Item | Value |
---|---|
geneid | 10863 |
ensemblid | ENSG00000042980.14 |
hgncid | 206 |
symbol | ADAM28 |
name | ADAM metallopeptidase domain 28 |
refseq_nuc | NM_014265.6 |
refseq_prot | NP_055080.2 |
ensembl_nuc | ENST00000265769.9 |
ensembl_prot | ENSP00000265769.4 |
mane_status | MANE Select |
chr | chr8 |
start | 24294069 |
end | 24359014 |
strand | + |
ver | v1.2 |
region | chr8:24294069-24359014 |
region5000 | chr8:24289069-24364014 |
regionname0 | ADAM28_chr8_24294069_24359014 |
regionname5000 | ADAM28_chr8_24289069_24364014 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 775 | 264 | 44 | 46 | 135 | 11 | 27 | 93 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0002 | 0/0 | 775 | 34 | 3 | 4 | 21 | 0 | 6 | 19 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0003 | 0/0 | 775 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0004 | 1/0 | 775 | 9 | 5 | 0 | 0 | 0 | 3 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0005 | 0/0 | 775 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0006 | 0/0 | 775 | 3 | 1 | 0 | 1 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0007 | 0/0 | 775 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0008 | 0/0 | 775 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0009 | 0/0 | 775 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0010 | 0/0 | 775 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0011 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0012 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0013 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0014 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0015 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0016 | 0/0 | 775 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0017 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0018 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0019 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
a0020 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | MLQGL others(770): Show |
chr8 | 24289069 | 24364014 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2325 | 210 | 41 | 36 | 98 | 7 | 27 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0001c0002 | 0/0 | 2325 | 48 | 0 | 9 | 36 | 3 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0001c0013 | 0/0 | 2325 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0001c0017 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0001c0025 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0001c0026 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0001c0034 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0002c0003 | 0/0 | 2325 | 27 | 1 | 1 | 20 | 0 | 5 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0002c0007 | 0/0 | 2325 | 4 | 2 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0002c0019 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0002c0031 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0002c0033 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0003c0005 | 0/0 | 2325 | 7 | 5 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0003c0006 | 0/0 | 2325 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0004c0004 | 1/0 | 2325 | 9 | 5 | 0 | 0 | 0 | 3 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0005c0008 | 0/0 | 2325 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0006c0012 | 0/0 | 2325 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0006c0023 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0007c0009 | 0/0 | 2325 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0008c0011 | 0/0 | 2325 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0008c0020 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0009c0010 | 0/0 | 2325 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0009c0028 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0010c0014 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0011c0032 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0012c0021 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0013c0024 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0014c0015 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0015c0027 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0016c0016 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0017c0029 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0018c0022 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0019c0018 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 | ||
a0020c0030 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ATGTT others(2320): Show |
chr8 | 24289069 | 24364014 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7032 | 59 | 7 | 5 | 42 | 1 | 4 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0002 | 0/0 | 7032 | 55 | 20 | 6 | 14 | 2 | 13 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0003 | 0/1 | 7032 | 38 | 4 | 11 | 12 | 3 | 7 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0004 | 0/0 | 7033 | 7 | 0 | 0 | 7 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0005 | 0/0 | 7033 | 9 | 1 | 2 | 6 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0006 | 0/0 | 7032 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0008 | 0/0 | 7032 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0009 | 0/0 | 7032 | 5 | 0 | 4 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0010 | 0/0 | 7008 | 4 | 0 | 4 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7003): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0011 | 0/0 | 7037 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7032): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0012 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0015 | 0/0 | 7033 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0016 | 0/0 | 7032 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0017 | 0/0 | 7030 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7025): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0018 | 0/0 | 7032 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0019 | 0/0 | 7033 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0021 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0022 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0025 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0027 | 0/0 | 7028 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7023): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0030 | 0/0 | 7049 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7044): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0032 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0034 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0036 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0037 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0038 | 0/0 | 7030 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7025): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0039 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0040 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0043 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0044 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0001t0047 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0001 | 0/0 | 7032 | 22 | 0 | 1 | 18 | 3 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0002 | 0/0 | 7032 | 6 | 0 | 6 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0003 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0004 | 0/0 | 7033 | 8 | 0 | 0 | 8 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0005 | 0/0 | 7033 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0008 | 0/0 | 7032 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0010 | 0/0 | 7008 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7003): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0012 | 0/0 | 7033 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0002t0014 | 0/0 | 7032 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0013t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0013t0013 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0017t0002 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0025t0042 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0001c0026t0001 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0001c0034t0024 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0001 | 0/0 | 7032 | 8 | 0 | 0 | 8 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0002 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0003 | 0/0 | 7032 | 11 | 0 | 0 | 7 | 0 | 4 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0004 | 0/0 | 7033 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0008 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0029 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0031 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0045 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0002c0003t0046 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0007t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0007t0003 | 0/0 | 7032 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0007t0026 | 0/0 | 7033 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0002c0019t0006 | 0/0 | 7032 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0031t0002 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0002c0033t0008 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0003c0005t0005 | 0/0 | 7033 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0003c0005t0006 | 0/0 | 7032 | 5 | 3 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0003c0006t0001 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0003c0006t0002 | 0/0 | 7032 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0003c0006t0013 | 0/0 | 7033 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
a0004c0004t0007 | 1/0 | 7019 | 7 | 3 | 0 | 0 | 0 | 3 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7014): Show |
chr8 | 24289069 | 24364014 |
a0004c0004t0020 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7033): Show |
chr8 | 24289069 | 24364014 |
a0004c0004t0041 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7029): Show |
chr8 | 24289069 | 24364014 |
a0005c0008t0002 | 0/0 | 7032 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0006c0012t0001 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0006c0012t0003 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0006c0023t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0007c0009t0003 | 0/0 | 7032 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0008c0011t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0008c0011t0006 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0008c0020t0023 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0009c0010t0002 | 0/0 | 7032 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0009c0028t0006 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0010c0014t0028 | 0/0 | 7024 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7019): Show |
chr8 | 24289069 | 24364014 |
a0011c0032t0033 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7029): Show |
chr8 | 24289069 | 24364014 |
a0012c0021t0001 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0013c0024t0003 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0014c0015t0002 | 0/0 | 7032 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0015c0027t0007 | 0/0 | 7019 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7014): Show |
chr8 | 24289069 | 24364014 |
a0016c0016t0003 | 0/0 | 7032 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0017c0029t0002 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0018c0022t0002 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0019c0018t0035 | 0/0 | 7032 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7027): Show |
chr8 | 24289069 | 24364014 |
a0020c0030t0004 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | ACTGG others(7028): Show |
chr8 | 24289069 | 24364014 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0010g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0012g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0015g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0015g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0016g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0018g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0018g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0019g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0021g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0022g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0025g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0027g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0030g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0032g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0034g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0036g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0037g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0038g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0039g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0040g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0043g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0044g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0001t0047g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0008g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0010g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0012g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0012g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0014g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0002t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0013t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0013t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0017t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0025t0042g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0026t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0001c0034t0024g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0029g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0031g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0045g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0003t0046g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0007t0026g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0019t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0031t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0002c0033t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0005t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0003c0006t0013g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0020g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0004c0004t0041g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0005c0008t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0005c0008t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0006c0012t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0006c0012t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0006c0023t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0007c0009t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0007c0009t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0007c0009t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0008c0011t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0008c0011t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0008c0020t0023g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0009c0010t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0009c0010t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0009c0028t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0010c0014t0028g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0011c0032t0033g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0012c0021t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0013c0024t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0014c0015t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0015c0027t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0016c0016t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0017c0029t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0018c0022t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0019c0018t0035g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
a0020c0030t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0286 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0219 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00140 | hp1 | a0010 | c0014 | t0028 | g0162 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0177 | EUR | GBR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0030 | EUR | FIN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00323 | hp2 | a0001 | c0001 | t0009 | g0103 | EUR | FIN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00423 | hp2 | a0001 | c0002 | t0004 | g0311 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00438 | hp2 | a0001 | c0001 | t0022 | g0043 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00609 | hp2 | a0001 | c0002 | t0012 | g0314 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0024 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0039 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00673 | hp1 | a0001 | c0001 | t0008 | g0197 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00733 | hp2 | a0003 | c0005 | t0006 | g0243 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00738 | hp2 | a0003 | c0005 | t0006 | g0241 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0222 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0305 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0215 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01074 | hp2 | a0001 | c0001 | t0043 | g0029 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01081 | hp1 | a0001 | c0001 | t0009 | g0131 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0163 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0192 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0221 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01167 | hp1 | a0002 | c0007 | t0003 | g0270 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01168 | hp1 | a0001 | c0001 | t0016 | g0007 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01169 | hp1 | a0002 | c0007 | t0003 | g0271 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01169 | hp2 | a0001 | c0001 | t0016 | g0007 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01192 | hp2 | a0001 | c0017 | t0002 | g0124 | AMR | PUR | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0310 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01258 | hp1 | a0001 | c0001 | t0037 | g0036 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01261 | hp2 | a0002 | c0019 | t0006 | g0229 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01346 | hp2 | a0001 | c0001 | t0009 | g0132 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0289 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0298 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0288 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01516 | hp2 | a0001 | c0026 | t0001 | g0073 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0301 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0135 | EUR | IBS | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01884 | hp1 | a0004 | c0004 | t0007 | g0064 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01891 | hp1 | a0005 | c0008 | t0002 | g0006 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01891 | hp2 | a0001 | c0001 | t0038 | g0123 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01934 | hp1 | a0001 | c0002 | t0010 | g0281 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01943 | hp1 | a0002 | c0003 | t0029 | g0262 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0193 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02015 | hp2 | a0006 | c0012 | t0003 | g0212 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02027 | hp1 | a0001 | c0001 | t0025 | g0159 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02040 | hp1 | a0001 | c0002 | t0004 | g0285 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0235 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02055 | hp1 | a0011 | c0032 | t0033 | g0247 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02055 | hp2 | a0003 | c0006 | t0002 | g0277 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02056 | hp2 | a0001 | c0002 | t0004 | g0290 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02071 | hp2 | a0002 | c0033 | t0008 | g0266 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02074 | hp2 | a0012 | c0021 | t0001 | g0100 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02080 | hp1 | a0013 | c0024 | t0003 | g0086 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02080 | hp2 | a0007 | c0009 | t0003 | g0001 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02083 | hp1 | a0001 | c0001 | t0015 | g0190 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0300 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02145 | hp1 | a0001 | c0001 | t0027 | g0182 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02145 | hp2 | a0003 | c0005 | t0006 | g0244 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02155 | hp1 | a0001 | c0034 | t0024 | g0296 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | CDX | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02257 | hp1 | a0004 | c0004 | t0007 | g0122 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02257 | hp2 | a0008 | c0020 | t0023 | g0246 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02258 | hp1 | a0001 | c0001 | t0044 | g0228 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02258 | hp2 | a0003 | c0006 | t0002 | g0275 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02280 | hp1 | a0004 | c0004 | t0020 | g0230 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02523 | hp2 | a0001 | c0001 | t0012 | g0028 | EAS | KHV | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02572 | hp1 | a0003 | c0006 | t0002 | g0276 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02615 | hp1 | a0006 | c0023 | t0002 | g0120 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02615 | hp2 | a0003 | c0005 | t0005 | g0018 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02630 | hp1 | a0014 | c0015 | t0002 | g0226 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02630 | hp2 | a0004 | c0004 | t0007 | g0166 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02698 | hp2 | a0002 | c0003 | t0046 | g0260 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02735 | hp2 | a0001 | c0001 | t0036 | g0218 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02809 | hp1 | a0002 | c0007 | t0026 | g0065 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02809 | hp2 | a0001 | c0013 | t0002 | g0168 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02895 | hp1 | a0008 | c0011 | t0002 | g0026 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02895 | hp2 | a0003 | c0006 | t0001 | g0279 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02922 | hp1 | a0005 | c0008 | t0002 | g0006 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02922 | hp2 | a0003 | c0006 | t0013 | g0273 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02965 | hp1 | a0001 | c0025 | t0042 | g0248 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02965 | hp2 | a0002 | c0007 | t0002 | g0116 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03130 | hp1 | a0004 | c0004 | t0041 | g0133 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03195 | hp1 | a0005 | c0008 | t0002 | g0006 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03195 | hp2 | a0015 | c0027 | t0007 | g0025 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03453 | hp1 | a0003 | c0005 | t0006 | g0240 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03486 | hp1 | a0001 | c0001 | t0017 | g0042 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03486 | hp2 | a0003 | c0006 | t0013 | g0274 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03490 | hp1 | a0016 | c0016 | t0003 | g0174 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03491 | hp1 | a0002 | c0003 | t0003 | g0019 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0204 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03492 | hp1 | a0002 | c0003 | t0003 | g0019 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03540 | hp1 | a0009 | c0010 | t0002 | g0239 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03540 | hp2 | a0005 | c0008 | t0002 | g0316 | AFR | GWD | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03579 | hp1 | a0003 | c0005 | t0005 | g0018 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03579 | hp2 | a0001 | c0001 | t0040 | g0074 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03669 | hp2 | a0002 | c0003 | t0003 | g0252 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03688 | hp1 | a0002 | c0003 | t0003 | g0253 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03831 | hp1 | a0004 | c0004 | t0007 | g0076 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03831 | hp2 | a0006 | c0012 | t0001 | g0078 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03834 | hp1 | a0001 | c0001 | t0039 | g0057 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03942 | hp1 | a0004 | c0004 | t0007 | g0075 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03942 | hp2 | a0004 | c0004 | t0007 | g0061 | SAS | BEB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG04204 | hp2 | a0002 | c0031 | t0002 | g0257 | SAS | STU | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | CHB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18906 | hp2 | a0003 | c0005 | t0006 | g0242 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18943 | hp1 | a0002 | c0003 | t0003 | g0267 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18943 | hp2 | a0001 | c0001 | t0018 | g0095 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18944 | hp2 | a0002 | c0003 | t0003 | g0259 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18945 | hp2 | a0002 | c0003 | t0008 | g0261 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18946 | hp2 | a0017 | c0029 | t0002 | g0297 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18948 | hp2 | a0001 | c0002 | t0005 | g0022 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0152 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18954 | hp2 | a0001 | c0001 | t0032 | g0010 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18961 | hp1 | a0001 | c0001 | t0030 | g0010 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18963 | hp1 | a0002 | c0003 | t0004 | g0255 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18965 | hp1 | a0001 | c0002 | t0004 | g0291 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18965 | hp2 | a0001 | c0001 | t0034 | g0005 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18967 | hp1 | a0002 | c0003 | t0002 | g0264 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18968 | hp1 | a0018 | c0022 | t0002 | g0180 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18969 | hp2 | a0001 | c0002 | t0004 | g0293 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18970 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18970 | hp2 | a0007 | c0009 | t0003 | g0178 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18971 | hp2 | a0001 | c0001 | t0011 | g0079 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18973 | hp1 | a0001 | c0002 | t0004 | g0236 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18979 | hp2 | a0001 | c0002 | t0008 | g0023 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0282 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18982 | hp2 | a0002 | c0003 | t0003 | g0251 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18986 | hp1 | a0001 | c0001 | t0011 | g0060 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18988 | hp1 | a0001 | c0001 | t0021 | g0150 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18989 | hp1 | a0001 | c0002 | t0005 | g0022 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18989 | hp2 | a0001 | c0001 | t0047 | g0066 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18990 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18993 | hp2 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18995 | hp1 | a0001 | c0001 | t0015 | g0170 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0258 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19005 | hp1 | a0001 | c0002 | t0014 | g0021 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0263 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19030 | hp2 | a0009 | c0028 | t0006 | g0245 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19054 | hp1 | a0001 | c0002 | t0014 | g0287 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19057 | hp2 | a0001 | c0002 | t0014 | g0021 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19060 | hp2 | a0019 | c0018 | t0035 | g0179 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19062 | hp1 | a0001 | c0001 | t0011 | g0077 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19062 | hp2 | a0002 | c0003 | t0031 | g0237 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19064 | hp2 | a0002 | c0003 | t0004 | g0250 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19067 | hp2 | a0002 | c0003 | t0003 | g0254 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19070 | hp2 | a0001 | c0002 | t0008 | g0023 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19074 | hp2 | a0007 | c0009 | t0003 | g0005 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19077 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19080 | hp1 | a0020 | c0030 | t0004 | g0299 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19080 | hp2 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19086 | hp2 | a0001 | c0002 | t0012 | g0313 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19087 | hp1 | a0002 | c0003 | t0003 | g0265 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19091 | hp2 | a0001 | c0001 | t0018 | g0110 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | YRI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | TSI | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | GIH | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20905 | hp2 | a0001 | c0001 | t0019 | g0037 | SAS | GIH | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02109 | hp1 | a0001 | c0001 | t0017 | g0161 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02486 | hp1 | a0009 | c0010 | t0002 | g0238 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03471 | hp1 | a0003 | c0006 | t0002 | g0278 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG06807 | hp1 | a0001 | c0013 | t0013 | g0167 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA21309 | hp1 | a0002 | c0003 | t0045 | g0272 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
