 | a0001c0001t0001 a0001c0001t0037 a0001c0002t0001 others(18): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
5_prime_UTR_variant | MODIFIER | c.-124_-123dupAA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 123 | chr3 | 15796643 | ||||||
chr3:15796643 | GT | G | 13 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0023 others(10): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-123delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 123 | chr3 | 15796643 | ||||||
chr3:15796752 | G | A | 1 | a0001c0002t0045 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-231C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 231 | chr3 | 15796752 | ||||||
chr3:15796808 | A | C | 1 | a0001c0002t0033 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-287T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 287 | chr3 | 15796808 | ||||||
chr3:15796828 | T | A | 4 | a0001c0003t0005 a0001c0003t0018 a0001c0003t0019 others(1): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-307A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 307 | chr3 | 15796828 | ||||||
chr3:15796920 | A | C | 1 | a0001c0001t0032 | 1 | NA18954.hp2 | 5_prime_UTR_variant | MODIFIER | c.-399T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 399 | chr3 | 15796920 | ||||||
chr3:15797051 | T | C | 1 | a0001c0005t0052 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-530A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 530 | chr3 | 15797051 | ||||||
chr3:15797102 | A | G | 1 | a0001c0005t0052 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-581T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 581 | chr3 | 15797102 | ||||||
chr3:15797203 | C | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(52): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
5_prime_UTR_variant | MODIFIER | c.-682G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 682 | chr3 | 15797203 | ||||||
chr3:15797204 | A | C | 1 | a0001c0001t0031 | 1 | HG01433.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-683T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797204 | |||||||
chr3:15797205 | A | C | 1 | a0001c0001t0030 | 1 | HG02895.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-684T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797205 | |||||||
chr3:15797209 | C | A | 4 | a0001c0001t0046 a0001c0002t0011 a0001c0007t0021 others(1): Show |
7 | HG01255.hp1 HG01993.hp2 HG02004.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-688G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 688 | chr3 | 15797209 | ||||||
chr3:15797209 | CA | C | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0014 others(38): Show |
244 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(241): Show |
5_prime_UTR_variant | MODIFIER | c.-689delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 689 | chr3 | 15797209 | ||||||
chr3:15797210 | A | C | 4 | a0001c0001t0046 a0001c0002t0011 a0001c0007t0021 others(1): Show |
7 | HG01255.hp1 HG01993.hp2 HG02004.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-689T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797210 | |||||||
chr3:15797213 | A | C | 2 | a0001c0001t0029 a0003c0013t0050 |
2 | HG01884.hp2 NA18967.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-692T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797213 | |||||||
chr3:15797248 | C | T | 1 | a0001c0001t0028 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-727G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 727 | chr3 | 15797248 | ||||||
chr3:15797254 | G | A | 9 | a0001c0001t0006 a0001c0003t0051 a0001c0004t0009 others(6): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-733C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797254 | |||||||
chr3:15797558 | T | A | 1 | a0001c0002t0054 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1037A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1037 | chr3 | 15797558 | ||||||
chr3:15797558 | T | TA | 5 | a0001c0004t0053 a0001c0005t0012 a0001c0005t0052 others(2): Show |
7 | HG02622.hp1 HG02647.hp2 HG03041.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-1038dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1038 | chr3 | 15797558 | ||||||
chr3:15797559 | A | T | 1 | a0001c0002t0027 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1038T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1038 | chr3 | 15797559 | ||||||
chr3:15797564 | A | G | 2 | a0001c0001t0016 a0001c0001t0057 |
4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-1043T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1043 | chr3 | 15797564 | ||||||
chr3:15797569 | A | G | 3 | a0001c0001t0015 a0001c0002t0022 a0001c0014t0026 |
5 | HG00639.hp2 HG02683.hp2 HG02965.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1048T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1048 | chr3 | 15797569 | ||||||
chr3:15797578 | A | G | 17 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0023 others(14): Show |
104 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
5_prime_UTR_variant | MODIFIER | c.-1057T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1057 | chr3 | 15797578 | ||||||
chr3:15797579 | A | G | 2 | a0001c0001t0024 a0001c0004t0025 |
2 | HG02723.hp2 NA19091.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1058T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1058 | chr3 | 15797579 | ||||||
chr3:15797646 | G | C | 1 | a0001c0001t0055 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1125C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1125 | chr3 | 15797646 | ||||||
chr3:15797657 | G | A | 1 | a0001c0005t0056 | 1 | HG03225.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1136C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797657 | |||||||
chr3:15797717 | C | T | 1 | a0001c0001t0023 | 1 | NA18969.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1196G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1196 | chr3 | 15797717 | ||||||
chr3:15797728 | T | C | 5 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0016 others(2): Show |
16 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1207A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797728 | |||||||
chr3:15797924 | A | C | 1 | a0001c0002t0022 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1403T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1403 | chr3 | 15797924 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:15670582 | A | T | 1 | a0001c0002t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2966-26T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670582 | |||||||
chr3:15670592 | C | T | 1 | a0001c0001t0037g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2966-36G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670592 | |||||||
chr3:15670629 | A | C | 1 | a0001c0004t0009g0295 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2966-73T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670629 | |||||||
chr3:15670696 | T | A | 1 | a0001c0001t0002g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2966-140A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670696 | |||||||
chr3:15670815 | A | G | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2966-259T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670815 | |||||||
chr3:15670862 | A | G | 7 | a0001c0001t0008g0330 a0001c0001t0008g0331 a0001c0001t0008g0334 others(4): Show |
7 | HG02896.hp2 HG03130.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2966-306T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670862 | |||||||
chr3:15671042 | C | T | 2 | a0001c0002t0001g0110 a0001c0002t0001g0111 |
2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2966-486G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671042 | |||||||
chr3:15671322 | C | T | 1 | a0001c0001t0008g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2966-766G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671322 | |||||||
chr3:15671353 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2966-797C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671353 | |||||||
chr3:15671364 | A | G | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2966-808T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671364 | |||||||
chr3:15671576 | T | C | 39 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(36): Show |
40 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.2966-1020A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671576 | |||||||
chr3:15671578 | G | GT | 17 | a0001c0002t0001g0120 a0001c0002t0001g0129 a0001c0002t0033g0014 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.2966-1023dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671578 | |||||||
chr3:15671578 | G | T | 1 | a0001c0003t0005g0283 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2966-1022C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671578 | |||||||
chr3:15671589 | G | T | 24 | a0001c0001t0002g0209 a0001c0003t0005g0278 a0001c0003t0005g0279 others(21): Show |
24 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2966-1033C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671589 | |||||||
chr3:15671618 | C | T | 1 | a0001c0002t0041g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2966-1062G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671618 | |||||||
chr3:15671668 | T | C | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2966-1112A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671668 | |||||||
chr3:15671836 | C | T | 10 | a0001c0001t0002g0186 a0001c0004t0009g0291 a0001c0004t0009g0292 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2966-1280G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671836 | |||||||
chr3:15671953 | A | G | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2966-1397T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671953 | |||||||
chr3:15672062 | T | C | 1 | a0001c0002t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2966-1506A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672062 | |||||||
chr3:15672146 | A | AT | 18 | a0001c0001t0002g0177 a0001c0001t0002g0209 a0001c0001t0004g0234 others(15): Show |
18 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2966-1591dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672146 | |||||||
chr3:15672146 | AT | A | 27 | a0001c0001t0003g0252 a0001c0003t0005g0278 a0001c0003t0005g0279 others(24): Show |
27 | HG01109.hp2 HG01168.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2966-1591delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672146 | |||||||
chr3:15672146 | ATT | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2966-1592_2966-159 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672146 | |||||||
chr3:15672172 | G | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2966-1616C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672172 | |||||||
chr3:15672215 | G | A | 1 | a0001c0003t0005g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2966-1659C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672215 | |||||||
chr3:15672419 | G | A | 8 | a0001c0004t0009g0292 a0001c0004t0009g0293 a0001c0004t0009g0294 others(5): Show |
8 | HG02257.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2966-1863C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672419 | |||||||
chr3:15672437 | C | A | 1 | a0001c0002t0001g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2966-1881G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672437 | |||||||
chr3:15672844 | C | T | 2 | a0001c0001t0008g0330 a0001c0001t0008g0331 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2966-2288G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672844 | |||||||
chr3:15672984 | G | A | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2966-2428C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672984 | |||||||
chr3:15673192 | T | C | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2966-2636A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673192 | |||||||
chr3:15673381 | G | A | 1 | a0001c0001t0003g0253 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2965+2517C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673381 | |||||||
chr3:15673438 | T | A | 1 | a0001c0001t0002g0177 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2965+2460A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673438 | |||||||
chr3:15673480 | C | T | 19 | a0001c0002t0001g0091 a0001c0002t0001g0100 a0001c0002t0001g0101 others(16): Show |
19 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.2965+2418G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673480 | |||||||
chr3:15673642 | A | G | 5 | a0001c0002t0017g0132 a0001c0002t0017g0133 a0001c0007t0021g0300 others(2): Show |
5 | HG00597.hp1 NA18956.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.2965+2256T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673642 | |||||||
chr3:15673649 | G | C | 127 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.2965+2249C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673649 | |||||||
chr3:15673650 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2965+2248T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673650 | |||||||
chr3:15673856 | A | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02155.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2965+2042T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673856 | |||||||
chr3:15673979 | C | T | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2965+1919G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673979 | |||||||
chr3:15674050 | T | C | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2965+1848A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674050 | |||||||
chr3:15674154 | A | C | 1 | a0001c0001t0004g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2965+1744T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674154 | |||||||
chr3:15674174 | C | CA | 16 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0241 others(13): Show |
16 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.2965+1723dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | |||||||
chr3:15674174 | C | CAAA | 13 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0283 others(10): Show |
13 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2965+1721_2965+172 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | |||||||
chr3:15674174 | C | CAAAAA | 25 | a0001c0001t0006g0307 a0001c0002t0001g0041 a0001c0002t0001g0043 others(22): Show |
25 | HG00099.hp2 HG00642.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2965+1719_2965+172 others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | |||||||
chr3:15674174 | C | CAAAAAA | 73 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
74 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.2965+1718_2965+172 others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | |||||||
chr3:15674174 | C | CAAAAAAA | 25 | a0001c0001t0037g0086 a0001c0002t0001g0024 a0001c0002t0001g0030 others(22): Show |
25 | HG00423.hp1 HG00673.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.2965+1717_2965+172 others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | |||||||
chr3:15674174 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0054g0320 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2965+1713_2965+172 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | |||||||
chr3:15674174 | CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2965+1714_2965+172 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | |||||||
chr3:15674196 | A | AAAAAAAA others(24): Show |
1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2965+1701_2965+170 others(35): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | |||||||
chr3:15674196 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0168 a0001c0001t0002g0178 |
2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | |||||||
chr3:15674196 | A | AAAAAAAA others(3): Show |
1 | a0004c0008t0002g0211 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2965+1701_2965+170 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | |||||||
chr3:15674196 | A | AAAAAAAA others(2): Show |
10 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0001t0002g0145 others(7): Show |
10 | HG00423.hp2 HG02132.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | |||||||
chr3:15674196 | A | AAAAAAAA others(1): Show |
34 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(31): Show |
34 | HG00597.hp2 HG01099.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | |||||||
chr3:15674196 | A | AAAAAAAG | 64 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0156 others(61): Show |
65 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | |||||||
chr3:15674196 | A | G | 3 | a0001c0001t0002g0186 a0001c0001t0002g0208 a0001c0001t0002g0209 |
3 | NA19001.hp2 NA19011.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2965+1702T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | |||||||
chr3:15674199 | G | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2965+1699C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674199 | |||||||
chr3:15674400 | GT | G | 311 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(308): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.2965+1497delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674400 | |||||||
chr3:15674498 | A | G | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2965+1400T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674498 | |||||||
chr3:15674543 | C | A | 1 | a0001c0001t0002g0144 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2965+1355G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674543 | |||||||
chr3:15674718 | G | C | 1 | a0001c0002t0001g0030 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2965+1180C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674718 | |||||||
chr3:15674746 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2965+1152C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674746 | |||||||
chr3:15674761 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2965+1137A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674761 | |||||||
chr3:15674821 | A | C | 1 | a0002c0006t0001g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2965+1077T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674821 | |||||||
chr3:15674896 | T | C | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2965+1002A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674896 | |||||||
chr3:15674955 | C | T | 109 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(106): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2965+943G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674955 | |||||||
chr3:15674960 | C | A | 1 | a0001c0004t0009g0297 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2965+938G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674960 | |||||||
chr3:15674977 | T | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2965+921A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674977 | |||||||
chr3:15675003 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2965+895G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675003 | |||||||
chr3:15675185 | C | T | 127 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.2965+713G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675185 | |||||||
chr3:15675266 | G | A | 4 | a0002c0006t0001g0042 a0002c0006t0001g0108 a0002c0006t0001g0109 others(1): Show |
4 | HG00642.hp1 HG01109.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2965+632C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675266 | |||||||
chr3:15675332 | G | T | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2965+566C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675332 | |||||||
chr3:15675391 | C | T | 150 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2965+507G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675391 | |||||||
chr3:15675534 | G | A | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2965+364C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675534 | |||||||
chr3:15675617 | G | C | 125 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2965+281C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675617 | |||||||
chr3:15675692 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2965+206G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675692 | |||||||
chr3:15676107 | G | A | 10 | a0001c0002t0001g0041 a0001c0002t0001g0043 a0001c0002t0001g0044 others(7): Show |
10 | HG00642.hp2 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2874-118C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676107 | |||||||
chr3:15676134 | G | A | 13 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(10): Show |
13 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.2874-145C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676134 | |||||||
chr3:15676186 | G | A | 123 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(120): Show |
124 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2874-197C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676186 | |||||||
chr3:15676195 | G | A | 1 | a0001c0001t0015g0325 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2874-206C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676195 | |||||||
chr3:15676265 | T | A | 1 | a0001c0002t0027g0008 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2874-276A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676265 | |||||||
chr3:15676337 | C | T | 126 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.2874-348G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676337 | |||||||
chr3:15676455 | C | T | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2874-466G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676455 | |||||||
chr3:15676637 | C | G | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2873+337G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676637 | |||||||
chr3:15676881 | A | G | 1 | a0001c0002t0017g0133 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2873+93T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676881 | |||||||
chr3:15676891 | A | G | 1 | a0001c0001t0003g0249 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2873+83T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676891 | |||||||
chr3:15677145 | T | A | 154 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(151): Show |
155 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.2791-89A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 25/27 | chr3 | 15677145 | |||||||
chr3:15677436 | GTTAATA | G | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2790+38_2790+43del others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 25/27 | chr3 | 15677436 | |||||||
chr3:15677701 | A | G | 3 | a0001c0001t0001g0072 a0001c0001t0003g0260 a0001c0001t0003g0261 |
3 | HG01069.hp1 HG01071.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2708-139T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677701 | |||||||
chr3:15677760 | A | G | 1 | a0001c0003t0005g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2708-198T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677760 | |||||||
chr3:15677772 | T | C | 45 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(42): Show |
46 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2708-210A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677772 | |||||||
chr3:15677813 | A | C | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2708-251T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677813 | |||||||
chr3:15677856 | C | T | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2708-294G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677856 | |||||||
chr3:15677869 | C | T | 2 | a0001c0001t0003g0257 a0001c0001t0003g0259 |
2 | HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2708-307G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677869 | |||||||
chr3:15677889 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2707+320A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677889 | |||||||
chr3:15677933 | A | C | 1 | a0001c0003t0019g0226 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2707+276T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677933 | |||||||
chr3:15677964 | A | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2707+245T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677964 | |||||||
chr3:15678421 | T | C | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2562-67A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15678421 | |||||||
chr3:15678615 | T | G | 121 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(118): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.2562-261A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15678615 | |||||||
chr3:15678881 | G | A | 109 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(106): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2561+420C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15678881 | |||||||
chr3:15679135 | C | CT | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2561+165dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15679135 | |||||||
chr3:15679447 | C | G | 1 | a0002c0006t0001g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2477+29G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/27 | chr3 | 15679447 | |||||||
chr3:15679467 | T | G | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2477+9A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/27 | chr3 | 15679467 | |||||||
chr3:15679647 | A | G | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2390-84T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679647 | |||||||
chr3:15679762 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2390-199G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679762 | |||||||
chr3:15679900 | A | ATTATT | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-338_2390-337i others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679900 | |||||||
chr3:15679903 | C | CCCTAAAT others(1): Show |
16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0283 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2390-341_2390-340i others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679903 | |||||||
chr3:15680765 | A | C | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1202T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680765 | |||||||
chr3:15680769 | G | C | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1206C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680769 | |||||||
chr3:15680771 | T | A | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1208A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680771 | |||||||
chr3:15680777 | C | G | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1214G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680777 | |||||||
chr3:15680778 | A | G | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1215T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680778 | |||||||
chr3:15680779 | C | G | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1216G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680779 | |||||||
chr3:15680880 | T | C | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2390-1317A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680880 | |||||||
chr3:15681015 | A | G | 1 | a0001c0001t0008g0335 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2390-1452T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681015 | |||||||
chr3:15681367 | C | G | 34 | a0001c0002t0017g0132 a0001c0002t0017g0133 a0001c0003t0005g0278 others(31): Show |
34 | HG00597.hp1 HG01109.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.2390-1804G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681367 | |||||||
chr3:15681378 | G | A | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2390-1815C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681378 | |||||||
chr3:15681670 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2390-2107T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681670 | |||||||
chr3:15681679 | T | A | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2390-2116A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681679 | |||||||
chr3:15681719 | T | C | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-2156A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681719 | |||||||
chr3:15681835 | C | T | 1 | a0001c0001t0002g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2390-2272G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681835 | |||||||
chr3:15681955 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2390-2392G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681955 | |||||||
chr3:15682078 | C | T | 1 | a0001c0001t0044g0188 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2390-2515G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682078 | |||||||
chr3:15682079 | G | A | 16 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(13): Show |
16 | HG00597.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.2390-2516C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682079 | |||||||
chr3:15682344 | C | T | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-2781G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682344 | |||||||
chr3:15682584 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2389+2642G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682584 | |||||||
chr3:15682619 | C | T | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2389+2607G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682619 | |||||||
chr3:15682626 | T | G | 125 | a0001c0001t0037g0086 a0001c0002t0001g0001 a0001c0002t0001g0018 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2389+2600A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682626 | |||||||
chr3:15682736 | G | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+2490C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682736 | |||||||
chr3:15682839 | T | C | 124 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(121): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.2389+2387A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682839 | |||||||
chr3:15683023 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+2203A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683023 | |||||||
chr3:15683172 | A | G | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2389+2054T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683172 | |||||||
chr3:15683304 | T | C | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2389+1922A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683304 | |||||||
chr3:15683597 | G | A | 3 | a0001c0001t0003g0250 a0001c0001t0003g0257 a0001c0001t0003g0259 |
3 | HG01167.hp1 HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2389+1629C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683597 | |||||||
chr3:15683856 | A | G | 2 | a0001c0001t0015g0323 a0001c0001t0015g0324 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2389+1370T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683856 | |||||||
chr3:15683945 | G | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2389+1281C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683945 | |||||||
chr3:15683965 | C | T | 8 | a0001c0002t0017g0132 a0001c0002t0017g0133 a0001c0005t0012g0317 others(5): Show |
8 | HG00597.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2389+1261G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683965 | |||||||
chr3:15684093 | A | C | 3 | a0001c0007t0021g0300 a0001c0007t0021g0301 a0001c0007t0043g0172 |
3 | NA18957.hp1 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+1133T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684093 | |||||||
chr3:15684104 | T | C | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2389+1122A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684104 | |||||||
chr3:15684210 | G | A | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2389+1016C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684210 | |||||||
chr3:15684271 | T | G | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2389+955A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684271 | |||||||
chr3:15684286 | T | C | 1 | a0001c0003t0005g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2389+940A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684286 | |||||||
chr3:15684298 | T | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2389+928A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684298 | |||||||
chr3:15684307 | A | G | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.2389+919T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684307 | |||||||
chr3:15684392 | A | G | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2389+834T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684392 | |||||||
chr3:15684486 | G | T | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2389+740C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684486 | |||||||
chr3:15684635 | T | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2389+591A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684635 | |||||||
chr3:15684654 | T | C | 124 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(121): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.2389+572A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684654 | |||||||
chr3:15684664 | T | C | 1 | a0001c0002t0017g0133 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2389+562A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684664 | |||||||
chr3:15684733 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2389+493T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684733 | |||||||
chr3:15684805 | C | G | 2 | a0001c0002t0001g0101 a0001c0002t0001g0104 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2389+421G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684805 | |||||||
chr3:15684858 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+368A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684858 | |||||||
chr3:15684983 | G | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2389+243C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684983 | |||||||
chr3:15685138 | T | G | 1 | a0001c0004t0009g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2389+88A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15685138 | |||||||
chr3:15685185 | T | C | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2389+41A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15685185 | |||||||
chr3:15685501 | A | G | 121 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(118): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.2170-56T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 20/27 | chr3 | 15685501 | |||||||
chr3:15685727 | A | G | 128 | a0001c0001t0037g0086 a0001c0002t0001g0001 a0001c0002t0001g0018 others(125): Show |
129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2169+275T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 20/27 | chr3 | 15685727 | |||||||
chr3:15686131 | C | G | 6 | a0001c0002t0001g0021 a0001c0002t0001g0038 a0001c0002t0001g0078 others(3): Show |
6 | NA18747.hp2 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2052-12G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686131 | |||||||
chr3:15686183 | C | T | 2 | a0001c0001t0015g0323 a0001c0001t0015g0324 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2051+39G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686183 | |||||||
chr3:15686195 | A | G | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2051+27T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686195 | |||||||
chr3:15686196 | T | G | 1 | a0001c0004t0009g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2051+26A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686196 | |||||||
chr3:15686316 | A | G | 112 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(109): Show |
113 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
splice_region_variant&intron_variant | LOW | c.1964-7T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686316 | |||||||
