Item | Value |
---|---|
geneid | 10350 |
ensemblid | ENSG00000154258.17 |
hgncid | 39 |
symbol | ABCA9 |
name | ATP binding cassette subfamily A member 9 |
refseq_nuc | NM_080283.4 |
refseq_prot | NP_525022.2 |
ensembl_nuc | ENST00000340001.9 |
ensembl_prot | ENSP00000342216.3 |
mane_status | MANE Select |
chr | chr17 |
start | 68974488 |
end | 69060927 |
strand | - |
ver | v1.2 |
region | chr17:68974488-69060927 |
region5000 | chr17:68969488-69065927 |
regionname0 | ABCA9_chr17_68974488_69060927 |
regionname5000 | ABCA9_chr17_68969488_69065927 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1624 | 108 | 23 | 11 | 52 | 8 | 14 | 40 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0002 | 0/1 | 1624 | 108 | 10 | 21 | 57 | 6 | 13 | 44 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0003 | 1/0 | 1624 | 34 | 23 | 3 | 0 | 0 | 7 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0004 | 0/0 | 1624 | 18 | 16 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0005 | 0/0 | 1624 | 14 | 0 | 4 | 9 | 0 | 1 | 8 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0006 | 0/0 | 1624 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0007 | 0/0 | 1624 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0008 | 0/0 | 1624 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0009 | 0/0 | 1049 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1044): Show |
chr17 | 68969488 | 69065927 |
a0010 | 0/0 | 1624 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0011 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0012 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0013 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0014 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0015 | 0/0 | 1624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0016 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0017 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0018 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0019 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0020 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0021 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0022 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
a0023 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | MSKRR others(1619): Show |
chr17 | 68969488 | 69065927 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4872 | 87 | 12 | 7 | 52 | 3 | 13 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0001c0007 | 0/0 | 4872 | 11 | 2 | 4 | 0 | 4 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0001c0008 | 0/0 | 4872 | 8 | 8 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0001c0021 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0001c0029 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0002c0002 | 0/1 | 4872 | 86 | 10 | 21 | 40 | 4 | 10 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0002c0004 | 0/0 | 4872 | 19 | 0 | 0 | 16 | 1 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0002c0026 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0002c0027 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0002c0028 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0003c0003 | 1/0 | 4872 | 34 | 23 | 3 | 0 | 0 | 7 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0004c0005 | 0/0 | 4872 | 18 | 16 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0005c0006 | 0/0 | 4872 | 14 | 0 | 4 | 9 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0006c0009 | 0/0 | 4872 | 5 | 2 | 3 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0007c0010 | 0/0 | 4872 | 5 | 0 | 5 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0008c0013 | 0/0 | 4872 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0008c0020 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0009c0012 | 0/0 | 4872 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0010c0011 | 0/0 | 4872 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0011c0014 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0012c0016 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0013c0022 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0014c0015 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0015c0024 | 0/0 | 4872 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0016c0017 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0017c0018 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0018c0019 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0019c0023 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0020c0030 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0021c0032 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0022c0025 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 | ||
a0023c0031 | 0/0 | 4872 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | ATGAG others(4867): Show |
chr17 | 68969488 | 69065927 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6377 | 78 | 8 | 4 | 50 | 3 | 13 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0001c0001t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0001c0001t0006 | 0/0 | 6371 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6366): Show |
chr17 | 68969488 | 69065927 |
a0001c0001t0008 | 0/0 | 6377 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0001c0001t0009 | 0/0 | 6377 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0001c0001t0011 | 0/0 | 6377 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0001c0001t0012 | 0/0 | 6377 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0001c0007t0001 | 0/0 | 6377 | 10 | 1 | 4 | 0 | 4 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0001c0007t0004 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0001c0008t0001 | 0/0 | 6377 | 8 | 8 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0001c0021t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0001c0029t0001 | 0/0 | 6377 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0002c0002t0002 | 0/1 | 6373 | 84 | 10 | 19 | 40 | 4 | 10 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0002c0002t0007 | 0/0 | 6373 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0002c0004t0002 | 0/0 | 6373 | 19 | 0 | 0 | 16 | 1 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0002c0026t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0002c0027t0002 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0002c0028t0002 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0003c0003t0001 | 1/0 | 6377 | 11 | 5 | 1 | 0 | 0 | 4 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0003c0003t0003 | 0/0 | 6373 | 10 | 7 | 2 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0003c0003t0004 | 0/0 | 6373 | 11 | 10 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0003c0003t0010 | 0/0 | 6377 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0003c0003t0013 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0004c0005t0003 | 0/0 | 6373 | 18 | 16 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0005c0006t0001 | 0/0 | 6377 | 14 | 0 | 4 | 9 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0006c0009t0005 | 0/0 | 6371 | 5 | 2 | 3 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6366): Show |
chr17 | 68969488 | 69065927 |
a0007c0010t0002 | 0/0 | 6373 | 5 | 0 | 5 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0008c0013t0003 | 0/0 | 6373 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0008c0020t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0009c0012t0001 | 0/0 | 6377 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0010c0011t0003 | 0/0 | 6373 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0011c0014t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0012c0016t0002 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0013c0022t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0014c0015t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0015c0024t0002 | 0/0 | 6373 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0016c0017t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0017c0018t0014 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0018c0019t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0019c0023t0003 | 0/0 | 6373 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0020c0030t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0021c0032t0001 | 0/0 | 6377 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6372): Show |
chr17 | 68969488 | 69065927 |
a0022c0025t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
a0023c0031t0002 | 0/0 | 6373 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | AGAAC others(6368): Show |
chr17 | 68969488 | 69065927 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0008g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0008g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0011g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0001t0012g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0007t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0008t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0021t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0001c0029t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0007g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0002t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0004t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0026t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0027t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0002c0028t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0003c0003t0013g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0004c0005t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0005c0006t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0009t0005g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0009t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0009t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0006c0009t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0010t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0010t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0010t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0010t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0007c0010t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0008c0013t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0008c0013t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0008c0020t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0009c0012t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0009c0012t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0010c0011t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0010c0011t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0011c0014t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0012c0016t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0013c0022t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0014c0015t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0015c0024t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0016c0017t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0017c0018t0014g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0018c0019t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0019c0023t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0020c0030t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0021c0032t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0022c0025t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
a0023c0031t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0029 | t0001 | g0195 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0068 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0076 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00140 | hp2 | a0001 | c0007 | t0001 | g0220 | EUR | GBR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00280 | hp1 | a0002 | c0004 | t0002 | g0257 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00280 | hp2 | a0001 | c0007 | t0001 | g0236 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00544 | hp2 | a0005 | c0006 | t0001 | g0014 | EAS | CHS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00639 | hp1 | a0002 | c0002 | t0007 | g0129 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00639 | hp2 | a0003 | c0003 | t0003 | g0038 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00642 | hp2 | a0001 | c0007 | t0001 | g0206 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00733 | hp1 | a0008 | c0013 | t0003 | g0058 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01069 | hp1 | a0006 | c0009 | t0005 | g0289 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01071 | hp1 | a0006 | c0009 | t0005 | g0015 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0130 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01074 | hp1 | a0005 | c0006 | t0001 | g0270 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01074 | hp2 | a0002 | c0002 | t0007 | g0128 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0035 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01106 | hp1 | a0006 | c0009 | t0005 | g0015 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0229 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01109 | hp2 | a0004 | c0005 | t0003 | g0285 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01167 | hp2 | a0009 | c0012 | t0001 | g0268 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01169 | hp2 | a0009 | c0012 | t0001 | g0278 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0145 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01257 | hp1 | a0007 | c0010 | t0002 | g0081 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01257 | hp2 | a0001 | c0001 | t0008 | g0246 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01258 | hp1 | a0001 | c0007 | t0001 | g0115 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0245 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01346 | hp1 | a0004 | c0005 | t0003 | g0001 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01361 | hp1 | a0003 | c0003 | t0003 | g0042 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01361 | hp2 | a0001 | c0007 | t0001 | g0137 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01496 | hp1 | a0001 | c0007 | t0001 | g0113 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01496 | hp2 | a0007 | c0010 | t0002 | g0118 | AMR | CLM | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01516 | hp1 | a0001 | c0007 | t0001 | g0012 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01516 | hp2 | a0002 | c0027 | t0002 | g0069 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01517 | hp1 | a0001 | c0007 | t0001 | g0012 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0136 | EUR | IBS | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01884 | hp1 | a0003 | c0003 | t0004 | g0026 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01891 | hp1 | a0001 | c0021 | t0003 | g0020 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01891 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0080 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01952 | hp2 | a0007 | c0010 | t0002 | g0141 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01975 | hp2 | a0005 | c0006 | t0001 | g0014 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01978 | hp1 | a0005 | c0006 | t0001 | g0271 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG01978 | hp2 | a0007 | c0010 | t0002 | g0150 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02004 | hp2 | a0005 | c0006 | t0001 | g0273 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02055 | hp2 | a0006 | c0009 | t0005 | g0288 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02071 | hp2 | a0002 | c0004 | t0002 | g0262 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02074 | hp2 | a0002 | c0004 | t0002 | g0135 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02083 | hp2 | a0002 | c0004 | t0002 | g0106 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02132 | hp2 | a0001 | c0001 | t0011 | g0244 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02145 | hp1 | a0011 | c0014 | t0003 | g0051 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0099 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02155 | hp1 | a0002 | c0004 | t0002 | g0110 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | CDX | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02258 | hp2 | a0012 | c0016 | t0002 | g0053 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02273 | hp1 | a0007 | c0010 | t0002 | g0140 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02280 | hp2 | a0001 | c0007 | t0001 | g0088 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02451 | hp1 | a0013 | c0022 | t0003 | g0019 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02451 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02572 | hp2 | a0001 | c0008 | t0001 | g0162 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0031 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02622 | hp1 | a0014 | c0015 | t0003 | g0052 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0028 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02630 | hp1 | a0004 | c0005 | t0003 | g0283 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02630 | hp2 | a0003 | c0003 | t0003 | g0040 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02647 | hp1 | a0001 | c0008 | t0001 | g0187 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02647 | hp2 | a0004 | c0005 | t0003 | g0282 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02698 | hp2 | a0003 | c0003 | t0003 | g0045 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02717 | hp1 | a0001 | c0008 | t0001 | g0191 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02717 | hp2 | a0003 | c0003 | t0004 | g0023 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02723 | hp2 | a0001 | c0008 | t0001 | g0176 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02735 | hp2 | a0015 | c0024 | t0002 | g0063 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02809 | hp1 | a0004 | c0005 | t0003 | g0280 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02809 | hp2 | a0016 | c0017 | t0003 | g0184 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02818 | hp1 | a0004 | c0005 | t0003 | g0265 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02818 | hp2 | a0003 | c0003 | t0004 | g0006 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02886 | hp1 | a0004 | c0005 | t0003 | g0269 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02886 | hp2 | a0001 | c0007 | t0004 | g0091 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02922 | hp1 | a0001 | c0008 | t0001 | g0186 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02922 | hp2 | a0004 | c0005 | t0003 | g0263 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02970 | hp1 | a0004 | c0005 | t0003 | g0281 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0100 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0021 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02976 | hp2 | a0003 | c0003 | t0004 | g0027 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0005 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03041 | hp2 | a0010 | c0011 | t0003 | g0049 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03098 | hp1 | a0008 | c0020 | t0003 | g0055 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03098 | hp2 | a0004 | c0005 | t0003 | g0266 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03130 | hp1 | a0003 | c0003 | t0004 | g0006 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03139 | hp1 | a0003 | c0003 | t0004 | g0024 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0084 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03195 | hp1 | a0001 | c0008 | t0001 | g0258 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03209 | hp1 | a0001 | c0008 | t0001 | g0185 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03209 | hp2 | a0003 | c0003 | t0003 | g0041 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03225 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03453 | hp1 | a0004 | c0005 | t0003 | g0267 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03453 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03486 | hp1 | a0004 | c0005 | t0003 | g0264 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0037 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03490 | hp2 | a0002 | c0028 | t0002 | g0079 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03491 | hp1 | a0003 | c0003 | t0001 | g0007 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0007 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03516 | hp1 | a0018 | c0019 | t0003 | g0056 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03516 | hp2 | a0019 | c0023 | t0003 | g0018 | AFR | ESN | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0120 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03579 | hp1 | a0003 | c0003 | t0003 | g0036 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03579 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03654 | hp1 | a0002 | c0004 | t0002 | g0260 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0085 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0134 | SAS | PJL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03834 | hp1 | a0003 | c0003 | t0004 | g0022 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0149 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03927 | hp2 | a0003 | c0003 | t0013 | g0025 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0121 | SAS | BEB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04115 | hp1 | a0005 | c0006 | t0001 | g0287 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04115 | hp2 | a0001 | c0007 | t0001 | g0156 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0119 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0086 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG04228 | hp2 | a0002 | c0004 | t0002 | g0083 | SAS | STU | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18522 | hp1 | a0003 | c0003 | t0003 | g0044 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18522 | hp2 | a0003 | c0003 | t0004 | g0005 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | CHB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18906 | hp1 | a0003 | c0003 | t0004 | g0029 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18957 | hp1 | a0002 | c0004 | t0002 | g0107 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18962 | hp2 | a0002 | c0004 | t0002 | g0207 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18967 | hp2 | a0002 | c0004 | t0002 | g0151 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18969 | hp1 | a0002 | c0004 | t0002 | g0108 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18974 | hp2 | a0005 | c0006 | t0001 | g0013 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18979 | hp1 | a0002 | c0004 | t0002 | g0178 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18979 | hp2 | a0002 | c0004 | t0002 | g0144 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18980 | hp2 | a0005 | c0006 | t0001 | g0276 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18982 | hp2 | a0002 | c0004 | t0002 | g0109 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18985 | hp1 | a0005 | c0006 | t0001 | g0279 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18987 | hp2 | a0002 | c0004 | t0002 | g0192 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18989 | hp1 | a0005 | c0006 | t0001 | g0277 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18993 | hp1 | a0005 | c0006 | t0001 | g0013 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19002 | hp1 | a0002 | c0026 | t0002 | g0071 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19002 | hp2 | a0005 | c0006 | t0001 | g0274 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19009 | hp2 | a0020 | c0030 | t0002 | g0200 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19011 | hp2 | a0002 | c0004 | t0002 | g0242 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19043 | hp1 | a0008 | c0013 | t0003 | g0057 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19043 | hp2 | a0006 | c0009 | t0005 | g0290 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19054 | hp1 | a0021 | c0032 | t0001 | g0221 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19066 | hp2 | a0001 | c0001 | t0009 | g0194 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19067 | hp1 | a0002 | c0004 | t0002 | g0152 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19068 | hp2 | a0002 | c0004 | t0002 | g0111 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19075 | hp2 | a0022 | c0025 | t0002 | g0059 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19083 | hp2 | a0002 | c0004 | t0002 | g0179 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19086 | hp1 | a0005 | c0006 | t0001 | g0275 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19087 | hp1 | a0023 | c0031 | t0002 | g0231 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19087 | hp2 | a0005 | c0006 | t0001 | g0272 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19240 | hp1 | a0010 | c0011 | t0003 | g0050 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA19240 | hp2 | a0003 | c0003 | t0003 | g0039 | AFR | YRI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20129 | hp1 | a0001 | c0008 | t0001 | g0188 | AFR | ASW | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ASW | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0131 | EUR | TSI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0030 | SAS | GIH | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02486 | hp2 | a0003 | c0003 | t0010 | g0033 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0046 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG02559 | hp2 | a0004 | c0005 | t0003 | g0284 | AFR | ACB | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG03471 | hp2 | a0017 | c0018 | t0014 | g0291 | AFR | MSL | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
HG06807 | hp2 | a0004 | c0005 | t0003 | g0001 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA20300 | hp2 | a0004 | c0005 | t0003 | g0286 | AFR | USA | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA21309 | hp1 | a0003 | c0003 | t0003 | g0043 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | LWK | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0112 | REF | REF | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0047 | REF | REF | ABCA9_chr17_68969488_69065927 | ABCA9 | chr17 | 68969488 | 69065927 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68986306 | C | T | 4 | a0004 a0011 a0016 others(1): Show |
21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
missense_variant | MODERATE | c.4066G>A | p.Gly1356Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/39 | 4141/6377 | 4066/4875 | 1356/1624 | chr17 | 68986306 | |||
chr17:68989851 | T | G | 7 | a0002 a0007 a0012 others(4): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
missense_variant | MODERATE | c.3917A>C | p.Lys1306Thr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/39 | 3992/6377 | 3917/4875 | 1306/1624 | chr17 | 68989851 | |||
chr17:68989875 | T | C | 1 | a0019 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.3893A>G | p.Asn1298Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/39 | 3968/6377 | 3893/4875 | 1298/1624 | chr17 | 68989875 | |||
chr17:69008235 | T | A | 1 | a0009 | 2 | HG01167.hp2 HG01169.hp2 |
stop_gained&splice_region_variant | HIGH | c.3148A>T | p.Lys1050* | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 24/39 | 3223/6377 | 3148/4875 | 1050/1624 | chr17 | 69008235 | |||
chr17:69016293 | G | A | 1 | a0020 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.2999C>T | p.Ser1000Leu | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/39 | 3074/6377 | 2999/4875 | 1000/1624 | chr17 | 69016293 | |||
chr17:69016309 | G | A | 2 | a0008 a0010 |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.2983C>T | p.Leu995Phe | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/39 | 3058/6377 | 2983/4875 | 995/1624 | chr17 | 69016309 | |||
chr17:69017778 | C | T | 1 | a0022 | 1 | NA19075.hp2 | missense_variant | MODERATE | c.2779G>A | p.Asp927Asn | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/39 | 2854/6377 | 2779/4875 | 927/1624 | chr17 | 69017778 | |||
chr17:69018533 | G | C | 3 | a0013 a0018 a0019 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.2647C>G | p.Leu883Val | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/39 | 2722/6377 | 2647/4875 | 883/1624 | chr17 | 69018533 | |||
chr17:69021789 | T | C | 1 | a0007 | 5 | HG01257.hp1 HG01496.hp2 HG01952.hp2 others(2): Show |
missense_variant | MODERATE | c.2354A>G | p.Asn785Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/39 | 2429/6377 | 2354/4875 | 785/1624 | chr17 | 69021789 | |||
chr17:69029202 | C | T | 1 | a0015 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1471G>A | p.Ala491Thr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/39 | 1546/6377 | 1471/4875 | 491/1624 | chr17 | 69029202 | |||
chr17:69033857 | T | C | 1 | a0023 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.1145A>G | p.Tyr382Cys | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/39 | 1220/6377 | 1145/4875 | 382/1624 | chr17 | 69033857 | |||
chr17:69035316 | C | T | 22 | a0001 a0002 a0004 others(19): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
missense_variant | MODERATE | c.1058G>A | p.Arg353His | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/39 | 1133/6377 | 1058/4875 | 353/1624 | chr17 | 69035316 | |||
chr17:69035396 | C | A | 1 | a0021 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.978G>T | p.Lys326Asn | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/39 | 1053/6377 | 978/4875 | 326/1624 | chr17 | 69035396 | |||
chr17:69035739 | A | G | 4 | a0006 a0008 a0017 others(1): Show |
10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
missense_variant | MODERATE | c.863T>C | p.Ile288Thr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 7/39 | 938/6377 | 863/4875 | 288/1624 | chr17 | 69035739 | |||
chr17:69043504 | C | T | 3 | a0004 a0005 a0009 |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
missense_variant | MODERATE | c.785G>A | p.Arg262Gln | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/39 | 860/6377 | 785/4875 | 262/1624 | chr17 | 69043504 | |||
chr17:69049311 | G | T | 4 | a0010 a0011 a0012 others(1): Show |
5 | HG02145.hp1 HG02258.hp2 HG02622.hp1 others(2): Show |
missense_variant | MODERATE | c.276C>A | p.Asn92Lys | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/39 | 351/6377 | 276/4875 | 92/1624 | chr17 | 69049311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68985116 | C | A | 2 | a0013c0022 a0018c0019 |
2 | HG02451.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.4221G>T | p.Ala1407Ala | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 33/39 | 4296/6377 | 4221/4875 | 1407/1624 | chr17 | 68985116 | |||