NA21309 | hp2 | a0008 | c0011 | t0006 | g0049 | AFR | LWK | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0223 | REF | REF | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
homoSapiens | grch38p0 | a0004 | c0004 | t0007 | g0134 | REF | REF | ADAM28_chr8_24289069_24364014 | ADAM28 | chr8 | 24289069 | 24364014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24294172 | T | A | 1 | a0010 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.23T>A | p.Val8Asp | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/23 | 104/7019 | 23/2328 | 8/775 | chr8 | 24294172 | |||
chr8:24311367 | T | A | 1 | a0014 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.313T>A | p.Cys105Ser | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/23 | 394/7019 | 313/2328 | 105/775 | chr8 | 24311367 | |||
chr8:24313423 | T | C | 1 | a0016 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.419T>C | p.Ile140Thr | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 500/7019 | 419/2328 | 140/775 | chr8 | 24313423 | |||
chr8:24313447 | G | T | 1 | a0005 | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.443G>T | p.Arg148Leu | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 524/7019 | 443/2328 | 148/775 | chr8 | 24313447 | |||
chr8:24313470 | T | C | 1 | a0007 | 3 | HG02080.hp2 NA18970.hp2 NA19074.hp2 |
missense_variant | MODERATE | c.466T>C | p.Phe156Leu | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 547/7019 | 466/2328 | 156/775 | chr8 | 24313470 | |||
chr8:24321225 | G | T | 3 | a0003 a0009 a0015 |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
missense_variant | MODERATE | c.656G>T | p.Arg219Met | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/23 | 737/7019 | 656/2328 | 219/775 | chr8 | 24321225 | |||
chr8:24335552 | A | G | 2 | a0005 a0011 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.1478A>G | p.Asn493Ser | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/23 | 1559/7019 | 1478/2328 | 493/775 | chr8 | 24335552 | |||
chr8:24339500 | G | C | 1 | a0019 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1602G>C | p.Arg534Ser | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1683/7019 | 1602/2328 | 534/775 | chr8 | 24339500 | |||
chr8:24339504 | G | A | 2 | a0017 a0020 |
2 | NA18946.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.1606G>A | p.Glu536Lys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1687/7019 | 1606/2328 | 536/775 | chr8 | 24339504 | |||
chr8:24339531 | C | T | 1 | a0013 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.1633C>T | p.Arg545Cys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1714/7019 | 1633/2328 | 545/775 | chr8 | 24339531 | |||
chr8:24341705 | C | A | 4 | a0002 a0005 a0008 others(1): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
missense_variant | MODERATE | c.1778C>A | p.Thr593Lys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/23 | 1859/7019 | 1778/2328 | 593/775 | chr8 | 24341705 | |||
chr8:24349882 | G | A | 1 | a0012 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2009G>A | p.Gly670Glu | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2090/7019 | 2009/2328 | 670/775 | chr8 | 24349882 | |||
chr8:24349923 | A | G | 1 | a0006 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.2050A>G | p.Met684Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2131/7019 | 2050/2328 | 684/775 | chr8 | 24349923 | |||
chr8:24349925 | G | A | 6 | a0002 a0006 a0009 others(3): Show |
42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
missense_variant | MODERATE | c.2052G>A | p.Met684Ile | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2133/7019 | 2052/2328 | 684/775 | chr8 | 24349925 | |||
chr8:24349959 | A | C | 1 | a0005 | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.2086A>C | p.Lys696Gln | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2167/7019 | 2086/2328 | 696/775 | chr8 | 24349959 | |||
chr8:24352045 | C | T | 1 | a0018 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.2237C>T | p.Ala746Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/23 | 2318/7019 | 2237/2328 | 746/775 | chr8 | 24352045 | |||
chr8:24353818 | G | A | 18 | a0001 a0002 a0003 others(15): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
missense_variant | MODERATE | c.2293G>A | p.Val765Met | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/23 | 2374/7019 | 2293/2328 | 765/775 | chr8 | 24353818 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24310238 | T | C | 1 | a0009c0010 | 2 | HG02486.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.303T>C | p.Ile101Ile | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/23 | 384/7019 | 303/2328 | 101/775 | chr8 | 24310238 | |||
chr8:24313472 | C | T | 1 | a0001c0034 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.468C>T | p.Phe156Phe | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 549/7019 | 468/2328 | 156/775 | chr8 | 24313472 | |||
chr8:24313538 | C | T | 10 | a0001c0002 a0001c0034 a0002c0003 others(7): Show |
92 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
synonymous_variant | LOW | c.534C>T | p.His178His | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/23 | 615/7019 | 534/2328 | 178/775 | chr8 | 24313538 | |||
chr8:24323926 | C | T | 1 | a0001c0026 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.813C>T | p.Phe271Phe | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/23 | 894/7019 | 813/2328 | 271/775 | chr8 | 24323926 | |||
chr8:24326575 | G | T | 1 | a0001c0025 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.912G>T | p.Thr304Thr | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/23 | 993/7019 | 912/2328 | 304/775 | chr8 | 24326575 | |||
chr8:24330044 | C | T | 1 | a0002c0033 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.1032C>T | p.Asn344Asn | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/23 | 1113/7019 | 1032/2328 | 344/775 | chr8 | 24330044 | |||
chr8:24331291 | G | A | 6 | a0001c0017 a0003c0005 a0003c0006 others(3): Show |
22 | HG00733.hp2 HG00738.hp2 HG01192.hp2 others(19): Show |
synonymous_variant | LOW | c.1245G>A | p.Val415Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/23 | 1326/7019 | 1245/2328 | 415/775 | chr8 | 24331291 | |||
chr8:24339521 | C | T | 4 | a0001c0013 a0003c0005 a0003c0006 others(1): Show |
17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.1623C>T | p.Tyr541Tyr | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/23 | 1704/7019 | 1623/2328 | 541/775 | chr8 | 24339521 | |||
chr8:24343562 | C | T | 1 | a0011c0032 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1968C>T | p.Cys656Cys | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/23 | 2049/7019 | 1968/2328 | 656/775 | chr8 | 24343562 | |||
chr8:24349886 | G | C | 9 | a0002c0003 a0002c0019 a0002c0033 others(6): Show |
36 | HG00621.hp2 HG01261.hp2 HG01943.hp1 others(33): Show |
synonymous_variant | LOW | c.2013G>C | p.Val671Val | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/23 | 2094/7019 | 2013/2328 | 671/775 | chr8 | 24349886 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24354444 | T | G | 1 | a0001c0001t0019 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*40T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 40 | chr8 | 24354444 | ||||||
chr8:24354480 | ACTAT | A | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(84): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*83_*86delATCT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 83 | INFO_REALIGN_3_PRIME | chr8 | 24354480 | |||||
chr8:24354495 | A | T | 1 | a0001c0001t0047 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*91A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 91 | chr8 | 24354495 | ||||||
chr8:24354507 | C | T | 1 | a0002c0003t0046 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 103 | chr8 | 24354507 | ||||||
chr8:24354527 | T | C | 17 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(14): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*123T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 123 | chr8 | 24354527 | ||||||
chr8:24354541 | T | A | 3 | a0001c0013t0013 a0002c0007t0026 a0003c0006t0013 |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*137T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 137 | chr8 | 24354541 | ||||||
chr8:24354632 | A | G | 1 | a0001c0001t0018 | 2 | NA18943.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 228 | chr8 | 24354632 | ||||||
chr8:24354695 | T | G | 1 | a0001c0001t0015 | 2 | HG02083.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*291T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 291 | chr8 | 24354695 | ||||||
chr8:24354863 | A | C | 4 | a0001c0013t0013 a0002c0003t0045 a0002c0007t0026 others(1): Show |
5 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 459 | chr8 | 24354863 | ||||||
chr8:24354951 | G | A | 21 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0016 others(18): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*547G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 547 | chr8 | 24354951 | ||||||
chr8:24355057 | G | A | 3 | a0001c0013t0013 a0002c0007t0026 a0003c0006t0013 |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*653G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 653 | chr8 | 24355057 | ||||||
chr8:24355087 | T | G | 1 | a0001c0001t0021 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 683 | chr8 | 24355087 | ||||||
chr8:24355221 | T | A | 88 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(85): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*817T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 817 | chr8 | 24355221 | ||||||
chr8:24355259 | T | A | 1 | a0002c0007t0026 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 855 | chr8 | 24355259 | ||||||
chr8:24355392 | C | CCTAT | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(84): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*992_*995dupTCTA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 996 | INFO_REALIGN_3_PRIME | chr8 | 24355392 | |||||
chr8:24355409 | T | G | 88 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(85): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*1005T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1005 | chr8 | 24355409 | ||||||
chr8:24355517 | C | CT | 9 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0012 others(6): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1124dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1125 | INFO_REALIGN_3_PRIME | chr8 | 24355517 | |||||
chr8:24355533 | G | T | 1 | a0001c0001t0044 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1129G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1129 | chr8 | 24355533 | ||||||
chr8:24355662 | A | AAGATAGA others(1): Show |
87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(84): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1262_*1269dupTAGA others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1270 | INFO_REALIGN_3_PRIME | chr8 | 24355662 | |||||
chr8:24355675 | C | T | 1 | a0001c0001t0043 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1271 | chr8 | 24355675 | ||||||
chr8:24355935 | G | T | 1 | a0001c0025t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1531 | chr8 | 24355935 | ||||||
chr8:24356052 | C | G | 5 | a0001c0001t0006 a0002c0019t0006 a0003c0005t0006 others(2): Show |
11 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1648 | chr8 | 24356052 | ||||||
chr8:24356091 | T | C | 1 | a0019c0018t0035 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1687T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1687 | chr8 | 24356091 | ||||||
chr8:24356241 | T | A | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(84): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1837T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1837 | chr8 | 24356241 | ||||||
chr8:24356248 | G | C | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1844G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1844 | chr8 | 24356248 | ||||||
chr8:24356409 | A | G | 1 | a0001c0001t0009 | 5 | HG00323.hp2 HG00741.hp1 HG01071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2005A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2005 | chr8 | 24356409 | ||||||
chr8:24356539 | T | C | 1 | a0002c0003t0029 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2135T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2135 | chr8 | 24356539 | ||||||
chr8:24356562 | C | G | 1 | a0001c0001t0025 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2158C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2158 | chr8 | 24356562 | ||||||
chr8:24356613 | C | T | 1 | a0001c0001t0016 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2209C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2209 | chr8 | 24356613 | ||||||
chr8:24356658 | C | T | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(83): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*2254C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2254 | chr8 | 24356658 | ||||||
chr8:24356686 | G | A | 3 | a0001c0013t0013 a0002c0007t0026 a0003c0006t0013 |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2282G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2282 | chr8 | 24356686 | ||||||
chr8:24356870 | C | CCTTTGGG others(30): Show |
1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2467_*2503dupCTTT others(33): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2504 | INFO_REALIGN_3_PRIME | chr8 | 24356870 | |||||
chr8:24356921 | G | C | 1 | a0002c0003t0031 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2517 | chr8 | 24356921 | ||||||
chr8:24357097 | A | G | 1 | a0001c0001t0039 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2693A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2693 | chr8 | 24357097 | ||||||
chr8:24357128 | ATT | A | 85 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(82): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*2727_*2728delTT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2727 | INFO_REALIGN_3_PRIME | chr8 | 24357128 | |||||
chr8:24357212 | T | C | 85 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(82): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*2808T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2808 | chr8 | 24357212 | ||||||
chr8:24357247 | G | A | 85 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(82): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*2843G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2843 | chr8 | 24357247 | ||||||
chr8:24357334 | A | G | 1 | a0001c0025t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2930A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2930 | chr8 | 24357334 | ||||||
chr8:24357422 | C | A | 21 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0016 others(18): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3018C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3018 | chr8 | 24357422 | ||||||
chr8:24357488 | A | G | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(83): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*3084A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3084 | chr8 | 24357488 | ||||||
chr8:24357562 | G | A | 1 | a0001c0001t0022 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3158G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3158 | chr8 | 24357562 | ||||||
chr8:24357662 | G | C | 1 | a0002c0003t0029 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3258G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3258 | chr8 | 24357662 | ||||||
chr8:24357713 | G | T | 1 | a0001c0034t0024 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3309G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3309 | chr8 | 24357713 | ||||||
chr8:24357755 | C | T | 2 | a0001c0001t0030 a0001c0001t0032 |
2 | NA18954.hp2 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3351C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3351 | chr8 | 24357755 | ||||||
chr8:24357775 | T | TTCTC | 88 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(85): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*3372_*3373insCTCT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3373 | INFO_REALIGN_3_PRIME | chr8 | 24357775 | |||||
chr8:24357865 | C | T | 1 | a0001c0034t0024 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3461C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3461 | chr8 | 24357865 | ||||||
chr8:24357914 | A | T | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(83): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*3510A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3510 | chr8 | 24357914 | ||||||
chr8:24357984 | TTATAGTT others(18): Show |
T | 2 | a0001c0001t0010 a0001c0002t0010 |
5 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3606_*3630delTATA others(21): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3606 | INFO_REALIGN_3_PRIME | chr8 | 24357984 | |||||
chr8:24358101 | A | C | 88 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(85): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*3697A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3697 | chr8 | 24358101 | ||||||
chr8:24358112 | T | TATG | 88 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(85): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*3710_*3711insGAT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3711 | INFO_REALIGN_3_PRIME | chr8 | 24358112 | |||||
chr8:24358137 | G | A | 1 | a0008c0020t0023 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3733G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3733 | chr8 | 24358137 | ||||||
chr8:24358137 | G | T | 1 | a0001c0001t0011 | 3 | NA18971.hp2 NA18986.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3733G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3733 | chr8 | 24358137 | ||||||
chr8:24358150 | T | C | 1 | a0001c0001t0037 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3746T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3746 | chr8 | 24358150 | ||||||
chr8:24358178 | G | C | 2 | a0001c0001t0030 a0001c0001t0032 |
2 | NA18954.hp2 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3774G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3774 | chr8 | 24358178 | ||||||
chr8:24358224 | T | A | 1 | a0001c0002t0014 | 3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3820T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3820 | chr8 | 24358224 | ||||||
chr8:24358284 | T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3880T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3880 | chr8 | 24358284 | ||||||
chr8:24358293 | G | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3889 | chr8 | 24358293 | ||||||
chr8:24358303 | T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3899T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3899 | chr8 | 24358303 | ||||||
chr8:24358306 | T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3902T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3902 | chr8 | 24358306 | ||||||
chr8:24358311 | C | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3907C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3907 | chr8 | 24358311 | ||||||
chr8:24358317 | T | TATAGAAT others(8): Show |
1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3913_*3914insATAG others(11): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3914 | chr8 | 24358317 | ||||||
chr8:24358318 | C | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3914C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3914 | chr8 | 24358318 | ||||||
chr8:24358318 | CATT | C | 2 | a0001c0001t0017 a0001c0001t0038 |
3 | HG01891.hp2 HG02109.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3915_*3917delATT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3915 | chr8 | 24358318 | ||||||
chr8:24358326 | A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3922A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3922 | chr8 | 24358326 | ||||||
chr8:24358327 | A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3923A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3923 | chr8 | 24358327 | ||||||
chr8:24358332 | T | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3928T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3928 | chr8 | 24358332 | ||||||
chr8:24358355 | A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3951A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3951 | chr8 | 24358355 | ||||||
chr8:24358366 | A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3962A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3962 | chr8 | 24358366 | ||||||
chr8:24358371 | A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3967A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3967 | chr8 | 24358371 | ||||||
chr8:24358372 | G | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3968G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3968 | chr8 | 24358372 | ||||||
chr8:24358374 | A | T | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3970A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3970 | chr8 | 24358374 | ||||||
chr8:24358376 | C | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3972C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3972 | chr8 | 24358376 | ||||||
chr8:24358379 | G | T | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(84): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*3975G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3975 | chr8 | 24358379 | ||||||
chr8:24358382 | G | C | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3978G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3978 | chr8 | 24358382 | ||||||
chr8:24358383 | T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3979T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3979 | chr8 | 24358383 | ||||||
chr8:24358387 | A | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3983A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 3983 | chr8 | 24358387 | ||||||
chr8:24358404 | T | A | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4000T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4000 | chr8 | 24358404 | ||||||
chr8:24358502 | T | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4098T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4098 | chr8 | 24358502 | ||||||
chr8:24358505 | GCTCCACC others(28): Show |
G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4102_*4136delCTCC others(31): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4102 | chr8 | 24358505 | ||||||
chr8:24358543 | A | C | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4139A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4139 | chr8 | 24358543 | ||||||
chr8:24358553 | C | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4149C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4149 | chr8 | 24358553 | ||||||
chr8:24358563 | A | G | 1 | a0001c0001t0030 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4159A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4159 | chr8 | 24358563 | ||||||
chr8:24358568 | C | T | 3 | a0001c0013t0013 a0002c0007t0026 a0003c0006t0013 |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4164C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4164 | chr8 | 24358568 | ||||||
chr8:24358648 | C | CT | 12 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0017 others(9): Show |
26 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4249dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4250 | INFO_REALIGN_3_PRIME | chr8 | 24358648 | |||||
chr8:24358711 | T | A | 1 | a0001c0001t0038 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4307T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4307 | chr8 | 24358711 | ||||||
chr8:24358734 | A | C | 1 | a0001c0001t0047 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4330A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4330 | chr8 | 24358734 | ||||||
chr8:24358755 | A | T | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(84): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*4351A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4351 | chr8 | 24358755 | ||||||
chr8:24358818 | C | T | 68 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(65): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*4414C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4414 | chr8 | 24358818 | ||||||
chr8:24358856 | T | C | 4 | a0001c0001t0008 a0001c0002t0008 a0002c0003t0008 others(1): Show |
6 | HG00673.hp1 HG02071.hp2 NA18945.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4452T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4452 | chr8 | 24358856 | ||||||
chr8:24358878 | A | G | 9 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0017 others(6): Show |
22 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4474A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4474 | chr8 | 24358878 | ||||||
chr8:24358935 | A | AAAACT | 1 | a0001c0001t0011 | 3 | NA18971.hp2 NA18986.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4533_*4537dupAACT others(1): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4538 | INFO_REALIGN_3_PRIME | chr8 | 24358935 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:24294203 | T | C | 1 | a0001c0001t0010g0024 | 1 | HG00639.hp2 | splice_region_variant&intron_variant | LOW | c.46+8T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24294203 | |||||||
chr8:24294636 | GTTTGAGT others(7): Show |
G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+446_46+459delAG others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24294636 | ||||||
chr8:24294678 | T | C | 1 | a0015c0027t0007g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.46+483T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24294678 | |||||||
chr8:24294725 | C | T | 93 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0002t0001g0003 others(90): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.46+530C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24294725 | |||||||
chr8:24295115 | T | G | 2 | a0001c0002t0004g0236 a0001c0002t0005g0235 |
2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.46+920T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295115 | |||||||
chr8:24295155 | T | C | 2 | a0002c0003t0003g0017 a0002c0003t0031g0237 |
3 | NA18993.hp2 NA19062.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.46+960T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295155 | |||||||
chr8:24295305 | C | G | 1 | a0001c0001t0005g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.46+1110C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295305 | |||||||
chr8:24295469 | GT | G | 40 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0025t0042g0248 others(37): Show |
46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.46+1281delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24295469 | ||||||
chr8:24295683 | G | A | 2 | a0009c0010t0002g0238 a0009c0010t0002g0239 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.46+1488G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295683 | |||||||