chr3:15686449 | A | C | 23 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(20): Show |
23 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1964-140T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686449 | |||||||
chr3:15686740 | C | T | 1 | a0001c0004t0009g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1964-431G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686740 | |||||||
chr3:15686845 | C | T | 1 | a0001c0002t0034g0075 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1964-536G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686845 | |||||||
chr3:15686901 | C | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0056 |
3 | HG00621.hp2 NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1964-592G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686901 | |||||||
chr3:15686902 | G | A | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG00408.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1964-593C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686902 | |||||||
chr3:15686912 | C | T | 6 | a0001c0001t0004g0236 a0001c0001t0004g0237 a0001c0001t0004g0238 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1964-603G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686912 | |||||||
chr3:15686946 | C | CT | 46 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(43): Show |
46 | HG00140.hp1 HG01109.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.1964-638dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686946 | |||||||
chr3:15686947 | T | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1964-638A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686947 | |||||||
chr3:15686982 | C | T | 16 | a0001c0002t0001g0080 a0001c0002t0001g0081 a0001c0002t0001g0088 others(13): Show |
16 | HG00639.hp2 HG02004.hp1 HG02273.hp2 others(13): Show |
intron_variant | MODIFIER | c.1964-673G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686982 | |||||||
chr3:15687099 | C | T | 3 | a0001c0003t0019g0225 a0001c0003t0019g0226 a0001c0003t0051g0311 |
3 | HG03209.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1964-790G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687099 | |||||||
chr3:15687104 | G | A | 2 | a0001c0001t0008g0330 a0001c0001t0008g0331 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1964-795C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687104 | |||||||
chr3:15687106 | C | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1964-797G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687106 | |||||||
chr3:15687180 | T | C | 274 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(271): Show |
276 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.1964-871A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687180 | |||||||
chr3:15687223 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1964-914T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687223 | |||||||
chr3:15687250 | C | G | 293 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(290): Show |
295 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.1964-941G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687250 | |||||||
chr3:15687308 | T | C | 7 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(4): Show |
7 | NA18940.hp2 NA18942.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1964-999A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687308 | |||||||
chr3:15687332 | G | GAT | 7 | a0001c0002t0017g0132 a0001c0002t0017g0133 a0001c0005t0012g0318 others(4): Show |
7 | HG00597.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1964-1025_1964-102 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687332 | |||||||
chr3:15687333 | A | T | 1 | a0001c0001t0008g0334 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1964-1024T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687333 | |||||||
chr3:15687547 | A | C | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1964-1238T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687547 | |||||||
chr3:15687566 | G | A | 1 | a0001c0002t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1964-1257C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687566 | |||||||
chr3:15687652 | T | TGGAACAT others(17): Show |
1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1964-1344_1964-134 others(28): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687652 | |||||||
chr3:15687656 | A | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1964-1347T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687656 | |||||||
chr3:15687659 | A | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1964-1350T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687659 | |||||||
chr3:15687684 | G | T | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1964-1375C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687684 | |||||||
chr3:15687817 | T | G | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1964-1508A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687817 | |||||||
chr3:15687890 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1964-1581T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687890 | |||||||
chr3:15688062 | T | C | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1964-1753A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688062 | |||||||
chr3:15688078 | T | C | 1 | a0001c0004t0009g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1964-1769A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688078 | |||||||
chr3:15688207 | C | G | 127 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1963+1812G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688207 | |||||||
chr3:15688246 | A | T | 7 | a0001c0002t0011g0231 a0001c0002t0011g0232 a0002c0006t0001g0042 others(4): Show |
7 | HG00642.hp1 HG01109.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1963+1773T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688246 | |||||||
chr3:15688274 | T | C | 1 | a0001c0001t0002g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1963+1745A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688274 | |||||||
chr3:15688750 | G | A | 127 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1963+1269C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688750 | |||||||
chr3:15688785 | T | C | 141 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(138): Show |
142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1963+1234A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688785 | |||||||
chr3:15688821 | A | G | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1963+1198T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688821 | |||||||
chr3:15688829 | A | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1963+1190T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688829 | |||||||
chr3:15688914 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1963+1105G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688914 | |||||||
chr3:15689372 | T | C | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1963+647A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689372 | |||||||
chr3:15689528 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1963+491C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689528 | |||||||
chr3:15689577 | A | G | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1963+442T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689577 | |||||||
chr3:15689759 | G | C | 1 | a0001c0001t0003g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1963+260C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689759 | |||||||
chr3:15690573 | G | T | 1 | a0001c0003t0005g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1762-353C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690573 | |||||||
chr3:15690653 | C | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1762-433G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690653 | |||||||
chr3:15690665 | A | C | 2 | a0001c0001t0006g0309 a0001c0001t0006g0310 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1762-445T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690665 | |||||||
chr3:15690714 | G | A | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1762-494C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690714 | |||||||
chr3:15690749 | G | T | 125 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1762-529C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690749 | |||||||
chr3:15690778 | G | C | 1 | a0001c0002t0001g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1762-558C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690778 | |||||||
chr3:15690786 | C | T | 1 | a0001c0001t0003g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1762-566G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690786 | |||||||
chr3:15690895 | A | G | 1 | a0001c0002t0001g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1762-675T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690895 | |||||||
chr3:15690896 | G | T | 1 | a0001c0002t0001g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1762-676C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690896 | |||||||
chr3:15691032 | T | G | 133 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1762-812A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691032 | |||||||
chr3:15691037 | A | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1762-817T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691037 | |||||||
chr3:15691125 | CT | C | 11 | a0001c0001t0002g0156 a0001c0001t0002g0216 a0001c0001t0004g0243 others(8): Show |
11 | HG00558.hp2 HG01169.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.1762-906delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691125 | |||||||
chr3:15691218 | G | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1762-998C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691218 | |||||||
chr3:15691280 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1762-1060A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691280 | |||||||
chr3:15691366 | G | A | 151 | a0001c0001t0002g0207 a0001c0002t0001g0001 a0001c0002t0001g0018 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1762-1146C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691366 | |||||||
chr3:15691489 | T | C | 1 | a0001c0004t0009g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1762-1269A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691489 | |||||||
chr3:15691654 | T | C | 5 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(2): Show |
5 | NA18942.hp2 NA18966.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-1434A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691654 | |||||||
chr3:15691707 | T | C | 38 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1762-1487A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691707 | |||||||
chr3:15691838 | G | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1762-1618C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691838 | |||||||
chr3:15691998 | G | A | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1762-1778C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691998 | |||||||
chr3:15692005 | TG | T | 7 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-1786delC | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692005 | |||||||
chr3:15692011 | ATGCCT | A | 7 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-1796_1762-179 others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692011 | |||||||
chr3:15692017 | G | C | 7 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-1797C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692017 | |||||||
chr3:15692045 | C | T | 135 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1762-1825G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692045 | |||||||
chr3:15692063 | C | G | 1 | a0001c0001t0002g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1762-1843G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692063 | |||||||
chr3:15692093 | A | T | 152 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(149): Show |
153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1762-1873T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692093 | |||||||
chr3:15692139 | C | T | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1762-1919G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692139 | |||||||
chr3:15692144 | T | TA | 121 | a0001c0001t0002g0146 a0001c0001t0002g0161 a0001c0001t0015g0324 others(118): Show |
122 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1762-1925dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692144 | |||||||
chr3:15692144 | T | TAA | 40 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(37): Show |
41 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1762-1926_1762-192 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692144 | |||||||
chr3:15692147 | A | T | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1762-1927T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692147 | |||||||
chr3:15692285 | C | A | 25 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(22): Show |
25 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1762-2065G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692285 | |||||||
chr3:15692337 | T | C | 1 | a0001c0001t0002g0198 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1762-2117A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692337 | |||||||
chr3:15692390 | T | C | 164 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(161): Show |
165 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1762-2170A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692390 | |||||||
chr3:15692589 | C | G | 154 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(151): Show |
155 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1761+2150G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692589 | |||||||
chr3:15692813 | T | C | 3 | a0001c0001t0004g0238 a0001c0001t0004g0240 a0001c0001t0004g0245 |
3 | HG02258.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1761+1926A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692813 | |||||||
chr3:15692814 | A | G | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1761+1925T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692814 | |||||||
chr3:15692863 | G | T | 1 | a0001c0001t0003g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1761+1876C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692863 | |||||||
chr3:15692946 | G | A | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+1793C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692946 | |||||||
chr3:15692948 | C | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1761+1791G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692948 | |||||||
chr3:15693146 | C | A | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1761+1593G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693146 | |||||||
chr3:15693194 | A | T | 2 | a0001c0002t0001g0040 a0001c0002t0035g0039 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1761+1545T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693194 | |||||||
chr3:15693206 | C | T | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1761+1533G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693206 | |||||||
chr3:15693246 | T | C | 1 | a0001c0001t0002g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1761+1493A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693246 | |||||||
chr3:15693327 | C | CAG | 13 | a0001c0002t0042g0131 a0001c0003t0005g0278 a0001c0003t0005g0279 others(10): Show |
13 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1761+1410_1761+141 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693327 | |||||||
chr3:15693376 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1761+1363G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693376 | |||||||
chr3:15693405 | A | C | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1761+1334T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693405 | |||||||
chr3:15693426 | G | A | 2 | a0001c0001t0008g0330 a0001c0001t0008g0331 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1761+1313C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693426 | |||||||
chr3:15693474 | A | G | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1761+1265T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693474 | |||||||
chr3:15693517 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1761+1222A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693517 | |||||||
chr3:15693544 | C | G | 161 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(158): Show |
162 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1761+1195G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693544 | |||||||
chr3:15693605 | A | ATGC | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1761+1131_1761+113 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693605 | |||||||
chr3:15693930 | G | A | 1 | a0001c0001t0008g0334 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1761+809C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693930 | |||||||
chr3:15694115 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1761+624A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694115 | |||||||
chr3:15694146 | T | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1761+593A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694146 | |||||||
chr3:15694214 | G | GA | 129 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1761+524dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694214 | |||||||
chr3:15694360 | C | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1761+379G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694360 | |||||||
chr3:15694493 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1761+246C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694493 | |||||||
chr3:15694612 | T | G | 1 | a0001c0002t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1761+127A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694612 | |||||||
chr3:15694717 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1761+22G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694717 | |||||||
chr3:15694723 | T | A | 1 | a0001c0001t0002g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1761+16A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694723 | |||||||
chr3:15694838 | T | A | 6 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(3): Show |
6 | HG01433.hp2 NA18940.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1687-25A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 16/27 | chr3 | 15694838 | |||||||
chr3:15695164 | G | A | 2 | a0001c0001t0002g0157 a0001c0005t0012g0317 |
2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1686+24C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 16/27 | chr3 | 15695164 | |||||||
chr3:15695304 | C | T | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1660-90G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695304 | |||||||
chr3:15695321 | C | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1660-107G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695321 | |||||||
chr3:15695424 | C | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1660-210G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695424 | |||||||
chr3:15695436 | G | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1660-222C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695436 | |||||||
chr3:15695510 | G | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1660-296C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695510 | |||||||
chr3:15695539 | C | G | 1 | a0001c0002t0001g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1660-325G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695539 | |||||||
chr3:15695549 | T | C | 2 | a0001c0002t0001g0105 a0001c0005t0012g0318 |
2 | HG00099.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1660-335A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695549 | |||||||
chr3:15695652 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1660-438C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695652 | |||||||
chr3:15695742 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1659+392A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695742 | |||||||
chr3:15695771 | C | T | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1659+363G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695771 | |||||||
chr3:15695807 | C | T | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1659+327G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695807 | |||||||
chr3:15696103 | T | C | 138 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1659+31A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15696103 | |||||||
chr3:15696317 | A | G | 1 | a0001c0001t0046g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1548-72T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696317 | |||||||
chr3:15696375 | C | T | 3 | a0001c0005t0012g0317 a0001c0010t0012g0315 a0001c0010t0012g0316 |
3 | HG02622.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1548-130G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696375 | |||||||
chr3:15696463 | G | A | 1 | a0001c0002t0001g0030 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1548-218C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696463 | |||||||
chr3:15696583 | C | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1548-338G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696583 | |||||||
chr3:15696620 | T | C | 1 | a0002c0006t0001g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1548-375A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696620 | |||||||
chr3:15696675 | A | T | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1548-430T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696675 | |||||||
chr3:15696808 | G | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1548-563C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696808 | |||||||
chr3:15696833 | A | C | 6 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(3): Show |
6 | NA18942.hp2 NA18951.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1548-588T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696833 | |||||||
chr3:15696882 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1548-637A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696882 | |||||||
chr3:15696952 | A | G | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1548-707T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696952 | |||||||
chr3:15697011 | G | A | 16 | a0001c0001t0002g0178 a0001c0001t0002g0180 a0001c0001t0002g0181 others(13): Show |
16 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.1548-766C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697011 | |||||||
chr3:15697066 | C | G | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-821G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697066 | |||||||
chr3:15697139 | G | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1548-894C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697139 | |||||||
chr3:15697214 | G | A | 1 | a0001c0003t0019g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1548-969C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697214 | |||||||
chr3:15697282 | G | C | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1548-1037C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697282 | |||||||
chr3:15697363 | T | C | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1548-1118A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697363 | |||||||
chr3:15697477 | A | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1548-1232T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697477 | |||||||
chr3:15697504 | G | A | 1 | a0001c0001t0003g0258 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1548-1259C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697504 | |||||||
chr3:15697511 | T | G | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-1266A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697511 | |||||||
chr3:15697612 | T | G | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1548-1367A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697612 | |||||||
chr3:15697674 | C | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-1429G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697674 | |||||||
chr3:15697697 | T | C | 255 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(252): Show |
257 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1548-1452A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697697 | |||||||
chr3:15697839 | C | T | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1548-1594G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697839 | |||||||
chr3:15697894 | T | C | 129 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1548-1649A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697894 | |||||||
chr3:15698017 | C | T | 8 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0020g0298 others(5): Show |
8 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1548-1772G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698017 | |||||||
chr3:15698077 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1548-1832A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698077 | |||||||
chr3:15698174 | C | T | 4 | a0001c0002t0001g0057 a0001c0002t0001g0093 a0001c0002t0001g0094 others(1): Show |
4 | HG00558.hp1 NA19000.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548-1929G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698174 | |||||||
chr3:15698177 | C | A | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1548-1932G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698177 | |||||||
chr3:15698270 | C | A | 23 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(20): Show |
23 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1548-2025G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698270 | |||||||
chr3:15698299 | A | C | 129 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1548-2054T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698299 | |||||||
chr3:15698314 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1548-2069G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698314 | |||||||
chr3:15698329 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1548-2084G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698329 | |||||||
chr3:15698336 | G | A | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1548-2091C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698336 | |||||||
chr3:15698368 | T | C | 249 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(246): Show |
251 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1548-2123A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698368 | |||||||
chr3:15698566 | G | A | 24 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1548-2321C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698566 | |||||||
chr3:15698578 | G | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1548-2333C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698578 | |||||||
chr3:15698675 | A | C | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1548-2430T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698675 | |||||||
chr3:15698872 | C | G | 120 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(117): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1548-2627G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698872 | |||||||
chr3:15698935 | C | G | 1 | a0001c0002t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1548-2690G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698935 | |||||||
chr3:15698951 | G | T | 133 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1548-2706C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698951 | |||||||
chr3:15699122 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1548-2877G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699122 | |||||||
chr3:15699211 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1548-2966G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699211 | |||||||
chr3:15699287 | C | T | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548-3042G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699287 | |||||||
chr3:15699392 | G | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-3147C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699392 | |||||||
chr3:15699396 | TCTAATTA others(3): Show |
T | 1 | a0001c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1548-3161_1548-315 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699396 | |||||||
chr3:15699502 | G | A | 129 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1548-3257C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699502 | |||||||
chr3:15699624 | A | G | 1 | a0001c0001t0008g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1548-3379T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699624 | |||||||
chr3:15699755 | G | A | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1548-3510C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699755 | |||||||
chr3:15699789 | A | C | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1548-3544T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699789 | |||||||
chr3:15699882 | T | C | 129 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1548-3637A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699882 | |||||||
chr3:15699932 | A | C | 266 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(263): Show |
268 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1548-3687T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699932 | |||||||
chr3:15699936 | G | A | 14 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1548-3691C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699936 | |||||||
chr3:15700092 | A | G | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1548-3847T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700092 | |||||||
chr3:15700169 | C | T | 24 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1548-3924G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700169 | |||||||
chr3:15700286 | G | A | 154 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(151): Show |
155 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1548-4041C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700286 | |||||||
chr3:15700300 | G | T | 1 | a0001c0001t0008g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1548-4055C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700300 | |||||||
chr3:15700304 | G | A | 7 | a0001c0001t0002g0143 a0001c0001t0002g0145 a0001c0001t0002g0167 others(4): Show |
7 | HG00423.hp2 HG02132.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-4059C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700304 | |||||||
chr3:15700306 | G | GC | 5 | a0001c0001t0002g0162 a0001c0001t0015g0324 a0001c0002t0001g0054 others(2): Show |
5 | HG02056.hp2 HG03927.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548-4062dupG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700306 | |||||||
chr3:15700458 | C | CA | 152 | a0001c0001t0002g0162 a0001c0001t0002g0194 a0001c0002t0001g0001 others(149): Show |
153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1548-4214dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700458 | |||||||
chr3:15700502 | G | A | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1548-4257C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700502 | |||||||
chr3:15700502 | G | C | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1548-4257C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700502 | |||||||
chr3:15700542 | G | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1548-4297C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700542 | |||||||
chr3:15700599 | T | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-4354A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700599 | |||||||
chr3:15700599 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1548-4354A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700599 | |||||||
chr3:15700632 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1548-4387C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700632 | |||||||
chr3:15700646 | C | T | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1548-4401G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700646 | |||||||
chr3:15700730 | C | T | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | HG00423.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1548-4485G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700730 | |||||||
chr3:15700731 | G | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-4486C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700731 | |||||||
chr3:15700782 | A | G | 45 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(42): Show |
46 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1548-4537T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700782 | |||||||
chr3:15700829 | A | G | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-4584T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700829 | |||||||
chr3:15700830 | A | G | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548-4585T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700830 | |||||||
chr3:15701002 | C | T | 1 | a0001c0002t0001g0051 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1548-4757G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701002 | |||||||
chr3:15701158 | T | C | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1548-4913A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701158 | |||||||
chr3:15701315 | T | C | 318 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(315): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1548-5070A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701315 | |||||||
chr3:15701401 | T | C | 1 | a0001c0002t0001g0053 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1548-5156A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701401 | |||||||
chr3:15701528 | C | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1548-5283G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701528 | |||||||
chr3:15701569 | A | T | 7 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(4): Show |
7 | HG01433.hp2 NA18940.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-5324T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701569 | |||||||
chr3:15701622 | CAAG | C | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-5380_1548-537 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701622 | |||||||
chr3:15701647 | A | AAAAT | 7 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0020g0298 others(4): Show |
7 | HG02145.hp2 HG02622.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-5406_1548-540 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701647 | |||||||
chr3:15701647 | A | AAAATAAA others(9): Show |
1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1548-5418_1548-540 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701647 | |||||||
chr3:15701696 | T | C | 10 | a0001c0002t0001g0041 a0001c0002t0001g0043 a0001c0002t0001g0044 others(7): Show |
10 | HG00642.hp2 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1548-5451A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701696 | |||||||
chr3:15701947 | A | G | 1 | a0001c0001t0023g0004 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1548-5702T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701947 | |||||||
chr3:15701972 | T | TTA | 14 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1548-5729_1548-572 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701972 | |||||||
chr3:15702139 | C | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+5785G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702139 | |||||||
chr3:15702214 | C | T | 177 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1547+5710G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702214 | |||||||
chr3:15702245 | C | G | 8 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0020g0298 others(5): Show |