chr17:68986286 | G | A | 1 | a0002c0028 | 1 | HG03490.hp2 | synonymous_variant | LOW | c.4086C>T | p.Gly1362Gly | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/39 | 4161/6377 | 4086/4875 | 1362/1624 | chr17 | 68986286 | |||
chr17:68989101 | A | G | 1 | a0019c0023 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.3973T>C | p.Leu1325Leu | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/39 | 4048/6377 | 3973/4875 | 1325/1624 | chr17 | 68989101 | |||
chr17:69007825 | A | G | 1 | a0002c0027 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.3369T>C | p.Tyr1123Tyr | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/39 | 3444/6377 | 3369/4875 | 1123/1624 | chr17 | 69007825 | |||
chr17:69007870 | G | A | 1 | a0001c0029 | 1 | HG00099.hp1 | splice_region_variant&synonymous_variant | LOW | c.3324C>T | p.Ile1108Ile | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/39 | 3399/6377 | 3324/4875 | 1108/1624 | chr17 | 69007870 | |||
chr17:69017776 | A | G | 1 | a0002c0026 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.2781T>C | p.Asp927Asp | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/39 | 2856/6377 | 2781/4875 | 927/1624 | chr17 | 69017776 | |||
chr17:69018501 | C | T | 1 | a0001c0021 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.2679G>A | p.Pro893Pro | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/39 | 2754/6377 | 2679/4875 | 893/1624 | chr17 | 69018501 | |||
chr17:69020504 | G | A | 1 | a0008c0020 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2484C>T | p.Ser828Ser | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/39 | 2559/6377 | 2484/4875 | 828/1624 | chr17 | 69020504 | |||
chr17:69032119 | T | C | 11 | a0001c0007 a0001c0029 a0002c0002 others(8): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
synonymous_variant | LOW | c.1434A>G | p.Lys478Lys | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/39 | 1509/6377 | 1434/4875 | 478/1624 | chr17 | 69032119 | |||
chr17:69035741 | A | G | 2 | a0001c0008 a0016c0017 |
9 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.861T>C | p.Leu287Leu | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 7/39 | 936/6377 | 861/4875 | 287/1624 | chr17 | 69035741 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68974507 | T | G | 1 | a0006c0009t0005 | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1408A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1408 | chr17 | 68974507 | ||||||
chr17:68974717 | G | A | 2 | a0001c0001t0006 a0006c0009t0005 |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1198 | chr17 | 68974717 | ||||||
chr17:68974782 | CAG | C | 2 | a0001c0001t0006 a0006c0009t0005 |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1131_*1132delCT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1131 | chr17 | 68974782 | ||||||
chr17:68974804 | G | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0007t0004 others(28): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1111 | chr17 | 68974804 | ||||||
chr17:68975001 | C | A | 1 | a0003c0003t0010 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 914 | chr17 | 68975001 | ||||||
chr17:68975016 | C | T | 1 | a0002c0002t0007 | 2 | HG00639.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*899G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 899 | chr17 | 68975016 | ||||||
chr17:68975100 | G | A | 3 | a0001c0001t0006 a0003c0003t0013 a0006c0009t0005 |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*815C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 815 | chr17 | 68975100 | ||||||
chr17:68975108 | G | T | 1 | a0001c0001t0008 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*807C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 807 | chr17 | 68975108 | ||||||
chr17:68975434 | G | C | 12 | a0002c0002t0002 a0002c0002t0007 a0002c0004t0002 others(9): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*481C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 481 | chr17 | 68975434 | ||||||
chr17:68975523 | A | G | 3 | a0001c0007t0004 a0003c0003t0004 a0003c0003t0013 |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*392T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 392 | chr17 | 68975523 | ||||||
chr17:68975554 | AAAAT | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0007t0004 others(28): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*357_*360delATTT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 357 | chr17 | 68975554 | ||||||
chr17:68975629 | A | G | 1 | a0001c0001t0009 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*286T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 286 | chr17 | 68975629 | ||||||
chr17:68975738 | T | C | 13 | a0001c0001t0011 a0002c0002t0002 a0002c0002t0007 others(10): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 177 | chr17 | 68975738 | ||||||
chr17:68975757 | C | T | 12 | a0002c0002t0002 a0002c0002t0007 a0002c0004t0002 others(9): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*158G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 158 | chr17 | 68975757 | ||||||
chr17:68975847 | T | G | 1 | a0001c0001t0012 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 68 | chr17 | 68975847 | ||||||
chr17:68975914 | T | G | 3 | a0001c0007t0004 a0003c0003t0004 a0003c0003t0013 |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 39/39 | 1 | chr17 | 68975914 | ||||||
chr17:69060910 | T | C | 2 | a0006c0009t0005 a0017c0018t0014 |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-58A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/39 | 9784 | chr17 | 69060910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:68976109 | A | T | 109 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.4776+26T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 38/38 | chr17 | 68976109 | |||||||
chr17:68976223 | A | ATT | 18 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(15): Show |
22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.4721-35_4721-34dup others(2): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976223 | |||||||
chr17:68976416 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.4721-226T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976416 | |||||||
chr17:68976479 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.4721-289C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976479 | |||||||
chr17:68976487 | C | T | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4721-297G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976487 | |||||||
chr17:68976505 | C | T | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-315G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976505 | |||||||
chr17:68976908 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01175.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.4721-718C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976908 | |||||||
chr17:68976977 | C | A | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4721-787G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68976977 | |||||||
chr17:68977003 | T | C | 6 | a0001c0008t0001g0185 a0001c0008t0001g0186 a0001c0008t0001g0187 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.4721-813A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977003 | |||||||
chr17:68977005 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4721-815C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977005 | |||||||
chr17:68977037 | TGAA | T | 109 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.4721-850_4721-848d others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977037 | |||||||
chr17:68977257 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4721-1067C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977257 | |||||||
chr17:68977297 | A | C | 15 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(12): Show |
15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4721-1107T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977297 | |||||||
chr17:68977338 | G | A | 17 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(14): Show |
21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4721-1148C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977338 | |||||||
chr17:68977365 | G | A | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4721-1175C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977365 | |||||||
chr17:68977477 | T | C | 1 | a0002c0002t0002g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4721-1287A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977477 | |||||||
chr17:68977555 | C | T | 6 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.4721-1365G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977555 | |||||||
chr17:68977599 | G | A | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4721-1409C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977599 | |||||||
chr17:68977697 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4721-1507G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977697 | |||||||
chr17:68977744 | T | C | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-1554A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977744 | |||||||
chr17:68977842 | T | A | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4721-1652A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977842 | |||||||
chr17:68977931 | T | C | 4 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4721-1741A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68977931 | |||||||
chr17:68978238 | T | C | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-2048A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978238 | |||||||
chr17:68978333 | C | T | 1 | a0001c0001t0006g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4721-2143G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978333 | |||||||
chr17:68978443 | T | C | 2 | a0001c0001t0003g0160 a0008c0020t0003g0055 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4721-2253A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978443 | |||||||
chr17:68978484 | G | A | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4721-2294C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978484 | |||||||
chr17:68978488 | T | C | 1 | a0006c0009t0005g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4721-2298A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978488 | |||||||
chr17:68978570 | C | A | 1 | a0010c0011t0003g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4721-2380G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978570 | |||||||
chr17:68978606 | C | T | 17 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(14): Show |
21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4721-2416G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978606 | |||||||
chr17:68978611 | G | A | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4721-2421C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978611 | |||||||
chr17:68978680 | C | T | 1 | a0002c0002t0002g0067 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4721-2490G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978680 | |||||||
chr17:68978692 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4721-2502C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978692 | |||||||
chr17:68978719 | A | G | 4 | a0002c0002t0002g0087 a0002c0002t0002g0120 a0002c0002t0002g0131 others(1): Show |
4 | HG01081.hp1 HG01169.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.4721-2529T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978719 | |||||||
chr17:68978737 | G | A | 1 | a0003c0003t0004g0005 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4721-2547C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978737 | |||||||
chr17:68978890 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4721-2700G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978890 | |||||||
chr17:68978934 | C | A | 109 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.4721-2744G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68978934 | |||||||
chr17:68979000 | C | T | 1 | a0001c0008t0001g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4721-2810G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979000 | |||||||
chr17:68979025 | T | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4721-2835A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979025 | |||||||
chr17:68979120 | A | G | 1 | a0001c0007t0001g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.4721-2930T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979120 | |||||||
chr17:68979141 | T | C | 4 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4721-2951A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979141 | |||||||
chr17:68979194 | T | G | 3 | a0002c0002t0002g0064 a0002c0004t0002g0108 a0002c0004t0002g0109 |
3 | HG02738.hp2 NA18969.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.4721-3004A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979194 | |||||||
chr17:68979302 | G | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4721-3112C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979302 | |||||||
chr17:68979308 | TC | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4721-3119delG | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979308 | |||||||
chr17:68979436 | T | C | 2 | a0002c0002t0002g0084 a0002c0004t0002g0260 |
2 | HG03139.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4720+3126A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979436 | |||||||
chr17:68979463 | C | T | 1 | a0002c0002t0002g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4720+3099G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979463 | |||||||
chr17:68979486 | G | A | 163 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(160): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.4720+3076C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979486 | |||||||
chr17:68979525 | T | TTTTTGAT others(43): Show |
4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+3036_4720+303 others(54): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979525 | |||||||
chr17:68979625 | T | C | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2937A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979625 | |||||||
chr17:68979626 | G | A | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2936C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979626 | |||||||
chr17:68979629 | A | G | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2933T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979629 | |||||||
chr17:68979632 | T | C | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2930A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979632 | |||||||
chr17:68979851 | T | C | 2 | a0013c0022t0003g0019 a0018c0019t0003g0056 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4720+2711A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68979851 | |||||||
chr17:68980005 | G | A | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4720+2557C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980005 | |||||||
chr17:68980006 | A | C | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4720+2556T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980006 | |||||||
chr17:68980262 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4720+2300C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980262 | |||||||
chr17:68980359 | T | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2203A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980359 | |||||||