chr8:24295685 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.46+1490C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295685 | |||||||
chr8:24295689 | G | A | 1 | a0001c0001t0016g0007 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.46+1494G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295689 | |||||||
chr8:24295788 | G | A | 1 | a0008c0011t0002g0026 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.46+1593G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24295788 | |||||||
chr8:24296145 | G | T | 2 | a0002c0007t0003g0270 a0002c0007t0003g0271 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.46+1950G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296145 | |||||||
chr8:24296176 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.46+1981G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296176 | |||||||
chr8:24296268 | A | C | 1 | a0001c0001t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.46+2073A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296268 | |||||||
chr8:24296312 | G | GT | 7 | a0001c0001t0002g0225 a0001c0001t0002g0227 a0001c0001t0002g0231 others(4): Show |
7 | HG01261.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+2123dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24296312 | ||||||
chr8:24296346 | C | T | 1 | a0001c0002t0008g0023 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.46+2151C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296346 | |||||||
chr8:24296427 | A | T | 25 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0002c0003t0001g0002 others(22): Show |
30 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.46+2232A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296427 | |||||||
chr8:24296433 | C | T | 43 | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0283 others(40): Show |
50 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.46+2238C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296433 | |||||||
chr8:24296641 | A | G | 2 | a0001c0002t0001g0315 a0001c0002t0008g0023 |
3 | NA18969.hp1 NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.46+2446A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296641 | |||||||
chr8:24296645 | T | C | 44 | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0283 others(41): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.46+2450T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296645 | |||||||
chr8:24296685 | C | A | 1 | a0001c0001t0012g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.46+2490C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296685 | |||||||
chr8:24296803 | T | C | 10 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.46+2608T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296803 | |||||||
chr8:24296884 | C | T | 1 | a0001c0001t0003g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.46+2689C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296884 | |||||||
chr8:24296936 | G | A | 53 | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0283 others(50): Show |
62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.46+2741G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24296936 | |||||||
chr8:24297075 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.46+2880G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297075 | |||||||
chr8:24297141 | C | T | 40 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0025t0042g0248 others(37): Show |
46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-2833C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297141 | |||||||
chr8:24297159 | G | GTTT | 40 | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0286 others(37): Show |
47 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.47-2808_47-2806dup others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24297159 | ||||||
chr8:24297159 | G | GTTTTT | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-2810_47-2806dup others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24297159 | ||||||
chr8:24297162 | T | G | 1 | a0001c0001t0043g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.47-2812T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297162 | |||||||
chr8:24297166 | TTTG | T | 39 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0025t0042g0248 others(36): Show |
45 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.47-2793_47-2791del others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24297166 | ||||||
chr8:24297169 | G | T | 162 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(159): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.47-2805G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297169 | |||||||
chr8:24297380 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0003g0030 a0001c0001t0003g0032 |
3 | HG00323.hp1 HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.47-2594T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297380 | |||||||
chr8:24297445 | T | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0002g0033 others(1): Show |
5 | HG01433.hp2 HG01934.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-2529T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297445 | |||||||
chr8:24297474 | C | T | 10 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-2500C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297474 | |||||||
chr8:24297641 | T | G | 4 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-2333T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297641 | |||||||
chr8:24297652 | A | G | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.47-2322A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297652 | |||||||
chr8:24297679 | G | A | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-2295G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297679 | |||||||
chr8:24297910 | G | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-2064G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24297910 | |||||||
chr8:24298155 | G | A | 53 | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0283 others(50): Show |
62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.47-1819G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298155 | |||||||
chr8:24298242 | A | T | 2 | a0002c0007t0003g0270 a0002c0007t0003g0271 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.47-1732A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298242 | |||||||
chr8:24298252 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.47-1722T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298252 | |||||||
chr8:24298419 | T | A | 91 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0002t0001g0003 others(88): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.47-1555T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298419 | |||||||
chr8:24298552 | G | T | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.47-1422G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298552 | |||||||
chr8:24298607 | T | C | 2 | a0001c0001t0019g0037 a0001c0001t0037g0036 |
2 | HG01258.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.47-1367T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298607 | |||||||
chr8:24298691 | C | T | 107 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(104): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.47-1283C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298691 | |||||||
chr8:24298874 | G | A | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.47-1100G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298874 | |||||||
chr8:24298892 | T | C | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.47-1082T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298892 | |||||||
chr8:24298893 | C | A | 1 | a0001c0001t0010g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.47-1081C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298893 | |||||||
chr8:24298959 | A | G | 45 | a0001c0001t0003g0135 a0001c0002t0001g0003 a0001c0002t0001g0280 others(42): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.47-1015A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24298959 | |||||||
chr8:24299031 | G | GA | 8 | a0001c0001t0002g0040 a0001c0001t0002g0137 a0001c0001t0002g0225 others(5): Show |
8 | HG02886.hp1 HG03486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-928dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24299031 | ||||||
chr8:24299031 | GAA | G | 11 | a0001c0025t0042g0248 a0003c0005t0005g0018 a0003c0005t0006g0240 others(8): Show |
12 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.47-929_47-928delAA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24299031 | ||||||
chr8:24299069 | T | G | 1 | a0001c0001t0003g0138 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.47-905T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299069 | |||||||
chr8:24299297 | G | T | 40 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0025t0042g0248 others(37): Show |
46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-677G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299297 | |||||||
chr8:24299462 | GT | G | 278 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(275): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.47-503delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 24299462 | ||||||
chr8:24299511 | T | A | 40 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0025t0042g0248 others(37): Show |
46 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-463T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299511 | |||||||
chr8:24299528 | A | G | 4 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0009g0131 others(1): Show |
4 | HG00733.hp1 HG01081.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-446A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299528 | |||||||
chr8:24299553 | A | T | 1 | a0001c0001t0003g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47-421A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299553 | |||||||
chr8:24299558 | A | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | NA18963.hp2 NA18994.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.47-416A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299558 | |||||||
chr8:24299634 | C | T | 94 | a0001c0001t0003g0135 a0001c0001t0003g0268 a0001c0001t0003g0269 others(91): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.47-340C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299634 | |||||||
chr8:24299692 | G | A | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-282G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299692 | |||||||
chr8:24299891 | T | C | 2 | a0002c0007t0003g0270 a0002c0007t0003g0271 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.47-83T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | chr8 | 24299891 | |||||||
chr8:24300130 | CAT | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+62_150+63delAT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24300130 | ||||||
chr8:24300149 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.150+72G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300149 | |||||||
chr8:24300317 | C | T | 1 | a0001c0001t0009g0222 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150+240C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300317 | |||||||
chr8:24300411 | T | C | 1 | a0001c0001t0043g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.150+334T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300411 | |||||||
chr8:24300480 | G | A | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+403G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300480 | |||||||
chr8:24300517 | C | T | 7 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(4): Show |
8 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+440C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300517 | |||||||
chr8:24300527 | C | T | 1 | a0001c0001t0010g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+450C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300527 | |||||||
chr8:24300561 | G | A | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+484G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300561 | |||||||
chr8:24300705 | C | T | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+628C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300705 | |||||||
chr8:24300814 | T | C | 1 | a0001c0002t0010g0281 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.150+737T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300814 | |||||||
chr8:24300838 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.150+761T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300838 | |||||||
chr8:24300842 | G | T | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+765G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300842 | |||||||
chr8:24300960 | C | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+883C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24300960 | |||||||
chr8:24301104 | A | G | 2 | a0003c0006t0001g0279 a0003c0006t0002g0278 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.150+1027A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301104 | |||||||
chr8:24301136 | T | G | 1 | a0001c0001t0003g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150+1059T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301136 | |||||||
chr8:24301326 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0005g0045 others(1): Show |
4 | HG00438.hp2 HG00558.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+1249G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301326 | |||||||
chr8:24301329 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.150+1252T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301329 | |||||||
chr8:24301362 | T | C | 91 | a0001c0001t0003g0135 a0001c0002t0001g0003 a0001c0002t0001g0038 others(88): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.150+1285T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301362 | |||||||
chr8:24301446 | G | T | 39 | a0001c0025t0042g0248 a0002c0003t0001g0002 a0002c0003t0001g0249 others(36): Show |
45 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.150+1369G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301446 | |||||||
chr8:24301725 | G | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0048 |
3 | HG03225.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.150+1648G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301725 | |||||||
chr8:24301968 | T | C | 1 | a0008c0011t0006g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+1891T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24301968 | |||||||
chr8:24302012 | G | C | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+1935G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302012 | |||||||
chr8:24302054 | C | A | 1 | a0001c0001t0002g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150+1977C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302054 | |||||||
chr8:24302071 | A | G | 2 | a0003c0005t0005g0018 a0009c0028t0006g0245 |
3 | HG02615.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.150+1994A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302071 | |||||||
chr8:24302229 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150+2152C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302229 | |||||||
chr8:24302295 | A | G | 1 | a0001c0001t0004g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.150+2218A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302295 | |||||||
chr8:24302376 | C | A | 2 | a0002c0007t0003g0270 a0002c0007t0003g0271 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.150+2299C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302376 | |||||||
chr8:24302503 | G | A | 1 | a0001c0001t0006g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.150+2426G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302503 | |||||||
chr8:24302547 | G | A | 52 | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0283 others(49): Show |
61 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.150+2470G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302547 | |||||||
chr8:24302734 | T | C | 44 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(41): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.150+2657T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302734 | |||||||
chr8:24302755 | C | T | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2678C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302755 | |||||||
chr8:24302768 | C | T | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.150+2691C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302768 | |||||||
chr8:24302770 | C | CT | 10 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2701dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24302770 | ||||||
chr8:24302778 | T | A | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0014c0015t0002g0226 |
5 | HG01891.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+2701T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302778 | |||||||
chr8:24302791 | T | C | 44 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(41): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.150+2714T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302791 | |||||||
chr8:24302817 | C | T | 34 | a0001c0025t0042g0248 a0002c0003t0001g0002 a0002c0003t0001g0249 others(31): Show |
40 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.150+2740C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302817 | |||||||
chr8:24302918 | C | G | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2841C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302918 | |||||||
chr8:24302939 | G | A | 1 | a0001c0001t0043g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.150+2862G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302939 | |||||||
chr8:24302973 | T | C | 45 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(42): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.150+2896T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24302973 | |||||||
chr8:24303010 | A | G | 23 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(20): Show |
28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.150+2933A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303010 | |||||||
chr8:24303019 | T | A | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+2942T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303019 | |||||||
chr8:24303541 | C | T | 23 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(20): Show |
28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.150+3464C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303541 | |||||||
chr8:24303715 | C | G | 45 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(42): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.150+3638C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24303715 | |||||||
chr8:24304047 | A | G | 38 | a0001c0025t0042g0248 a0002c0003t0001g0002 a0002c0003t0001g0249 others(35): Show |
44 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.150+3970A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304047 | |||||||
chr8:24304053 | G | A | 1 | a0001c0002t0004g0285 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.150+3976G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304053 | |||||||
chr8:24304148 | C | T | 10 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+4071C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304148 | |||||||
chr8:24304234 | A | C | 38 | a0001c0025t0042g0248 a0002c0003t0001g0002 a0002c0003t0001g0249 others(35): Show |
44 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.150+4157A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304234 | |||||||
chr8:24304251 | T | C | 3 | a0001c0001t0002g0040 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | HG02004.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.150+4174T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304251 | |||||||
chr8:24304487 | G | C | 2 | a0001c0001t0002g0053 a0001c0001t0006g0054 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.150+4410G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304487 | |||||||
chr8:24304526 | G | A | 2 | a0002c0003t0001g0249 a0002c0003t0004g0250 |
2 | NA18985.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.150+4449G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304526 | |||||||
chr8:24304587 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.150+4510T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304587 | |||||||
chr8:24304590 | G | T | 4 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4513G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304590 | |||||||
chr8:24304603 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.150+4526C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304603 | |||||||
chr8:24304701 | T | C | 93 | a0001c0001t0003g0135 a0001c0002t0001g0003 a0001c0002t0001g0038 others(90): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.150+4624T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304701 | |||||||
chr8:24304738 | T | TACCTCTA others(42): Show |
1 | a0002c0003t0045g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+4711_150+4759d others(51): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304738 | ||||||
chr8:24304875 | A | C | 1 | a0001c0001t0017g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.150+4798A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304875 | |||||||
chr8:24304881 | A | T | 4 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4804A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304881 | |||||||
chr8:24304916 | C | CA | 35 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0001g0145 others(32): Show |
41 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(38): Show |
intron_variant | MODIFIER | c.150+4854dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304916 | ||||||
chr8:24304916 | CA | C | 17 | a0001c0001t0001g0118 a0001c0001t0002g0040 a0001c0001t0002g0051 others(14): Show |
17 | HG01192.hp2 HG01891.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.150+4854delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304916 | ||||||
chr8:24304930 | A | AAAAATAG | 50 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(47): Show |
59 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.150+4854_150+4855i others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24304930 | ||||||
chr8:24304932 | T | G | 54 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(51): Show |
63 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.150+4855T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24304932 | |||||||
chr8:24305063 | T | G | 1 | a0001c0002t0012g0313 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.151-4831T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305063 | |||||||
chr8:24305110 | TG | T | 15 | a0001c0025t0042g0248 a0002c0007t0003g0270 a0002c0007t0003g0271 others(12): Show |
16 | HG00733.hp2 HG00738.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.151-4783delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305110 | |||||||
chr8:24305117 | T | A | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-4777T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305117 | |||||||
chr8:24305174 | T | G | 2 | a0002c0007t0003g0270 a0002c0007t0003g0271 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.151-4720T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305174 | |||||||
chr8:24305264 | C | T | 24 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(21): Show |
29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-4630C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305264 | |||||||
chr8:24305268 | C | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-4626C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305268 | |||||||
chr8:24305269 | G | A | 4 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0002c0019t0006g0229 others(1): Show |
4 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-4625G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305269 | |||||||
chr8:24305355 | AGTGTGTG others(7): Show |
A | 10 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-4531_151-4518d others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305355 | ||||||
chr8:24305451 | C | CT | 26 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0113 others(23): Show |
28 | HG00099.hp2 HG00738.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-4417dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | ||||||
chr8:24305451 | C | CTT | 14 | a0001c0001t0038g0123 a0001c0002t0001g0280 a0001c0002t0001g0286 others(11): Show |
14 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.151-4418_151-4417d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | ||||||
chr8:24305451 | C | CTTT | 37 | a0001c0001t0003g0135 a0001c0002t0001g0003 a0001c0002t0001g0283 others(34): Show |
44 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.151-4419_151-4417d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | ||||||
chr8:24305451 | C | CTTTT | 26 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0284 others(23): Show |
30 | HG00621.hp2 HG01261.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-4420_151-4417d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | ||||||
chr8:24305451 | C | CTTTTT | 5 | a0001c0002t0001g0038 a0002c0003t0002g0264 a0002c0003t0003g0019 others(2): Show |
6 | HG02071.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-4421_151-4417d others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | ||||||
chr8:24305451 | CT | C | 27 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0153 others(24): Show |
28 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.151-4417delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24305451 | ||||||
chr8:24305468 | TTTTTTTT others(3): Show |
T | 1 | a0005c0008t0002g0316 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.151-4425_151-4416d others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305468 | |||||||
chr8:24305477 | T | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0145 others(11): Show |
15 | HG00438.hp1 HG02074.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.151-4417T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305477 | |||||||
chr8:24305478 | A | T | 91 | a0001c0001t0002g0225 a0001c0001t0002g0227 a0001c0001t0002g0231 others(88): Show |
104 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.151-4416A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305478 | |||||||
chr8:24305641 | A | G | 69 | a0001c0001t0003g0135 a0001c0002t0001g0003 a0001c0002t0001g0038 others(66): Show |
81 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.151-4253A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305641 | |||||||
chr8:24305654 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.151-4240G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305654 | |||||||
chr8:24305691 | C | T | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-4203C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305691 | |||||||
chr8:24305767 | A | T | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-4127A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305767 | |||||||
chr8:24305852 | TA | T | 90 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(87): Show |
99 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.151-4041delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24305852 | |||||||
chr8:24306006 | G | A | 2 | a0009c0010t0002g0238 a0009c0010t0002g0239 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.151-3888G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306006 | |||||||
chr8:24306061 | A | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3833A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306061 | |||||||
chr8:24306064 | C | T | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-3830C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306064 | |||||||
chr8:24306117 | G | C | 13 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0002c0019t0006g0229 others(10): Show |
15 | HG01261.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.151-3777G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306117 | |||||||
chr8:24306156 | G | T | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3738G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306156 | |||||||
chr8:24306190 | C | A | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3704C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306190 | |||||||
chr8:24306213 | C | A | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.151-3681C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306213 | |||||||
chr8:24306213 | C | T | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.151-3681C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306213 | |||||||
chr8:24306214 | G | A | 9 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(6): Show |