8 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1547+5679G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702245 | |||||||
chr3:15702337 | A | G | 175 | a0001c0001t0003g0256 a0001c0001t0006g0302 a0001c0001t0006g0303 others(172): Show |
176 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1547+5587T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702337 | |||||||
chr3:15702357 | G | A | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | NA18969.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1547+5567C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702357 | |||||||
chr3:15702383 | C | T | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547+5541G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702383 | |||||||
chr3:15702419 | G | A | 1 | a0001c0001t0002g0221 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1547+5505C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702419 | |||||||
chr3:15702443 | C | G | 3 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0011g0230 |
3 | NA18948.hp2 NA18967.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1547+5481G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702443 | |||||||
chr3:15702659 | T | C | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547+5265A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702659 | |||||||
chr3:15702689 | G | C | 1 | a0001c0002t0001g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1547+5235C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702689 | |||||||
chr3:15702899 | A | G | 120 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(117): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1547+5025T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702899 | |||||||
chr3:15703303 | A | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1547+4621T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703303 | |||||||
chr3:15703422 | A | G | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547+4502T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703422 | |||||||
chr3:15703595 | C | G | 1 | a0001c0001t0028g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1547+4329G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703595 | |||||||
chr3:15703653 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1547+4271G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703653 | |||||||
chr3:15703746 | G | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+4178C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703746 | |||||||
chr3:15703915 | A | G | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1547+4009T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703915 | |||||||
chr3:15704041 | T | C | 1 | a0001c0001t0006g0304 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1547+3883A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704041 | |||||||
chr3:15704197 | T | C | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02155.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1547+3727A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704197 | |||||||
chr3:15704204 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1547+3720T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704204 | |||||||
chr3:15704299 | T | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | NA18986.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1547+3625A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704299 | |||||||
chr3:15704703 | AT | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547+3220delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704703 | |||||||
chr3:15704727 | T | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1547+3197A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704727 | |||||||
chr3:15704767 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1547+3157T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704767 | |||||||
chr3:15704830 | C | A | 1 | a0001c0001t0003g0258 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1547+3094G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704830 | |||||||
chr3:15704878 | C | A | 1 | a0001c0002t0001g0073 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1547+3046G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704878 | |||||||
chr3:15704927 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1547+2997A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704927 | |||||||
chr3:15705089 | C | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1547+2835G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705089 | |||||||
chr3:15705236 | A | C | 1 | a0001c0001t0002g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1547+2688T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705236 | |||||||
chr3:15705318 | C | T | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1547+2606G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705318 | |||||||
chr3:15705336 | G | C | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547+2588C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705336 | |||||||
chr3:15705353 | G | A | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1547+2571C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705353 | |||||||
chr3:15705430 | G | A | 146 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(143): Show |
147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1547+2494C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705430 | |||||||
chr3:15705453 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1547+2471A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705453 | |||||||
chr3:15705696 | A | G | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1547+2228T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705696 | |||||||
chr3:15705858 | G | GCAC | 122 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(119): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1547+2065_1547+206 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705858 | |||||||
chr3:15706047 | C | CA | 177 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1547+1876dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706047 | |||||||
chr3:15706047 | CAAAA | C | 3 | a0001c0001t0010g0272 a0001c0001t0010g0273 a0001c0001t0010g0274 |
3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1547+1873_1547+187 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706047 | |||||||
chr3:15706071 | T | G | 1 | a0001c0001t0058g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1547+1853A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706071 | |||||||
chr3:15706073 | G | T | 37 | a0001c0001t0002g0134 a0001c0001t0002g0156 a0001c0001t0002g0157 others(34): Show |
37 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1547+1851C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706073 | |||||||
chr3:15706102 | T | G | 3 | a0001c0001t0015g0323 a0001c0001t0015g0324 a0001c0001t0015g0325 |
3 | HG02683.hp2 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1547+1822A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706102 | |||||||
chr3:15706197 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1547+1727G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706197 | |||||||
chr3:15706236 | C | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547+1688G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706236 | |||||||
chr3:15706359 | C | A | 1 | a0001c0002t0001g0081 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1547+1565G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706359 | |||||||
chr3:15706359 | C | T | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547+1565G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706359 | |||||||
chr3:15706410 | G | A | 2 | a0001c0002t0001g0110 a0001c0002t0001g0111 |
2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1547+1514C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706410 | |||||||
chr3:15706417 | ACTC | A | 151 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1547+1504_1547+150 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706417 | |||||||
chr3:15706522 | C | T | 22 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(19): Show |
22 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1547+1402G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706522 | |||||||
chr3:15706533 | A | G | 22 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(19): Show |
22 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1547+1391T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706533 | |||||||
chr3:15706537 | T | C | 1 | a0001c0002t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1547+1387A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706537 | |||||||
chr3:15706539 | A | G | 1 | a0001c0002t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1547+1385T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706539 | |||||||
chr3:15706654 | T | G | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1547+1270A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706654 | |||||||
chr3:15706723 | C | T | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | NA19005.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1547+1201G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706723 | |||||||
chr3:15706886 | T | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+1038A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706886 | |||||||
chr3:15706892 | A | T | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1547+1032T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706892 | |||||||
chr3:15706945 | A | C | 1 | a0001c0001t0003g0255 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1547+979T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706945 | |||||||
chr3:15707071 | G | A | 24 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1547+853C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707071 | |||||||
chr3:15707155 | T | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+769A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707155 | |||||||
chr3:15707249 | G | A | 4 | a0001c0001t0016g0326 a0001c0001t0016g0327 a0001c0001t0016g0329 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+675C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707249 | |||||||
chr3:15707258 | GA | G | 135 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1547+665delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707258 | |||||||
chr3:15707400 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1547+524G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707400 | |||||||
chr3:15707459 | A | G | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547+465T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707459 | |||||||
chr3:15707493 | C | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1547+431G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707493 | |||||||
chr3:15707706 | C | T | 131 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(128): Show |
132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1547+218G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707706 | |||||||
chr3:15707807 | A | ATT | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547+116_1547+117i others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707807 | |||||||
chr3:15707841 | C | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+83G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707841 | |||||||
chr3:15707845 | T | C | 100 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(97): Show |
101 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1547+79A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707845 | |||||||
chr3:15708103 | G | A | 1 | a0001c0001t0008g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1407-39C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708103 | |||||||
chr3:15708549 | G | A | 137 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(134): Show |
138 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1407-485C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708549 | |||||||
chr3:15708573 | T | C | 4 | a0001c0001t0016g0326 a0001c0001t0016g0327 a0001c0001t0016g0329 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1407-509A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708573 | |||||||
chr3:15708586 | G | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1407-522C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708586 | |||||||
chr3:15708663 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1407-599C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708663 | |||||||
chr3:15708696 | G | A | 124 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1407-632C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708696 | |||||||
chr3:15708761 | G | A | 127 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1407-697C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708761 | |||||||
chr3:15708837 | A | C | 257 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(254): Show |
259 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1407-773T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708837 | |||||||
chr3:15708985 | C | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1406+683G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708985 | |||||||
chr3:15709182 | G | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406+486C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15709182 | |||||||
chr3:15709377 | T | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1406+291A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15709377 | |||||||
chr3:15709534 | G | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1406+134C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15709534 | |||||||
chr3:15709820 | T | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338-84A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15709820 | |||||||
chr3:15709821 | G | A | 1 | a0001c0002t0001g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1338-85C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15709821 | |||||||
chr3:15709900 | A | G | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1338-164T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15709900 | |||||||
chr3:15710036 | G | GT | 289 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(286): Show |
291 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.1338-301dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710036 | |||||||
chr3:15710076 | T | A | 148 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1338-340A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710076 | |||||||
chr3:15710077 | T | C | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.1338-341A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710077 | |||||||
chr3:15710142 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1338-406G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710142 | |||||||
chr3:15710398 | G | C | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1338-662C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710398 | |||||||
chr3:15710446 | C | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1338-710G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710446 | |||||||
chr3:15710487 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1337+724G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710487 | |||||||
chr3:15710621 | T | C | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1337+590A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710621 | |||||||
chr3:15710780 | T | C | 1 | a0001c0002t0022g0003 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1337+431A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710780 | |||||||
chr3:15711068 | C | T | 1 | a0001c0002t0013g0015 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1337+143G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15711068 | |||||||
chr3:15711098 | T | C | 2 | a0001c0001t0004g0234 a0001c0001t0004g0235 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1337+113A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15711098 | |||||||
chr3:15711125 | GAATT | G | 5 | a0001c0001t0003g0252 a0001c0001t0003g0253 a0001c0001t0003g0254 others(2): Show |
5 | NA18957.hp2 NA18961.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.1337+82_1337+85del others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15711125 | |||||||
chr3:15711322 | C | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1274-48G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711322 | |||||||
chr3:15711323 | T | C | 129 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1274-49A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711323 | |||||||
chr3:15711593 | T | C | 120 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(117): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1274-319A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711593 | |||||||
chr3:15711792 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1273+348A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711792 | |||||||
chr3:15711843 | C | G | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+297G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711843 | |||||||
chr3:15711843 | C | T | 129 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1273+297G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711843 | |||||||
chr3:15711865 | A | AT | 124 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1273+274dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711865 | |||||||
chr3:15711865 | A | ATT | 7 | a0001c0002t0001g0030 a0001c0002t0001g0068 a0001c0002t0001g0069 others(4): Show |
7 | HG00673.hp1 HG02145.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273+273_1273+274d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711865 | |||||||
chr3:15711885 | G | A | 1 | a0007c0011t0003g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1273+255C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711885 | |||||||
chr3:15711963 | T | C | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273+177A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711963 | |||||||
chr3:15712002 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1273+138G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15712002 | |||||||
chr3:15712029 | T | G | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1273+111A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15712029 | |||||||
chr3:15712134 | A | G | 124 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
splice_region_variant&intron_variant | LOW | c.1273+6T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15712134 | |||||||
chr3:15712245 | G | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191-23C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712245 | |||||||
chr3:15712361 | A | G | 120 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(117): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1191-139T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712361 | |||||||
chr3:15712389 | G | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1191-167C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712389 | |||||||
chr3:15712557 | C | T | 2 | a0001c0001t0008g0333 a0001c0001t0008g0338 |
2 | NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1191-335G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712557 | |||||||
chr3:15712568 | A | G | 1 | a0001c0001t0006g0306 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1191-346T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712568 | |||||||
chr3:15712740 | T | C | 257 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(254): Show |
259 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1191-518A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712740 | |||||||
chr3:15713031 | A | G | 133 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1190+496T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15713031 | |||||||
chr3:15713342 | C | T | 155 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(152): Show |
156 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1190+185G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15713342 | |||||||
chr3:15713478 | C | T | 20 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1190+49G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15713478 | |||||||
chr3:15713669 | C | A | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1076-28G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713669 | |||||||
chr3:15713696 | G | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1076-55C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713696 | |||||||
chr3:15713862 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1076-221A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713862 | |||||||
chr3:15713889 | A | C | 3 | a0001c0002t0001g0057 a0001c0002t0001g0093 a0001c0002t0001g0094 |
3 | HG00558.hp1 NA19000.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1076-248T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713889 | |||||||
chr3:15713900 | A | G | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1076-259T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713900 | |||||||
chr3:15713983 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1076-342G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713983 | |||||||
chr3:15714299 | G | A | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1075+279C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714299 | |||||||
chr3:15714532 | G | GA | 33 | a0001c0001t0001g0072 a0001c0001t0002g0140 a0001c0001t0002g0157 others(30): Show |
33 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1075+45dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714532 | |||||||
chr3:15714532 | G | GAA | 114 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(111): Show |
115 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1075+44_1075+45dup others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714532 | |||||||
chr3:15714532 | G | GAAA | 10 | a0001c0002t0001g0063 a0001c0002t0001g0065 a0001c0002t0001g0094 others(7): Show |
10 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075+43_1075+45dup others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714532 | |||||||
chr3:15714552 | A | C | 1 | a0001c0001t0006g0312 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1075+26T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714552 | |||||||
chr3:15714661 | G | T | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.997-5C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15714661 | |||||||
chr3:15714708 | A | T | 177 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(174): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.997-52T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15714708 | |||||||
chr3:15714835 | G | A | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.997-179C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15714835 | |||||||
chr3:15715048 | AT | A | 3 | a0001c0001t0001g0072 a0001c0001t0003g0260 a0001c0001t0003g0261 |
3 | HG01069.hp1 HG01071.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.997-393delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715048 | |||||||
chr3:15715291 | G | A | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.997-635C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715291 | |||||||
chr3:15715453 | T | G | 8 | a0001c0001t0002g0134 a0001c0001t0002g0156 a0001c0001t0002g0157 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.997-797A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715453 | |||||||
chr3:15715526 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.997-870A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715526 | |||||||
chr3:15715559 | T | C | 3 | a0001c0003t0019g0225 a0001c0003t0019g0226 a0001c0003t0051g0311 |
3 | HG03209.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.997-903A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715559 | |||||||
chr3:15715766 | G | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-1110C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715766 | |||||||
chr3:15716068 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.997-1412G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716068 | |||||||
chr3:15716069 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.997-1413C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716069 | |||||||
chr3:15716124 | A | C | 1 | a0001c0001t0028g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.997-1468T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716124 | |||||||
chr3:15716281 | C | CT | 12 | a0001c0001t0002g0138 a0001c0001t0002g0168 a0001c0001t0002g0217 others(9): Show |
12 | HG01109.hp2 HG02602.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.997-1626dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716281 | |||||||
chr3:15716281 | CT | C | 20 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0216 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.997-1626delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716281 | |||||||
chr3:15716394 | T | C | 130 | a0001c0001t0002g0174 a0001c0002t0001g0001 a0001c0002t0001g0018 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.997-1738A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716394 | |||||||
chr3:15716642 | T | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.997-1986A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716642 | |||||||
chr3:15716674 | C | T | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG00408.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.997-2018G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716674 | |||||||
chr3:15716775 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.997-2119T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716775 | |||||||
chr3:15716822 | C | T | 1 | a0001c0002t0001g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.997-2166G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716822 | |||||||
chr3:15717003 | T | G | 1 | a0001c0001t0002g0203 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.997-2347A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717003 | |||||||
chr3:15717502 | T | G | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.997-2846A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717502 | |||||||
chr3:15717543 | T | G | 125 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.997-2887A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717543 | |||||||
chr3:15717733 | C | T | 252 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.997-3077G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717733 | |||||||
chr3:15717764 | T | A | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.997-3108A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717764 | |||||||
chr3:15717853 | T | A | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.996+3062A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717853 | |||||||
chr3:15717856 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.996+3059G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717856 | |||||||
chr3:15717899 | T | C | 20 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.996+3016A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717899 | |||||||
chr3:15717984 | A | G | 254 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(251): Show |
256 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.996+2931T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717984 | |||||||
chr3:15718073 | A | G | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.996+2842T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718073 | |||||||
chr3:15718098 | A | G | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.996+2817T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718098 | |||||||
chr3:15718123 | T | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.996+2792A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718123 | |||||||
chr3:15718149 | A | G | 3 | a0001c0001t0015g0323 a0001c0001t0015g0324 a0001c0001t0015g0325 |
3 | HG02683.hp2 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.996+2766T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718149 | |||||||
chr3:15718290 | T | C | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+2625A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718290 | |||||||
chr3:15718442 | T | A | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.996+2473A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718442 | |||||||
chr3:15718490 | C | T | 1 | a0001c0001t0004g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.996+2425G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718490 | |||||||
chr3:15718550 | T | C | 1 | a0002c0006t0001g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.996+2365A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718550 | |||||||
chr3:15718733 | A | C | 1 | a0001c0001t0002g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.996+2182T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718733 | |||||||
chr3:15718789 | A | G | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.996+2126T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718789 | |||||||
chr3:15718833 | C | T | 252 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.996+2082G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718833 | |||||||
chr3:15718955 | C | T | 254 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(251): Show |
256 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.996+1960G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718955 | |||||||
chr3:15718967 | A | G | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.996+1948T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718967 | |||||||
chr3:15719014 | A | G | 3 | a0001c0002t0011g0231 a0001c0002t0011g0232 a0003c0015t0011g0229 |
3 | HG01255.hp1 HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.996+1901T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719014 | |||||||
chr3:15719252 | C | T | 2 | a0001c0001t0004g0243 a0001c0001t0004g0244 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.996+1663G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719252 | |||||||
chr3:15719455 | C | A | 254 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(251): Show |
256 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.996+1460G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719455 | |||||||
chr3:15719820 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.996+1095T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719820 | |||||||
chr3:15719852 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.996+1063G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719852 | |||||||
chr3:15720155 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.996+760A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720155 | |||||||
chr3:15720218 | C | CA | 20 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(17): Show |
20 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.996+696dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720218 | |||||||
chr3:15720228 | C | A | 1 | a0001c0004t0009g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.996+687G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720228 | |||||||
chr3:15720272 | T | A | 1 | a0001c0001t0004g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.996+643A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720272 | |||||||
chr3:15720554 | G | GACAAATG others(29): Show |
1 | a0002c0006t0001g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.996+325_996+360dup others(36): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720554 | |||||||
chr3:15720613 | C | A | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.996+302G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720613 | |||||||
chr3:15720698 | CCCA | C | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.996+214_996+216del others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720698 | |||||||
chr3:15720702 | T | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.996+213A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720702 | |||||||
chr3:15721189 | C | G | 45 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(42): Show |
46 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.784-62G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721189 | |||||||
chr3:15721235 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.784-108G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721235 | |||||||
chr3:15721340 | G | A | 135 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.784-213C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721340 | |||||||
chr3:15721363 | G | T | 3 | a0001c0001t0010g0272 a0001c0001t0010g0273 a0001c0001t0010g0274 |
3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.784-236C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721363 | |||||||
chr3:15721395 | A | G | 1 | a0001c0001t0003g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.784-268T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721395 | |||||||
chr3:15721413 | C | T | 135 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.784-286G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721413 | |||||||
chr3:15721588 | A | G | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.784-461T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721588 | |||||||
chr3:15721636 | T | A | 5 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(2): Show |
5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-509A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721636 | |||||||
chr3:15721848 | G | A | 3 | a0001c0005t0012g0317 a0001c0010t0012g0315 a0001c0010t0012g0316 |
3 | HG02622.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.784-721C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721848 | |||||||
chr3:15721990 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.784-863G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721990 | |||||||
chr3:15722024 | C | T | 7 | a0001c0001t0002g0134 a0001c0001t0002g0156 a0001c0001t0002g0157 others(4): Show |
7 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-897G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722024 | |||||||
chr3:15722066 | A | G | 46 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(43): Show |
47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.784-939T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722066 | |||||||
chr3:15722277 | T | C | 1 | a0001c0001t0004g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.784-1150A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722277 | |||||||
chr3:15722464 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.784-1337G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722464 | |||||||
chr3:15722591 | A | G | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.784-1464T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722591 | |||||||
chr3:15722592 | T | C | 1 | a0001c0001t0058g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.784-1465A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722592 | |||||||
chr3:15722921 | C | G | 276 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(273): Show |
278 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.783+1461G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722921 | |||||||
chr3:15723084 | A | AT | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1297_783+1298i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723084 | |||||||
chr3:15723085 | A | C | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1297T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723085 | |||||||
chr3:15723086 | T | C | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1296A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723086 | |||||||
chr3:15723119 | C | T | 11 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1263G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723119 | |||||||