chr17:68980364 | A | G | 164 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.4720+2198T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980364 | |||||||
chr17:68980365 | G | A | 12 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(9): Show |
14 | HG00733.hp1 HG01884.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.4720+2197C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980365 | |||||||
chr17:68980377 | T | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2185A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980377 | |||||||
chr17:68980387 | G | A | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2175C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980387 | |||||||
chr17:68980388 | T | G | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2174A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980388 | |||||||
chr17:68980394 | T | A | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2168A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980394 | |||||||
chr17:68980397 | C | A | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2165G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980397 | |||||||
chr17:68980398 | G | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2164C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980398 | |||||||
chr17:68980416 | C | T | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4720+2146G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980416 | |||||||
chr17:68980421 | A | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2141T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980421 | |||||||
chr17:68980425 | T | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2137A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980425 | |||||||
chr17:68980434 | G | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2128C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980434 | |||||||
chr17:68980435 | G | A | 10 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(7): Show |
10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.4720+2127C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980435 | |||||||
chr17:68980451 | T | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4720+2111A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980451 | |||||||
chr17:68980467 | T | G | 14 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(11): Show |
14 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4720+2095A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980467 | |||||||
chr17:68980493 | T | C | 18 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(15): Show |
22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.4720+2069A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980493 | |||||||
chr17:68980498 | C | T | 1 | a0002c0002t0002g0125 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4720+2064G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980498 | |||||||
chr17:68980499 | G | A | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+2063C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980499 | |||||||
chr17:68980758 | C | T | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+1804G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980758 | |||||||
chr17:68980883 | G | A | 1 | a0002c0004t0002g0262 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4720+1679C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980883 | |||||||
chr17:68980928 | T | TA | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4720+1633dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980928 | |||||||
chr17:68980928 | TA | T | 24 | a0001c0001t0001g0171 a0001c0001t0001g0216 a0001c0001t0001g0247 others(21): Show |
25 | HG00639.hp2 HG00733.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.4720+1633delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980928 | |||||||
chr17:68980953 | C | T | 1 | a0002c0002t0002g0095 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4720+1609G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68980953 | |||||||
chr17:68981127 | C | G | 217 | a0001c0001t0001g0017 a0001c0001t0001g0158 a0001c0001t0001g0159 others(214): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.4720+1435G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981127 | |||||||
chr17:68981173 | C | T | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+1389G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981173 | |||||||
chr17:68981196 | A | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01175.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.4720+1366T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981196 | |||||||
chr17:68981210 | T | C | 6 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.4720+1352A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981210 | |||||||
chr17:68981337 | GAAAA | G | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4720+1221_4720+122 others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981337 | |||||||
chr17:68981426 | A | G | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+1136T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981426 | |||||||
chr17:68981456 | C | T | 2 | a0001c0001t0003g0160 a0008c0020t0003g0055 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4720+1106G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981456 | |||||||
chr17:68981835 | C | CA | 119 | a0001c0001t0001g0159 a0001c0001t0001g0171 a0001c0001t0001g0214 others(116): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.4720+726dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981835 | |||||||
chr17:68981835 | C | CAA | 24 | a0001c0007t0004g0091 a0002c0002t0002g0060 a0002c0002t0002g0066 others(21): Show |
26 | HG00733.hp2 HG01192.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.4720+725_4720+726d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981835 | |||||||
chr17:68981835 | CA | C | 9 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0210 others(6): Show |
9 | HG00323.hp2 HG00733.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.4720+726delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981835 | |||||||
chr17:68981870 | C | T | 1 | a0005c0006t0001g0276 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4720+692G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981870 | |||||||
chr17:68981909 | T | C | 4 | a0005c0006t0001g0013 a0005c0006t0001g0272 a0005c0006t0001g0275 others(1): Show |
5 | NA18974.hp2 NA18985.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.4720+653A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981909 | |||||||
chr17:68981921 | A | C | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4720+641T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981921 | |||||||
chr17:68981928 | TG | T | 18 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(15): Show |
22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.4720+633delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68981928 | |||||||
chr17:68982031 | G | T | 4 | a0001c0001t0001g0017 a0003c0003t0001g0035 a0003c0003t0001g0046 others(1): Show |
4 | HG01099.hp2 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4720+531C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68982031 | |||||||
chr17:68982178 | G | A | 14 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(11): Show |
14 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4720+384C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68982178 | |||||||
chr17:68982199 | T | C | 3 | a0003c0003t0003g0040 a0003c0003t0003g0041 a0003c0003t0003g0042 |
3 | HG01361.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4720+363A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 37/38 | chr17 | 68982199 | |||||||
chr17:68982866 | A | C | 54 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(51): Show |
62 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.4641-225T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982866 | |||||||
chr17:68982882 | T | C | 3 | a0001c0007t0004g0091 a0003c0003t0004g0024 a0003c0003t0004g0028 |
3 | HG02622.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4641-241A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982882 | |||||||
chr17:68982906 | T | C | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4641-265A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982906 | |||||||
chr17:68982954 | G | A | 7 | a0002c0004t0002g0111 a0002c0004t0002g0178 a0002c0004t0002g0179 others(4): Show |
7 | HG02818.hp1 NA18962.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.4641-313C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68982954 | |||||||
chr17:68983046 | G | A | 50 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(47): Show |
58 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.4641-405C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983046 | |||||||
chr17:68983078 | C | T | 54 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(51): Show |
62 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.4641-437G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983078 | |||||||
chr17:68983131 | A | G | 4 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4641-490T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983131 | |||||||
chr17:68983350 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4640+359A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983350 | |||||||
chr17:68983537 | T | C | 1 | a0007c0010t0002g0150 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4640+172A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983537 | |||||||
chr17:68983558 | T | G | 164 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.4640+151A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 36/38 | chr17 | 68983558 | |||||||
chr17:68983973 | G | A | 1 | a0001c0007t0001g0236 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4499+83C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 35/38 | chr17 | 68983973 | |||||||
chr17:68984226 | T | G | 1 | a0002c0002t0002g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4380-51A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984226 | |||||||
chr17:68984272 | C | A | 1 | a0002c0002t0002g0095 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4380-97G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984272 | |||||||
chr17:68984402 | T | C | 2 | a0001c0001t0003g0160 a0008c0020t0003g0055 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4380-227A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984402 | |||||||
chr17:68984498 | C | T | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4380-323G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984498 | |||||||
chr17:68984567 | T | C | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4379+318A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984567 | |||||||
chr17:68984581 | G | A | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4379+304C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984581 | |||||||
chr17:68984661 | A | T | 1 | a0019c0023t0003g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4379+224T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984661 | |||||||
chr17:68984878 | A | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | NA19009.hp1 NA19067.hp2 |
splice_region_variant&intron_variant | LOW | c.4379+7T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 34/38 | chr17 | 68984878 | |||||||
chr17:68985338 | G | C | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4209-210C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985338 | |||||||
chr17:68985345 | C | T | 109 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.4209-217G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985345 | |||||||
chr17:68985379 | T | G | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4209-251A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985379 | |||||||
chr17:68985457 | A | G | 7 | a0001c0001t0001g0017 a0003c0003t0001g0021 a0003c0003t0001g0032 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4209-329T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985457 | |||||||
chr17:68985491 | G | A | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4209-363C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985491 | |||||||
chr17:68985504 | C | G | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4209-376G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985504 | |||||||
chr17:68985511 | A | G | 109 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.4209-383T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985511 | |||||||
chr17:68985615 | C | T | 1 | a0001c0029t0001g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4209-487G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985615 | |||||||
chr17:68985826 | G | A | 3 | a0001c0007t0004g0091 a0003c0003t0004g0024 a0003c0003t0004g0028 |
3 | HG02622.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4208+338C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985826 | |||||||
chr17:68985919 | G | A | 1 | a0011c0014t0003g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4208+245C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985919 | |||||||
chr17:68985932 | T | C | 2 | a0001c0008t0001g0162 a0001c0008t0001g0176 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4208+232A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985932 | |||||||
chr17:68985955 | G | GA | 12 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(9): Show |
12 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.4208+208dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985955 | |||||||
chr17:68985982 | T | C | 1 | a0003c0003t0004g0005 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4208+182A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985982 | |||||||
chr17:68985998 | C | T | 17 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(14): Show |
21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4208+166G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 32/38 | chr17 | 68985998 | |||||||
chr17:68986489 | C | T | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4048-165G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68986489 | |||||||
chr17:68986850 | T | C | 12 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(9): Show |
12 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.4048-526A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68986850 | |||||||
chr17:68986906 | G | A | 2 | a0013c0022t0003g0019 a0018c0019t0003g0056 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4048-582C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68986906 | |||||||
chr17:68987160 | T | G | 1 | a0002c0004t0002g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4048-836A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987160 | |||||||
chr17:68987295 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4048-971G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987295 | |||||||
chr17:68987369 | T | A | 1 | a0003c0003t0004g0024 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4048-1045A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987369 | |||||||
chr17:68987612 | A | G | 165 | a0001c0001t0001g0248 a0001c0001t0003g0160 a0001c0001t0006g0008 others(162): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.4048-1288T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987612 | |||||||