11 | HG01891.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3680G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306214 | |||||||
chr8:24306280 | G | T | 1 | a0001c0001t0004g0115 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.151-3614G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306280 | |||||||
chr8:24306349 | CAAATAAA others(5): Show |
C | 22 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(19): Show |
27 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.151-3539_151-3528d others(14): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306349 | ||||||
chr8:24306351 | A | AATATATA others(3): Show |
3 | a0001c0002t0004g0291 a0001c0002t0010g0281 a0005c0008t0002g0006 |
3 | HG01891.hp1 HG01934.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(5): Show |
7 | a0001c0002t0001g0283 a0001c0002t0001g0306 a0001c0002t0001g0307 others(4): Show |
7 | HG00423.hp2 HG00741.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(14): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(7): Show |
2 | a0001c0025t0042g0248 a0005c0008t0002g0006 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(9): Show |
5 | a0001c0002t0001g0280 a0001c0002t0001g0309 a0001c0002t0008g0023 others(2): Show |
6 | HG00408.hp1 HG02165.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(18): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(11): Show |
7 | a0001c0002t0001g0038 a0001c0002t0001g0294 a0001c0002t0001g0295 others(4): Show |
7 | HG00558.hp2 HG01496.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(20): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(53): Show |
4 | a0003c0005t0006g0241 a0003c0005t0006g0242 a0003c0005t0006g0243 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(62): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(13): Show |
1 | a0001c0002t0001g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.151-3540_151-3539i others(22): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(87): Show |
1 | a0003c0005t0005g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.151-3540_151-3539i others(96): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(15): Show |
8 | a0001c0002t0001g0292 a0001c0002t0001g0303 a0001c0002t0001g0308 others(5): Show |
8 | HG00621.hp1 HG00673.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(24): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(89): Show |
1 | a0003c0005t0005g0018 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-3540_151-3539i others(98): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(17): Show |
4 | a0001c0002t0002g0302 a0001c0002t0002g0310 a0001c0002t0004g0285 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(19): Show |
4 | a0001c0002t0001g0284 a0001c0002t0001g0301 a0001c0002t0014g0021 others(1): Show |
4 | HG01517.hp1 HG02155.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3540_151-3539i others(28): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(21): Show |
3 | a0001c0002t0001g0003 a0001c0002t0004g0290 a0001c0002t0005g0022 |
3 | HG02056.hp2 NA18971.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(75): Show |
1 | a0015c0027t0007g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151-3540_151-3539i others(84): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(31): Show |
2 | a0001c0002t0004g0236 a0003c0006t0002g0276 |
2 | HG02572.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(40): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(67): Show |
1 | a0009c0010t0002g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151-3540_151-3539i others(76): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | AATATATA others(17): Show |
2 | a0001c0002t0001g0003 a0001c0002t0001g0312 |
2 | NA18951.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.151-3540_151-3539i others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306351 | A | ATATATAT others(14): Show |
1 | a0001c0002t0004g0293 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.151-3543_151-3542i others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306351 | |||||||
chr8:24306351 | A | ATATATAT others(16): Show |
1 | a0020c0030t0004g0299 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.151-3543_151-3542i others(25): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306351 | |||||||
chr8:24306351 | A | ATATATAT others(20): Show |
1 | a0001c0002t0001g0288 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.151-3543_151-3542i others(29): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306351 | |||||||
chr8:24306351 | AATAAATA others(35): Show |
A | 4 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3539_151-3498d others(44): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306351 | ||||||
chr8:24306353 | TAAATAAA others(3): Show |
T | 5 | a0001c0002t0001g0286 a0001c0002t0002g0020 a0001c0002t0002g0289 others(2): Show |
6 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-3539_151-3530d others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306353 | ||||||
chr8:24306355 | A | T | 60 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(57): Show |
67 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.151-3539A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306355 | |||||||
chr8:24306356 | A | ATATATAT others(21): Show |
1 | a0001c0001t0044g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151-3536_151-3535i others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306356 | ||||||
chr8:24306357 | T | TATATATA others(23): Show |
1 | a0002c0019t0006g0229 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.151-3536_151-3535i others(32): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306357 | ||||||
chr8:24306357 | T | TATATATA others(55): Show |
1 | a0014c0015t0002g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.151-3536_151-3535i others(64): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306357 | ||||||
chr8:24306357 | T | TATATATA others(21): Show |
1 | a0001c0001t0002g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151-3536_151-3535i others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306357 | ||||||
chr8:24306359 | A | T | 60 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(57): Show |
68 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.151-3535A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306359 | |||||||
chr8:24306361 | T | A | 4 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0002c0019t0006g0229 others(1): Show |
4 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-3533T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306361 | |||||||
chr8:24306361 | T | TAAATATA others(21): Show |
3 | a0001c0001t0002g0148 a0001c0001t0003g0214 a0001c0001t0005g0098 |
3 | HG02083.hp2 HG03209.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.151-3516_151-3489d others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306361 | ||||||
chr8:24306363 | A | AAT | 11 | a0001c0001t0001g0109 a0001c0001t0002g0004 a0001c0001t0002g0040 others(8): Show |
13 | HG00408.hp2 HG02004.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.151-3510_151-3509d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306363 | ||||||
chr8:24306363 | A | T | 63 | a0001c0001t0009g0215 a0001c0002t0001g0003 a0001c0002t0001g0038 others(60): Show |
72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.151-3531A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306363 | |||||||
chr8:24306365 | T | A | 1 | a0001c0001t0002g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.151-3529T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306365 | |||||||
chr8:24306367 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.151-3527T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306367 | |||||||
chr8:24306367 | T | TATATAAA others(87): Show |
1 | a0009c0028t0006g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-3522_151-3521i others(96): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306367 | ||||||
chr8:24306369 | T | A | 5 | a0003c0005t0005g0018 a0003c0005t0006g0241 a0003c0005t0006g0242 others(2): Show |
6 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-3525T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306369 | |||||||
chr8:24306369 | T | TAAATATA others(85): Show |
1 | a0003c0005t0006g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.151-3524_151-3523i others(94): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306369 | ||||||
chr8:24306371 | T | TATATATA others(69): Show |
1 | a0009c0010t0002g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.151-3511_151-3510i others(78): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24306371 | ||||||
chr8:24306373 | T | A | 1 | a0009c0010t0002g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151-3521T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306373 | |||||||
chr8:24306385 | TTTAAAA | T | 2 | a0001c0002t0002g0020 a0001c0002t0002g0289 |
3 | HG01069.hp1 HG01071.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.151-3508_151-3503d others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306385 | |||||||
chr8:24306386 | T | A | 76 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(73): Show |
88 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.151-3508T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306386 | |||||||
chr8:24306389 | A | T | 52 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(49): Show |
59 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.151-3505A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306389 | |||||||
chr8:24306391 | A | T | 5 | a0001c0002t0001g0306 a0001c0002t0001g0315 a0001c0002t0002g0305 others(2): Show |
5 | HG00609.hp2 HG00741.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-3503A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306391 | |||||||
chr8:24306393 | T | A | 13 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0002c0019t0006g0229 others(10): Show |
15 | HG01261.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.151-3501T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306393 | |||||||
chr8:24306716 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.151-3178C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306716 | |||||||
chr8:24306813 | C | A | 1 | a0001c0001t0002g0062 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.151-3081C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306813 | |||||||
chr8:24306890 | C | A | 80 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(77): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-3004C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306890 | |||||||
chr8:24306922 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.151-2972A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306922 | |||||||
chr8:24306989 | T | C | 1 | a0018c0022t0002g0180 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.151-2905T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24306989 | |||||||
chr8:24307025 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.151-2869T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307025 | |||||||
chr8:24307147 | C | T | 1 | a0008c0020t0023g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-2747C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307147 | |||||||
chr8:24307180 | T | A | 1 | a0004c0004t0007g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151-2714T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307180 | |||||||
chr8:24307193 | C | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-2701C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307193 | |||||||
chr8:24307236 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151-2658T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307236 | |||||||
chr8:24307245 | C | A | 1 | a0015c0027t0007g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151-2649C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307245 | |||||||
chr8:24307380 | G | T | 1 | a0001c0001t0002g0108 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.151-2514G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307380 | |||||||
chr8:24307647 | A | G | 8 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0002c0007t0003g0270 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-2247A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307647 | |||||||
chr8:24307898 | C | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-1996C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307898 | |||||||
chr8:24307965 | G | A | 1 | a0002c0003t0003g0267 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.151-1929G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24307965 | |||||||
chr8:24308001 | C | G | 80 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(77): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-1893C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308001 | |||||||
chr8:24308042 | G | A | 80 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(77): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-1852G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308042 | |||||||
chr8:24308187 | G | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-1707G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308187 | |||||||
chr8:24308193 | TCTTA | T | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-1697_151-1694d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24308193 | ||||||
chr8:24308259 | C | G | 1 | a0001c0001t0005g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.151-1635C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308259 | |||||||
chr8:24308312 | A | T | 1 | a0001c0001t0002g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.151-1582A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308312 | |||||||
chr8:24308356 | ATCTTTCC others(14): Show |
A | 51 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(48): Show |
60 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.151-1536_151-1516d others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 24308356 | ||||||
chr8:24308536 | A | G | 1 | a0001c0002t0001g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.151-1358A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308536 | |||||||
chr8:24308583 | G | A | 80 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(77): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-1311G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308583 | |||||||
chr8:24308774 | G | A | 4 | a0001c0001t0002g0056 a0001c0001t0002g0063 a0001c0001t0039g0057 others(1): Show |
4 | HG03704.hp2 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-1120G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308774 | |||||||
chr8:24308786 | T | A | 1 | a0002c0003t0003g0254 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.151-1108T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308786 | |||||||
chr8:24308824 | G | T | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.151-1070G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308824 | |||||||
chr8:24308869 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.151-1025C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308869 | |||||||
chr8:24308875 | C | T | 90 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(87): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.151-1019C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308875 | |||||||
chr8:24308907 | G | A | 24 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(21): Show |
29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-987G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308907 | |||||||
chr8:24308914 | G | T | 4 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-980G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308914 | |||||||
chr8:24308967 | A | C | 80 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(77): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-927A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24308967 | |||||||
chr8:24309000 | T | C | 54 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(51): Show |
63 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.151-894T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309000 | |||||||
chr8:24309037 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151-857A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309037 | |||||||
chr8:24309128 | G | C | 2 | a0002c0007t0003g0270 a0002c0007t0003g0271 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.151-766G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309128 | |||||||
chr8:24309135 | A | G | 3 | a0001c0001t0002g0040 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | HG02004.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.151-759A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309135 | |||||||
chr8:24309270 | A | G | 75 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(72): Show |
89 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.151-624A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309270 | |||||||
chr8:24309324 | T | C | 92 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(89): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.151-570T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309324 | |||||||
chr8:24309543 | T | C | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-351T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309543 | |||||||
chr8:24309566 | C | G | 3 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0008c0011t0006g0049 |
3 | HG02717.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.151-328C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309566 | |||||||
chr8:24309694 | G | C | 2 | a0003c0006t0013g0273 a0003c0006t0013g0274 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.151-200G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309694 | |||||||
chr8:24309760 | G | A | 80 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(77): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-134G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309760 | |||||||
chr8:24309776 | T | C | 80 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(77): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.151-118T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309776 | |||||||
chr8:24309803 | G | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-91G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | chr8 | 24309803 | |||||||
chr8:24309979 | C | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.227+9C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 3/22 | chr8 | 24309979 | |||||||
chr8:24310096 | T | A | 1 | a0001c0001t0002g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.228-67T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 3/22 | chr8 | 24310096 | |||||||
chr8:24310545 | A | ATT | 68 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(65): Show |
80 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.306+306_306+307dup others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 24310545 | ||||||
chr8:24310551 | A | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+310A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310551 | |||||||
chr8:24310569 | T | C | 4 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0002c0019t0006g0229 others(1): Show |
4 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+328T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310569 | |||||||
chr8:24310938 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.307-423A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310938 | |||||||
chr8:24310945 | A | T | 4 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-416A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24310945 | |||||||
chr8:24311010 | G | A | 5 | a0001c0025t0042g0248 a0002c0007t0003g0270 a0002c0007t0003g0271 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-351G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311010 | |||||||
chr8:24311014 | T | G | 1 | a0004c0004t0007g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307-347T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311014 | |||||||
chr8:24311025 | A | T | 5 | a0001c0025t0042g0248 a0002c0007t0003g0270 a0002c0007t0003g0271 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-336A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311025 | |||||||
chr8:24311042 | T | C | 10 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.307-319T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311042 | |||||||
chr8:24311048 | T | C | 5 | a0001c0025t0042g0248 a0002c0007t0003g0270 a0002c0007t0003g0271 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-313T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311048 | |||||||
chr8:24311126 | C | A | 1 | a0001c0002t0004g0290 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.307-235C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311126 | |||||||
chr8:24311134 | A | G | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-227A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311134 | |||||||
chr8:24311228 | T | A | 4 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-133T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311228 | |||||||
chr8:24311310 | C | T | 1 | a0001c0001t0009g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.307-51C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311310 | |||||||
chr8:24311311 | G | A | 1 | a0001c0001t0010g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307-50G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4/22 | chr8 | 24311311 | |||||||
chr8:24311564 | C | A | 5 | a0001c0025t0042g0248 a0002c0007t0003g0270 a0002c0007t0003g0271 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+127C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311564 | |||||||
chr8:24311614 | T | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383+177T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311614 | |||||||
chr8:24311677 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383+240A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311677 | |||||||
chr8:24311754 | G | A | 5 | a0001c0025t0042g0248 a0002c0007t0003g0270 a0002c0007t0003g0271 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+317G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311754 | |||||||
chr8:24311863 | C | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383+426C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311863 | |||||||
chr8:24311886 | C | T | 1 | a0006c0012t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.383+449C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24311886 | |||||||
chr8:24312141 | A | C | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.383+704A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312141 | |||||||
chr8:24312327 | T | C | 11 | a0001c0025t0042g0248 a0003c0005t0005g0018 a0003c0005t0006g0240 others(8): Show |
12 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.383+890T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312327 | |||||||
chr8:24312330 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.383+893A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312330 | |||||||
chr8:24312444 | A | G | 11 | a0001c0025t0042g0248 a0003c0005t0005g0018 a0003c0005t0006g0240 others(8): Show |
12 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.384-944A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312444 | |||||||
chr8:24312637 | A | G | 1 | a0002c0003t0001g0263 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.384-751A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312637 | |||||||
chr8:24312669 | G | A | 1 | a0002c0003t0002g0264 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.384-719G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312669 | |||||||
chr8:24312681 | T | C | 1 | a0003c0006t0002g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.384-707T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312681 | |||||||
chr8:24312745 | G | T | 10 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.384-643G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312745 | |||||||
chr8:24312746 | C | CT | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-641dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr8 | 24312746 | ||||||
chr8:24312757 | T | C | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.384-631T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312757 | |||||||
chr8:24312911 | T | C | 103 | a0001c0001t0002g0227 a0001c0001t0038g0123 a0001c0001t0044g0228 others(100): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.384-477T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24312911 | |||||||
chr8:24313225 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.384-163A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24313225 | |||||||
chr8:24313292 | T | C | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-96T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24313292 | |||||||
chr8:24313375 | C | A | 1 | a0001c0001t0047g0066 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.384-13C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | chr8 | 24313375 | |||||||
chr8:24313609 | C | T | 6 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(3): Show |
6 | HG00597.hp2 HG00609.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+29C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313609 | |||||||
chr8:24313757 | T | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0112 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.576+177T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313757 | |||||||
chr8:24313758 | A | AT | 55 | a0001c0001t0002g0148 a0001c0001t0003g0204 a0001c0002t0001g0003 others(52): Show |
62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.576+194dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24313758 | ||||||
chr8:24313758 | A | T | 23 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(20): Show |
28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.576+178A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313758 | |||||||
chr8:24313758 | AT | A | 11 | a0001c0001t0002g0069 a0001c0001t0006g0068 a0003c0005t0006g0240 others(8): Show |
11 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+194delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24313758 | ||||||
chr8:24313856 | T | C | 318 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(315): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.576+276T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313856 | |||||||
chr8:24313919 | A | G | 83 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+339A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24313919 | |||||||
chr8:24314026 | A | G | 83 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+446A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314026 | |||||||
chr8:24314049 | A | G | 83 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+469A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314049 | |||||||
chr8:24314131 | G | C | 4 | a0001c0017t0002g0124 a0005c0008t0002g0006 a0005c0008t0002g0316 others(1): Show |
6 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+551G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314131 | |||||||
chr8:24314157 | C | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+577C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314157 | |||||||
chr8:24314190 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.576+610A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314190 | |||||||
chr8:24314340 | A | T | 1 | a0001c0001t0003g0157 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.576+760A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314340 | |||||||
chr8:24314408 | T | C | 4 | a0001c0001t0002g0056 a0001c0001t0002g0063 a0001c0001t0039g0057 others(1): Show |
4 | HG03704.hp2 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+828T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314408 | |||||||
chr8:24314414 | T | C | 2 | a0002c0007t0002g0116 a0002c0007t0026g0065 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.576+834T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314414 | |||||||
chr8:24314515 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.576+935A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314515 | |||||||
chr8:24314534 | C | G | 1 | a0016c0016t0003g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.576+954C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314534 | |||||||
chr8:24314667 | T | C | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1087T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314667 | |||||||
chr8:24314822 | T | G | 1 | a0001c0001t0002g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.576+1242T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314822 | |||||||
chr8:24314924 | C | CA | 39 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0071 others(36): Show |