chr3:15723192 | T | G | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.783+1190A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723192 | |||||||
chr3:15723248 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.783+1134C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723248 | |||||||
chr3:15723411 | T | C | 1 | a0001c0007t0021g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.783+971A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723411 | |||||||
chr3:15723459 | A | T | 1 | a0001c0007t0021g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.783+923T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723459 | |||||||
chr3:15723503 | G | A | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.783+879C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723503 | |||||||
chr3:15723632 | T | TA | 20 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(17): Show |
20 | HG00408.hp2 HG01433.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.783+749dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723632 | |||||||
chr3:15723760 | C | G | 1 | a0002c0006t0001g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.783+622G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723760 | |||||||
chr3:15723881 | G | A | 263 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(260): Show |
265 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.783+501C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723881 | |||||||
chr3:15723988 | T | C | 1 | a0001c0001t0003g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.783+394A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723988 | |||||||
chr3:15724717 | G | A | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.641-193C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724717 | |||||||
chr3:15724767 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.641-243G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724767 | |||||||
chr3:15724802 | G | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.641-278C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724802 | |||||||
chr3:15724873 | T | G | 25 | a0001c0001t0037g0086 a0001c0002t0001g0025 a0001c0002t0001g0026 others(22): Show |
25 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.641-349A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724873 | |||||||
chr3:15724981 | G | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.641-457C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724981 | |||||||
chr3:15725186 | T | C | 17 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(14): Show |
17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.641-662A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725186 | |||||||
chr3:15725364 | C | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-840G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725364 | |||||||
chr3:15725380 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.641-856G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725380 | |||||||
chr3:15725453 | C | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.641-929G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725453 | |||||||
chr3:15725515 | CATCTTGT others(12): Show |
C | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-1010_641-992de others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725515 | |||||||
chr3:15725534 | T | A | 6 | a0001c0002t0001g0040 a0001c0002t0013g0015 a0001c0002t0013g0016 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-1010A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725534 | |||||||
chr3:15725578 | A | AT | 99 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.641-1055dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725578 | |||||||
chr3:15725614 | G | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.641-1090C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725614 | |||||||
chr3:15725796 | C | T | 130 | a0001c0001t0037g0086 a0001c0002t0001g0001 a0001c0002t0001g0018 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.641-1272G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725796 | |||||||
chr3:15726095 | C | T | 124 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(121): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.641-1571G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726095 | |||||||
chr3:15726257 | G | T | 4 | a0001c0002t0001g0080 a0001c0002t0001g0088 a0001c0002t0022g0003 others(1): Show |
4 | HG00639.hp2 HG02004.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-1733C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726257 | |||||||
chr3:15726315 | T | C | 12 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-1791A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726315 | |||||||
chr3:15726317 | G | C | 1 | a0001c0001t0003g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.641-1793C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726317 | |||||||
chr3:15726339 | C | T | 275 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(272): Show |
277 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.641-1815G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726339 | |||||||
chr3:15726349 | TA | T | 90 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(87): Show |
91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.641-1826delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726349 | |||||||
chr3:15726438 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.641-1914C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726438 | |||||||
chr3:15726479 | C | T | 1 | a0001c0002t0001g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.641-1955G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726479 | |||||||
chr3:15726580 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.641-2056A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726580 | |||||||
chr3:15726584 | G | C | 138 | a0001c0001t0037g0086 a0001c0002t0001g0001 a0001c0002t0001g0018 others(135): Show |
139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.641-2060C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726584 | |||||||
chr3:15726590 | A | T | 138 | a0001c0001t0037g0086 a0001c0002t0001g0001 a0001c0002t0001g0018 others(135): Show |
139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.641-2066T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726590 | |||||||
chr3:15726618 | G | A | 99 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.641-2094C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726618 | |||||||
chr3:15726698 | A | C | 5 | a0001c0002t0001g0001 a0001c0002t0001g0121 a0001c0002t0001g0123 others(2): Show |
6 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-2174T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726698 | |||||||
chr3:15726762 | T | G | 3 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 |
3 | HG01934.hp1 HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.641-2238A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726762 | |||||||
chr3:15726786 | T | C | 277 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.641-2262A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726786 | |||||||
chr3:15726812 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-2288G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726812 | |||||||
chr3:15726820 | C | G | 46 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(43): Show |
47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.641-2296G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726820 | |||||||
chr3:15727019 | AAAG | A | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-2498_641-2496d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727019 | |||||||
chr3:15727072 | C | A | 130 | a0001c0001t0037g0086 a0001c0002t0001g0001 a0001c0002t0001g0018 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.641-2548G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727072 | |||||||
chr3:15727241 | T | C | 124 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(121): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.641-2717A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727241 | |||||||
chr3:15727270 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.641-2746A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727270 | |||||||
chr3:15727296 | G | T | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.641-2772C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727296 | |||||||
chr3:15727364 | C | T | 1 | a0001c0002t0048g0275 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.641-2840G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727364 | |||||||
chr3:15727403 | C | A | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.641-2879G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727403 | |||||||
chr3:15727549 | A | C | 2 | a0001c0001t0010g0263 a0001c0001t0010g0264 |
2 | HG01934.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.641-3025T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727549 | |||||||
chr3:15727564 | C | CA | 22 | a0001c0001t0002g0146 a0001c0001t0002g0203 a0001c0001t0002g0207 others(19): Show |
22 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.641-3041dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | |||||||
chr3:15727564 | C | CAA | 106 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(103): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.641-3042_641-3041d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | |||||||
chr3:15727564 | C | CAAA | 13 | a0001c0001t0002g0156 a0001c0001t0002g0159 a0001c0001t0002g0185 others(10): Show |
13 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-3043_641-3041d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | |||||||
chr3:15727564 | CA | C | 17 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.641-3041delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | |||||||
chr3:15727564 | CAA | C | 119 | a0001c0001t0006g0312 a0001c0002t0001g0001 a0001c0002t0001g0018 others(116): Show |
120 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.641-3042_641-3041d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | |||||||
chr3:15727564 | CAAA | C | 6 | a0001c0002t0001g0073 a0001c0002t0001g0076 a0001c0002t0001g0077 others(3): Show |
6 | HG00099.hp2 HG02015.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.641-3043_641-3041d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | |||||||
chr3:15727583 | A | G | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.641-3059T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727583 | |||||||
chr3:15727587 | A | G | 138 | a0001c0001t0037g0086 a0001c0002t0001g0001 a0001c0002t0001g0018 others(135): Show |
139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.641-3063T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727587 | |||||||
chr3:15727592 | A | C | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-3068T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727592 | |||||||
chr3:15727596 | A | C | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-3072T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727596 | |||||||
chr3:15727793 | A | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-3269T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727793 | |||||||
chr3:15727883 | T | C | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-3359A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727883 | |||||||
chr3:15728012 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.641-3488T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728012 | |||||||
chr3:15728092 | T | C | 1 | a0001c0002t0001g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.641-3568A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728092 | |||||||
chr3:15728104 | C | T | 1 | a0001c0001t0002g0207 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.641-3580G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728104 | |||||||
chr3:15728108 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.641-3584T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728108 | |||||||
chr3:15728153 | AT | A | 14 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-3630delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728153 | |||||||
chr3:15728292 | GTAAT | G | 235 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(232): Show |
237 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.641-3772_641-3769d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728292 | |||||||
chr3:15728301 | T | C | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-3777A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728301 | |||||||
chr3:15728327 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | NA18983.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.641-3803G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728327 | |||||||
chr3:15728385 | C | G | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.641-3861G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728385 | |||||||
chr3:15729141 | T | C | 291 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(288): Show |
293 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.641-4617A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729141 | |||||||
chr3:15729165 | G | A | 4 | a0001c0001t0002g0204 a0001c0001t0002g0221 a0001c0001t0002g0222 others(1): Show |
4 | HG00621.hp1 HG02129.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-4641C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729165 | |||||||
chr3:15729287 | T | C | 1 | a0001c0001t0008g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-4763A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729287 | |||||||
chr3:15729613 | C | T | 4 | a0001c0002t0001g0058 a0001c0002t0001g0060 a0001c0002t0001g0061 others(1): Show |
4 | NA18948.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-5089G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729613 | |||||||
chr3:15729709 | T | G | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.641-5185A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729709 | |||||||
chr3:15729784 | G | C | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.641-5260C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729784 | |||||||
chr3:15729842 | T | C | 1 | a0001c0002t0001g0073 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.641-5318A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729842 | |||||||
chr3:15729865 | T | C | 277 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.641-5341A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729865 | |||||||
chr3:15729902 | A | T | 1 | a0001c0001t0002g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.641-5378T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729902 | |||||||
chr3:15730181 | C | T | 1 | a0002c0006t0001g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.640+5229G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730181 | |||||||
chr3:15730653 | C | T | 7 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+4757G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730653 | |||||||
chr3:15730794 | A | C | 47 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0018 others(44): Show |
48 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.640+4616T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730794 | |||||||
chr3:15730799 | G | A | 1 | a0001c0001t0008g0334 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.640+4611C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730799 | |||||||
chr3:15730827 | T | C | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.640+4583A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730827 | |||||||
chr3:15731035 | C | T | 1 | a0001c0007t0021g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.640+4375G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731035 | |||||||
chr3:15731141 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.640+4269T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731141 | |||||||
chr3:15731304 | GA | G | 14 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+4105delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731304 | |||||||
chr3:15731314 | GT | G | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+4095delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731314 | |||||||
chr3:15731520 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.640+3890C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731520 | |||||||
chr3:15731586 | T | C | 1 | a0001c0001t0028g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.640+3824A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731586 | |||||||
chr3:15731811 | T | C | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3599A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731811 | |||||||
chr3:15731848 | C | CA | 70 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0139 others(67): Show |
70 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.640+3561dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | |||||||
chr3:15731848 | C | CAA | 9 | a0001c0001t0002g0143 a0001c0001t0002g0162 a0001c0001t0004g0241 others(6): Show |
9 | HG02132.hp1 HG02486.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+3560_640+3561d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | |||||||
chr3:15731848 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0006g0309 a0001c0001t0006g0310 a0001c0004t0009g0293 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3554_640+3561d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | |||||||
chr3:15731848 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0305 others(3): Show |
6 | HG01192.hp2 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3552_640+3561d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | |||||||
chr3:15731848 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0006g0306 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.640+3551_640+3561d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | |||||||
chr3:15731848 | C | CAAAAAAA others(5): Show |
1 | a0005c0012t0006g0308 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+3550_640+3561d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | |||||||
chr3:15731859 | AAAAAAAA others(9): Show |
A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.640+3535_640+3550d others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731859 | |||||||
chr3:15731874 | A | AAG | 22 | a0001c0001t0003g0262 a0001c0001t0010g0264 a0001c0002t0001g0074 others(19): Show |
22 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.640+3535_640+3536i others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | |||||||
chr3:15731874 | A | AAGG | 7 | a0001c0002t0001g0038 a0001c0002t0001g0073 a0001c0002t0001g0078 others(4): Show |
7 | NA18944.hp2 NA18965.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+3535_640+3536i others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | |||||||
chr3:15731874 | A | G | 1 | a0001c0003t0005g0278 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.640+3536T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | |||||||
chr3:15731874 | AG | A | 40 | a0001c0001t0002g0140 a0001c0001t0002g0152 a0001c0001t0002g0154 others(37): Show |
40 | HG00408.hp1 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.640+3535delC | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | |||||||
chr3:15731875 | G | A | 182 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(179): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.640+3535C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731875 | |||||||
chr3:15731876 | G | A | 109 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(106): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.640+3534C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731876 | |||||||
chr3:15731877 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.640+3533C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731877 | |||||||
chr3:15731882 | G | T | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+3528C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731882 | |||||||
chr3:15731883 | G | T | 7 | a0001c0001t0002g0135 a0001c0001t0002g0141 a0001c0001t0002g0142 others(4): Show |
7 | HG01099.hp1 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+3527C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731883 | |||||||
chr3:15731884 | G | GT | 8 | a0001c0003t0005g0282 a0001c0003t0005g0283 a0001c0003t0005g0284 others(5): Show |
8 | HG01168.hp2 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.640+3525_640+3526i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731884 | |||||||
chr3:15731884 | G | T | 9 | a0001c0003t0005g0278 a0001c0003t0018g0227 a0001c0003t0018g0228 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+3526C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731884 | |||||||
chr3:15732304 | T | C | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.640+3106A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732304 | |||||||
chr3:15732500 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.640+2910C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732500 | |||||||
chr3:15732515 | C | T | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.640+2895G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732515 | |||||||
chr3:15732823 | G | A | 4 | a0001c0001t0016g0326 a0001c0001t0016g0327 a0001c0001t0016g0329 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2587C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732823 | |||||||
chr3:15732840 | A | T | 1 | a0001c0001t0004g0240 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.640+2570T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732840 | |||||||
chr3:15732845 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.640+2565A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732845 | |||||||
chr3:15732937 | G | A | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.640+2473C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732937 | |||||||
chr3:15733096 | G | A | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.640+2314C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733096 | |||||||
chr3:15733120 | GTGCCGC | G | 4 | a0001c0001t0002g0135 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG01099.hp1 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2284_640+2289d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733120 | |||||||
chr3:15733271 | A | G | 4 | a0001c0002t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
4 | HG00673.hp1 NA18962.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2139T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733271 | |||||||
chr3:15733287 | G | A | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+2123C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733287 | |||||||
chr3:15733318 | A | G | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.640+2092T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733318 | |||||||
chr3:15733388 | T | A | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.640+2022A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733388 | |||||||
chr3:15733418 | G | A | 4 | a0001c0001t0002g0204 a0001c0001t0002g0221 a0001c0001t0002g0222 others(1): Show |
4 | HG00621.hp1 HG02129.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+1992C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733418 | |||||||
chr3:15733566 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.640+1844C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733566 | |||||||
chr3:15733661 | T | C | 3 | a0001c0001t0010g0272 a0001c0001t0010g0273 a0001c0001t0010g0274 |
3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.640+1749A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733661 | |||||||
chr3:15733766 | C | T | 1 | a0001c0001t0015g0324 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.640+1644G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733766 | |||||||
chr3:15733909 | A | G | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.640+1501T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733909 | |||||||
chr3:15733918 | T | C | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.640+1492A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733918 | |||||||
chr3:15733939 | T | C | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG02735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.640+1471A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733939 | |||||||
chr3:15733955 | T | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.640+1455A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733955 | |||||||
chr3:15734012 | C | G | 1 | a0007c0011t0003g0251 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.640+1398G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734012 | |||||||
chr3:15734087 | T | C | 8 | a0001c0001t0002g0134 a0001c0001t0002g0156 a0001c0001t0002g0157 others(5): Show |
8 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+1323A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734087 | |||||||
chr3:15734090 | A | G | 2 | a0001c0002t0001g0040 a0001c0002t0035g0039 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.640+1320T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734090 | |||||||
chr3:15734094 | T | A | 2 | a0001c0002t0001g0040 a0001c0002t0035g0039 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.640+1316A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734094 | |||||||
chr3:15734142 | T | C | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+1268A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734142 | |||||||
chr3:15734187 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.640+1223A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734187 | |||||||
chr3:15734191 | G | T | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.640+1219C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734191 | |||||||
chr3:15734265 | C | T | 7 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0241 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+1145G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734265 | |||||||
chr3:15734280 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.640+1130G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734280 | |||||||
chr3:15734337 | G | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+1073C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734337 | |||||||
chr3:15734357 | C | A | 1 | a0001c0002t0013g0016 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.640+1053G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734357 | |||||||
chr3:15734361 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.640+1049A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734361 | |||||||
chr3:15734376 | C | A | 1 | a0001c0001t0016g0327 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.640+1034G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734376 | |||||||
chr3:15734456 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.640+954A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734456 | |||||||
chr3:15734516 | A | G | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+894T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734516 | |||||||
chr3:15734667 | C | T | 1 | a0001c0002t0011g0232 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.640+743G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734667 | |||||||
chr3:15734686 | T | G | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.640+724A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734686 | |||||||
chr3:15734719 | C | T | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.640+691G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734719 | |||||||
chr3:15734913 | CTG | C | 236 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(233): Show |
238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.640+495_640+496del others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734913 | |||||||
chr3:15735017 | G | A | 252 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.640+393C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15735017 | |||||||
chr3:15735177 | A | G | 236 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(233): Show |
238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.640+233T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15735177 | |||||||
chr3:15735643 | G | A | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-146C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735643 | |||||||
chr3:15735838 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.553-341G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735838 | |||||||
chr3:15735840 | T | C | 3 | a0001c0002t0001g0100 a0001c0002t0001g0110 a0001c0002t0001g0111 |
3 | HG00733.hp2 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.553-343A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735840 | |||||||
chr3:15735916 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.553-419C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735916 | |||||||
chr3:15735982 | A | G | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-485T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735982 | |||||||
chr3:15736232 | T | C | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.553-735A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736232 | |||||||
chr3:15736284 | C | T | 2 | a0001c0002t0001g0018 a0001c0002t0001g0019 |
2 | NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.552+749G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736284 | |||||||
chr3:15736353 | G | C | 2 | a0001c0001t0002g0189 a0004c0008t0002g0211 |
2 | HG02071.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.552+680C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736353 | |||||||
chr3:15736454 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+579G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736454 | |||||||
chr3:15737276 | T | C | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-43A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737276 | |||||||
chr3:15737312 | G | T | 12 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.352-79C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737312 | |||||||
chr3:15737375 | A | T | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-142T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737375 | |||||||
chr3:15737521 | A | AAAAGAAA others(137): Show |
1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-289_352-288ins others(144): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737521 | |||||||
chr3:15737522 | G | GAAGAAAT others(137): Show |
277 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(274): Show |
279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.352-290_352-289ins others(144): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737522 | |||||||
chr3:15737522 | G | T | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-289C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737522 | |||||||
chr3:15737608 | G | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-375C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737608 | |||||||
chr3:15737687 | C | A | 252 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.352-454G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737687 | |||||||
chr3:15737707 | C | T | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.352-474G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737707 | |||||||
chr3:15737899 | TA | T | 207 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0140 others(204): Show |
208 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.352-667delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737899 | |||||||
chr3:15737925 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.352-692C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737925 | |||||||
chr3:15738162 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.352-929G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738162 | |||||||
chr3:15738163 | G | A | 21 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.352-930C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738163 | |||||||
chr3:15738304 | G | A | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.352-1071C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738304 | |||||||
chr3:15738349 | G | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-1116C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738349 | |||||||
chr3:15738350 | T | A | 1 | a0001c0002t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.352-1117A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738350 | |||||||
chr3:15738355 | G | A | 15 | a0001c0002t0001g0080 a0001c0002t0001g0081 a0001c0002t0001g0088 others(12): Show |
15 | HG00639.hp2 HG02004.hp1 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.352-1122C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738355 | |||||||
chr3:15738531 | C | T | 1 | a0001c0003t0005g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.352-1298G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738531 | |||||||
chr3:15738576 | G | A | 1 | a0001c0001t0016g0329 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.352-1343C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738576 | |||||||
chr3:15738588 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.352-1355C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738588 | |||||||
chr3:15738608 | C | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.352-1375G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738608 | |||||||
chr3:15738660 | G | A | 3 | a0001c0001t0002g0141 a0001c0002t0042g0131 a0001c0014t0026g0007 |
3 | HG01993.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-1427C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738660 | |||||||
chr3:15738665 | C | A | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-1432G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738665 | |||||||
chr3:15738770 | A | T | 1 | a0001c0001t0058g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.352-1537T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738770 | |||||||
chr3:15738875 | A | G | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-1642T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738875 | |||||||
chr3:15738911 | T | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.352-1678A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738911 | |||||||
chr3:15739016 | T | C | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-1783A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739016 | |||||||
chr3:15739082 | T | C | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-1849A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739082 | |||||||
chr3:15739149 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-1916A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739149 | |||||||
chr3:15739429 | C | T | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-2196G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739429 | |||||||
chr3:15739498 | C | T | 236 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(233): Show |
238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.352-2265G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739498 | |||||||
chr3:15739652 | A | C | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.352-2419T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739652 | |||||||
chr3:15739776 | A | T | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.352-2543T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739776 | |||||||
chr3:15739797 | A | C | 1 | a0001c0001t0002g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.352-2564T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739797 | |||||||
chr3:15739848 | C | T | 1 | a0001c0002t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.352-2615G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739848 | |||||||
chr3:15739853 | G | A | 2 | a0001c0001t0003g0254 a0001c0005t0012g0317 |