chr17:68987736 | G | A | 6 | a0002c0002t0002g0009 a0002c0002t0002g0093 a0002c0002t0002g0101 others(3): Show |
7 | HG00544.hp1 HG02165.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4047+1291C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987736 | |||||||
chr17:68987736 | G | GT | 14 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0243 others(11): Show |
17 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.4047+1290dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987736 | |||||||
chr17:68987739 | TTTTTTTG others(20): Show |
T | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4047+1261_4047+128 others(31): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987739 | |||||||
chr17:68987745 | TG | T | 10 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(7): Show |
10 | HG01361.hp1 HG02630.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.4047+1281delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987745 | |||||||
chr17:68987746 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4047+1281C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987746 | |||||||
chr17:68987758 | G | T | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4047+1269C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987758 | |||||||
chr17:68987758 | GTTTGTTT others(5): Show |
G | 5 | a0001c0001t0001g0165 a0001c0001t0001g0235 a0001c0001t0001g0240 others(2): Show |
5 | HG00323.hp2 HG01081.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4047+1257_4047+126 others(16): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987758 | |||||||
chr17:68987761 | TG | T | 65 | a0001c0007t0004g0091 a0002c0002t0002g0002 a0002c0002t0002g0009 others(62): Show |
68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.4047+1265delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987761 | |||||||
chr17:68987761 | TGTTTG | T | 49 | a0001c0001t0001g0248 a0002c0002t0002g0003 a0002c0002t0002g0004 others(46): Show |
54 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.4047+1261_4047+126 others(9): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987761 | |||||||
chr17:68987762 | G | T | 18 | a0001c0001t0003g0160 a0001c0021t0003g0020 a0002c0002t0002g0099 others(15): Show |
18 | HG00639.hp2 HG01361.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.4047+1265C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987762 | |||||||
chr17:68987762 | GTTTGT | G | 6 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.4047+1260_4047+126 others(9): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987762 | |||||||
chr17:68987764 | T | G | 2 | a0001c0021t0003g0020 a0003c0003t0004g0005 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4047+1263A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987764 | |||||||
chr17:68987765 | T | G | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
12 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.4047+1262A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987765 | |||||||
chr17:68987766 | G | T | 86 | a0001c0001t0003g0160 a0001c0007t0004g0091 a0001c0021t0003g0020 others(83): Show |
91 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.4047+1261C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987766 | |||||||
chr17:68987767 | T | G | 1 | a0008c0020t0003g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4047+1260A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987767 | |||||||
chr17:68987774 | G | T | 146 | a0001c0001t0001g0248 a0001c0001t0003g0160 a0001c0001t0006g0008 others(143): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.4047+1253C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987774 | |||||||
chr17:68987822 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.4047+1205C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987822 | |||||||
chr17:68987860 | G | A | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4047+1167C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987860 | |||||||
chr17:68987953 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4047+1074C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987953 | |||||||
chr17:68987991 | T | C | 49 | a0001c0001t0003g0160 a0001c0007t0004g0091 a0001c0021t0003g0020 others(46): Show |
55 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.4047+1036A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68987991 | |||||||
chr17:68988039 | C | T | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.4047+988G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988039 | |||||||
chr17:68988083 | A | G | 17 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(14): Show |
21 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.4047+944T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988083 | |||||||
chr17:68988119 | G | T | 2 | a0003c0003t0001g0007 a0003c0003t0001g0030 |
3 | HG03491.hp1 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.4047+908C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988119 | |||||||
chr17:68988236 | G | GT | 16 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(13): Show |
20 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.4047+790dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988236 | |||||||
chr17:68988288 | T | C | 49 | a0001c0001t0003g0160 a0001c0007t0004g0091 a0001c0021t0003g0020 others(46): Show |
55 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.4047+739A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988288 | |||||||
chr17:68988347 | T | C | 30 | a0001c0007t0004g0091 a0001c0021t0003g0020 a0003c0003t0004g0005 others(27): Show |
36 | HG01109.hp2 HG01346.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.4047+680A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988347 | |||||||
chr17:68988597 | A | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4047+430T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988597 | |||||||
chr17:68988670 | C | T | 1 | a0006c0009t0005g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4047+357G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988670 | |||||||
chr17:68988744 | G | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4047+283C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988744 | |||||||
chr17:68988869 | A | G | 1 | a0019c0023t0003g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4047+158T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 31/38 | chr17 | 68988869 | |||||||
chr17:68989199 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0203 |
3 | HG00323.hp1 HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3956-81G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989199 | |||||||
chr17:68989225 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3956-107T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989225 | |||||||
chr17:68989242 | C | CCT | 6 | a0001c0001t0001g0261 a0002c0002t0002g0154 a0003c0003t0003g0045 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3956-126_3956-125d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989242 | |||||||
chr17:68989242 | C | CCTCT | 6 | a0002c0002t0002g0065 a0002c0002t0002g0101 a0002c0002t0002g0155 others(3): Show |
6 | HG00544.hp1 HG02074.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.3956-128_3956-125d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989242 | |||||||
chr17:68989256 | T | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0197 |
3 | HG02071.hp1 HG03831.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3956-138A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCA | 7 | a0001c0001t0001g0062 a0001c0001t0001g0161 a0001c0001t0001g0202 others(4): Show |
7 | HG00099.hp1 HG02004.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.3956-140_3956-139d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCACA | 3 | a0001c0001t0001g0181 a0001c0008t0001g0188 a0022c0025t0002g0059 |
3 | HG04204.hp2 NA19075.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3956-142_3956-139d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCTCA | 3 | a0001c0001t0003g0160 a0003c0003t0003g0043 a0008c0020t0003g0055 |
3 | HG03098.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3956-139_3956-138i others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCTCACA | 9 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(6): Show |
9 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCTCTCA | 38 | a0002c0002t0002g0002 a0002c0002t0002g0016 a0002c0002t0002g0066 others(35): Show |
40 | HG00408.hp2 HG00438.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCTCTCAC others(1): Show |
44 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(41): Show |
49 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCTCTCAC others(3): Show |
9 | a0002c0002t0002g0076 a0002c0002t0002g0102 a0002c0002t0002g0121 others(6): Show |
9 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.3956-139_3956-138i others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCTCTCAC others(5): Show |
2 | a0002c0002t0002g0130 a0002c0002t0002g0145 |
2 | HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.3956-139_3956-138i others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | T | TCTCTCAC others(9): Show |
2 | a0002c0002t0002g0117 a0002c0002t0002g0146 |
2 | NA18953.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3956-139_3956-138i others(18): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | TCA | T | 37 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0169 others(34): Show |
44 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.3956-140_3956-139d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | TCACA | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0243 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.3956-142_3956-139d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | TCACACA | T | 14 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(11): Show |
16 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.3956-144_3956-139d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989256 | TCACACAC others(3): Show |
T | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3956-148_3956-139d others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989256 | |||||||
chr17:68989258 | A | T | 10 | a0002c0002t0002g0009 a0002c0002t0002g0093 a0002c0002t0002g0120 others(7): Show |
11 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3956-140T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989258 | |||||||
chr17:68989260 | A | T | 20 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0002c0002t0002g0009 others(17): Show |
26 | HG01109.hp2 HG01346.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3956-142T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989260 | |||||||
chr17:68989262 | A | T | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0021t0003g0020 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3956-144T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989262 | |||||||
chr17:68989264 | A | T | 13 | a0001c0007t0004g0091 a0001c0021t0003g0020 a0003c0003t0004g0005 others(10): Show |
15 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.3956-146T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989264 | |||||||
chr17:68989266 | A | T | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.3956-148T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989266 | |||||||
chr17:68989268 | A | T | 5 | a0001c0007t0004g0091 a0003c0003t0004g0024 a0003c0003t0004g0028 others(2): Show |
5 | HG00733.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3956-150T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989268 | |||||||
chr17:68989295 | C | CA | 4 | a0002c0002t0002g0004 a0002c0002t0002g0078 a0002c0004t0002g0262 others(1): Show |
4 | HG02071.hp2 HG04115.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.3956-178_3956-177i others(3): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989295 | |||||||
chr17:68989418 | A | T | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3956-300T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989418 | |||||||
chr17:68989525 | G | A | 1 | a0001c0007t0001g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3955+288C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989525 | |||||||
chr17:68989550 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0224 a0001c0001t0012g0229 |
3 | HG01109.hp1 HG02486.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3955+263T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989550 | |||||||
chr17:68989672 | A | G | 15 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(12): Show |
15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3955+141T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989672 | |||||||
chr17:68989706 | C | T | 6 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3955+107G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989706 | |||||||
chr17:68989796 | G | A | 2 | a0002c0002t0002g0117 a0002c0002t0002g0146 |
2 | NA18953.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3955+17C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 30/38 | chr17 | 68989796 | |||||||
chr17:68990015 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0210 |
3 | NA18946.hp1 NA18957.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.3838-85G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990015 | |||||||
chr17:68990223 | C | G | 1 | a0002c0002t0002g0102 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3838-293G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990223 | |||||||
chr17:68990244 | C | T | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0241 others(2): Show |
5 | HG00408.hp1 HG02132.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.3838-314G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990244 | |||||||
chr17:68990488 | C | G | 1 | a0002c0004t0002g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3837+349G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990488 | |||||||
chr17:68990562 | A | C | 55 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(52): Show |
63 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.3837+275T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 29/38 | chr17 | 68990562 | |||||||
chr17:68991061 | A | T | 164 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.3717-104T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991061 | |||||||
chr17:68991088 | A | G | 6 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3717-131T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991088 | |||||||
chr17:68991113 | C | G | 164 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.3717-156G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991113 | |||||||
chr17:68991275 | A | C | 109 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.3717-318T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991275 | |||||||
chr17:68991405 | C | A | 1 | a0002c0002t0002g0089 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3717-448G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991405 | |||||||
chr17:68991480 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3717-523C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991480 | |||||||
chr17:68991705 | C | A | 15 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(12): Show |
15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3716+470G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 28/38 | chr17 | 68991705 | |||||||