39 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.576+1358dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24314924 | ||||||
chr8:24314924 | CAA | C | 79 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(76): Show |
91 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.576+1357_576+1358d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24314924 | ||||||
chr8:24314998 | A | G | 80 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(77): Show |
92 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.576+1418A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24314998 | |||||||
chr8:24315229 | T | A | 1 | a0001c0017t0002g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.576+1649T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315229 | |||||||
chr8:24315271 | C | A | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+1691C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315271 | |||||||
chr8:24315358 | A | G | 81 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(78): Show |
93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+1778A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315358 | |||||||
chr8:24315489 | C | T | 1 | a0008c0011t0002g0026 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.576+1909C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315489 | |||||||
chr8:24315656 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.576+2076T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315656 | |||||||
chr8:24315723 | C | G | 31 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(28): Show |
36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.576+2143C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315723 | |||||||
chr8:24315910 | C | T | 1 | a0001c0001t0004g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.576+2330C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315910 | |||||||
chr8:24315912 | T | G | 4 | a0001c0017t0002g0124 a0005c0008t0002g0006 a0005c0008t0002g0316 others(1): Show |
6 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+2332T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24315912 | |||||||
chr8:24316053 | A | G | 2 | a0003c0005t0005g0018 a0009c0028t0006g0245 |
3 | HG02615.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.576+2473A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316053 | |||||||
chr8:24316060 | CCATT | C | 41 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(38): Show |
47 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.576+2481_576+2484d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316060 | |||||||
chr8:24316061 | C | CATTT | 21 | a0001c0001t0001g0090 a0001c0001t0002g0058 a0001c0001t0002g0117 others(18): Show |
21 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.576+2512_576+2515d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24316061 | ||||||
chr8:24316061 | C | CATTTATT others(1): Show |
3 | a0001c0017t0002g0124 a0003c0005t0005g0018 a0005c0008t0002g0006 |
3 | HG01192.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.576+2508_576+2515d others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24316061 | ||||||
chr8:24316061 | C | T | 33 | a0001c0002t0014g0021 a0001c0002t0014g0287 a0002c0003t0001g0002 others(30): Show |
39 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.576+2481C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316061 | |||||||
chr8:24316097 | T | C | 2 | a0009c0010t0002g0238 a0009c0010t0002g0239 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.576+2517T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316097 | |||||||
chr8:24316359 | A | T | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.576+2779A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316359 | |||||||
chr8:24316369 | T | C | 2 | a0001c0001t0003g0135 a0001c0001t0009g0222 |
2 | HG00741.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.576+2789T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316369 | |||||||
chr8:24316426 | T | C | 79 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(76): Show |
93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+2846T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316426 | |||||||
chr8:24316532 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0048 |
3 | HG03225.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.576+2952A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316532 | |||||||
chr8:24316753 | A | C | 1 | a0001c0001t0038g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.576+3173A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316753 | |||||||
chr8:24316811 | A | G | 84 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.576+3231A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316811 | |||||||
chr8:24316851 | C | T | 79 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(76): Show |
93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+3271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316851 | |||||||
chr8:24316858 | G | A | 83 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.576+3278G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316858 | |||||||
chr8:24316863 | A | G | 1 | a0002c0003t0029g0262 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.576+3283A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316863 | |||||||
chr8:24316916 | C | T | 2 | a0001c0002t0004g0291 a0001c0002t0004g0311 |
2 | HG00423.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.577-3320C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24316916 | |||||||
chr8:24316998 | A | AG | 83 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.577-3236dupG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24316998 | ||||||
chr8:24317017 | T | C | 83 | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.577-3219T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317017 | |||||||
chr8:24317095 | A | C | 2 | a0009c0010t0002g0238 a0009c0010t0002g0239 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.577-3141A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317095 | |||||||
chr8:24317409 | G | C | 31 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(28): Show |
36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2827G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317409 | |||||||
chr8:24317409 | G | T | 44 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(41): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.577-2827G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317409 | |||||||
chr8:24317506 | T | G | 31 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(28): Show |
36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2730T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317506 | |||||||
chr8:24317540 | GA | G | 10 | a0001c0001t0002g0056 a0001c0001t0002g0063 a0001c0001t0011g0060 others(7): Show |
10 | HG03704.hp2 HG03831.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-2691delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 24317540 | ||||||
chr8:24317550 | C | A | 2 | a0001c0002t0014g0021 a0001c0002t0014g0287 |
3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.577-2686C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317550 | |||||||
chr8:24317591 | A | G | 31 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(28): Show |
36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2645A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317591 | |||||||
chr8:24317694 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.577-2542C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317694 | |||||||
chr8:24317739 | A | C | 45 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(42): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.577-2497A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317739 | |||||||
chr8:24317829 | G | A | 31 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(28): Show |
36 | HG00621.hp2 HG01943.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.577-2407G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317829 | |||||||
chr8:24317853 | C | T | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.577-2383C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317853 | |||||||
chr8:24317924 | A | C | 79 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(76): Show |
93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.577-2312A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24317924 | |||||||
chr8:24318010 | T | C | 79 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(76): Show |
93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.577-2226T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318010 | |||||||
chr8:24318013 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.577-2223C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318013 | |||||||
chr8:24318024 | T | A | 48 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(45): Show |
57 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.577-2212T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318024 | |||||||
chr8:24318385 | T | C | 1 | a0001c0002t0001g0292 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.577-1851T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318385 | |||||||
chr8:24318449 | G | A | 1 | a0003c0005t0006g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.577-1787G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318449 | |||||||
chr8:24318475 | T | C | 67 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(64): Show |
77 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.577-1761T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318475 | |||||||
chr8:24318653 | T | C | 1 | a0016c0016t0003g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.577-1583T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318653 | |||||||
chr8:24318765 | C | T | 25 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(22): Show |
30 | HG00621.hp2 HG01192.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.577-1471C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318765 | |||||||
chr8:24318809 | C | T | 24 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(21): Show |
29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.577-1427C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318809 | |||||||
chr8:24318816 | G | A | 30 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(27): Show |
37 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.577-1420G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318816 | |||||||
chr8:24318934 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0080 others(4): Show |
8 | NA18939.hp1 NA18941.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-1302G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318934 | |||||||
chr8:24318965 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0002g0062 a0001c0001t0002g0104 |
3 | NA18998.hp2 NA19011.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.577-1271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24318965 | |||||||
chr8:24319112 | C | T | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.577-1124C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319112 | |||||||
chr8:24319146 | T | C | 2 | a0009c0010t0002g0238 a0009c0010t0002g0239 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.577-1090T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319146 | |||||||
chr8:24319168 | C | T | 1 | a0002c0033t0008g0266 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.577-1068C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319168 | |||||||
chr8:24319495 | CAT | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0048 |
3 | HG03225.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.577-740_577-739del others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319495 | |||||||
chr8:24319535 | G | A | 48 | a0001c0017t0002g0124 a0001c0025t0042g0248 a0002c0003t0001g0002 others(45): Show |
56 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.577-701G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319535 | |||||||
chr8:24319551 | C | T | 23 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(20): Show |
28 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.577-685C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319551 | |||||||
chr8:24319730 | G | C | 47 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(44): Show |
55 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.577-506G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319730 | |||||||
chr8:24319751 | C | A | 3 | a0001c0002t0001g0294 a0001c0002t0004g0293 a0001c0002t0008g0023 |
4 | NA18967.hp2 NA18969.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-485C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319751 | |||||||
chr8:24319805 | T | C | 45 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(42): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.577-431T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319805 | |||||||
chr8:24319893 | T | A | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.577-343T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24319893 | |||||||
chr8:24320041 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.577-195G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24320041 | |||||||
chr8:24320206 | G | A | 1 | a0001c0001t0021g0150 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.577-30G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | 24320206 | |||||||
chr8:24320322 | T | C | 1 | a0001c0001t0027g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.648+15T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320322 | |||||||
chr8:24320409 | T | C | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.648+102T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320409 | |||||||
chr8:24320429 | A | C | 23 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0002g0027 others(20): Show |
23 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.648+122A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320429 | |||||||
chr8:24320459 | T | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+152T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320459 | |||||||
chr8:24320478 | A | ATTT | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.648+171_648+172ins others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320478 | |||||||
chr8:24320574 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.648+267A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320574 | |||||||
chr8:24320814 | A | G | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.649-404A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24320814 | |||||||
chr8:24321150 | G | A | 1 | a0004c0004t0007g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.649-68G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 7/22 | chr8 | 24321150 | |||||||
chr8:24321347 | T | A | 1 | a0001c0001t0017g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.720+58T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321347 | |||||||
chr8:24321680 | A | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+391A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321680 | |||||||
chr8:24321691 | C | T | 48 | a0001c0017t0002g0124 a0001c0025t0042g0248 a0002c0003t0001g0002 others(45): Show |
56 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.720+402C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321691 | |||||||
chr8:24321743 | A | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+454A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321743 | |||||||
chr8:24321922 | C | A | 47 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(44): Show |
55 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.720+633C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24321922 | |||||||
chr8:24322073 | A | G | 19 | a0002c0007t0002g0116 a0002c0007t0026g0065 a0003c0005t0005g0018 others(16): Show |
20 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.720+784A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322073 | |||||||
chr8:24322116 | A | G | 192 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(189): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.720+827A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322116 | |||||||
chr8:24322123 | A | T | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+834A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322123 | |||||||
chr8:24322128 | C | T | 1 | a0008c0011t0006g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+839C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322128 | |||||||
chr8:24322168 | T | C | 1 | a0015c0027t0007g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.720+879T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322168 | |||||||
chr8:24322196 | A | G | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.720+907A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322196 | |||||||
chr8:24322305 | G | T | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.720+1016G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322305 | |||||||
chr8:24322355 | G | A | 1 | a0001c0002t0004g0290 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.720+1066G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322355 | |||||||
chr8:24322382 | T | C | 3 | a0001c0001t0006g0068 a0004c0004t0007g0064 a0008c0011t0006g0049 |
3 | HG01884.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.720+1093T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322382 | |||||||
chr8:24322389 | G | A | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.720+1100G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322389 | |||||||
chr8:24322398 | A | C | 2 | a0001c0001t0002g0203 a0001c0001t0010g0024 |
2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.720+1109A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322398 | |||||||
chr8:24322509 | C | T | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.720+1220C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322509 | |||||||
chr8:24322702 | A | G | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.721-1132A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322702 | |||||||
chr8:24322802 | T | A | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.721-1032T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322802 | |||||||
chr8:24322861 | C | A | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0008c0020t0023g0246 |
3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.721-973C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24322861 | |||||||
chr8:24323145 | G | A | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.721-689G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323145 | |||||||
chr8:24323184 | A | G | 17 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.721-650A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323184 | |||||||
chr8:24323289 | C | T | 23 | a0001c0025t0042g0248 a0002c0007t0003g0270 a0002c0007t0003g0271 others(20): Show |
26 | HG00733.hp2 HG00738.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.721-545C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323289 | |||||||
chr8:24323415 | C | A | 30 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(27): Show |
37 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.721-419C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323415 | |||||||
chr8:24323442 | T | C | 1 | a0001c0001t0037g0036 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.721-392T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323442 | |||||||
chr8:24323485 | A | G | 1 | a0008c0020t0023g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.721-349A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323485 | |||||||
chr8:24323610 | A | C | 24 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(21): Show |
29 | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.721-224A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323610 | |||||||
chr8:24323633 | T | C | 1 | a0004c0004t0020g0230 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.721-201T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 8/22 | chr8 | 24323633 | |||||||
chr8:24324120 | G | C | 2 | a0003c0006t0001g0279 a0003c0006t0002g0278 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.890+117G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324120 | |||||||
chr8:24324166 | T | A | 28 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(25): Show |
33 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.890+163T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324166 | |||||||
chr8:24324167 | A | G | 2 | a0003c0006t0001g0279 a0003c0006t0002g0278 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.890+164A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324167 | |||||||
chr8:24324167 | A | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.890+164A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324167 | |||||||
chr8:24324231 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.890+228A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324231 | |||||||
chr8:24324381 | A | G | 1 | a0001c0001t0003g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.890+378A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324381 | |||||||
chr8:24324405 | G | A | 2 | a0001c0001t0003g0204 a0001c0001t0003g0211 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.890+402G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324405 | |||||||
chr8:24324459 | G | T | 1 | a0002c0003t0003g0265 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.890+456G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324459 | |||||||
chr8:24324653 | G | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.890+650G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324653 | |||||||
chr8:24324670 | T | C | 2 | a0004c0004t0007g0075 a0004c0004t0007g0076 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.890+667T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324670 | |||||||
chr8:24324910 | T | C | 1 | a0001c0001t0015g0170 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.890+907T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24324910 | |||||||
chr8:24325132 | A | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.890+1129A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325132 | |||||||
chr8:24325142 | T | C | 16 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(13): Show |
17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.890+1139T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325142 | |||||||
chr8:24325349 | T | C | 1 | a0001c0001t0019g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.891-1205T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325349 | |||||||
chr8:24325574 | T | C | 2 | a0001c0001t0002g0129 a0001c0026t0001g0073 |
2 | HG01516.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.891-980T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325574 | |||||||
chr8:24325736 | C | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-818C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325736 | |||||||
chr8:24325835 | T | G | 16 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(13): Show |
17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.891-719T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325835 | |||||||
chr8:24325871 | C | CA | 16 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0082 others(13): Show |
16 | HG00438.hp2 HG01081.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.891-654dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | C | CAAAAAAA others(3): Show |
1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-663_891-654dup others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | C | CAAAAAAA others(15): Show |
1 | a0003c0006t0013g0273 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.891-675_891-654dup others(22): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | C | CAAAAAAA others(16): Show |
1 | a0003c0006t0013g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.891-676_891-654dup others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | C | CAAAAAAA others(17): Show |
2 | a0003c0006t0002g0275 a0003c0006t0002g0276 |
2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.891-677_891-654dup others(24): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | C | CAAAAAAA others(18): Show |
1 | a0003c0006t0001g0279 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.891-678_891-654dup others(25): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | C | CAAAAAAA others(19): Show |
1 | a0003c0006t0002g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.891-679_891-654dup others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | C | CAAAAAAA others(23): Show |
1 | a0003c0006t0002g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.891-654_891-653ins others(30): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | CA | C | 108 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(105): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.891-654delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325871 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0055 |
3 | NA18944.hp1 NA18972.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.891-669_891-654del others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325871 | ||||||
chr8:24325882 | A | AAAACAAA others(5): Show |
2 | a0001c0002t0004g0285 a0001c0002t0005g0235 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.891-669_891-668ins others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325882 | ||||||
chr8:24325883 | A | AAAACAAA others(5): Show |
2 | a0001c0001t0001g0181 a0001c0001t0004g0149 |
2 | HG02523.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.891-668_891-667ins others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325883 | ||||||
chr8:24325883 | A | AAACAAAC others(4): Show |
39 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(36): Show |
46 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.891-669_891-668ins others(11): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325883 | ||||||
chr8:24325883 | A | AACAAACA others(3): Show |
1 | a0001c0002t0004g0291 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.891-670_891-669ins others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325883 | ||||||
chr8:24325884 | A | AACAAACA others(3): Show |
2 | a0001c0002t0001g0292 a0001c0002t0002g0305 |
2 | HG00673.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.891-669_891-668ins others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325884 | ||||||
chr8:24325886 | A | C | 2 | a0001c0002t0004g0285 a0001c0002t0005g0235 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.891-668A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325886 | |||||||
chr8:24325887 | A | AACAAACA others(3): Show |
3 | a0002c0003t0001g0256 a0002c0003t0003g0254 a0002c0003t0029g0262 |
3 | HG00621.hp2 HG01943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.891-666_891-665ins others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325887 | ||||||
chr8:24325887 | A | ACAAACAA others(2): Show |
22 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(19): Show |
27 | HG01192.hp2 HG02071.hp2 HG02698.hp2 others(24): Show |
intron_variant | MODIFIER | c.891-667_891-666ins others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325887 | |||||||
chr8:24325887 | A | C | 42 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(39): Show |
49 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.891-667A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325887 | |||||||
chr8:24325888 | A | C | 2 | a0001c0002t0001g0292 a0001c0002t0002g0305 |
2 | HG00673.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.891-666A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325888 | |||||||
chr8:24325889 | A | AAAAAAAA others(22): Show |
1 | a0003c0005t0005g0018 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.891-654_891-653ins others(29): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | 24325889 | ||||||
chr8:24325889 | A | C | 5 | a0003c0005t0006g0240 a0003c0005t0006g0241 a0003c0005t0006g0242 others(2): Show |
5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.891-665A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325889 | |||||||
chr8:24325891 | A | C | 27 | a0001c0002t0001g0303 a0001c0002t0001g0306 a0001c0017t0002g0124 others(24): Show |
32 | HG00621.hp1 HG00621.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.891-663A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325891 | |||||||
chr8:24325893 | A | C | 1 | a0001c0001t0003g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.891-661A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325893 | |||||||
chr8:24325904 | A | C | 1 | a0001c0001t0006g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.891-650A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24325904 | |||||||