2 | HG03209.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.352-2620C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739853 | |||||||
chr3:15740029 | TAAAC | T | 6 | a0001c0002t0001g0040 a0001c0002t0013g0015 a0001c0002t0013g0016 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-2800_352-2797d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740029 | |||||||
chr3:15740113 | G | C | 236 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(233): Show |
238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.352-2880C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740113 | |||||||
chr3:15740298 | A | C | 99 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.352-3065T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740298 | |||||||
chr3:15740304 | C | T | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-3071G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740304 | |||||||
chr3:15740357 | A | G | 6 | a0001c0002t0001g0040 a0001c0002t0013g0015 a0001c0002t0013g0016 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-3124T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740357 | |||||||
chr3:15740552 | G | C | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.352-3319C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740552 | |||||||
chr3:15740667 | C | T | 252 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.352-3434G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740667 | |||||||
chr3:15740831 | C | T | 5 | a0001c0002t0007g0082 a0001c0002t0007g0083 a0001c0002t0007g0084 others(2): Show |
5 | NA18944.hp2 NA18950.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-3598G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740831 | |||||||
chr3:15740834 | T | G | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 |
3 | HG01978.hp1 HG02148.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.352-3601A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740834 | |||||||
chr3:15740928 | C | T | 4 | a0001c0001t0002g0184 a0001c0001t0010g0272 a0001c0001t0010g0273 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-3695G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740928 | |||||||
chr3:15740995 | T | G | 1 | a0001c0001t0002g0144 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.352-3762A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740995 | |||||||
chr3:15741025 | C | T | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-3792G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741025 | |||||||
chr3:15741042 | T | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-3809A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741042 | |||||||
chr3:15741060 | G | A | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.352-3827C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741060 | |||||||
chr3:15741068 | G | A | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.352-3835C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741068 | |||||||
chr3:15741143 | G | A | 1 | a0001c0002t0017g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.352-3910C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741143 | |||||||
chr3:15741198 | CAAAAAAA | C | 48 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(45): Show |
49 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.352-3972_352-3966d others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741198 | |||||||
chr3:15741204 | A | C | 182 | a0001c0001t0001g0072 a0001c0001t0002g0178 a0001c0001t0002g0179 others(179): Show |
183 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.352-3971T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741204 | |||||||
chr3:15741205 | A | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-3972T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741205 | |||||||
chr3:15741424 | C | T | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-4191G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741424 | |||||||
chr3:15741697 | C | CTTTTTT | 7 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0309 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-4470_352-4465d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0006g0312 a0001c0004t0009g0293 |
2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.352-4474_352-4465d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0004g0234 a0001c0001t0004g0235 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.352-4476_352-4465d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | C | CTTTTTTT others(6): Show |
2 | a0001c0003t0051g0311 a0001c0004t0009g0295 |
2 | HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.352-4477_352-4465d others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0004g0244 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.352-4481_352-4465d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0243 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.352-4482_352-4465d others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CT | C | 16 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0003g0254 others(13): Show |
16 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-4465delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTT | C | 14 | a0001c0001t0003g0270 a0001c0001t0008g0333 a0001c0001t0008g0337 others(11): Show |
14 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.352-4466_352-4465d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTT | C | 14 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0164 others(11): Show |
14 | HG01168.hp2 HG01433.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.352-4467_352-4465d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTT | C | 31 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0139 others(28): Show |
32 | HG00423.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.352-4468_352-4465d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTT | C | 36 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(33): Show |
36 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.352-4469_352-4465d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTT | C | 13 | a0001c0002t0001g0022 a0001c0002t0001g0024 a0001c0002t0001g0091 others(10): Show |
13 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.352-4470_352-4465d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT | C | 9 | a0001c0001t0001g0072 a0001c0001t0004g0242 a0001c0002t0001g0030 others(6): Show |
9 | HG00738.hp2 HG02602.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-4471_352-4465d others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0006g0307 a0001c0001t0037g0086 a0001c0002t0001g0026 others(19): Show |
22 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.352-4472_352-4465d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(2): Show |
C | 64 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0019 others(61): Show |
65 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.352-4473_352-4465d others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(3): Show |
C | 8 | a0001c0002t0001g0056 a0001c0002t0001g0067 a0001c0002t0001g0073 others(5): Show |
8 | HG00621.hp2 HG02965.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-4474_352-4465d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.352-4475_352-4465d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0002g0178 a0001c0001t0002g0195 a0001c0001t0002g0201 others(3): Show |
6 | HG00597.hp2 HG01884.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.352-4479_352-4465d others(17): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(9): Show |
C | 44 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(41): Show |
44 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.352-4480_352-4465d others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0002g0186 a0001c0001t0002g0203 a0001c0001t0002g0205 others(2): Show |
5 | HG01069.hp2 HG03490.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-4481_352-4465d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(12): Show |
C | 1 | a0001c0002t0001g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.352-4483_352-4465d others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(13): Show |
C | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.352-4484_352-4465d others(22): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0002g0162 a0001c0001t0004g0248 |
2 | HG03225.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.352-4485_352-4465d others(23): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(15): Show |
C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-4486_352-4465d others(24): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741697 | CTTTTTTT others(19): Show |
C | 6 | a0001c0001t0004g0236 a0001c0001t0004g0237 a0001c0001t0004g0238 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.352-4490_352-4465d others(28): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | |||||||
chr3:15741848 | T | C | 3 | a0001c0004t0009g0296 a0001c0004t0009g0297 a0001c0004t0025g0006 |
3 | HG02723.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.352-4615A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741848 | |||||||
chr3:15741865 | T | C | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-4632A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741865 | |||||||
chr3:15741874 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.352-4641A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741874 | |||||||
chr3:15741881 | C | T | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.352-4648G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741881 | |||||||
chr3:15741883 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.352-4650G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741883 | |||||||
chr3:15741893 | C | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-4660G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741893 | |||||||
chr3:15741935 | C | T | 2 | a0001c0002t0001g0101 a0001c0002t0001g0104 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.352-4702G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741935 | |||||||
chr3:15741948 | G | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.352-4715C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741948 | |||||||
chr3:15741964 | C | G | 230 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(227): Show |
232 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.352-4731G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741964 | |||||||
chr3:15742011 | T | C | 14 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.352-4778A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742011 | |||||||
chr3:15742019 | G | A | 1 | a0001c0001t0002g0198 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.352-4786C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742019 | |||||||
chr3:15742089 | A | G | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-4856T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742089 | |||||||
chr3:15742126 | G | A | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.352-4893C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742126 | |||||||
chr3:15742157 | A | AC | 4 | a0001c0001t0002g0199 a0001c0002t0001g0018 a0001c0002t0001g0100 others(1): Show |
4 | HG00738.hp1 HG00741.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-4925dupG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742157 | |||||||
chr3:15742180 | G | A | 241 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(238): Show |
243 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.352-4947C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742180 | |||||||
chr3:15742194 | G | A | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-4961C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742194 | |||||||
chr3:15742195 | C | T | 3 | a0001c0002t0001g0100 a0001c0002t0001g0110 a0001c0002t0001g0111 |
3 | HG00733.hp2 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.352-4962G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742195 | |||||||
chr3:15742269 | C | T | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-5036G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742269 | |||||||
chr3:15742356 | C | T | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-5123G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742356 | |||||||
chr3:15742357 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-5124C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742357 | |||||||
chr3:15742389 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-5156C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742389 | |||||||
chr3:15742394 | G | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.352-5161C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742394 | |||||||
chr3:15742408 | A | G | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-5175T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742408 | |||||||
chr3:15742411 | C | T | 1 | a0001c0001t0003g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.352-5178G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742411 | |||||||
chr3:15742428 | G | A | 23 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.352-5195C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742428 | |||||||
chr3:15742434 | G | A | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.352-5201C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742434 | |||||||
chr3:15742465 | C | T | 3 | a0001c0002t0001g0100 a0001c0002t0001g0110 a0001c0002t0001g0111 |
3 | HG00733.hp2 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.352-5232G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742465 | |||||||
chr3:15742470 | C | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-5237G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742470 | |||||||
chr3:15742471 | G | A | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-5238C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742471 | |||||||
chr3:15742506 | G | A | 48 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(45): Show |
49 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.352-5273C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742506 | |||||||
chr3:15742515 | G | A | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-5282C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742515 | |||||||
chr3:15742534 | C | T | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-5301G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742534 | |||||||
chr3:15742538 | C | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5305G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742538 | |||||||
chr3:15742579 | A | G | 1 | a0001c0001t0006g0307 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.352-5346T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742579 | |||||||
chr3:15742594 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.352-5361G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742594 | |||||||
chr3:15742595 | G | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-5362C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742595 | |||||||
chr3:15742614 | G | A | 40 | a0001c0001t0002g0151 a0001c0001t0002g0178 a0001c0001t0002g0179 others(37): Show |
40 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.352-5381C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742614 | |||||||
chr3:15742619 | CT | C | 335 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(332): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.352-5387delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742619 | |||||||
chr3:15742621 | G | A | 6 | a0001c0002t0001g0021 a0001c0002t0001g0038 a0001c0002t0001g0078 others(3): Show |
6 | NA18747.hp2 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-5388C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742621 | |||||||
chr3:15742624 | A | C | 1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5391T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742624 | |||||||
chr3:15742625 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5392C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742625 | |||||||
chr3:15742659 | A | G | 1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5426T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742659 | |||||||
chr3:15742669 | T | C | 1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5436A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742669 | |||||||
chr3:15742671 | C | CCCGGCCA others(693): Show |
1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5439_352-5438i others(702): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742671 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
4 | a0001c0005t0012g0318 a0001c0005t0056g0322 a0001c0010t0012g0315 others(1): Show |
4 | HG02622.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
3 | a0001c0002t0011g0231 a0001c0002t0011g0232 a0003c0015t0011g0229 |
3 | HG01255.hp1 HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(746): Show |
1 | a0001c0001t0008g0337 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(755): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0001t0002g0144 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(729): Show |
1 | a0001c0003t0005g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(738): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(792): Show |
1 | a0001c0003t0051g0311 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(801): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(791): Show |
10 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(791): Show |
1 | a0001c0004t0009g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(792): Show |
1 | a0001c0001t0006g0307 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(801): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(791): Show |
2 | a0001c0001t0006g0309 a0001c0001t0006g0310 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(791): Show |
8 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
2 | a0001c0001t0002g0178 a0001c0001t0032g0013 |
2 | NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(744): Show |
3 | a0001c0001t0004g0240 a0001c0001t0004g0241 a0001c0001t0004g0242 |
3 | HG02258.hp2 HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0001t0015g0324 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
12 | a0001c0001t0003g0257 a0001c0001t0004g0234 a0001c0001t0004g0235 others(9): Show |
12 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(731): Show |
1 | a0001c0003t0005g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(740): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(747): Show |
1 | a0001c0001t0002g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(756): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(744): Show |
1 | a0001c0002t0001g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(745): Show |
1 | a0001c0002t0017g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(754): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
3 | a0001c0001t0002g0165 a0001c0002t0017g0133 a0004c0008t0002g0211 |
3 | NA18956.hp1 NA18998.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(744): Show |
1 | a0001c0002t0048g0275 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
5 | a0001c0002t0001g0027 a0001c0002t0001g0110 a0001c0002t0001g0124 others(2): Show |
5 | HG00741.hp2 HG01978.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
2 | a0001c0001t0008g0333 a0001c0001t0008g0338 |
2 | NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
7 | a0001c0001t0015g0323 a0001c0001t0015g0325 a0001c0001t0016g0326 others(4): Show |
7 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
3 | a0001c0001t0008g0334 a0001c0001t0008g0335 a0001c0001t0008g0336 |
3 | HG02896.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0001t0008g0331 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0002t0001g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0002t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
26 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0252 others(23): Show |
26 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0001t0010g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0001t0002g0201 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0002t0034g0075 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(729): Show |
1 | a0001c0009t0005g0281 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(738): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(744): Show |
1 | a0004c0008t0002g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0001t0002g0215 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0001t0002g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0001t0002g0142 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
86 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(83): Show |
87 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(728): Show |
8 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(5): Show |
8 | HG01109.hp2 HG01168.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(737): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(728): Show |
1 | a0001c0003t0005g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(737): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0002t0001g0052 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0002t0035g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(743): Show |
1 | a0001c0002t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(693): Show |
1 | a0001c0002t0027g0008 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(702): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0001t0002g0220 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
2 | a0001c0002t0001g0120 a0001c0002t0001g0129 |
2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0001t0037g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(791): Show |
2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCC others(742): Show |
1 | a0001c0001t0003g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | AGCCAGCT others(791): Show |
1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742674 | A | C | 1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5441T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | |||||||
chr3:15742736 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5503G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742736 | |||||||
chr3:15742769 | G | A | 2 | a0001c0001t0004g0234 a0001c0001t0004g0235 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.352-5536C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742769 | |||||||
chr3:15742773 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.352-5540C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742773 | |||||||
chr3:15742781 | A | G | 262 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(259): Show |
264 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.352-5548T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742781 | |||||||
chr3:15742803 | C | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5570G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742803 | |||||||
chr3:15742814 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.352-5581C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742814 | |||||||
chr3:15742817 | C | T | 2 | a0001c0002t0001g0077 a0001c0002t0001g0123 |
2 | HG02015.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.352-5584G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742817 | |||||||
chr3:15742897 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.352-5664C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742897 | |||||||
chr3:15742900 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-5667G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742900 | |||||||
chr3:15742909 | C | T | 3 | a0001c0007t0021g0300 a0001c0007t0021g0301 a0003c0013t0050g0290 |
3 | HG01884.hp2 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5676G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742909 | |||||||
chr3:15742915 | T | C | 5 | a0001c0005t0020g0298 a0001c0005t0020g0299 a0001c0007t0021g0300 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-5682A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742915 | |||||||
chr3:15742996 | T | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5763A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742996 | |||||||
chr3:15743355 | A | AAAAC | 9 | a0001c0002t0001g0041 a0001c0002t0001g0043 a0001c0002t0001g0044 others(6): Show |
9 | HG00642.hp1 HG01071.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-6126_352-6123d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743355 | |||||||
chr3:15743370 | ACAAAC | A | 3 | a0001c0007t0021g0300 a0001c0007t0021g0301 a0003c0013t0050g0290 |
3 | HG01884.hp2 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-6142_352-6138d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743370 | |||||||
chr3:15743375 | C | A | 1 | a0001c0001t0014g0002 | 2 | NA18945.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.352-6142G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743375 | |||||||
chr3:15743375 | C | CA | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-6143dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743375 | |||||||
chr3:15743384 | A | C | 230 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(227): Show |
232 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.352-6151T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743384 | |||||||
chr3:15743539 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-6306G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743539 | |||||||
chr3:15743545 | A | AAC | 16 | a0001c0001t0002g0143 a0001c0001t0002g0196 a0001c0001t0002g0199 others(13): Show |
16 | HG00733.hp1 HG01099.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.352-6314_352-6313d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | A | AACAC | 4 | a0001c0001t0002g0195 a0001c0002t0001g0026 a0001c0002t0001g0103 others(1): Show |
4 | HG00642.hp2 HG01192.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-6316_352-6313d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | A | AACACACA others(9): Show |
1 | a0002c0006t0001g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.352-6328_352-6313d others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | AAC | A | 80 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.352-6314_352-6313d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | AACAC | A | 61 | a0001c0001t0002g0145 a0001c0001t0002g0174 a0001c0001t0002g0175 others(58): Show |
61 | HG00639.hp2 HG00738.hp2 HG01891.hp1 others(58): Show |
intron_variant | MODIFIER | c.352-6316_352-6313d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | AACACAC | A | 31 | a0001c0001t0002g0134 a0001c0001t0002g0139 a0001c0001t0002g0141 others(28): Show |
33 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.352-6318_352-6313d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | AACACACA others(1): Show |
A | 41 | a0001c0001t0001g0072 a0001c0001t0002g0135 a0001c0001t0002g0142 others(38): Show |
41 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.352-6320_352-6313d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | AACACACA others(3): Show |
A | 4 | a0001c0001t0002g0155 a0001c0001t0002g0159 a0001c0002t0001g0048 others(1): Show |
4 | HG01891.hp2 HG02293.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-6322_352-6313d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743545 | AACACACA others(7): Show |
A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.352-6326_352-6313d others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | |||||||
chr3:15743580 | A | ACACACAC others(9): Show |
2 | a0001c0003t0005g0278 a0001c0003t0005g0279 |
2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.352-6348_352-6347i others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | |||||||
chr3:15743580 | A | ACACACAC others(5): Show |
1 | a0001c0003t0005g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.352-6348_352-6347i others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | |||||||
chr3:15743580 | A | ACACACAC others(3): Show |
3 | a0001c0003t0005g0286 a0001c0003t0005g0289 a0001c0009t0005g0281 |
3 | HG02055.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.352-6348_352-6347i others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | |||||||
chr3:15743580 | A | ACACACAC others(1): Show |
5 | a0001c0003t0005g0282 a0001c0003t0005g0283 a0001c0003t0005g0285 others(2): Show |
5 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-6348_352-6347i others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | |||||||
chr3:15743580 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.352-6347T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | |||||||
chr3:15743582 | ACACACAC others(10): Show |
A | 1 | a0001c0001t0004g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.352-6366_352-6350d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743582 | |||||||
chr3:15743593 | C | T | 2 | a0001c0001t0003g0250 a0001c0001t0003g0257 |
2 | HG01167.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.352-6360G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743593 | |||||||
chr3:15743645 | G | A | 2 | a0001c0001t0003g0249 a0001c0001t0003g0269 |
2 | HG00733.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.352-6412C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743645 | |||||||
chr3:15743679 | T | C | 1 | a0001c0001t0002g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.352-6446A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743679 | |||||||
chr3:15743749 | G | A | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.352-6516C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743749 | |||||||
chr3:15743827 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.352-6594G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743827 | |||||||
chr3:15744046 | G | C | 2 | a0001c0001t0002g0210 a0001c0001t0046g0233 |
2 | NA18952.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.352-6813C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744046 | |||||||
chr3:15744148 | T | C | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.352-6915A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744148 | |||||||
chr3:15744251 | T | G | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.352-7018A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744251 | |||||||
chr3:15744406 | C | A | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-7173G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744406 | |||||||
chr3:15744455 | G | A | 1 | a0001c0001t0010g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.352-7222C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744455 | |||||||
chr3:15744473 | C | CT | 111 | a0001c0001t0002g0141 a0001c0001t0002g0156 a0001c0001t0002g0194 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(108): Show |
intron_variant | MODIFIER | c.352-7241dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744473 | |||||||
chr3:15744473 | C | CTT | 97 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(94): Show |
98 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.352-7242_352-7241d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744473 | |||||||
chr3:15744597 | G | A | 1 | a0001c0002t0007g0092 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.351+7153C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744597 | |||||||
chr3:15744623 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.351+7127C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744623 | |||||||
chr3:15744664 | T | G | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.351+7086A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744664 | |||||||
chr3:15744771 | G | A | 1 | a0001c0001t0028g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.351+6979C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744771 | |||||||
chr3:15744774 | T | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.351+6976A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744774 | |||||||
chr3:15745046 | T | C | 1 | a0001c0002t0001g0051 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.351+6704A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745046 | |||||||
chr3:15745151 | T | C | 4 | a0001c0001t0002g0214 a0001c0001t0002g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG02886.hp2 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+6599A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745151 | |||||||
chr3:15745621 | A | G | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+6129T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745621 | |||||||
chr3:15745667 | G | C | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.351+6083C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745667 | |||||||
chr3:15745721 | A | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+6029T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745721 | |||||||
chr3:15745722 | ATT | A | 29 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(26): Show |
29 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.351+6026_351+6027d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745722 | |||||||
chr3:15745777 | C | T | 19 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(16): Show |
19 | HG01109.hp2 HG01168.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+5973G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745777 | |||||||
chr3:15745785 | G | A | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+5965C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745785 | |||||||
chr3:15745805 | T | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+5945A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745805 | |||||||
chr3:15745836 | C | T | 1 | a0001c0002t0013g0016 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.351+5914G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745836 | |||||||
chr3:15746042 | T | C | 3 | a0001c0002t0001g0057 a0001c0002t0001g0093 a0001c0002t0001g0094 |
3 | HG00558.hp1 NA19000.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.351+5708A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746042 | |||||||
chr3:15746333 | C | T | 292 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(289): Show |
294 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.351+5417G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746333 | |||||||
chr3:15746379 | T | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+5371A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746379 | |||||||
chr3:15746388 | T | C | 1 | a0001c0003t0018g0228 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.351+5362A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746388 | |||||||
chr3:15746405 | G | A | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.351+5345C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746405 | |||||||
chr3:15746491 | G | C | 1 | a0001c0002t0039g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.351+5259C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746491 | |||||||
chr3:15746528 | T | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+5222A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746528 | |||||||
chr3:15746550 | C | T | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.351+5200G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746550 | |||||||
chr3:15746631 | A | C | 1 | a0001c0002t0036g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.351+5119T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746631 | |||||||
chr3:15746985 | A | G | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+4765T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746985 | |||||||
chr3:15747166 | CT | C | 27 | a0001c0001t0002g0175 a0001c0001t0002g0177 a0001c0001t0016g0326 others(24): Show |
27 | HG00140.hp1 HG01109.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.351+4583delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747166 | |||||||
chr3:15747198 | T | C | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.351+4552A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747198 | |||||||