chr17:68992375 | T | C | 4 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3625-109A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992375 | |||||||
chr17:68992493 | T | C | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3625-227A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992493 | |||||||
chr17:68992525 | A | G | 55 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(52): Show |
63 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.3625-259T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992525 | |||||||
chr17:68992604 | G | A | 18 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(15): Show |
22 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3625-338C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992604 | |||||||
chr17:68992786 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3624+230G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992786 | |||||||
chr17:68992808 | T | C | 4 | a0001c0001t0001g0017 a0003c0003t0001g0035 a0003c0003t0001g0046 others(1): Show |
4 | HG01099.hp2 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3624+208A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992808 | |||||||
chr17:68992825 | AG | A | 142 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(139): Show |
153 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.3624+190delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992825 | |||||||
chr17:68992825 | AGG | A | 16 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(13): Show |
20 | HG01109.hp2 HG01346.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.3624+189_3624+190d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992825 | |||||||
chr17:68992826 | G | A | 4 | a0002c0002t0002g0010 a0002c0002t0002g0068 a0002c0004t0002g0257 others(1): Show |
5 | HG00099.hp2 HG00280.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.3624+190C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992826 | |||||||
chr17:68992852 | C | CGT | 25 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0001c0021t0003g0020 others(22): Show |
31 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.3624+162_3624+163d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992852 | |||||||
chr17:68992852 | C | T | 2 | a0013c0022t0003g0019 a0018c0019t0003g0056 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3624+164G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992852 | |||||||
chr17:68992861 | G | GTGTGTGT others(23): Show |
10 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(7): Show |
12 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.3624+154_3624+155i others(32): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992861 | |||||||
chr17:68992863 | GTGTGTGC others(19): Show |
G | 1 | a0004c0005t0003g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3624+127_3624+152d others(28): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992863 | |||||||
chr17:68992965 | C | T | 1 | a0002c0002t0002g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3624+51G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 27/38 | chr17 | 68992965 | |||||||
chr17:68993231 | C | T | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3556-147G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993231 | |||||||
chr17:68993349 | C | A | 15 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(12): Show |
15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3556-265G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993349 | |||||||
chr17:68993519 | A | G | 6 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3556-435T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993519 | |||||||
chr17:68993679 | C | T | 1 | a0002c0004t0002g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3556-595G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993679 | |||||||
chr17:68993826 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3556-742G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993826 | |||||||
chr17:68993949 | C | T | 10 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0094 others(7): Show |
14 | HG02040.hp2 HG02080.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.3556-865G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68993949 | |||||||
chr17:68994003 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0008g0245 a0001c0001t0008g0246 |
3 | HG00323.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3556-919C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994003 | |||||||
chr17:68994096 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 |
3 | HG02074.hp1 HG02135.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3556-1012C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994096 | |||||||
chr17:68994370 | C | A | 1 | a0005c0006t0001g0276 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3556-1286G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994370 | |||||||
chr17:68994381 | C | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0209 |
2 | NA19004.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3556-1297G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994381 | |||||||
chr17:68994417 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0224 a0001c0001t0012g0229 |
3 | HG01109.hp1 HG02486.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3556-1333G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994417 | |||||||
chr17:68994490 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0163 |
3 | HG03490.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3555+1405G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994490 | |||||||
chr17:68994516 | C | T | 1 | a0022c0025t0002g0059 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3555+1379G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994516 | |||||||
chr17:68994715 | C | A | 11 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0094 others(8): Show |
15 | HG02040.hp2 HG02080.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.3555+1180G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994715 | |||||||
chr17:68994764 | G | C | 15 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(12): Show |
15 | HG00639.hp2 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3555+1131C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994764 | |||||||
chr17:68994794 | G | C | 2 | a0009c0012t0001g0268 a0009c0012t0001g0278 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3555+1101C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994794 | |||||||
chr17:68994816 | T | G | 1 | a0008c0013t0003g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3555+1079A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994816 | |||||||
chr17:68994862 | G | A | 2 | a0002c0002t0002g0099 a0002c0002t0002g0120 |
2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3555+1033C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994862 | |||||||
chr17:68994882 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0234 |
2 | HG02165.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.3555+1013C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994882 | |||||||
chr17:68994889 | C | T | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0010c0011t0003g0049 others(1): Show |
4 | HG00733.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.3555+1006G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68994889 | |||||||
chr17:68995075 | T | C | 11 | a0001c0007t0004g0091 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.3555+820A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995075 | |||||||
chr17:68995079 | A | G | 5 | a0004c0005t0003g0001 a0004c0005t0003g0264 a0004c0005t0003g0266 others(2): Show |
9 | HG01346.hp1 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3555+816T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995079 | |||||||
chr17:68995433 | C | T | 1 | a0001c0007t0001g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3555+462G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995433 | |||||||
chr17:68995451 | C | T | 4 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3555+444G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995451 | |||||||
chr17:68995489 | C | T | 4 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3555+406G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995489 | |||||||
chr17:68995541 | T | G | 1 | a0001c0001t0001g0189 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3555+354A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995541 | |||||||
chr17:68995655 | T | C | 1 | a0019c0023t0003g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3555+240A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995655 | |||||||
chr17:68995698 | TG | T | 161 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(158): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.3555+196delC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995698 | |||||||
chr17:68995886 | A | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0235 |
2 | HG01081.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3555+9T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 26/38 | chr17 | 68995886 | |||||||
chr17:68996156 | T | A | 1 | a0012c0016t0002g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3436-142A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996156 | |||||||
chr17:68996376 | G | T | 2 | a0013c0022t0003g0019 a0018c0019t0003g0056 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3436-362C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996376 | |||||||
chr17:68996566 | C | T | 30 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0004c0005t0003g0001 others(27): Show |
36 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3436-552G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996566 | |||||||
chr17:68996575 | T | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-561A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996575 | |||||||
chr17:68996584 | G | A | 30 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0004c0005t0003g0001 others(27): Show |
36 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3436-570C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996584 | |||||||
chr17:68996664 | A | T | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-650T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996664 | |||||||
chr17:68996684 | T | C | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-670A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996684 | |||||||
chr17:68996763 | G | A | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-749C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68996763 | |||||||
chr17:68997034 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-1020C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997034 | |||||||
chr17:68997157 | C | G | 2 | a0001c0008t0001g0186 a0003c0003t0001g0034 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3436-1143G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997157 | |||||||
chr17:68997182 | C | T | 20 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(17): Show |
22 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.3436-1168G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997182 | |||||||
chr17:68997190 | C | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-1176G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997190 | |||||||
chr17:68997594 | C | CT | 9 | a0001c0001t0001g0224 a0001c0001t0001g0250 a0001c0001t0012g0229 others(6): Show |
12 | HG00280.hp1 HG01109.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.3436-1581dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997594 | |||||||
chr17:68997594 | CT | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0190 others(73): Show |
82 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.3436-1581delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997594 | |||||||
chr17:68997594 | CTTT | C | 24 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0004c0005t0003g0001 others(21): Show |
30 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.3436-1583_3436-158 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997594 | |||||||
chr17:68997602 | T | C | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-1588A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997602 | |||||||
chr17:68997707 | A | C | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3436-1693T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997707 | |||||||
chr17:68997814 | C | T | 7 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3436-1800G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997814 | |||||||
chr17:68997828 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3436-1814T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997828 | |||||||
chr17:68997988 | T | C | 10 | a0001c0008t0001g0162 a0001c0008t0001g0176 a0001c0008t0001g0185 others(7): Show |
10 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3436-1974A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997988 | |||||||
chr17:68997999 | G | A | 21 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(18): Show |
23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3436-1985C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68997999 | |||||||
chr17:68998021 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3436-2007C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998021 | |||||||
chr17:68998050 | A | G | 1 | a0008c0020t0003g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3436-2036T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998050 | |||||||
chr17:68998103 | C | T | 4 | a0008c0013t0003g0057 a0008c0020t0003g0055 a0010c0011t0003g0049 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.3436-2089G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998103 | |||||||
chr17:68998157 | G | A | 6 | a0001c0008t0001g0185 a0001c0008t0001g0186 a0001c0008t0001g0187 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436-2143C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998157 | |||||||
chr17:68998266 | A | G | 30 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0004c0005t0003g0001 others(27): Show |
36 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3436-2252T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998266 | |||||||
chr17:68998309 | A | G | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3436-2295T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998309 | |||||||
chr17:68998366 | T | C | 1 | a0003c0003t0003g0045 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3436-2352A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998366 | |||||||
chr17:68998417 | C | A | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3436-2403G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998417 | |||||||
chr17:68998419 | T | A | 21 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(18): Show |
23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3436-2405A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998419 | |||||||
chr17:68998479 | A | G | 10 | a0001c0008t0001g0162 a0001c0008t0001g0176 a0001c0008t0001g0185 others(7): Show |
10 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3436-2465T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998479 | |||||||
chr17:68998508 | G | A | 8 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(5): Show |
8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3436-2494C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998508 | |||||||