chr8:24326005 | T | C | 1 | a0003c0006t0002g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.891-549T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326005 | |||||||
chr8:24326059 | C | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-495C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326059 | |||||||
chr8:24326132 | C | G | 1 | a0001c0001t0003g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.891-422C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326132 | |||||||
chr8:24326257 | A | G | 90 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(87): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.891-297A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326257 | |||||||
chr8:24326305 | T | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-249T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326305 | |||||||
chr8:24326386 | C | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891-168C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326386 | |||||||
chr8:24326543 | C | T | 16 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(13): Show |
17 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.891-11C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | chr8 | 24326543 | |||||||
chr8:24326664 | A | C | 2 | a0004c0004t0007g0075 a0004c0004t0007g0076 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.972+29A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326664 | |||||||
chr8:24326754 | C | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+119C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326754 | |||||||
chr8:24326804 | A | T | 1 | a0001c0001t0001g0013 | 2 | NA18955.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.972+169A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326804 | |||||||
chr8:24326809 | T | G | 17 | a0001c0025t0042g0248 a0003c0005t0005g0018 a0003c0005t0006g0240 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.972+174T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326809 | |||||||
chr8:24326893 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+258A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326893 | |||||||
chr8:24326978 | G | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+343G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326978 | |||||||
chr8:24326979 | A | C | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+344A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326979 | |||||||
chr8:24326982 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0034 |
3 | HG01433.hp2 HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.972+347G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24326982 | |||||||
chr8:24327116 | G | T | 45 | a0001c0017t0002g0124 a0002c0003t0001g0002 a0002c0003t0001g0249 others(42): Show |
53 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.972+481G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327116 | |||||||
chr8:24327152 | G | A | 8 | a0001c0025t0042g0248 a0003c0006t0001g0279 a0003c0006t0002g0275 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.972+517G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327152 | |||||||
chr8:24327154 | A | C | 7 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.972+519A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327154 | |||||||
chr8:24327236 | C | T | 3 | a0001c0001t0011g0060 a0001c0001t0011g0077 a0001c0001t0011g0079 |
3 | NA18971.hp2 NA18986.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.972+601C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327236 | |||||||
chr8:24327312 | C | T | 1 | a0001c0017t0002g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.972+677C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327312 | |||||||
chr8:24327421 | T | C | 1 | a0001c0002t0002g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.972+786T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327421 | |||||||
chr8:24327425 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0112 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.972+790G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327425 | |||||||
chr8:24327444 | C | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+809C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327444 | |||||||
chr8:24327448 | G | A | 3 | a0001c0025t0042g0248 a0005c0008t0002g0006 a0005c0008t0002g0316 |
5 | HG01891.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+813G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327448 | |||||||
chr8:24327621 | G | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+986G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327621 | |||||||
chr8:24327661 | A | T | 3 | a0001c0001t0002g0130 a0001c0001t0009g0131 a0001c0001t0009g0132 |
3 | HG00733.hp1 HG01081.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.972+1026A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327661 | |||||||
chr8:24327667 | G | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1032G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327667 | |||||||
chr8:24327711 | A | G | 1 | a0004c0004t0007g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972+1076A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327711 | |||||||
chr8:24327740 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.972+1105A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327740 | |||||||
chr8:24327822 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1187A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327822 | |||||||
chr8:24327986 | A | G | 1 | a0001c0001t0003g0083 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.972+1351A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24327986 | |||||||
chr8:24328006 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.972+1371T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328006 | |||||||
chr8:24328008 | A | G | 1 | a0001c0001t0015g0170 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.972+1373A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328008 | |||||||
chr8:24328018 | C | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1383C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328018 | |||||||
chr8:24328027 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.972+1392C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328027 | |||||||
chr8:24328114 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.972+1479T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328114 | |||||||
chr8:24328148 | A | G | 2 | a0001c0001t0005g0192 a0001c0001t0005g0193 |
2 | HG01109.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.972+1513A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328148 | |||||||
chr8:24328150 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.972+1515A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328150 | |||||||
chr8:24328183 | A | C | 1 | a0002c0003t0045g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.972+1548A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328183 | |||||||
chr8:24328444 | G | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0146 a0001c0001t0001g0155 others(9): Show |
13 | HG00558.hp2 HG02074.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.973-1541G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328444 | |||||||
chr8:24328465 | A | C | 1 | a0008c0020t0023g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.973-1520A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328465 | |||||||
chr8:24328484 | A | T | 1 | a0001c0001t0006g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.973-1501A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328484 | |||||||
chr8:24328488 | T | G | 3 | a0001c0002t0001g0308 a0001c0002t0005g0022 a0001c0034t0024g0296 |
4 | HG02155.hp1 NA18948.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-1497T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328488 | |||||||
chr8:24328500 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0099 a0012c0021t0001g0100 |
3 | HG02074.hp2 HG02165.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.973-1485C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328500 | |||||||
chr8:24328577 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.973-1408G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328577 | |||||||
chr8:24328607 | C | G | 93 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(90): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.973-1378C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328607 | |||||||
chr8:24328615 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.973-1370C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328615 | |||||||
chr8:24328671 | T | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-1314T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328671 | |||||||
chr8:24328853 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.973-1132G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328853 | |||||||
chr8:24328894 | T | C | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-1091T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328894 | |||||||
chr8:24328921 | C | CA | 86 | a0001c0001t0001g0106 a0001c0001t0001g0181 a0001c0001t0004g0149 others(83): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.973-1052dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24328921 | ||||||
chr8:24328929 | A | AG | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-1056_973-1055i others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328929 | |||||||
chr8:24328976 | G | C | 1 | a0001c0001t0003g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.973-1009G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24328976 | |||||||
chr8:24329129 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-856A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329129 | |||||||
chr8:24329200 | T | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-785T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329200 | |||||||
chr8:24329349 | T | C | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-636T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329349 | |||||||
chr8:24329383 | T | C | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-602T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329383 | |||||||
chr8:24329436 | C | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-549C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329436 | |||||||
chr8:24329595 | G | GAGCTTGT others(5): Show |
1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-390_973-389ins others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329595 | |||||||
chr8:24329596 | G | C | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-389G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329596 | |||||||
chr8:24329614 | A | C | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-371A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329614 | |||||||
chr8:24329615 | T | A | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-370T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329615 | |||||||
chr8:24329616 | C | T | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.973-369C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329616 | |||||||
chr8:24329654 | A | G | 1 | a0019c0018t0035g0179 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.973-331A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329654 | |||||||
chr8:24329769 | C | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-216C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329769 | |||||||
chr8:24329807 | A | G | 2 | a0001c0002t0002g0302 a0001c0002t0002g0310 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.973-178A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329807 | |||||||
chr8:24329830 | ACT | A | 3 | a0001c0001t0001g0084 a0001c0001t0002g0089 a0001c0001t0017g0042 |
3 | HG03139.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.973-144_973-143del others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329830 | ||||||
chr8:24329847 | C | CTG | 6 | a0001c0001t0003g0224 a0001c0001t0005g0192 a0001c0002t0002g0020 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.973-118_973-117dup others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329847 | ||||||
chr8:24329859 | GTGTGTGT others(3): Show |
G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-116_973-107del others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329859 | ||||||
chr8:24329867 | G | T | 1 | a0006c0023t0002g0120 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.973-118G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329867 | |||||||
chr8:24329869 | T | G | 2 | a0006c0023t0002g0120 a0015c0027t0007g0025 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.973-116T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329869 | |||||||
chr8:24329869 | TTG | T | 3 | a0001c0001t0003g0204 a0002c0007t0002g0116 a0002c0007t0026g0065 |
3 | HG02809.hp1 HG02965.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.973-99_973-98delTG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329869 | ||||||
chr8:24329871 | G | T | 1 | a0015c0027t0007g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.973-114G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329871 | |||||||
chr8:24329880 | TGTGTGTG others(1): Show |
T | 15 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(12): Show |
16 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.973-103_973-96delT others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329880 | ||||||
chr8:24329882 | TGTGTGAG others(1): Show |
T | 3 | a0001c0017t0002g0124 a0002c0007t0003g0270 a0002c0007t0003g0271 |
3 | HG01167.hp1 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.973-101_973-94delT others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329882 | ||||||
chr8:24329882 | TGTGTGAG others(3): Show |
T | 26 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(23): Show |
33 | HG00621.hp2 HG01891.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.973-101_973-92delT others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329882 | ||||||
chr8:24329884 | T | A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0092 a0001c0001t0002g0027 others(3): Show |
6 | HG01106.hp2 HG02300.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.973-101T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329884 | |||||||
chr8:24329884 | T | TGA | 21 | a0001c0001t0001g0090 a0001c0001t0001g0109 a0001c0001t0001g0127 others(18): Show |
21 | HG00140.hp1 HG00733.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.973-100_973-99insA others(1): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329884 | ||||||
chr8:24329884 | TGTGA | T | 6 | a0001c0001t0002g0154 a0001c0001t0005g0098 a0001c0001t0021g0150 others(3): Show |
6 | HG02074.hp2 HG02083.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.973-99_973-96delTG others(2): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329884 | ||||||
chr8:24329884 | TGTGAGAG others(3): Show |
T | 1 | a0015c0027t0007g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.973-99_973-90delTG others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 24329884 | ||||||
chr8:24329886 | T | A | 256 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(253): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.973-99T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329886 | |||||||
chr8:24329897 | G | T | 45 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(42): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.973-88G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329897 | |||||||
chr8:24329908 | A | G | 6 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(3): Show |
7 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-77A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329908 | |||||||
chr8:24329929 | T | C | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-56T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329929 | |||||||
chr8:24329932 | T | A | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.973-53T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | 24329932 | |||||||
chr8:24330203 | C | T | 1 | a0001c0001t0009g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1103+88C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330203 | |||||||
chr8:24330374 | G | A | 1 | a0001c0017t0002g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1103+259G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330374 | |||||||
chr8:24330394 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1103+279C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330394 | |||||||
chr8:24330559 | C | T | 45 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(42): Show |
52 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1103+444C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330559 | |||||||
chr8:24330744 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1104-406T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330744 | |||||||
chr8:24330750 | A | C | 46 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(43): Show |
53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1104-400A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330750 | |||||||
chr8:24330834 | A | G | 93 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(90): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1104-316A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24330834 | |||||||
chr8:24331007 | G | A | 1 | a0001c0002t0001g0292 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1104-143G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 11/22 | chr8 | 24331007 | |||||||
chr8:24331331 | T | C | 96 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0181 others(93): Show |
111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
splice_region_variant&intron_variant | LOW | c.1281+4T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331331 | |||||||
chr8:24331445 | C | T | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1281+118C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331445 | |||||||
chr8:24331537 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1281+210A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331537 | |||||||
chr8:24331588 | G | A | 1 | a0001c0001t0043g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1281+261G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331588 | |||||||
chr8:24331636 | A | G | 92 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(89): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1281+309A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331636 | |||||||
chr8:24331675 | C | T | 75 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(72): Show |
89 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1281+348C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331675 | |||||||
chr8:24331687 | T | C | 75 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(72): Show |
89 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1281+360T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331687 | |||||||
chr8:24331735 | A | C | 1 | a0001c0001t0002g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1281+408A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331735 | |||||||
chr8:24331770 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1281+443C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24331770 | |||||||
chr8:24332024 | C | A | 1 | a0001c0001t0040g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1282-636C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332024 | |||||||
chr8:24332142 | A | C | 1 | a0002c0003t0045g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1282-518A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332142 | |||||||
chr8:24332376 | T | C | 5 | a0002c0007t0002g0116 a0002c0007t0026g0065 a0008c0011t0002g0026 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-284T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332376 | |||||||
chr8:24332406 | A | C | 1 | a0001c0001t0006g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1282-254A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332406 | |||||||
chr8:24332414 | T | C | 1 | a0004c0004t0007g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1282-246T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332414 | |||||||
chr8:24332499 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1282-161C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332499 | |||||||
chr8:24332537 | A | G | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1282-123A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332537 | |||||||
chr8:24332544 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1282-116C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332544 | |||||||
chr8:24332624 | A | G | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282-36A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 12/22 | chr8 | 24332624 | |||||||
chr8:24332779 | TATG | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+33_1371+35del others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24332779 | ||||||
chr8:24332866 | A | G | 1 | a0001c0001t0037g0036 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1371+117A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24332866 | |||||||
chr8:24332921 | T | G | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | NA18955.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1371+172T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24332921 | |||||||
chr8:24332982 | A | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+233A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24332982 | |||||||
chr8:24333002 | T | C | 1 | a0001c0002t0001g0280 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1371+253T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333002 | |||||||
chr8:24333050 | C | G | 96 | a0001c0001t0001g0181 a0001c0001t0004g0149 a0001c0002t0001g0003 others(93): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1371+301C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333050 | |||||||
chr8:24333099 | G | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+350G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333099 | |||||||
chr8:24333155 | A | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+406A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333155 | |||||||
chr8:24333170 | C | T | 2 | a0001c0002t0014g0021 a0001c0002t0014g0287 |
3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1371+421C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333170 | |||||||
chr8:24333691 | G | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+942G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333691 | |||||||
chr8:24333713 | G | A | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+964G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333713 | |||||||
chr8:24333781 | C | G | 1 | a0001c0001t0006g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1371+1032C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333781 | |||||||
chr8:24333815 | T | C | 1 | a0008c0020t0023g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1371+1066T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333815 | |||||||
chr8:24333970 | C | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+1221C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24333970 | |||||||
chr8:24333983 | GTT | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+1237_1371+123 others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24333983 | ||||||
chr8:24334065 | G | A | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1371+1316G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334065 | |||||||
chr8:24334247 | G | A | 1 | a0010c0014t0028g0162 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1372-1199G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334247 | |||||||
chr8:24334271 | A | G | 5 | a0003c0005t0006g0240 a0003c0005t0006g0241 a0003c0005t0006g0242 others(2): Show |
5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1372-1175A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334271 | |||||||
chr8:24334325 | T | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-1121T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334325 | |||||||
chr8:24334398 | C | T | 1 | a0009c0010t0002g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1372-1048C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334398 | |||||||
chr8:24334447 | A | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-999A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334447 | |||||||
chr8:24334493 | CT | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-951delT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24334493 | ||||||
chr8:24334615 | T | G | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-831T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334615 | |||||||
chr8:24334616 | C | G | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-830C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334616 | |||||||
chr8:24334868 | G | A | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-578G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24334868 | |||||||
chr8:24335166 | G | GT | 10 | a0001c0001t0044g0228 a0003c0005t0005g0018 a0003c0005t0006g0240 others(7): Show |
13 | HG00733.hp2 HG00738.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1372-268dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 24335166 | ||||||
chr8:24335309 | A | C | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-137A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24335309 | |||||||
chr8:24335344 | T | C | 2 | a0002c0007t0002g0116 a0002c0007t0026g0065 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1372-102T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | chr8 | 24335344 | |||||||
chr8:24335675 | C | T | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567+34C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335675 | |||||||
chr8:24335749 | T | C | 1 | a0006c0012t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1567+108T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335749 | |||||||
chr8:24335751 | T | C | 317 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(314): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1567+110T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335751 | |||||||
chr8:24335835 | C | T | 1 | a0001c0001t0009g0215 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1567+194C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335835 | |||||||
chr8:24335839 | A | G | 1 | a0001c0001t0005g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1567+198A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335839 | |||||||
chr8:24335948 | T | C | 1 | a0001c0001t0015g0170 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1567+307T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24335948 | |||||||
chr8:24336039 | G | GGT | 4 | a0001c0001t0003g0199 a0001c0001t0006g0141 a0001c0001t0010g0024 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+418_1567+419d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336039 | ||||||
chr8:24336039 | GGT | G | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567+418_1567+419d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336039 | ||||||
chr8:24336043 | T | G | 3 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567+402T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336043 | |||||||
chr8:24336137 | G | A | 1 | a0001c0001t0006g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1567+496G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336137 | |||||||
chr8:24336301 | T | C | 9 | a0001c0013t0002g0168 a0001c0013t0013g0167 a0003c0006t0001g0279 others(6): Show |
9 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1567+660T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336301 | |||||||
chr8:24336349 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1567+708T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336349 | |||||||
chr8:24336366 | G | T | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1567+725G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336366 | |||||||
chr8:24336411 | G | T | 2 | a0002c0003t0003g0254 a0002c0003t0029g0262 |
2 | HG01943.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1567+770G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336411 | |||||||
chr8:24336443 | C | T | 46 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0031 others(43): Show |
48 | HG00323.hp1 HG01074.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1567+802C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336443 | |||||||
chr8:24336512 | G | A | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+871G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336512 | |||||||