chr3:15747406 | T | C | 1 | a0001c0002t0048g0275 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.351+4344A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747406 | |||||||
chr3:15747447 | G | T | 46 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0018 others(43): Show |
47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.351+4303C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747447 | |||||||
chr3:15747457 | C | T | 1 | a0001c0001t0003g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.351+4293G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747457 | |||||||
chr3:15747463 | C | G | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.351+4287G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747463 | |||||||
chr3:15747474 | GTTATTTA others(3): Show |
G | 1 | a0001c0002t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.351+4266_351+4275d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747474 | |||||||
chr3:15747564 | A | G | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+4186T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747564 | |||||||
chr3:15747735 | C | T | 129 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.351+4015G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747735 | |||||||
chr3:15747836 | G | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.351+3914C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747836 | |||||||
chr3:15747881 | G | C | 1 | a0001c0001t0002g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.351+3869C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747881 | |||||||
chr3:15747939 | A | T | 1 | a0001c0002t0001g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.351+3811T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747939 | |||||||
chr3:15747971 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.351+3779C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747971 | |||||||
chr3:15748063 | T | A | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+3687A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748063 | |||||||
chr3:15748128 | T | G | 1 | a0001c0001t0002g0177 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.351+3622A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748128 | |||||||
chr3:15748130 | A | T | 1 | a0001c0001t0002g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.351+3620T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748130 | |||||||
chr3:15748193 | T | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+3557A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748193 | |||||||
chr3:15748208 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.351+3542C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748208 | |||||||
chr3:15748215 | A | G | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+3535T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748215 | |||||||
chr3:15748489 | C | T | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.351+3261G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748489 | |||||||
chr3:15748547 | C | T | 1 | a0001c0002t0039g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.351+3203G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748547 | |||||||
chr3:15748663 | T | C | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.351+3087A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748663 | |||||||
chr3:15748895 | A | T | 5 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0147 others(2): Show |
5 | HG00597.hp1 NA18956.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2855T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748895 | |||||||
chr3:15748896 | T | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+2854A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748896 | |||||||
chr3:15748951 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.351+2799C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748951 | |||||||
chr3:15748992 | T | G | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.351+2758A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748992 | |||||||
chr3:15749093 | A | ATGTTTTT others(1): Show |
37 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(34): Show |
38 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.351+2656_351+2657i others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749093 | |||||||
chr3:15749095 | G | GT | 11 | a0001c0001t0004g0242 a0001c0001t0006g0313 a0001c0002t0042g0131 others(8): Show |
11 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2654dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTT | 7 | a0001c0003t0005g0278 a0001c0003t0005g0282 a0001c0003t0005g0283 others(4): Show |
7 | HG01168.hp2 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2653_351+2654d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTT | 7 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0003t0005g0279 others(4): Show |
7 | HG01109.hp2 HG02129.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2652_351+2654d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(2): Show |
9 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0167 others(6): Show |
9 | HG01433.hp2 HG03195.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(3): Show |
1 | a0001c0002t0017g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.351+2654_351+2655i others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(2): Show |
17 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0184 others(14): Show |
17 | HG00408.hp1 HG01069.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(3): Show |
13 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0183 others(10): Show |
13 | HG02040.hp1 HG02523.hp2 HG03239.hp1 others(10): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(4): Show |
11 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0191 others(8): Show |
11 | HG02071.hp2 NA18747.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(5): Show |
5 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0186 others(2): Show |
5 | HG00597.hp2 HG00673.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0180 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.351+2654_351+2655i others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(7): Show |
2 | a0001c0001t0002g0204 a0001c0001t0002g0208 |
2 | HG00621.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.351+2654_351+2655i others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | GTTTTTTT others(11): Show |
1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.351+2654_351+2655i others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | G | T | 1 | a0001c0001t0002g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.351+2655C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | GTTTTTGT | G | 28 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0040 others(25): Show |
28 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.351+2648_351+2654d others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749095 | GTTTTTGT others(1): Show |
G | 96 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(93): Show |
97 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.351+2647_351+2654d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | |||||||
chr3:15749101 | G | T | 159 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(156): Show |
160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.351+2649C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749101 | |||||||
chr3:15749101 | GT | G | 9 | a0001c0001t0008g0333 a0001c0001t0008g0338 a0001c0001t0015g0323 others(6): Show |
9 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2648delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749101 | |||||||
chr3:15749169 | G | C | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.351+2581C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749169 | |||||||
chr3:15749197 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.351+2553C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749197 | |||||||
chr3:15749268 | G | A | 135 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.351+2482C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749268 | |||||||
chr3:15749271 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.351+2479G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749271 | |||||||
chr3:15749302 | C | T | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2448G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749302 | |||||||
chr3:15749315 | T | C | 3 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0056 |
3 | HG00621.hp2 NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.351+2435A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749315 | |||||||
chr3:15749334 | G | A | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.351+2416C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749334 | |||||||
chr3:15749358 | C | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+2392G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749358 | |||||||
chr3:15749360 | C | T | 4 | a0001c0001t0016g0326 a0001c0001t0016g0327 a0001c0001t0016g0329 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2390G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749360 | |||||||
chr3:15749493 | C | A | 3 | a0001c0007t0021g0300 a0001c0007t0021g0301 a0003c0013t0050g0290 |
3 | HG01884.hp2 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+2257G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749493 | |||||||
chr3:15749601 | T | C | 2 | a0001c0001t0003g0249 a0001c0001t0003g0269 |
2 | HG00733.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.351+2149A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749601 | |||||||
chr3:15749772 | G | A | 127 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.351+1978C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749772 | |||||||
chr3:15750046 | G | A | 39 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(36): Show |
40 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.351+1704C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750046 | |||||||
chr3:15750164 | A | G | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.351+1586T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750164 | |||||||
chr3:15750243 | C | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+1507G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750243 | |||||||
chr3:15750339 | A | C | 1 | a0001c0001t0003g0268 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.351+1411T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750339 | |||||||
chr3:15750447 | C | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+1303G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750447 | |||||||
chr3:15750808 | G | A | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.351+942C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750808 | |||||||
chr3:15750889 | A | G | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+861T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750889 | |||||||
chr3:15750967 | T | G | 292 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(289): Show |
294 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.351+783A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750967 | |||||||
chr3:15751004 | G | A | 1 | a0001c0002t0054g0320 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.351+746C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751004 | |||||||
chr3:15751030 | A | G | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.351+720T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751030 | |||||||
chr3:15751114 | T | C | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+636A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751114 | |||||||
chr3:15751241 | A | G | 129 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(126): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.351+509T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751241 | |||||||
chr3:15751305 | A | G | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.351+445T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751305 | |||||||
chr3:15751504 | T | G | 2 | a0001c0003t0018g0227 a0001c0003t0018g0228 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.351+246A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751504 | |||||||
chr3:15751558 | C | T | 2 | a0001c0003t0005g0278 a0001c0003t0005g0279 |
2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.351+192G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751558 | |||||||
chr3:15751561 | G | A | 25 | a0001c0001t0037g0086 a0001c0002t0001g0025 a0001c0002t0001g0026 others(22): Show |
25 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.351+189C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751561 | |||||||
chr3:15751565 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+185G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751565 | |||||||
chr3:15751671 | T | C | 1 | a0001c0001t0037g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.351+79A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751671 | |||||||
chr3:15751988 | A | G | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-168T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15751988 | |||||||
chr3:15752049 | A | G | 25 | a0001c0001t0037g0086 a0001c0002t0001g0025 a0001c0002t0001g0026 others(22): Show |
25 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-229T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752049 | |||||||
chr3:15752182 | A | G | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.281-362T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752182 | |||||||
chr3:15752291 | C | T | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.281-471G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752291 | |||||||
chr3:15752335 | T | C | 21 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(18): Show |
21 | HG00408.hp2 HG01433.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-515A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752335 | |||||||
chr3:15752356 | T | C | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-536A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752356 | |||||||
chr3:15752508 | G | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.281-688C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752508 | |||||||
chr3:15752558 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.281-738C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752558 | |||||||
chr3:15752820 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.281-1000C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752820 | |||||||
chr3:15752829 | A | T | 1 | a0001c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-1009T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752829 | |||||||
chr3:15752880 | G | T | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-1060C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752880 | |||||||
chr3:15753012 | T | C | 1 | a0001c0001t0028g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-1192A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753012 | |||||||
chr3:15753060 | T | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.281-1240A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753060 | |||||||
chr3:15753193 | G | A | 15 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(12): Show |
15 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-1373C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753193 | |||||||
chr3:15753266 | A | G | 1 | a0001c0004t0009g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.281-1446T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753266 | |||||||
chr3:15753495 | A | G | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-1675T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753495 | |||||||
chr3:15753504 | C | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-1684G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753504 | |||||||
chr3:15753507 | A | G | 1 | a0001c0002t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.281-1687T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753507 | |||||||
chr3:15753663 | AG | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-1844delC | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753663 | |||||||
chr3:15753671 | G | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.281-1851C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753671 | |||||||
chr3:15753723 | G | GCCCA | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1904_281-1903i others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753723 | |||||||
chr3:15753725 | T | C | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1905A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753725 | |||||||
chr3:15753727 | G | C | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1907C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753727 | |||||||
chr3:15753729 | A | G | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1909T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753729 | |||||||
chr3:15753760 | T | C | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-1940A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753760 | |||||||
chr3:15753869 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.281-2049C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753869 | |||||||
chr3:15753893 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.281-2073C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753893 | |||||||
chr3:15753955 | G | A | 1 | a0001c0004t0025g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-2135C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753955 | |||||||
chr3:15754041 | C | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-2221G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754041 | |||||||
chr3:15754158 | T | A | 1 | a0001c0002t0001g0081 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.281-2338A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754158 | |||||||
chr3:15754170 | T | C | 1 | a0004c0008t0002g0166 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.281-2350A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754170 | |||||||
chr3:15754187 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.281-2367G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754187 | |||||||
chr3:15754290 | T | G | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-2470A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754290 | |||||||
chr3:15754518 | A | C | 1 | a0001c0001t0003g0259 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.281-2698T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754518 | |||||||
chr3:15754527 | A | G | 1 | a0001c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-2707T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754527 | |||||||
chr3:15754706 | C | T | 1 | a0001c0002t0001g0021 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.281-2886G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754706 | |||||||
chr3:15754839 | G | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.281-3019C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754839 | |||||||
chr3:15754892 | A | G | 292 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(289): Show |
294 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.281-3072T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754892 | |||||||
chr3:15754986 | C | T | 143 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(140): Show |
144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.281-3166G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754986 | |||||||
chr3:15754998 | G | A | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.281-3178C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754998 | |||||||
chr3:15754999 | C | T | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-3179G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754999 | |||||||
chr3:15755173 | C | A | 23 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.281-3353G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755173 | |||||||
chr3:15755208 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.281-3388C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755208 | |||||||
chr3:15755339 | A | G | 43 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(40): Show |
43 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.281-3519T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755339 | |||||||
chr3:15755346 | G | A | 125 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.281-3526C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755346 | |||||||
chr3:15755453 | G | A | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.281-3633C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755453 | |||||||
chr3:15755690 | G | A | 21 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.281-3870C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755690 | |||||||
chr3:15755729 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.281-3909C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755729 | |||||||
chr3:15755947 | A | G | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-4127T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755947 | |||||||
chr3:15756133 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.281-4313C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756133 | |||||||
chr3:15756279 | T | C | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-4459A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756279 | |||||||
chr3:15756382 | T | C | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.281-4562A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756382 | |||||||
chr3:15756399 | A | G | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.281-4579T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756399 | |||||||
chr3:15756430 | C | T | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-4610G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756430 | |||||||
chr3:15756533 | A | T | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-4713T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756533 | |||||||
chr3:15756535 | G | T | 2 | a0001c0002t0001g0067 a0001c0002t0038g0059 |
2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281-4715C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756535 | |||||||
chr3:15756589 | C | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-4769G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756589 | |||||||
chr3:15756725 | G | C | 22 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.281-4905C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756725 | |||||||
chr3:15756739 | A | G | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.281-4919T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756739 | |||||||
chr3:15756834 | G | A | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281-5014C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756834 | |||||||
chr3:15757210 | T | C | 2 | a0001c0001t0008g0333 a0001c0001t0008g0338 |
2 | NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.281-5390A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757210 | |||||||
chr3:15757486 | G | A | 1 | a0001c0002t0001g0020 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.281-5666C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757486 | |||||||
chr3:15757682 | G | A | 24 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(21): Show |
24 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.281-5862C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757682 | |||||||
chr3:15757723 | C | A | 1 | a0001c0002t0001g0020 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.281-5903G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757723 | |||||||
chr3:15757800 | C | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281-5980G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757800 | |||||||
chr3:15757908 | T | C | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-6088A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757908 | |||||||
chr3:15758078 | G | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.281-6258C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758078 | |||||||
chr3:15758391 | G | A | 3 | a0001c0001t0002g0156 a0001c0001t0002g0158 a0001c0001t0002g0160 |
3 | HG02622.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.281-6571C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758391 | |||||||
chr3:15758468 | T | G | 53 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(50): Show |
53 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.281-6648A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758468 | |||||||
chr3:15758486 | T | C | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-6666A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758486 | |||||||
chr3:15758740 | A | G | 1 | a0001c0001t0006g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-6920T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758740 | |||||||
chr3:15758866 | C | T | 11 | a0001c0001t0008g0333 a0001c0001t0008g0337 a0001c0001t0008g0338 others(8): Show |
11 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-7046G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758866 | |||||||
chr3:15759233 | C | T | 134 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.280+7001G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759233 | |||||||
chr3:15759301 | T | C | 254 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(251): Show |
256 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.280+6933A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759301 | |||||||
chr3:15759326 | C | CA | 23 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.280+6907dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759326 | |||||||
chr3:15759693 | C | A | 24 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(21): Show |
24 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.280+6541G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759693 | |||||||
chr3:15760032 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+6202C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760032 | |||||||
chr3:15760056 | ACTAT | A | 23 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.280+6174_280+6177d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760056 | |||||||
chr3:15760161 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.280+6073C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760161 | |||||||
chr3:15760336 | A | G | 1 | a0001c0003t0005g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.280+5898T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760336 | |||||||
chr3:15760390 | A | G | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280+5844T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760390 | |||||||
chr3:15760624 | A | T | 51 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(48): Show |
51 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.280+5610T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760624 | |||||||
chr3:15760697 | G | C | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+5537C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760697 | |||||||
chr3:15760892 | C | T | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.280+5342G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760892 | |||||||
chr3:15761064 | G | T | 1 | a0001c0002t0001g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+5170C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761064 | |||||||
chr3:15761337 | T | C | 40 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(37): Show |
41 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.280+4897A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761337 | |||||||
chr3:15761740 | T | G | 1 | a0001c0010t0012g0316 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.280+4494A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761740 | |||||||
chr3:15761757 | C | G | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.280+4477G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761757 | |||||||
chr3:15761762 | G | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+4472C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761762 | |||||||
chr3:15761797 | T | A | 1 | a0001c0002t0001g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280+4437A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761797 | |||||||
chr3:15761998 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.280+4236G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761998 | |||||||
chr3:15762154 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280+4080G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762154 | |||||||
chr3:15762188 | T | TA | 34 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0252 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.280+4045dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762188 | |||||||
chr3:15762189 | A | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+4045T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762189 | |||||||
chr3:15762189 | AAAAAAAA others(23): Show |
A | 3 | a0001c0002t0001g0079 a0001c0007t0021g0300 a0001c0007t0021g0301 |
3 | NA19001.hp1 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.280+4015_280+4044d others(32): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762189 | |||||||
chr3:15762190 | AAAAAAAA others(22): Show |
A | 124 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(121): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.280+4015_280+4043d others(31): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762190 | |||||||
chr3:15762191 | AAAAAAAA others(21): Show |
A | 9 | a0001c0002t0001g0112 a0001c0002t0001g0119 a0001c0002t0001g0121 others(6): Show |
9 | HG01361.hp1 HG01361.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.280+4015_280+4042d others(30): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762191 | |||||||
chr3:15762203 | A | C | 4 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
4 | HG01934.hp1 HG02273.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+4031T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762203 | |||||||
chr3:15762207 | A | C | 1 | a0001c0001t0029g0010 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.280+4027T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762207 | |||||||
chr3:15762209 | A | AC | 11 | a0001c0001t0003g0262 a0001c0001t0004g0234 a0001c0001t0004g0235 others(8): Show |
11 | HG01891.hp1 HG02056.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.280+4024_280+4025i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762209 | |||||||
chr3:15762209 | A | C | 2 | a0001c0001t0004g0243 a0001c0001t0004g0244 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.280+4025T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762209 | |||||||
chr3:15762212 | A | AAAC | 52 | a0001c0001t0002g0135 a0001c0001t0002g0142 a0001c0001t0002g0148 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.280+4021_280+4022i others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762212 | |||||||
chr3:15762212 | AAC | A | 6 | a0001c0004t0009g0291 a0001c0004t0009g0293 a0001c0004t0009g0297 others(3): Show |
6 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+4020_280+4021d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762212 | |||||||
chr3:15762213 | AC | A | 3 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 |
3 | HG01884.hp1 HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.280+4020delG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762213 | |||||||
chr3:15762214 | C | A | 83 | a0001c0001t0002g0135 a0001c0001t0002g0142 a0001c0001t0002g0148 others(80): Show |
83 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.280+4020G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762214 | |||||||
chr3:15762214 | C | CAA | 43 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(40): Show |
44 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.280+4018_280+4019d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762214 | |||||||
chr3:15762217 | A | C | 5 | a0001c0002t0001g0129 a0001c0003t0018g0227 a0001c0003t0018g0228 others(2): Show |
5 | HG01081.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+4017T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762217 | |||||||
chr3:15762219 | C | A | 43 | a0001c0001t0002g0186 a0001c0001t0002g0208 a0001c0001t0006g0302 others(40): Show |
43 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.280+4015G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762219 | |||||||
chr3:15762221 | A | AC | 48 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(45): Show |
48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.280+4012_280+4013i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762221 | |||||||
chr3:15762221 | A | ACAAC | 3 | a0001c0001t0002g0186 a0001c0001t0002g0208 a0001c0001t0049g0277 |
3 | NA19011.hp2 NA19087.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.280+4012_280+4013i others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762221 | |||||||
chr3:15762222 | A | C | 50 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(47): Show |
51 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.280+4012T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762222 | |||||||
chr3:15762223 | A | C | 6 | a0001c0001t0010g0263 a0001c0001t0010g0264 a0001c0001t0010g0272 others(3): Show |
6 | HG01934.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+4011T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762223 | |||||||
chr3:15762224 | A | C | 24 | a0001c0001t0003g0266 a0001c0001t0003g0270 a0001c0001t0004g0234 others(21): Show |
24 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.280+4010T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762224 | |||||||
chr3:15762492 | T | C | 1 | a0001c0002t0027g0008 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.280+3742A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762492 | |||||||
chr3:15762834 | T | C | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+3400A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762834 | |||||||
chr3:15762835 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+3399G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762835 | |||||||
chr3:15763046 | T | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280+3188A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763046 | |||||||
chr3:15763051 | T | G | 53 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(50): Show |
53 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.280+3183A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763051 | |||||||
chr3:15763244 | T | C | 3 | a0001c0002t0011g0231 a0001c0002t0011g0232 a0003c0015t0011g0229 |
3 | HG01255.hp1 HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.280+2990A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763244 | |||||||
chr3:15763550 | A | G | 4 | a0001c0002t0001g0058 a0001c0002t0001g0060 a0001c0002t0001g0061 others(1): Show |
4 | NA18948.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+2684T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763550 | |||||||
chr3:15763658 | A | G | 251 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(248): Show |
253 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.280+2576T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763658 | |||||||
chr3:15763689 | G | A | 1 | a0001c0002t0011g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280+2545C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763689 | |||||||
chr3:15763717 | A | G | 294 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(291): Show |
296 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.280+2517T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763717 | |||||||
chr3:15763753 | G | A | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+2481C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763753 | |||||||