chr17:68998646 | A | C | 115 | a0001c0007t0001g0088 a0001c0007t0001g0113 a0001c0007t0001g0115 others(112): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.3436-2632T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998646 | |||||||
chr17:68998647 | TATTA | T | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-2637_3436-263 others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998647 | |||||||
chr17:68998828 | A | C | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-2814T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998828 | |||||||
chr17:68998832 | C | CT | 8 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(5): Show |
8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3436-2819dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998832 | |||||||
chr17:68998832 | CT | C | 12 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0001c0008t0001g0162 others(9): Show |
13 | HG02055.hp1 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.3436-2819delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998832 | |||||||
chr17:68998835 | T | C | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436-2821A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998835 | |||||||
chr17:68998981 | C | G | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-2967G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68998981 | |||||||
chr17:68999102 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3436-3088C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999102 | |||||||
chr17:68999123 | T | TATC | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3436-3110_3436-310 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999123 | |||||||
chr17:68999192 | C | T | 6 | a0001c0007t0001g0088 a0007c0010t0002g0081 a0007c0010t0002g0118 others(3): Show |
6 | HG01257.hp1 HG01496.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.3436-3178G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999192 | |||||||
chr17:68999232 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3436-3218G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999232 | |||||||
chr17:68999238 | C | T | 8 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(5): Show |
8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3436-3224G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999238 | |||||||
chr17:68999271 | T | C | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3436-3257A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999271 | |||||||
chr17:68999437 | C | T | 1 | a0002c0002t0002g0064 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3436-3423G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999437 | |||||||
chr17:68999498 | T | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3436-3484A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999498 | |||||||
chr17:68999543 | T | C | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-3529A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999543 | |||||||
chr17:68999575 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3436-3561G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999575 | |||||||
chr17:68999605 | A | C | 2 | a0008c0013t0003g0058 a0014c0015t0003g0052 |
2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3436-3591T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999605 | |||||||
chr17:68999640 | G | C | 1 | a0021c0032t0001g0221 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3436-3626C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999640 | |||||||
chr17:68999696 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3436-3682G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999696 | |||||||
chr17:68999773 | T | A | 1 | a0002c0002t0002g0130 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3436-3759A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999773 | |||||||
chr17:68999845 | T | A | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-3831A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999845 | |||||||
chr17:68999987 | C | T | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3436-3973G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999987 | |||||||
chr17:68999999 | G | T | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-3985C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 68999999 | |||||||
chr17:69000056 | T | G | 7 | a0001c0001t0001g0017 a0003c0003t0001g0021 a0003c0003t0001g0032 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3436-4042A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000056 | |||||||
chr17:69000159 | G | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0203 |
3 | HG00323.hp1 HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3436-4145C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000159 | |||||||
chr17:69000200 | C | T | 1 | a0012c0016t0002g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3436-4186G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000200 | |||||||
chr17:69000251 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-4237G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000251 | |||||||
chr17:69000386 | C | T | 1 | a0002c0002t0002g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3436-4372G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000386 | |||||||
chr17:69000602 | T | C | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3436-4588A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000602 | |||||||
chr17:69000607 | T | C | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3436-4593A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000607 | |||||||
chr17:69000608 | G | A | 1 | a0006c0009t0005g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3436-4594C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000608 | |||||||
chr17:69000694 | T | C | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3436-4680A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000694 | |||||||
chr17:69000735 | A | G | 1 | a0003c0003t0003g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3436-4721T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000735 | |||||||
chr17:69000755 | A | G | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436-4741T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000755 | |||||||
chr17:69000757 | G | A | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3436-4743C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000757 | |||||||
chr17:69000763 | G | A | 4 | a0001c0021t0003g0020 a0008c0013t0003g0057 a0008c0013t0003g0058 others(1): Show |
4 | HG00733.hp1 HG01891.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3436-4749C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000763 | |||||||
chr17:69000782 | A | G | 1 | a0003c0003t0003g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3436-4768T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000782 | |||||||
chr17:69000803 | CAGTGGTT others(3): Show |
C | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-4799_3436-479 others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000803 | |||||||
chr17:69000816 | T | G | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3436-4802A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000816 | |||||||
chr17:69000856 | T | A | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3436-4842A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000856 | |||||||
chr17:69000871 | T | C | 21 | a0001c0021t0003g0020 a0004c0005t0003g0001 a0004c0005t0003g0263 others(18): Show |
25 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.3436-4857A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000871 | |||||||
chr17:69000933 | T | TTGG | 51 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0001c0021t0003g0020 others(48): Show |
59 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.3436-4920_3436-491 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69000933 | |||||||
chr17:69001130 | G | A | 1 | a0004c0005t0003g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3436-5116C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001130 | |||||||
chr17:69001147 | T | C | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3436-5133A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001147 | |||||||
chr17:69001215 | C | T | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3436-5201G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001215 | |||||||
chr17:69001477 | A | G | 21 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(18): Show |
23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3436-5463T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001477 | |||||||
chr17:69001578 | C | T | 1 | a0008c0013t0003g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3436-5564G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001578 | |||||||
chr17:69001841 | C | G | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3436-5827G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001841 | |||||||
chr17:69001954 | G | A | 21 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(18): Show |
23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3435+5805C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001954 | |||||||
chr17:69001975 | A | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+5784T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69001975 | |||||||
chr17:69002033 | G | A | 1 | a0002c0002t0002g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3435+5726C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002033 | |||||||
chr17:69002081 | T | C | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+5678A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002081 | |||||||
chr17:69002083 | A | G | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+5676T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002083 | |||||||
chr17:69002101 | T | C | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+5658A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002101 | |||||||
chr17:69002171 | T | C | 1 | a0002c0002t0002g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3435+5588A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002171 | |||||||
chr17:69002220 | A | G | 1 | a0002c0004t0002g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3435+5539T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002220 | |||||||
chr17:69002260 | C | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+5499G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002260 | |||||||
chr17:69002277 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3435+5482G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002277 | |||||||
chr17:69002294 | G | A | 11 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0003c0003t0004g0005 others(8): Show |
13 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.3435+5465C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002294 | |||||||
chr17:69002425 | G | A | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3435+5334C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002425 | |||||||
chr17:69002438 | A | T | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3435+5321T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002438 | |||||||
chr17:69002563 | TGTG | T | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+5193_3435+519 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002563 | |||||||
chr17:69002603 | G | A | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+5156C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002603 | |||||||
chr17:69002604 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+5155C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002604 | |||||||
chr17:69002604 | G | C | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+5155C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002604 | |||||||
chr17:69002634 | C | T | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3435+5125G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002634 | |||||||
chr17:69002712 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3435+5047A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002712 | |||||||
chr17:69002793 | G | A | 1 | a0003c0003t0003g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3435+4966C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002793 | |||||||
chr17:69002942 | C | A | 7 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3435+4817G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69002942 | |||||||
chr17:69003008 | G | T | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3435+4751C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003008 | |||||||
chr17:69003026 | A | G | 5 | a0002c0002t0002g0009 a0002c0002t0002g0093 a0002c0002t0002g0154 others(2): Show |
6 | HG00544.hp1 NA18954.hp1 NA19060.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+4733T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003026 | |||||||
chr17:69003045 | C | A | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+4714G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003045 | |||||||
chr17:69003061 | C | T | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+4698G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003061 | |||||||
chr17:69003070 | C | T | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+4689G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003070 | |||||||
chr17:69003072 | G | A | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+4687C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003072 | |||||||
chr17:69003484 | T | G | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+4275A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003484 | |||||||
chr17:69003487 | A | G | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3435+4272T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003487 | |||||||
chr17:69003524 | G | A | 1 | a0003c0003t0004g0024 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3435+4235C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003524 | |||||||
chr17:69003613 | G | A | 2 | a0005c0006t0001g0274 a0005c0006t0001g0277 |
2 | NA18989.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.3435+4146C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003613 | |||||||
chr17:69003624 | T | G | 1 | a0002c0002t0002g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3435+4135A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003624 | |||||||
chr17:69003656 | C | T | 22 | a0001c0001t0012g0229 a0001c0021t0003g0020 a0003c0003t0003g0036 others(19): Show |
24 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.3435+4103G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003656 | |||||||
chr17:69003740 | C | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+4019G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003740 | |||||||
chr17:69003757 | A | G | 1 | a0017c0018t0014g0291 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3435+4002T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003757 | |||||||
chr17:69003826 | C | G | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+3933G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003826 | |||||||
chr17:69003947 | G | A | 2 | a0001c0001t0001g0181 a0007c0010t0002g0118 |
2 | HG01496.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3435+3812C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003947 | |||||||