chr8:24336580 | C | CA | 56 | a0001c0001t0001g0035 a0001c0001t0001g0090 a0001c0001t0001g0181 others(53): Show |
63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1567+958dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | ||||||
chr8:24336580 | CA | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0071 others(5): Show |
8 | HG00558.hp1 HG03041.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567+958delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | ||||||
chr8:24336580 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0097 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1567+945_1567+958d others(16): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | ||||||
chr8:24336580 | CAAAAAAA others(10): Show |
C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+942_1567+958d others(19): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336580 | ||||||
chr8:24336590 | AAAAAAAA others(3): Show |
A | 5 | a0003c0005t0006g0240 a0003c0005t0006g0241 a0003c0005t0006g0242 others(2): Show |
5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567+965_1567+974d others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24336590 | ||||||
chr8:24336599 | AG | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG02004.hp1 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+959delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336599 | |||||||
chr8:24336646 | T | C | 1 | a0002c0031t0002g0257 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1567+1005T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336646 | |||||||
chr8:24336669 | A | G | 101 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(98): Show |
116 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1567+1028A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336669 | |||||||
chr8:24336697 | G | A | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567+1056G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336697 | |||||||
chr8:24336756 | C | T | 1 | a0001c0001t0006g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567+1115C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336756 | |||||||
chr8:24336956 | G | A | 10 | a0001c0002t0001g0286 a0001c0002t0001g0288 a0001c0002t0001g0301 others(7): Show |
11 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1567+1315G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24336956 | |||||||
chr8:24337035 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1567+1394A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337035 | |||||||
chr8:24337166 | C | G | 82 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(79): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1567+1525C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337166 | |||||||
chr8:24337191 | A | G | 85 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(82): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1567+1550A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337191 | |||||||
chr8:24337206 | G | C | 83 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1567+1565G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337206 | |||||||
chr8:24337253 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1567+1612T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337253 | |||||||
chr8:24337522 | G | T | 1 | a0006c0023t0002g0120 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1567+1881G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337522 | |||||||
chr8:24337538 | T | C | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1567+1897T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337538 | |||||||
chr8:24337606 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1860A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337606 | |||||||
chr8:24337614 | G | A | 1 | a0001c0001t0010g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1568-1852G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337614 | |||||||
chr8:24337707 | G | C | 1 | a0006c0012t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1568-1759G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337707 | |||||||
chr8:24337963 | T | G | 3 | a0001c0001t0001g0084 a0001c0001t0002g0089 a0001c0001t0017g0042 |
3 | HG03139.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1568-1503T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337963 | |||||||
chr8:24337976 | A | C | 1 | a0008c0020t0023g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1568-1490A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337976 | |||||||
chr8:24337978 | G | C | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1568-1488G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24337978 | |||||||
chr8:24338036 | G | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1430G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338036 | |||||||
chr8:24338167 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1299A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338167 | |||||||
chr8:24338170 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1296A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338170 | |||||||
chr8:24338195 | C | T | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1271C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338195 | |||||||
chr8:24338227 | ATTAG | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1235_1568-123 others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24338227 | ||||||
chr8:24338243 | G | A | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1568-1223G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338243 | |||||||
chr8:24338314 | A | G | 46 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(43): Show |
53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1568-1152A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338314 | |||||||
chr8:24338368 | A | G | 1 | a0002c0003t0008g0261 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1568-1098A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338368 | |||||||
chr8:24338380 | A | C | 5 | a0003c0005t0006g0240 a0003c0005t0006g0241 a0003c0005t0006g0242 others(2): Show |
5 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-1086A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338380 | |||||||
chr8:24338399 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1067A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338399 | |||||||
chr8:24338406 | A | C | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1060A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338406 | |||||||
chr8:24338426 | CTCCCTGA others(54): Show |
C | 1 | a0001c0001t0003g0030 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1568-995_1568-935d others(63): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24338426 | ||||||
chr8:24338433 | A | C | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1033A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338433 | |||||||
chr8:24338435 | T | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-1031T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338435 | |||||||
chr8:24338533 | T | C | 1 | a0002c0003t0045g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1568-933T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338533 | |||||||
chr8:24338577 | A | T | 46 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(43): Show |
53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1568-889A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338577 | |||||||
chr8:24338579 | TAAA | T | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-884_1568-882d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 24338579 | ||||||
chr8:24338607 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-859A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338607 | |||||||
chr8:24338701 | A | T | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-765A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338701 | |||||||
chr8:24338779 | G | C | 5 | a0002c0007t0002g0116 a0002c0007t0026g0065 a0008c0011t0002g0026 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-687G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338779 | |||||||
chr8:24338834 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0002g0062 a0001c0001t0002g0104 |
3 | NA18998.hp2 NA19011.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1568-632G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338834 | |||||||
chr8:24338844 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-622A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24338844 | |||||||
chr8:24339118 | G | A | 318 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(315): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1568-348G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339118 | |||||||
chr8:24339202 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-264A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339202 | |||||||
chr8:24339225 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1568-241A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339225 | |||||||
chr8:24339277 | T | C | 1 | a0001c0001t0043g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1568-189T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339277 | |||||||
chr8:24339368 | G | A | 4 | a0003c0005t0006g0241 a0003c0005t0006g0242 a0003c0005t0006g0243 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-98G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339368 | |||||||
chr8:24339385 | C | T | 82 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(79): Show |
96 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1568-81C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339385 | |||||||
chr8:24339419 | T | C | 1 | a0002c0019t0006g0229 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1568-47T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339419 | |||||||
chr8:24339424 | A | G | 8 | a0001c0001t0001g0118 a0001c0001t0002g0148 a0001c0001t0002g0160 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1568-42A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | chr8 | 24339424 | |||||||
chr8:24339837 | G | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+269G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24339837 | |||||||
chr8:24339857 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1670+289A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24339857 | |||||||
chr8:24339983 | T | C | 1 | a0001c0017t0002g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1670+415T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24339983 | |||||||
chr8:24340020 | T | A | 1 | a0008c0020t0023g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1670+452T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340020 | |||||||
chr8:24340056 | A | T | 18 | a0001c0013t0002g0168 a0001c0013t0013g0167 a0001c0017t0002g0124 others(15): Show |
19 | HG00733.hp2 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670+488A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340056 | |||||||
chr8:24340134 | G | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+566G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340134 | |||||||
chr8:24340168 | T | A | 1 | a0001c0001t0003g0030 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1670+600T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340168 | |||||||
chr8:24340322 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1670+754C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340322 | |||||||
chr8:24340383 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1670+815G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340383 | |||||||
chr8:24340438 | T | C | 1 | a0003c0005t0005g0018 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1670+870T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340438 | |||||||
chr8:24340442 | G | A | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
40 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1670+874G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340442 | |||||||
chr8:24340469 | G | T | 2 | a0004c0004t0007g0075 a0004c0004t0007g0076 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1670+901G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340469 | |||||||
chr8:24340656 | A | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-942A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340656 | |||||||
chr8:24340717 | G | T | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
40 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1671-881G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24340717 | |||||||
chr8:24341001 | G | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-597G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341001 | |||||||
chr8:24341011 | G | C | 83 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1671-587G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341011 | |||||||
chr8:24341037 | A | G | 2 | a0002c0007t0002g0116 a0002c0007t0026g0065 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1671-561A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341037 | |||||||
chr8:24341058 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1671-540T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341058 | |||||||
chr8:24341108 | T | G | 5 | a0001c0001t0002g0114 a0001c0001t0002g0117 a0001c0001t0002g0119 others(2): Show |
5 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-490T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341108 | |||||||
chr8:24341117 | C | A | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1671-481C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341117 | |||||||
chr8:24341194 | T | C | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-404T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341194 | |||||||
chr8:24341309 | C | A | 1 | a0009c0028t0006g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1671-289C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341309 | |||||||
chr8:24341346 | A | G | 1 | a0003c0005t0005g0018 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1671-252A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341346 | |||||||
chr8:24341348 | G | A | 3 | a0001c0001t0002g0148 a0001c0001t0003g0224 a0001c0001t0004g0169 |
3 | HG03688.hp2 HG04204.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1671-250G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341348 | |||||||
chr8:24341390 | A | T | 30 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(27): Show |
35 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1671-208A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341390 | |||||||
chr8:24341401 | A | G | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-197A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341401 | |||||||
chr8:24341496 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0002g0089 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1671-102C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341496 | |||||||
chr8:24341550 | G | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1671-48G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341550 | |||||||
chr8:24341561 | A | G | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1671-37A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341561 | |||||||
chr8:24341578 | C | A | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1671-20C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341578 | |||||||
chr8:24341586 | C | G | 2 | a0001c0002t0014g0021 a0001c0002t0014g0287 |
3 | NA19005.hp1 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1671-12C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 15/22 | chr8 | 24341586 | |||||||
chr8:24341805 | G | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1830+48G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341805 | |||||||
chr8:24341841 | T | C | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1830+84T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341841 | |||||||
chr8:24341869 | G | A | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1830+112G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341869 | |||||||
chr8:24341878 | T | C | 1 | a0001c0002t0004g0291 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1830+121T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341878 | |||||||
chr8:24341904 | G | T | 1 | a0002c0003t0003g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1830+147G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341904 | |||||||
chr8:24341933 | C | A | 5 | a0002c0007t0002g0116 a0002c0007t0026g0065 a0008c0011t0002g0026 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1830+176C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341933 | |||||||
chr8:24341958 | G | T | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1830+201G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341958 | |||||||
chr8:24341998 | A | C | 1 | a0015c0027t0007g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1830+241A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24341998 | |||||||
chr8:24342040 | G | A | 1 | a0002c0003t0001g0249 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1830+283G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342040 | |||||||
chr8:24342084 | C | T | 1 | a0002c0003t0046g0260 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1830+327C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342084 | |||||||
chr8:24342111 | C | T | 1 | a0002c0003t0003g0259 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1830+354C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342111 | |||||||
chr8:24342440 | G | A | 1 | a0001c0002t0001g0038 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1831-661G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342440 | |||||||
chr8:24342481 | A | G | 47 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(44): Show |
56 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1831-620A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342481 | |||||||
chr8:24342635 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1831-466C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342635 | |||||||
chr8:24342722 | A | G | 82 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(79): Show |
96 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1831-379A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342722 | |||||||
chr8:24342761 | G | C | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1831-340G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342761 | |||||||
chr8:24342762 | A | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1831-339A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342762 | |||||||
chr8:24342797 | G | A | 2 | a0001c0001t0003g0014 a0001c0001t0003g0194 |
3 | HG03516.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1831-304G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342797 | |||||||
chr8:24342961 | C | T | 44 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(41): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1831-140C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342961 | |||||||
chr8:24342978 | T | G | 1 | a0003c0005t0006g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1831-123T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 16/22 | chr8 | 24342978 | |||||||
chr8:24343261 | A | G | 82 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(79): Show |
96 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1911+80A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 17/22 | chr8 | 24343261 | |||||||
chr8:24343477 | G | T | 2 | a0002c0007t0002g0116 a0002c0007t0026g0065 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1912-29G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 17/22 | chr8 | 24343477 | |||||||
chr8:24343761 | C | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+177C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343761 | |||||||
chr8:24343762 | G | A | 1 | a0001c0001t0038g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1990+178G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343762 | |||||||
chr8:24343805 | T | A | 1 | a0011c0032t0033g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1990+221T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343805 | |||||||
chr8:24343911 | C | G | 3 | a0001c0001t0001g0084 a0001c0001t0002g0089 a0001c0001t0017g0042 |
3 | HG03139.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1990+327C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24343911 | |||||||
chr8:24343931 | A | AT | 84 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1990+351dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24343931 | ||||||
chr8:24344035 | G | A | 24 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0082 others(21): Show |
24 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1990+451G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344035 | |||||||
chr8:24344087 | C | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+503C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344087 | |||||||
chr8:24344175 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1990+591G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344175 | |||||||
chr8:24344241 | C | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+657C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344241 | |||||||
chr8:24344263 | AG | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(41): Show |
46 | HG00438.hp1 HG00558.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1990+682delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24344263 | ||||||
chr8:24344334 | C | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+750C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344334 | |||||||
chr8:24344385 | A | C | 46 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(43): Show |
53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1990+801A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344385 | |||||||
chr8:24344414 | G | A | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+830G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344414 | |||||||
chr8:24344453 | A | G | 3 | a0001c0001t0025g0159 a0002c0007t0003g0270 a0002c0007t0003g0271 |
3 | HG01167.hp1 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1990+869A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344453 | |||||||
chr8:24344465 | A | G | 1 | a0006c0023t0002g0120 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1990+881A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344465 | |||||||
chr8:24344481 | G | A | 4 | a0001c0013t0002g0168 a0001c0013t0013g0167 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp2 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1990+897G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344481 | |||||||
chr8:24344514 | G | C | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+930G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344514 | |||||||
chr8:24344546 | T | G | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990+962T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344546 | |||||||
chr8:24344622 | A | G | 1 | a0001c0025t0042g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1990+1038A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344622 | |||||||
chr8:24344669 | T | C | 46 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(43): Show |
53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1990+1085T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344669 | |||||||
chr8:24344724 | CTT | C | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+1142_1990+114 others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24344724 | ||||||
chr8:24344761 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1990+1177A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344761 | |||||||
chr8:24344828 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1990+1244T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344828 | |||||||
chr8:24344838 | G | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+1254G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24344838 | |||||||
chr8:24345028 | C | CA | 6 | a0001c0001t0001g0118 a0001c0001t0002g0063 a0001c0001t0002g0137 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1990+1458dupA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24345028 | ||||||
chr8:24345028 | CA | C | 52 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0181 others(49): Show |
59 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1990+1458delA | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24345028 | ||||||
chr8:24345028 | CAAAA | C | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+1455_1990+145 others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24345028 | ||||||
chr8:24345079 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1990+1495T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345079 | |||||||
chr8:24345247 | A | G | 102 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(99): Show |
117 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1990+1663A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345247 | |||||||
chr8:24345342 | A | C | 5 | a0002c0007t0002g0116 a0002c0007t0026g0065 a0008c0011t0002g0026 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1990+1758A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345342 | |||||||
chr8:24345514 | C | G | 1 | a0002c0003t0045g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1990+1930C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345514 | |||||||
chr8:24345578 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1990+1994A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345578 | |||||||
chr8:24345623 | T | C | 9 | a0001c0013t0002g0168 a0001c0013t0013g0167 a0003c0006t0001g0279 others(6): Show |
9 | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1990+2039T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345623 | |||||||
chr8:24345672 | A | G | 28 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(25): Show |
33 | HG00621.hp2 HG01261.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1990+2088A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345672 | |||||||
chr8:24345707 | G | A | 3 | a0008c0011t0002g0026 a0008c0011t0006g0049 a0009c0028t0006g0245 |
3 | HG02895.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2123G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345707 | |||||||
chr8:24345751 | T | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990+2167T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345751 | |||||||
chr8:24345816 | G | A | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+2232G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345816 | |||||||
chr8:24345902 | T | C | 38 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(35): Show |
45 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1990+2318T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24345902 | |||||||
chr8:24346032 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1990+2448C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346032 | |||||||
chr8:24346098 | G | A | 1 | a0001c0001t0011g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1990+2514G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346098 | |||||||
chr8:24346162 | T | G | 8 | a0003c0005t0005g0018 a0003c0005t0006g0240 a0003c0005t0006g0241 others(5): Show |
9 | HG00733.hp2 HG00738.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1990+2578T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346162 | |||||||
chr8:24346354 | G | T | 2 | a0008c0011t0002g0026 a0008c0011t0006g0049 |
2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2770G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346354 | |||||||
chr8:24346366 | C | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+2782C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346366 | |||||||
chr8:24346368 | T | C | 2 | a0008c0011t0002g0026 a0008c0011t0006g0049 |
2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2784T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346368 | |||||||
chr8:24346443 | C | T | 2 | a0008c0011t0002g0026 a0008c0011t0006g0049 |
2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1990+2859C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346443 | |||||||
chr8:24346523 | G | T | 3 | a0001c0001t0002g0203 a0001c0001t0010g0024 a0001c0001t0010g0221 |
3 | HG00639.hp2 HG01109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1990+2939G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346523 | |||||||
chr8:24346571 | T | G | 83 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1990+2987T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346571 | |||||||