chr3:15763865 | T | G | 1 | a0001c0002t0001g0029 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.280+2369A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763865 | |||||||
chr3:15763874 | T | C | 1 | a0001c0002t0001g0032 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.280+2360A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763874 | |||||||
chr3:15763982 | C | T | 1 | a0001c0001t0057g0328 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.280+2252G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763982 | |||||||
chr3:15764203 | A | G | 1 | a0002c0006t0001g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.280+2031T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764203 | |||||||
chr3:15764386 | T | A | 1 | a0001c0001t0002g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280+1848A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764386 | |||||||
chr3:15764541 | GA | G | 150 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(147): Show |
151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.280+1692delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764541 | |||||||
chr3:15764569 | A | T | 1 | a0001c0001t0002g0185 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280+1665T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764569 | |||||||
chr3:15764755 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+1479G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764755 | |||||||
chr3:15764964 | A | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.280+1270T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764964 | |||||||
chr3:15764982 | C | CTGTT | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+1251_280+1252i others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764982 | |||||||
chr3:15764998 | C | T | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+1236G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764998 | |||||||
chr3:15765013 | A | C | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.280+1221T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765013 | |||||||
chr3:15765181 | T | A | 1 | a0001c0002t0001g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.280+1053A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765181 | |||||||
chr3:15765314 | A | G | 2 | a0001c0002t0001g0076 a0001c0002t0001g0077 |
2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.280+920T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765314 | |||||||
chr3:15765486 | G | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+748C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765486 | |||||||
chr3:15765612 | C | T | 1 | a0001c0001t0016g0326 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.280+622G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765612 | |||||||
chr3:15765690 | A | G | 1 | a0001c0001t0006g0312 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.280+544T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765690 | |||||||
chr3:15765702 | T | C | 1 | a0001c0002t0001g0098 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.280+532A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765702 | |||||||
chr3:15765722 | C | A | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.280+512G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765722 | |||||||
chr3:15765839 | C | A | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.280+395G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765839 | |||||||
chr3:15765847 | CA | C | 60 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(57): Show |
60 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.280+386delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765847 | |||||||
chr3:15765847 | CAA | C | 179 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.280+385_280+386del others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765847 | |||||||
chr3:15765881 | G | A | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.280+353C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765881 | |||||||
chr3:15765907 | G | A | 6 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0052g0314 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+327C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765907 | |||||||
chr3:15765919 | C | A | 50 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(47): Show |
50 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.280+315G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765919 | |||||||
chr3:15766052 | A | G | 1 | a0001c0002t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.280+182T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766052 | |||||||
chr3:15766091 | T | C | 2 | a0001c0001t0004g0243 a0001c0001t0004g0244 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.280+143A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766091 | |||||||
chr3:15766108 | T | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.280+126A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766108 | |||||||
chr3:15766185 | A | G | 4 | a0001c0002t0013g0015 a0001c0002t0013g0016 a0001c0002t0013g0017 others(1): Show |
4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+49T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766185 | |||||||
chr3:15766218 | T | A | 134 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.280+16A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766218 | |||||||
chr3:15766326 | G | A | 1 | a0001c0002t0045g0224 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.202-14C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766326 | |||||||
chr3:15766496 | C | A | 1 | a0001c0002t0001g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.202-184G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766496 | |||||||
chr3:15766581 | A | G | 99 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.202-269T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766581 | |||||||
chr3:15766646 | T | C | 12 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-334A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766646 | |||||||
chr3:15766690 | A | C | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.202-378T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766690 | |||||||
chr3:15766851 | TGATA | T | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.202-543_202-540del others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766851 | |||||||
chr3:15766947 | G | C | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-635C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766947 | |||||||
chr3:15767097 | T | C | 2 | a0001c0002t0001g0040 a0001c0002t0035g0039 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.202-785A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767097 | |||||||
chr3:15767165 | A | C | 134 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.202-853T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767165 | |||||||
chr3:15767200 | C | T | 7 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0241 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-888G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767200 | |||||||
chr3:15767329 | TACTC | T | 23 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-1021_202-1018d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767329 | |||||||
chr3:15767352 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.202-1040G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767352 | |||||||
chr3:15767383 | A | T | 262 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(259): Show |
264 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.202-1071T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767383 | |||||||
chr3:15767600 | G | A | 1 | a0001c0002t0007g0090 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.202-1288C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767600 | |||||||
chr3:15767657 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.202-1345C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767657 | |||||||
chr3:15767682 | A | G | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.202-1370T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767682 | |||||||
chr3:15767700 | T | TA | 10 | a0001c0001t0003g0250 a0001c0001t0003g0269 a0001c0001t0008g0331 others(7): Show |
10 | HG00140.hp1 HG01167.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-1389dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | T | TAA | 6 | a0001c0001t0003g0257 a0001c0001t0003g0259 a0001c0001t0003g0262 others(3): Show |
6 | HG01243.hp1 HG02056.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-1390_202-1389d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0003g0255 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.202-1399_202-1389d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0003g0252 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.202-1400_202-1389d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | T | TAAAAAAA others(12): Show |
1 | a0001c0001t0016g0327 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.202-1407_202-1389d others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TA | T | 21 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0270 others(18): Show |
21 | HG00099.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.202-1389delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAA | T | 9 | a0001c0002t0001g0102 a0001c0002t0001g0106 a0001c0002t0001g0107 others(6): Show |
9 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-1390_202-1389d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAA | T | 7 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0040 others(4): Show |
7 | HG01255.hp1 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-1391_202-1389d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAA | T | 15 | a0001c0002t0001g0022 a0001c0002t0001g0099 a0001c0002t0001g0100 others(12): Show |
15 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.202-1392_202-1389d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAA | T | 7 | a0001c0002t0001g0103 a0001c0002t0001g0105 a0001c0002t0001g0110 others(4): Show |
7 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-1393_202-1389d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(3): Show |
T | 4 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0004g0242 others(1): Show |
4 | HG02486.hp1 HG02602.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-1398_202-1389d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(4): Show |
T | 5 | a0001c0001t0004g0234 a0001c0001t0004g0241 a0001c0001t0004g0243 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-1399_202-1389d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(5): Show |
T | 9 | a0001c0003t0005g0279 a0001c0003t0005g0284 a0001c0003t0005g0286 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.202-1400_202-1389d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(6): Show |
T | 12 | a0001c0003t0005g0278 a0001c0003t0005g0282 a0001c0003t0005g0283 others(9): Show |
12 | HG01168.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-1401_202-1389d others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(10): Show |
T | 19 | a0001c0001t0002g0134 a0001c0001t0002g0142 a0001c0001t0002g0151 others(16): Show |
20 | HG00597.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.202-1405_202-1389d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(11): Show |
T | 80 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(77): Show |
80 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.202-1406_202-1389d others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(12): Show |
T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.202-1407_202-1389d others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(14): Show |
T | 1 | a0001c0001t0004g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202-1409_202-1389d others(23): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(19): Show |
T | 7 | a0001c0002t0001g0021 a0001c0002t0001g0081 a0001c0002t0001g0091 others(4): Show |
7 | HG02300.hp1 HG02300.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-1414_202-1389d others(28): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767700 | TAAAAAAA others(20): Show |
T | 86 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(83): Show |
87 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.202-1415_202-1389d others(29): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | |||||||
chr3:15767751 | G | A | 1 | a0001c0004t0009g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.202-1439C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767751 | |||||||
chr3:15767783 | G | C | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-1471C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767783 | |||||||
chr3:15767786 | G | C | 1 | a0001c0002t0001g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.202-1474C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767786 | |||||||
chr3:15767813 | G | A | 6 | a0001c0002t0001g0040 a0001c0002t0013g0015 a0001c0002t0013g0016 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-1501C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767813 | |||||||
chr3:15767908 | CAACAAA | C | 11 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(8): Show |
11 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-1602_202-1597d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767908 | |||||||
chr3:15767910 | AC | A | 15 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-1599delG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767910 | |||||||
chr3:15767914 | A | C | 15 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-1602T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767914 | |||||||
chr3:15768098 | A | G | 2 | a0001c0002t0001g0018 a0001c0002t0001g0019 |
2 | NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.202-1786T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768098 | |||||||
chr3:15768390 | C | T | 24 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(21): Show |
24 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.202-2078G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768390 | |||||||
chr3:15768613 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202-2301A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768613 | |||||||
chr3:15768640 | A | C | 1 | a0001c0002t0042g0131 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.202-2328T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768640 | |||||||
chr3:15768687 | T | C | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | NA18969.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.202-2375A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768687 | |||||||
chr3:15768777 | G | A | 2 | a0001c0002t0001g0099 a0001c0002t0001g0102 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.202-2465C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768777 | |||||||
chr3:15768802 | A | G | 134 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.202-2490T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768802 | |||||||
chr3:15769071 | G | A | 1 | a0001c0001t0046g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.202-2759C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769071 | |||||||
chr3:15769091 | A | G | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-2779T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769091 | |||||||
chr3:15769098 | C | T | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.202-2786G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769098 | |||||||
chr3:15769136 | A | G | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-2824T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769136 | |||||||
chr3:15769158 | G | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-2846C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769158 | |||||||
chr3:15769410 | C | T | 2 | a0001c0001t0010g0272 a0001c0001t0010g0274 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.202-3098G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769410 | |||||||
chr3:15769426 | A | T | 4 | a0001c0002t0001g0058 a0001c0002t0001g0060 a0001c0002t0001g0061 others(1): Show |
4 | NA18948.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3114T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769426 | |||||||
chr3:15769540 | A | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-3228T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769540 | |||||||
chr3:15769725 | G | A | 4 | a0001c0002t0013g0015 a0001c0002t0013g0016 a0001c0002t0013g0017 others(1): Show |
4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3413C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769725 | |||||||
chr3:15769840 | A | G | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-3528T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769840 | |||||||
chr3:15770007 | C | T | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202-3695G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770007 | |||||||
chr3:15770033 | A | G | 1 | a0001c0002t0039g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.202-3721T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770033 | |||||||
chr3:15770034 | A | T | 1 | a0001c0002t0039g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.202-3722T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770034 | |||||||
chr3:15770037 | T | A | 1 | a0001c0002t0039g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.202-3725A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770037 | |||||||
chr3:15770037 | T | TA | 7 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0222 others(4): Show |
7 | HG00621.hp1 HG02129.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-3726dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770037 | |||||||
chr3:15770119 | T | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.202-3807A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770119 | |||||||
chr3:15770342 | GAA | G | 21 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.202-4032_202-4031d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770342 | |||||||
chr3:15770396 | T | C | 1 | a0001c0001t0004g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202-4084A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770396 | |||||||
chr3:15770413 | C | CAT | 86 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(83): Show |
87 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.202-4103_202-4102d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | |||||||
chr3:15770413 | C | CATAT | 13 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0141 others(10): Show |
13 | HG01099.hp1 HG01891.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.202-4105_202-4102d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | |||||||
chr3:15770413 | C | T | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202-4101G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | |||||||
chr3:15770413 | CAT | C | 38 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(35): Show |
38 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.202-4103_202-4102d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | |||||||
chr3:15770567 | C | T | 43 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(40): Show |
44 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-4255G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770567 | |||||||
chr3:15770578 | T | C | 42 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(39): Show |
42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.202-4266A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770578 | |||||||
chr3:15770751 | G | A | 3 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0001t0024g0005 |
3 | HG01069.hp2 NA18948.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.202-4439C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770751 | |||||||
chr3:15770836 | G | A | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-4524C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770836 | |||||||
chr3:15770873 | G | C | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-4561C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770873 | |||||||
chr3:15771015 | G | C | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-4703C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771015 | |||||||
chr3:15771324 | C | G | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-5012G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771324 | |||||||
chr3:15771409 | C | CA | 102 | a0001c0001t0001g0072 a0001c0001t0015g0325 a0001c0001t0037g0086 others(99): Show |
103 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.202-5098dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771409 | |||||||
chr3:15771409 | C | CAA | 23 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0100 others(20): Show |
23 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-5099_202-5098d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771409 | |||||||
chr3:15771409 | CA | C | 40 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(37): Show |
40 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.202-5098delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771409 | |||||||
chr3:15771462 | A | G | 2 | a0001c0009t0005g0280 a0001c0009t0005g0281 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.202-5150T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771462 | |||||||
chr3:15771514 | G | C | 1 | a0001c0002t0001g0112 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202-5202C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771514 | |||||||
chr3:15771560 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.202-5248T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771560 | |||||||
chr3:15771739 | C | A | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-5427G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771739 | |||||||
chr3:15771740 | G | T | 23 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-5428C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771740 | |||||||
chr3:15771869 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.202-5557A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771869 | |||||||
chr3:15771916 | A | G | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-5604T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771916 | |||||||
chr3:15772109 | T | C | 46 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0018 others(43): Show |
47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.202-5797A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772109 | |||||||
chr3:15772453 | C | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-6141G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772453 | |||||||
chr3:15772549 | T | G | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-6237A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772549 | |||||||
chr3:15772732 | G | A | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-6420C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772732 | |||||||
chr3:15772747 | C | T | 9 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-6435G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772747 | |||||||
chr3:15772782 | G | C | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202-6470C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772782 | |||||||
chr3:15772789 | C | T | 5 | a0001c0005t0012g0318 a0001c0005t0052g0314 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-6477G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772789 | |||||||
chr3:15772790 | G | T | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.202-6478C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772790 | |||||||
chr3:15772812 | G | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.202-6500C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772812 | |||||||
chr3:15773135 | TA | T | 13 | a0001c0001t0002g0183 a0001c0003t0005g0278 a0001c0003t0005g0279 others(10): Show |
13 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.202-6824delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773135 | |||||||
chr3:15773228 | T | C | 30 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(27): Show |
30 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.202-6916A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773228 | |||||||
chr3:15773279 | G | A | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202-6967C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773279 | |||||||
chr3:15773400 | G | A | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-7088C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773400 | |||||||
chr3:15773403 | T | C | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.202-7091A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773403 | |||||||
chr3:15773592 | G | A | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | NA18969.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.202-7280C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773592 | |||||||
chr3:15773947 | G | T | 1 | a0001c0001t0046g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.202-7635C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773947 | |||||||
chr3:15774042 | C | T | 1 | a0001c0002t0048g0275 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.202-7730G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774042 | |||||||
chr3:15774229 | T | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-7917A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774229 | |||||||
chr3:15774250 | A | G | 4 | a0001c0002t0013g0015 a0001c0002t0013g0016 a0001c0002t0013g0017 others(1): Show |
4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-7938T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774250 | |||||||
chr3:15774281 | C | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-7969G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774281 | |||||||
chr3:15774644 | A | G | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-8332T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774644 | |||||||
chr3:15774717 | A | G | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-8405T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774717 | |||||||
chr3:15774819 | C | T | 135 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.202-8507G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774819 | |||||||
chr3:15774849 | G | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-8537C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774849 | |||||||
chr3:15774985 | T | TCCTGCCT others(30): Show |
101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-8710_202-8674d others(39): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774985 | |||||||
chr3:15775029 | A | C | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-8717T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775029 | |||||||
chr3:15775040 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.202-8728G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775040 | |||||||
chr3:15775297 | G | A | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202-8985C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775297 | |||||||
chr3:15775378 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.202-9066G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775378 | |||||||
chr3:15775540 | T | C | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-9228A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775540 | |||||||
chr3:15775561 | A | C | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-9249T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775561 | |||||||
chr3:15775660 | A | G | 1 | a0001c0002t0033g0014 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202-9348T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775660 | |||||||
chr3:15775811 | C | A | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-9499G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775811 | |||||||
chr3:15775811 | C | T | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.202-9499G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775811 | |||||||
chr3:15775876 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.202-9564G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775876 | |||||||
chr3:15775917 | A | G | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202-9605T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775917 | |||||||
chr3:15775995 | T | G | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.202-9683A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775995 | |||||||
chr3:15776095 | T | A | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-9783A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776095 | |||||||
chr3:15776134 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.202-9822T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776134 | |||||||
chr3:15776623 | G | C | 1 | a0001c0002t0001g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.202-10311C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776623 | |||||||
chr3:15776936 | T | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-10624A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776936 | |||||||
chr3:15777071 | C | T | 23 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-10759G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777071 | |||||||
chr3:15777084 | G | T | 1 | a0001c0002t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.202-10772C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777084 | |||||||
chr3:15777107 | C | T | 1 | a0001c0002t0035g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.202-10795G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777107 | |||||||
chr3:15777140 | A | G | 292 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(289): Show |
294 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.202-10828T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777140 | |||||||
chr3:15777222 | T | C | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.202-10910A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777222 | |||||||
chr3:15777271 | CA | C | 21 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0010g0263 others(18): Show |
21 | HG01109.hp2 HG01168.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.202-10960delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777271 | |||||||
chr3:15777271 | CAA | C | 211 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(208): Show |
213 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.202-10961_202-1096 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777271 | |||||||
chr3:15777271 | CAAA | C | 45 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(42): Show |
45 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.202-10962_202-1096 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777271 | |||||||
chr3:15777388 | C | T | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-11076G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777388 | |||||||
chr3:15777577 | CAT | C | 3 | a0001c0003t0005g0285 a0001c0003t0005g0287 a0001c0003t0005g0288 |
3 | HG02280.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.202-11267_202-1126 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777577 | |||||||
chr3:15777586 | T | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-11274A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777586 | |||||||
chr3:15777684 | G | A | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-11372C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777684 | |||||||
chr3:15777812 | C | G | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-11500G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777812 | |||||||
chr3:15777849 | T | TAC | 30 | a0001c0001t0003g0254 a0001c0001t0003g0266 a0001c0001t0028g0009 others(27): Show |
31 | HG00642.hp1 HG01515.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.202-11539_202-1153 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACAC | 41 | a0001c0001t0003g0255 a0001c0001t0003g0267 a0001c0001t0004g0234 others(38): Show |
41 | HG00099.hp1 HG00423.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.202-11541_202-1153 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACAC | 35 | a0001c0001t0003g0249 a0001c0001t0003g0268 a0001c0001t0003g0269 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.202-11543_202-1153 others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACACA others(1): Show |
26 | a0001c0001t0001g0072 a0001c0001t0003g0270 a0001c0001t0004g0235 others(23): Show |
26 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-11545_202-1153 others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACACA others(3): Show |
15 | a0001c0001t0003g0271 a0001c0001t0008g0330 a0001c0001t0008g0334 others(12): Show |
15 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-11547_202-1153 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACACA others(5): Show |
7 | a0001c0001t0008g0335 a0001c0002t0001g0020 a0001c0002t0001g0037 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-11549_202-1153 others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACACA others(7): Show |
5 | a0001c0001t0016g0329 a0001c0001t0057g0328 a0001c0002t0001g0054 others(2): Show |
5 | HG01109.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-11551_202-1153 others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACACA others(9): Show |
1 | a0003c0015t0011g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.202-11553_202-1153 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACACA others(11): Show |
1 | a0001c0001t0008g0336 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.202-11555_202-1153 others(22): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | T | TACACACA others(15): Show |
2 | a0001c0002t0001g0029 a0001c0002t0001g0055 |
2 | HG00558.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.202-11559_202-1153 others(26): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | TAC | T | 14 | a0001c0001t0003g0252 a0001c0001t0003g0256 a0001c0001t0003g0260 others(11): Show |
14 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.202-11539_202-1153 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | TACAC | T | 7 | a0001c0001t0002g0134 a0001c0001t0002g0159 a0001c0001t0002g0160 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-11541_202-1153 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | TACACAC | T | 14 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0003g0250 others(11): Show |
14 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.202-11543_202-1153 others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | TACACACA others(3): Show |
T | 6 | a0001c0001t0002g0156 a0001c0001t0002g0174 a0001c0004t0009g0295 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-11547_202-1153 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | TACACACA others(5): Show |
T | 53 | a0001c0001t0002g0135 a0001c0001t0002g0140 a0001c0001t0002g0141 others(50): Show |
54 | HG00408.hp2 HG00423.hp2 HG01433.hp2 others(51): Show |
intron_variant | MODIFIER | c.202-11549_202-1153 others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | TACACACA others(7): Show |
T | 12 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(9): Show |
12 | HG02258.hp1 HG02647.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-11551_202-1153 others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777849 | TACACACA others(9): Show |
T | 39 | a0001c0001t0002g0175 a0001c0001t0002g0178 a0001c0001t0002g0179 others(36): Show |
39 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.202-11553_202-1153 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | |||||||
chr3:15777886 | A | C | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-11574T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777886 | |||||||
chr3:15777888 | ACACACAC others(8): Show |
A | 1 | a0001c0001t0002g0223 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.202-11591_202-1157 others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777888 | |||||||
chr3:15777892 | ACACACAC others(4): Show |
A | 1 | a0001c0001t0002g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.202-11591_202-1158 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777892 | |||||||
chr3:15777902 | A | C | 1 | a0001c0014t0026g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.202-11590T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777902 | |||||||
chr3:15777903 | C | CACACA | 5 | a0001c0002t0001g0032 a0001c0002t0001g0057 a0001c0002t0001g0080 others(2): Show |
5 | HG01255.hp2 HG02004.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-11592_202-1159 others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | |||||||
chr3:15777903 | C | CACACACA others(2): Show |
4 | a0001c0001t0010g0263 a0001c0001t0010g0264 a0001c0002t0001g0058 others(1): Show |
4 | HG01361.hp2 HG01934.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-11592_202-1159 others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | |||||||
chr3:15777903 | C | CACACACA others(4): Show |
2 | a0001c0002t0001g0041 a0001c0002t0048g0275 |
2 | HG01099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.202-11592_202-1159 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | |||||||
chr3:15777903 | C | CACACACA others(10): Show |
1 | a0001c0002t0038g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.202-11592_202-1159 others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | |||||||
chr3:15777998 | T | C | 1 | a0001c0002t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.202-11686A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777998 | |||||||
chr3:15778006 | C | G | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-11694G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778006 | |||||||
chr3:15778455 | A | C | 5 | a0001c0005t0020g0298 a0001c0005t0020g0299 a0001c0007t0021g0300 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-12143T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778455 | |||||||
chr3:15778469 | T | C | 4 | a0001c0002t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
4 | HG00673.hp1 NA18962.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-12157A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778469 | |||||||
chr3:15778545 | G | C | 9 | a0001c0002t0001g0041 a0001c0002t0001g0043 a0001c0002t0001g0044 others(6): Show |
9 | HG00642.hp1 HG01071.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-12233C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778545 | |||||||
chr3:15778730 | C | T | 12 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-12418G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778730 | |||||||
chr3:15778865 | G | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.202-12553C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778865 | |||||||
chr3:15779162 | A | G | 1 | a0001c0002t0017g0133 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.202-12850T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779162 | |||||||
chr3:15779284 | G | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-12972C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779284 | |||||||
chr3:15779429 | T | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 |
3 | NA18950.hp2 NA18998.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.202-13117A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779429 | |||||||
chr3:15779565 | T | C | 2 | a0001c0002t0042g0131 a0001c0014t0026g0007 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.202-13253A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779565 | |||||||
chr3:15779614 | T | C | 149 | a0001c0001t0001g0072 a0001c0001t0006g0302 a0001c0001t0006g0303 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.202-13302A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779614 | |||||||
chr3:15779635 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-13323G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779635 | |||||||
chr3:15779759 | T | C | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-13447A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779759 | |||||||
chr3:15779763 | T | C | 1 | a0003c0015t0011g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.202-13451A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779763 | |||||||
chr3:15779779 | C | T | 3 | a0001c0004t0009g0296 a0001c0004t0009g0297 a0001c0004t0025g0006 |
3 | HG02723.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.202-13467G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779779 | |||||||
chr3:15779836 | A | T | 1 | a0001c0001t0008g0337 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.202-13524T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779836 | |||||||
chr3:15779980 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-13668G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779980 | |||||||
chr3:15780001 | T | C | 1 | a0001c0002t0017g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.202-13689A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780001 | |||||||
chr3:15780007 | G | C | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-13695C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780007 | |||||||
chr3:15780080 | T | C | 100 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(97): Show |
101 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.202-13768A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780080 | |||||||
chr3:15780191 | C | T | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.202-13879G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780191 | |||||||
chr3:15780276 | C | A | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-13964G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780276 | |||||||
chr3:15780401 | T | C | 1 | a0001c0001t0004g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202-14089A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780401 | |||||||
chr3:15780410 | C | T | 1 | a0001c0001t0003g0258 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.202-14098G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780410 | |||||||
chr3:15780488 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.202-14176A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780488 | |||||||
chr3:15780717 | A | G | 1 | a0001c0001t0008g0331 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.202-14405T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780717 | |||||||
chr3:15780804 | A | G | 5 | a0001c0002t0001g0129 a0001c0003t0018g0227 a0001c0003t0018g0228 others(2): Show |
5 | HG01081.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+14419T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780804 | |||||||
chr3:15780932 | A | T | 1 | a0001c0001t0002g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.201+14291T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780932 | |||||||
chr3:15781659 | G | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG02155.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.201+13564C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781659 | |||||||
chr3:15781667 | A | C | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+13556T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781667 | |||||||
chr3:15781787 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.201+13436A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781787 | |||||||
chr3:15781949 | A | G | 102 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(99): Show |
103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.201+13274T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781949 | |||||||
chr3:15781951 | T | A | 1 | a0001c0001t0008g0337 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.201+13272A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781951 | |||||||
chr3:15782035 | A | G | 292 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(289): Show |
294 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.201+13188T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782035 | |||||||
chr3:15782043 | T | C | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+13180A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782043 | |||||||
chr3:15782073 | T | C | 1 | a0001c0002t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.201+13150A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782073 | |||||||
chr3:15782114 | A | G | 1 | a0001c0001t0004g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.201+13109T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782114 | |||||||
chr3:15782189 | C | T | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+13034G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782189 | |||||||
chr3:15782424 | A | T | 16 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(13): Show |
16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+12799T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782424 | |||||||
chr3:15782436 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.201+12787C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782436 | |||||||
chr3:15782525 | C | G | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201+12698G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782525 | |||||||
chr3:15782619 | T | C | 10 | a0001c0002t0001g0021 a0001c0002t0001g0038 a0001c0002t0001g0073 others(7): Show |
10 | HG02015.hp2 HG02129.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+12604A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782619 | |||||||
chr3:15782623 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201+12600C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782623 | |||||||
chr3:15782649 | T | C | 1 | a0001c0001t0006g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.201+12574A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782649 | |||||||
chr3:15782803 | C | A | 4 | a0001c0002t0013g0015 a0001c0002t0013g0016 a0001c0002t0013g0017 others(1): Show |
4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+12420G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782803 | |||||||
chr3:15782836 | T | C | 1 | a0001c0001t0008g0338 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.201+12387A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782836 | |||||||
chr3:15783040 | T | A | 1 | a0001c0002t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.201+12183A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783040 | |||||||
chr3:15783118 | A | C | 6 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(3): Show |
6 | HG00558.hp2 HG02056.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+12105T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783118 | |||||||
chr3:15783188 | A | C | 1 | a0001c0002t0001g0049 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.201+12035T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783188 | |||||||
chr3:15783325 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+11898C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783325 | |||||||
chr3:15783329 | T | C | 102 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(99): Show |
103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.201+11894A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783329 | |||||||
chr3:15783353 | T | G | 155 | a0001c0001t0001g0072 a0001c0001t0006g0302 a0001c0001t0006g0303 others(152): Show |
156 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.201+11870A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783353 | |||||||
chr3:15783383 | T | C | 1 | a0001c0001t0004g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.201+11840A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783383 | |||||||
chr3:15783681 | G | A | 24 | a0001c0001t0037g0086 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.201+11542C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783681 | |||||||
chr3:15784501 | TA | T | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.201+10721delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784501 | |||||||
chr3:15784601 | G | GACCAATA others(9): Show |
261 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(258): Show |
263 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.201+10621_201+1062 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784601 | |||||||
chr3:15784832 | A | G | 291 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(288): Show |
293 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.201+10391T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784832 | |||||||
chr3:15784849 | C | G | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+10374G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784849 | |||||||
chr3:15784903 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.201+10320T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784903 | |||||||
chr3:15784925 | A | G | 273 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(270): Show |
275 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.201+10298T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784925 | |||||||
chr3:15784936 | C | G | 14 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.201+10287G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784936 | |||||||
chr3:15785107 | T | C | 12 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+10116A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785107 | |||||||
chr3:15785216 | G | A | 2 | a0001c0001t0002g0178 a0001c0001t0032g0013 |
2 | NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.201+10007C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785216 | |||||||
chr3:15785337 | C | A | 5 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(2): Show |
5 | HG00423.hp2 NA18986.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+9886G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785337 | |||||||
chr3:15785535 | T | C | 2 | a0001c0002t0001g0040 a0001c0002t0035g0039 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.201+9688A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785535 | |||||||
chr3:15785699 | A | AT | 9 | a0001c0002t0001g0041 a0001c0002t0001g0043 a0001c0002t0001g0044 others(6): Show |
9 | HG00642.hp1 HG01071.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+9523dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785699 | |||||||
chr3:15785937 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.201+9286A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785937 | |||||||
chr3:15786028 | G | A | 4 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0119 others(1): Show |
4 | HG01243.hp2 HG02300.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+9195C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786028 | |||||||
chr3:15786047 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.201+9176C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786047 | |||||||
chr3:15786105 | A | T | 1 | a0001c0001t0002g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.201+9118T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786105 | |||||||
chr3:15786157 | C | A | 236 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(233): Show |
238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.201+9066G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786157 | |||||||
chr3:15786200 | A | C | 2 | a0001c0002t0001g0040 a0001c0002t0035g0039 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.201+9023T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786200 | |||||||
chr3:15786361 | T | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.201+8862A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786361 | |||||||
chr3:15786395 | T | C | 1 | a0001c0002t0017g0133 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.201+8828A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786395 | |||||||
chr3:15786757 | C | T | 252 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.201+8466G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786757 | |||||||
chr3:15787090 | C | T | 2 | a0001c0001t0004g0234 a0001c0001t0004g0235 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.201+8133G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787090 | |||||||
chr3:15787094 | G | A | 1 | a0001c0005t0012g0317 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.201+8129C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787094 | |||||||
chr3:15787304 | G | T | 262 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(259): Show |
264 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.201+7919C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787304 | |||||||
chr3:15787425 | A | C | 252 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.201+7798T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787425 | |||||||
chr3:15787435 | G | A | 26 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(23): Show |
26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.201+7788C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787435 | |||||||
chr3:15787620 | A | G | 133 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.201+7603T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787620 | |||||||
chr3:15787820 | A | G | 1 | a0001c0001t0003g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.201+7403T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787820 | |||||||
chr3:15787824 | T | C | 3 | a0001c0001t0010g0272 a0001c0001t0010g0273 a0001c0001t0010g0274 |
3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.201+7399A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787824 | |||||||
chr3:15787859 | C | T | 5 | a0001c0005t0012g0317 a0001c0005t0012g0318 a0001c0005t0056g0322 others(2): Show |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+7364G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787859 | |||||||
chr3:15787894 | T | C | 1 | a0001c0002t0001g0098 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.201+7329A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787894 | |||||||
chr3:15788198 | A | G | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+7025T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788198 | |||||||
chr3:15788218 | T | C | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.201+7005A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788218 | |||||||
chr3:15788407 | C | T | 1 | a0001c0002t0017g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.201+6816G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788407 | |||||||
chr3:15788510 | G | A | 3 | a0001c0001t0010g0272 a0001c0001t0010g0273 a0001c0001t0010g0274 |
3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.201+6713C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788510 | |||||||
chr3:15788730 | T | C | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.201+6493A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788730 | |||||||
chr3:15788765 | C | T | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.201+6458G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788765 | |||||||
chr3:15788766 | G | A | 1 | a0001c0001t0002g0220 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.201+6457C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788766 | |||||||
chr3:15788811 | G | T | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.201+6412C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788811 | |||||||
chr3:15788902 | C | T | 1 | a0001c0001t0008g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.201+6321G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788902 | |||||||
chr3:15788905 | C | T | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.201+6318G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788905 | |||||||
chr3:15788908 | A | C | 18 | a0001c0001t0003g0256 a0001c0001t0006g0302 a0001c0001t0006g0303 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.201+6315T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788908 | |||||||
chr3:15789085 | C | G | 1 | a0001c0002t0001g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.201+6138G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789085 | |||||||
chr3:15789090 | C | CT | 12 | a0001c0003t0005g0278 a0001c0003t0005g0279 a0001c0003t0005g0282 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.201+6132dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789090 | |||||||
chr3:15789164 | C | T | 8 | a0001c0001t0006g0304 a0001c0001t0006g0305 a0001c0001t0006g0306 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+6059G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789164 | |||||||
chr3:15789369 | C | T | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+5854G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789369 | |||||||
chr3:15789413 | C | T | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.201+5810G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789413 | |||||||
chr3:15789437 | T | A | 2 | a0001c0002t0001g0129 a0001c0002t0042g0131 |
2 | HG01081.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.201+5786A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789437 | |||||||
chr3:15789437 | TAAAAA | T | 12 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+5781_201+5785d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789437 | |||||||
chr3:15789443 | AAAAAG | A | 11 | a0001c0004t0009g0291 a0001c0004t0009g0292 a0001c0004t0009g0293 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.201+5775_201+5779d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789443 | |||||||
chr3:15789519 | T | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+5704A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789519 | |||||||
chr3:15789564 | C | A | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+5659G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789564 | |||||||
chr3:15789641 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.201+5582T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789641 | |||||||
chr3:15789780 | T | A | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+5443A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789780 | |||||||
chr3:15790018 | T | C | 151 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(148): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.201+5205A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790018 | |||||||
chr3:15790138 | G | A | 101 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(98): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.201+5085C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790138 | |||||||
chr3:15790152 | TAA | T | 5 | a0001c0001t0003g0252 a0001c0001t0003g0253 a0001c0001t0003g0254 others(2): Show |
5 | NA18957.hp2 NA18961.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+5069_201+5070d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790152 | |||||||
chr3:15790200 | C | T | 7 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(4): Show |
7 | NA18940.hp2 NA18942.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+5023G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790200 | |||||||
chr3:15790263 | T | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.201+4960A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790263 | |||||||
chr3:15790422 | T | A | 1 | a0001c0007t0043g0172 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.201+4801A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790422 | |||||||
chr3:15790518 | T | C | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+4705A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790518 | |||||||
chr3:15790542 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.201+4681A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790542 | |||||||
chr3:15790784 | T | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.201+4439A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790784 | |||||||
chr3:15790828 | T | C | 99 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(96): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.201+4395A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790828 | |||||||
chr3:15790848 | T | C | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+4375A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790848 | |||||||
chr3:15790876 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+4347T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790876 | |||||||
chr3:15790910 | C | T | 128 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(125): Show |
129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.201+4313G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790910 | |||||||
chr3:15791040 | C | T | 96 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(93): Show |
97 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.201+4183G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791040 | |||||||
chr3:15791054 | C | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+4169G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791054 | |||||||
chr3:15791216 | C | T | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 |
3 | HG01978.hp1 HG02148.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.201+4007G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791216 | |||||||
chr3:15791352 | TAACTTCA others(28): Show |
T | 16 | a0001c0001t0008g0330 a0001c0001t0008g0331 a0001c0001t0008g0333 others(13): Show |
16 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+3836_201+3870d others(37): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791352 | |||||||
chr3:15791823 | C | T | 1 | a0001c0002t0001g0030 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.201+3400G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791823 | |||||||
chr3:15791833 | C | T | 2 | a0001c0010t0012g0315 a0001c0010t0012g0316 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.201+3390G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791833 | |||||||
chr3:15791945 | T | C | 3 | a0001c0004t0009g0296 a0001c0004t0009g0297 a0001c0004t0025g0006 |
3 | HG02723.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.201+3278A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791945 | |||||||
chr3:15792033 | T | C | 13 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(10): Show |
13 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.201+3190A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792033 | |||||||
chr3:15792059 | T | A | 1 | a0001c0001t0002g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+3164A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792059 | |||||||
chr3:15792060 | C | A | 1 | a0001c0001t0002g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+3163G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792060 | |||||||
chr3:15792107 | GA | G | 10 | a0001c0003t0005g0282 a0001c0003t0005g0283 a0001c0005t0012g0317 others(7): Show |
10 | HG01168.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+3115delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792107 | |||||||
chr3:15792146 | C | T | 252 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(249): Show |
254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.201+3077G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792146 | |||||||
chr3:15792166 | C | T | 1 | a0003c0015t0011g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.201+3057G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792166 | |||||||
chr3:15792396 | C | G | 263 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(260): Show |
265 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.201+2827G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792396 | |||||||
chr3:15792554 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.201+2669G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792554 | |||||||
chr3:15792813 | T | G | 2 | a0001c0007t0021g0300 a0001c0007t0021g0301 |
2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+2410A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792813 | |||||||
chr3:15792852 | A | T | 1 | a0001c0002t0001g0029 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.201+2371T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792852 | |||||||
chr3:15793089 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.201+2134G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793089 | |||||||
chr3:15793163 | A | C | 1 | a0001c0002t0036g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.201+2060T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793163 | |||||||
chr3:15793189 | A | G | 1 | a0001c0001t0002g0178 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.201+2034T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793189 | |||||||
chr3:15793239 | G | A | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.201+1984C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793239 | |||||||
chr3:15793322 | A | C | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 |
3 | HG01978.hp1 HG02148.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.201+1901T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793322 | |||||||
chr3:15793568 | A | G | 3 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 |
3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.201+1655T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793568 | |||||||
chr3:15793653 | A | C | 1 | a0001c0001t0003g0249 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.201+1570T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793653 | |||||||
chr3:15793688 | C | T | 1 | a0001c0001t0006g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.201+1535G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793688 | |||||||
chr3:15793720 | C | T | 1 | a0001c0001t0006g0302 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.201+1503G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793720 | |||||||
chr3:15793813 | C | T | 1 | a0001c0002t0001g0021 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.201+1410G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793813 | |||||||
chr3:15793882 | A | T | 1 | a0001c0002t0001g0020 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.201+1341T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793882 | |||||||
chr3:15794070 | T | G | 1 | a0001c0002t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.201+1153A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794070 | |||||||
chr3:15794076 | A | AATAC | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.201+1143_201+1146d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794076 | |||||||
chr3:15794155 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.201+1068A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794155 | |||||||
chr3:15794211 | A | G | 4 | a0001c0003t0018g0227 a0001c0003t0018g0228 a0001c0003t0019g0225 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+1012T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794211 | |||||||
chr3:15794309 | G | A | 3 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 |
3 | HG02129.hp1 NA18964.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.201+914C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794309 | |||||||
chr3:15794328 | T | TA | 107 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(104): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.201+894dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794328 | |||||||
chr3:15794328 | T | TAA | 128 | a0001c0001t0001g0072 a0001c0001t0002g0176 a0001c0001t0002g0177 others(125): Show |
129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.201+893_201+894dup others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794328 | |||||||
chr3:15794392 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.201+831T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794392 | |||||||
chr3:15794411 | C | G | 1 | a0001c0005t0052g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.201+812G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794411 | |||||||
chr3:15794461 | C | T | 2 | a0001c0003t0005g0278 a0001c0003t0005g0279 |
2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.201+762G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794461 | |||||||
chr3:15794489 | C | T | 1 | a0006c0016t0047g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+734G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794489 | |||||||
chr3:15794589 | TA | T | 235 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(232): Show |
237 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.201+633delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794589 | |||||||
chr3:15794597 | A | T | 2 | a0001c0005t0020g0298 a0001c0005t0020g0299 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.201+626T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794597 | |||||||
chr3:15794627 | A | G | 2 | a0001c0002t0001g0018 a0001c0002t0001g0019 |
2 | NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.201+596T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794627 | |||||||
chr3:15794822 | A | T | 1 | a0003c0013t0050g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+401T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794822 | |||||||
chr3:15794891 | T | C | 1 | a0001c0005t0056g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.201+332A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794891 | |||||||
chr3:15794995 | G | A | 9 | a0001c0002t0001g0001 a0001c0002t0001g0121 a0001c0002t0001g0122 others(6): Show |
10 | HG00140.hp2 HG00741.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.201+228C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794995 | |||||||
chr3:15795184 | C | A | 1 | a0001c0005t0012g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201+39G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15795184 | |||||||
chr3:15795198 | G | A | 1 | a0001c0003t0005g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.201+25C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15795198 | |||||||
chr3:15795216 | G | GT | 13 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(10): Show |
13 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.201+6dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15795216 | |||||||
chr3:15795461 | G | C | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.118-155C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795461 | |||||||
chr3:15795473 | T | C | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.118-167A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795473 | |||||||
chr3:15795514 | C | T | 4 | a0001c0002t0013g0015 a0001c0002t0013g0016 a0001c0002t0013g0017 others(1): Show |
4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-208G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795514 | |||||||
chr3:15795558 | T | C | 1 | a0001c0001t0004g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118-252A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795558 | |||||||
chr3:15795861 | A | C | 21 | a0001c0001t0006g0302 a0001c0001t0006g0303 a0001c0001t0006g0304 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.117+544T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795861 | |||||||
chr3:15795913 | T | C | 17 | a0001c0002t0001g0129 a0001c0003t0005g0278 a0001c0003t0005g0279 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.117+492A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795913 | |||||||
chr3:15796031 | T | C | 51 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(48): Show |
51 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.117+374A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796031 | |||||||
chr3:15796070 | T | C | 2 | a0001c0002t0017g0132 a0001c0002t0017g0133 |
2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.117+335A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796070 | |||||||
chr3:15796149 | A | G | 126 | a0001c0001t0001g0072 a0001c0001t0037g0086 a0001c0002t0001g0001 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.117+256T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796149 | |||||||
chr3:15796277 | C | T | 278 | a0001c0001t0001g0072 a0001c0001t0002g0134 a0001c0001t0002g0135 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.117+128G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796277 |