chr8:24346614 | C | G | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+3030C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346614 | |||||||
chr8:24346708 | G | A | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1990+3124G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346708 | |||||||
chr8:24346712 | A | G | 1 | a0008c0011t0006g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1990+3128A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346712 | |||||||
chr8:24346812 | T | G | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-3052T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346812 | |||||||
chr8:24346827 | C | T | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-3037C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346827 | |||||||
chr8:24346880 | G | A | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-2984G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346880 | |||||||
chr8:24346997 | C | T | 2 | a0008c0011t0002g0026 a0008c0011t0006g0049 |
2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1991-2867C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24346997 | |||||||
chr8:24347018 | G | A | 100 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(97): Show |
115 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1991-2846G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347018 | |||||||
chr8:24347081 | A | ATGCTTTC others(21): Show |
1 | a0001c0001t0025g0159 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1991-2780_1991-275 others(32): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24347081 | ||||||
chr8:24347130 | C | G | 1 | a0001c0001t0027g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1991-2734C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347130 | |||||||
chr8:24347363 | A | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-2501A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347363 | |||||||
chr8:24347435 | C | T | 317 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(314): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1991-2429C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347435 | |||||||
chr8:24347457 | C | G | 1 | a0001c0017t0002g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1991-2407C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347457 | |||||||
chr8:24347603 | G | C | 2 | a0001c0001t0001g0099 a0012c0021t0001g0100 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1991-2261G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347603 | |||||||
chr8:24347629 | A | G | 30 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(27): Show |
35 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.1991-2235A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347629 | |||||||
chr8:24347690 | G | A | 2 | a0001c0017t0002g0124 a0001c0025t0042g0248 |
2 | HG01192.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1991-2174G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347690 | |||||||
chr8:24347690 | G | T | 1 | a0002c0003t0003g0254 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1991-2174G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347690 | |||||||
chr8:24347724 | T | G | 46 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(43): Show |
53 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1991-2140T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347724 | |||||||
chr8:24347815 | GACC | G | 3 | a0008c0011t0002g0026 a0008c0011t0006g0049 a0009c0028t0006g0245 |
3 | HG02895.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1991-2047_1991-204 others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 24347815 | ||||||
chr8:24347829 | A | G | 18 | a0001c0013t0002g0168 a0001c0013t0013g0167 a0001c0017t0002g0124 others(15): Show |
19 | HG00733.hp2 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1991-2035A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347829 | |||||||
chr8:24347838 | G | C | 83 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1991-2026G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24347838 | |||||||
chr8:24348011 | G | A | 15 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0002g0056 others(12): Show |
15 | HG00423.hp1 HG00733.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1991-1853G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348011 | |||||||
chr8:24348071 | A | C | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-1793A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348071 | |||||||
chr8:24348102 | C | T | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | NA18955.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1991-1762C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348102 | |||||||
chr8:24348219 | A | T | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
40 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1991-1645A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348219 | |||||||
chr8:24348271 | C | T | 1 | a0002c0019t0006g0229 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1991-1593C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348271 | |||||||
chr8:24348301 | C | T | 44 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(41): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1991-1563C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348301 | |||||||
chr8:24348314 | A | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1550A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348314 | |||||||
chr8:24348357 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1991-1507T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348357 | |||||||
chr8:24348362 | G | A | 44 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(41): Show |
51 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1991-1502G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348362 | |||||||
chr8:24348372 | C | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1492C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348372 | |||||||
chr8:24348454 | G | A | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1410G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348454 | |||||||
chr8:24348523 | C | T | 37 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1991-1341C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348523 | |||||||
chr8:24348524 | A | G | 83 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(80): Show |
97 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1991-1340A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348524 | |||||||
chr8:24348560 | T | G | 1 | a0001c0002t0004g0290 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1991-1304T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348560 | |||||||
chr8:24348616 | C | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0080 others(11): Show |
15 | HG02015.hp1 HG02056.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1991-1248C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348616 | |||||||
chr8:24348773 | G | A | 2 | a0002c0007t0002g0116 a0002c0007t0026g0065 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1991-1091G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348773 | |||||||
chr8:24348780 | T | C | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-1084T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348780 | |||||||
chr8:24348791 | G | C | 3 | a0001c0001t0001g0189 a0001c0002t0012g0313 a0001c0002t0012g0314 |
3 | HG00609.hp2 HG02074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1991-1073G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348791 | |||||||
chr8:24348913 | G | A | 81 | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(78): Show |
95 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1991-951G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348913 | |||||||
chr8:24348933 | C | A | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-931C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348933 | |||||||
chr8:24348956 | C | T | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-908C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348956 | |||||||
chr8:24348996 | G | A | 2 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1991-868G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24348996 | |||||||
chr8:24349013 | G | A | 17 | a0001c0013t0002g0168 a0001c0013t0013g0167 a0002c0003t0004g0255 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1991-851G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349013 | |||||||
chr8:24349068 | C | A | 2 | a0002c0007t0002g0116 a0002c0007t0026g0065 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1991-796C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349068 | |||||||
chr8:24349170 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1991-694C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349170 | |||||||
chr8:24349214 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1991-650C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349214 | |||||||
chr8:24349231 | T | C | 1 | a0001c0001t0002g0195 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1991-633T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349231 | |||||||
chr8:24349506 | A | G | 1 | a0002c0003t0003g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1991-358A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349506 | |||||||
chr8:24349520 | A | T | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-344A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349520 | |||||||
chr8:24349523 | A | C | 1 | a0001c0001t0006g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1991-341A>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349523 | |||||||
chr8:24349591 | G | A | 35 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(32): Show |
42 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1991-273G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349591 | |||||||
chr8:24349647 | G | T | 2 | a0001c0001t0002g0144 a0001c0001t0004g0149 |
2 | NA18972.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1991-217G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349647 | |||||||
chr8:24349710 | A | G | 1 | a0001c0001t0004g0115 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1991-154A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349710 | |||||||
chr8:24349718 | A | G | 36 | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(33): Show |
43 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1991-146A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | chr8 | 24349718 | |||||||
chr8:24350101 | G | A | 38 | a0001c0001t0003g0183 a0001c0001t0003g0196 a0001c0001t0008g0197 others(35): Show |
45 | HG00621.hp2 HG00673.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.2099+129G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350101 | |||||||
chr8:24350160 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2099+188A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350160 | |||||||
chr8:24350161 | T | C | 50 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0001t0001g0208 others(47): Show |
57 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2099+189T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350161 | |||||||
chr8:24350227 | A | G | 2 | a0003c0006t0001g0279 a0003c0006t0002g0278 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2099+255A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350227 | |||||||
chr8:24350381 | G | A | 1 | a0001c0001t0003g0217 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2099+409G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350381 | |||||||
chr8:24350426 | A | G | 170 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(167): Show |
188 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.2099+454A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350426 | |||||||
chr8:24350431 | AG | A | 3 | a0001c0013t0013g0167 a0003c0006t0013g0273 a0003c0006t0013g0274 |
3 | HG02922.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2099+460delG | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350431 | |||||||
chr8:24350481 | T | C | 90 | a0001c0001t0001g0072 a0001c0001t0001g0096 a0001c0001t0001g0142 others(87): Show |
100 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2099+509T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350481 | |||||||
chr8:24350505 | T | C | 93 | a0001c0001t0001g0072 a0001c0001t0001g0096 a0001c0001t0001g0142 others(90): Show |
103 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.2099+533T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350505 | |||||||
chr8:24350547 | A | G | 9 | a0001c0001t0006g0141 a0002c0019t0006g0229 a0003c0005t0006g0240 others(6): Show |
9 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2099+575A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350547 | |||||||
chr8:24350625 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0039g0057 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2100-607T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350625 | |||||||
chr8:24350674 | C | T | 13 | a0001c0001t0006g0141 a0001c0013t0013g0167 a0002c0007t0026g0065 others(10): Show |
13 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.2100-558C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350674 | |||||||
chr8:24350845 | G | A | 1 | a0003c0005t0005g0018 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2100-387G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350845 | |||||||
chr8:24350858 | AACG | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0083 a0001c0001t0047g0066 |
3 | NA18952.hp1 NA18985.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2100-373_2100-371d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350858 | |||||||
chr8:24350860 | C | T | 303 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(300): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.2100-372C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350860 | |||||||
chr8:24350864 | GTT | G | 30 | a0001c0001t0004g0094 a0001c0001t0004g0115 a0001c0001t0004g0125 others(27): Show |
30 | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.2100-343_2100-342d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | ||||||
chr8:24350864 | GTTT | G | 84 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0002g0004 others(81): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.2100-344_2100-342d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | ||||||
chr8:24350864 | GTTTT | G | 24 | a0001c0001t0001g0101 a0001c0001t0001g0202 a0001c0001t0002g0129 others(21): Show |
26 | HG00140.hp2 HG00597.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2100-345_2100-342d others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | ||||||
chr8:24350864 | GTTTTT | G | 170 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(167): Show |
186 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2100-346_2100-342d others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 24350864 | ||||||
chr8:24350865 | T | G | 3 | a0001c0001t0003g0041 a0001c0001t0003g0083 a0001c0001t0047g0066 |
3 | NA18952.hp1 NA18985.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2100-367T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350865 | |||||||
chr8:24350867 | T | G | 3 | a0001c0001t0003g0041 a0001c0001t0003g0083 a0001c0001t0047g0066 |
3 | NA18952.hp1 NA18985.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2100-365T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350867 | |||||||
chr8:24350875 | T | G | 26 | a0001c0001t0004g0094 a0001c0001t0004g0115 a0001c0001t0004g0125 others(23): Show |
26 | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.2100-357T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350875 | |||||||
chr8:24350876 | T | C | 3 | a0001c0001t0001g0046 a0001c0002t0001g0280 a0001c0002t0001g0284 |
3 | HG00408.hp1 NA18612.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2100-356T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350876 | |||||||
chr8:24350876 | T | G | 113 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0002g0004 others(110): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2100-356T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350876 | |||||||
chr8:24350877 | T | G | 110 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0001g0101 others(107): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.2100-355T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350877 | |||||||
chr8:24350878 | T | G | 193 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(190): Show |
211 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.2100-354T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350878 | |||||||
chr8:24350879 | T | G | 168 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(165): Show |
184 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2100-353T>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350879 | |||||||
chr8:24350949 | A | G | 3 | a0001c0001t0008g0197 a0001c0002t0008g0023 a0002c0003t0008g0261 |
4 | HG00673.hp1 NA18945.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2100-283A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24350949 | |||||||
chr8:24351081 | A | G | 14 | a0001c0001t0005g0045 a0001c0001t0005g0098 a0001c0001t0005g0143 others(11): Show |
15 | HG01109.hp1 HG02004.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.2100-151A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24351081 | |||||||
chr8:24351093 | C | T | 74 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0002g0004 others(71): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.2100-139C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24351093 | |||||||
chr8:24351136 | C | T | 306 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(303): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2100-96C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | chr8 | 24351136 | |||||||
chr8:24351334 | G | A | 200 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(197): Show |
218 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2178+24G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351334 | |||||||
chr8:24351421 | C | A | 74 | a0001c0001t0001g0031 a0001c0001t0002g0004 a0001c0001t0002g0154 others(71): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.2178+111C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351421 | |||||||
chr8:24351432 | A | G | 1 | a0004c0004t0007g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178+122A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351432 | |||||||
chr8:24351478 | C | T | 1 | a0001c0001t0011g0060 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2178+168C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351478 | |||||||
chr8:24351498 | T | A | 5 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0105 others(2): Show |
5 | HG02004.hp1 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2178+188T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351498 | |||||||
chr8:24351541 | C | G | 1 | a0001c0001t0017g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2178+231C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351541 | |||||||
chr8:24351567 | G | A | 3 | a0003c0006t0002g0275 a0003c0006t0002g0276 a0003c0006t0002g0277 |
3 | HG02055.hp2 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2178+257G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351567 | |||||||
chr8:24351596 | A | T | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2178+286A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351596 | |||||||
chr8:24351759 | A | ATCATTTA others(17): Show |
282 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(279): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2179-226_2179-203d others(26): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 24351759 | ||||||
chr8:24351772 | T | C | 1 | a0001c0001t0004g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2179-215T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351772 | |||||||
chr8:24351834 | C | T | 9 | a0001c0001t0002g0097 a0001c0001t0002g0108 a0001c0001t0002g0203 others(6): Show |
10 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.2179-153C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351834 | |||||||
chr8:24351969 | A | G | 1 | a0001c0001t0003g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2179-18A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 20/22 | chr8 | 24351969 | |||||||
chr8:24352093 | C | T | 1 | a0001c0001t0006g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2244+41C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352093 | |||||||
chr8:24352378 | C | T | 67 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0001t0003g0001 others(64): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2244+326C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352378 | |||||||
chr8:24352379 | T | C | 1 | a0001c0002t0001g0286 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2244+327T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352379 | |||||||
chr8:24352405 | C | A | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244+353C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352405 | |||||||
chr8:24352583 | C | T | 3 | a0002c0007t0003g0270 a0002c0007t0003g0271 a0011c0032t0033g0247 |
3 | HG01167.hp1 HG01169.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2244+531C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352583 | |||||||
chr8:24352612 | T | C | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244+560T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352612 | |||||||
chr8:24352679 | T | C | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244+627T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352679 | |||||||
chr8:24352809 | G | A | 8 | a0002c0019t0006g0229 a0003c0005t0006g0240 a0003c0005t0006g0241 others(5): Show |
8 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.2244+757G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352809 | |||||||
chr8:24352871 | A | G | 20 | a0001c0001t0005g0045 a0001c0001t0005g0098 a0001c0001t0005g0143 others(17): Show |
22 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.2244+819A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352871 | |||||||
chr8:24352911 | ATCT | A | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-854_2245-852d others(5): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24352911 | ||||||
chr8:24352924 | G | GTAAC | 20 | a0001c0001t0005g0045 a0001c0001t0005g0098 a0001c0001t0005g0143 others(17): Show |
22 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.2245-843_2245-842i others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24352924 | ||||||
chr8:24352928 | G | C | 307 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(304): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2245-842G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352928 | |||||||
chr8:24352942 | T | C | 3 | a0001c0013t0013g0167 a0003c0006t0013g0273 a0003c0006t0013g0274 |
3 | HG02922.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2245-828T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352942 | |||||||
chr8:24352960 | C | G | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-810C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24352960 | |||||||
chr8:24353038 | C | A | 8 | a0001c0001t0002g0175 a0001c0001t0002g0225 a0001c0001t0002g0231 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2245-732C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353038 | |||||||
chr8:24353055 | A | G | 1 | a0001c0001t0003g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2245-715A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353055 | |||||||
chr8:24353135 | A | G | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-635A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353135 | |||||||
chr8:24353147 | C | T | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-623C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353147 | |||||||
chr8:24353202 | A | AAG | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-567_2245-566d others(4): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24353202 | ||||||
chr8:24353240 | G | A | 310 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(307): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2245-530G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353240 | |||||||
chr8:24353285 | G | C | 306 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(303): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2245-485G>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353285 | |||||||
chr8:24353292 | T | A | 4 | a0001c0013t0013g0167 a0002c0007t0026g0065 a0003c0006t0013g0273 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-478T>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353292 | |||||||
chr8:24353309 | T | TAAGAGTC others(11): Show |
1 | a0001c0001t0003g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2245-457_2245-440d others(20): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24353309 | ||||||
chr8:24353428 | A | AT | 306 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(303): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2245-335dupT | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 24353428 | ||||||
chr8:24353579 | T | C | 311 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.2245-191T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353579 | |||||||
chr8:24353598 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2245-172C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353598 | |||||||
chr8:24353656 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2245-114T>C | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353656 | |||||||
chr8:24353681 | A | T | 1 | a0002c0007t0026g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2245-89A>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353681 | |||||||
chr8:24353725 | C | T | 1 | a0001c0002t0004g0300 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2245-45C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353725 | |||||||
chr8:24353765 | C | T | 309 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(306): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
splice_region_variant&intron_variant | LOW | c.2245-5C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | chr8 | 24353765 | |||||||
chr8:24353844 | A | G | 1 | a0001c0001t0003g0083 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2307+12A>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24353844 | |||||||
chr8:24353916 | A | AAAAACTT others(21): Show |
1 | a0001c0001t0002g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2307+86_2307+113du others(29): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 24353916 | ||||||
chr8:24353983 | G | A | 10 | a0001c0001t0006g0054 a0001c0001t0006g0068 a0002c0019t0006g0229 others(7): Show |
10 | HG00733.hp2 HG00738.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2307+151G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24353983 | |||||||
chr8:24354045 | C | A | 275 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2307+213C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354045 | |||||||
chr8:24354175 | C | T | 19 | a0001c0001t0005g0045 a0001c0001t0005g0098 a0001c0001t0005g0143 others(16): Show |
21 | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.2308-209C>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354175 | |||||||
chr8:24354203 | G | A | 276 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2308-181G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354203 | |||||||
chr8:24354221 | C | A | 1 | a0001c0002t0002g0305 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2308-163C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354221 | |||||||
chr8:24354221 | C | G | 309 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(306): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.2308-163C>G | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354221 | |||||||
chr8:24354226 | C | A | 310 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(307): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2308-158C>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354226 | |||||||
chr8:24354247 | G | A | 2 | a0001c0001t0003g0219 a0001c0001t0003g0233 |
2 | HG00099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2308-137G>A | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354247 | |||||||
chr8:24354356 | G | T | 33 | a0001c0001t0004g0094 a0001c0001t0004g0115 a0001c0001t0004g0125 others(30): Show |
33 | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.2308-28G>T | ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | chr8 | 24354356 | |||||||
chr8:24354371 | A | ATGTC | 311 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
splice_region_variant&intron_variant | LOW | c.2308-11_2308-8dupG others(3): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 24354371 |