chr17:69003954 | G | C | 1 | a0002c0002t0002g0136 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3435+3805C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69003954 | |||||||
chr17:69004006 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3435+3753C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004006 | |||||||
chr17:69004077 | C | T | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+3682G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004077 | |||||||
chr17:69004149 | C | T | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3435+3610G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004149 | |||||||
chr17:69004207 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3435+3552A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004207 | |||||||
chr17:69004466 | C | T | 115 | a0001c0007t0001g0088 a0001c0007t0001g0113 a0001c0007t0001g0115 others(112): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.3435+3293G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004466 | |||||||
chr17:69004697 | G | T | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+3062C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004697 | |||||||
chr17:69004774 | C | T | 1 | a0003c0003t0003g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3435+2985G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004774 | |||||||
chr17:69004786 | T | C | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3435+2973A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004786 | |||||||
chr17:69004793 | G | T | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+2966C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004793 | |||||||
chr17:69004825 | T | C | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3435+2934A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004825 | |||||||
chr17:69004854 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+2905C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004854 | |||||||
chr17:69004893 | G | A | 1 | a0007c0010t0002g0150 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3435+2866C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004893 | |||||||
chr17:69004896 | T | C | 167 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3435+2863A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004896 | |||||||
chr17:69004942 | C | T | 10 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(7): Show |
10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3435+2817G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004942 | |||||||
chr17:69004992 | C | T | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3435+2767G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69004992 | |||||||
chr17:69005078 | T | C | 9 | a0003c0003t0004g0005 a0003c0003t0004g0006 a0003c0003t0004g0022 others(6): Show |
11 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.3435+2681A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005078 | |||||||
chr17:69005108 | G | T | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3435+2651C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005108 | |||||||
chr17:69005141 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+2618G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005141 | |||||||
chr17:69005173 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3435+2586T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005173 | |||||||
chr17:69005190 | C | A | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3435+2569G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005190 | |||||||
chr17:69005377 | A | G | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3435+2382T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005377 | |||||||
chr17:69005427 | A | G | 215 | a0001c0001t0001g0017 a0001c0001t0001g0158 a0001c0001t0001g0159 others(212): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.3435+2332T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005427 | |||||||
chr17:69005579 | T | C | 1 | a0002c0002t0002g0117 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3435+2180A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005579 | |||||||
chr17:69005597 | C | T | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3435+2162G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005597 | |||||||
chr17:69005612 | G | A | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+2147C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005612 | |||||||
chr17:69005623 | A | G | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3435+2136T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69005623 | |||||||
chr17:69006042 | C | A | 166 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(163): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.3435+1717G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006042 | |||||||
chr17:69006069 | A | T | 1 | a0022c0025t0002g0059 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3435+1690T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006069 | |||||||
chr17:69006169 | C | G | 20 | a0002c0002t0002g0016 a0002c0002t0002g0086 a0002c0002t0002g0089 others(17): Show |
20 | HG00408.hp2 HG00438.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.3435+1590G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006169 | |||||||
chr17:69006517 | G | A | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3435+1242C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006517 | |||||||
chr17:69006717 | A | C | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3435+1042T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006717 | |||||||
chr17:69006905 | T | C | 2 | a0008c0013t0003g0057 a0008c0013t0003g0058 |
2 | HG00733.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+854A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006905 | |||||||
chr17:69006913 | G | T | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3435+846C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69006913 | |||||||
chr17:69007084 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3435+675A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007084 | |||||||
chr17:69007108 | A | T | 2 | a0003c0003t0003g0043 a0003c0003t0003g0045 |
2 | HG02698.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3435+651T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007108 | |||||||
chr17:69007144 | G | A | 114 | a0001c0007t0001g0088 a0001c0007t0001g0113 a0001c0007t0001g0115 others(111): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.3435+615C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007144 | |||||||
chr17:69007204 | C | T | 23 | a0001c0007t0001g0156 a0002c0002t0002g0003 a0002c0002t0002g0004 others(20): Show |
27 | HG02040.hp2 HG02074.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.3435+555G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007204 | |||||||
chr17:69007293 | C | T | 3 | a0001c0007t0001g0113 a0001c0007t0001g0115 a0001c0007t0001g0137 |
3 | HG01258.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.3435+466G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007293 | |||||||
chr17:69007332 | C | T | 2 | a0002c0002t0002g0114 a0002c0002t0002g0219 |
2 | HG01255.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.3435+427G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007332 | |||||||
chr17:69007333 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.3435+426C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007333 | |||||||
chr17:69007387 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01175.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.3435+372G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007387 | |||||||
chr17:69007518 | T | C | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3435+241A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007518 | |||||||
chr17:69007645 | A | G | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3435+114T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007645 | |||||||
chr17:69007683 | T | C | 1 | a0001c0007t0001g0012 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3435+76A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007683 | |||||||
chr17:69007727 | G | A | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3435+32C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 25/38 | chr17 | 69007727 | |||||||
chr17:69007931 | T | C | 23 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(20): Show |
27 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.3322-59A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 24/38 | chr17 | 69007931 | |||||||
chr17:69008245 | A | G | 7 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3148-10T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008245 | |||||||
chr17:69008342 | ATAT | A | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3148-110_3148-108d others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008342 | |||||||
chr17:69008352 | G | A | 1 | a0001c0008t0001g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3148-117C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008352 | |||||||
chr17:69008352 | G | C | 2 | a0002c0002t0002g0100 a0002c0002t0002g0122 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3148-117C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008352 | |||||||
chr17:69008368 | C | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3148-133G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008368 | |||||||
chr17:69008436 | T | G | 1 | a0002c0002t0002g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3148-201A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008436 | |||||||
chr17:69008448 | G | A | 2 | a0002c0002t0002g0124 a0002c0002t0002g0125 |
2 | HG02132.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3148-213C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008448 | |||||||
chr17:69008633 | G | A | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148-398C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008633 | |||||||
chr17:69008902 | G | T | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148-667C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69008902 | |||||||
chr17:69009053 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3148-818G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009053 | |||||||
chr17:69009118 | TA | T | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3148-884delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009118 | |||||||
chr17:69009120 | T | C | 1 | a0002c0004t0002g0257 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3148-885A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009120 | |||||||
chr17:69009262 | G | A | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148-1027C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009262 | |||||||
chr17:69009358 | G | T | 2 | a0006c0009t0005g0015 a0006c0009t0005g0289 |
3 | HG01069.hp1 HG01071.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.3148-1123C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009358 | |||||||
chr17:69009403 | CTTCCGTG others(11): Show |
C | 13 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(10): Show |
14 | HG01175.hp2 HG02572.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.3148-1186_3148-116 others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009403 | |||||||
chr17:69009554 | C | T | 21 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(18): Show |
23 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3148-1319G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009554 | |||||||
chr17:69009567 | T | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0222 a0001c0001t0001g0233 others(1): Show |
4 | HG02080.hp1 NA18967.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.3148-1332A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009567 | |||||||
chr17:69009617 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3148-1382G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009617 | |||||||
chr17:69009893 | A | G | 1 | a0002c0002t0002g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3148-1658T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009893 | |||||||
chr17:69009916 | T | C | 1 | a0002c0002t0002g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3148-1681A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009916 | |||||||
chr17:69009991 | C | T | 20 | a0002c0002t0002g0002 a0002c0002t0002g0060 a0002c0002t0002g0061 others(17): Show |
22 | HG00099.hp2 HG01192.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.3148-1756G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69009991 | |||||||
chr17:69010097 | C | A | 4 | a0004c0005t0003g0001 a0004c0005t0003g0264 a0004c0005t0003g0266 others(1): Show |
8 | HG01346.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3148-1862G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010097 | |||||||
chr17:69010175 | T | TA | 129 | a0001c0001t0001g0180 a0001c0007t0001g0088 a0001c0007t0001g0115 others(126): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.3147+1800dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010175 | |||||||
chr17:69010175 | TA | T | 6 | a0001c0001t0001g0254 a0003c0003t0004g0023 a0005c0006t0001g0013 others(3): Show |
7 | HG02717.hp2 NA18974.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.3147+1800delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010175 | |||||||
chr17:69010319 | G | A | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3147+1657C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010319 | |||||||
chr17:69010399 | A | G | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3147+1577T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010399 | |||||||
chr17:69010415 | T | C | 1 | a0002c0002t0002g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3147+1561A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010415 | |||||||
chr17:69010527 | A | T | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3147+1449T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010527 | |||||||
chr17:69010705 | A | G | 11 | a0001c0021t0003g0020 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3147+1271T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010705 | |||||||
chr17:69010722 | G | A | 1 | a0003c0003t0004g0005 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3147+1254C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010722 | |||||||
chr17:69010873 | C | T | 166 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(163): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.3147+1103G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69010873 | |||||||
chr17:69011044 | C | T | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3147+932G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011044 | |||||||
chr17:69011197 | G | T | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3147+779C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011197 | |||||||
chr17:69011553 | C | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3147+423G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011553 | |||||||
chr17:69011652 | T | G | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3147+324A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 23/38 | chr17 | 69011652 | |||||||
chr17:69012095 | T | C | 1 | a0002c0002t0002g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3040-12A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012095 | |||||||
chr17:69012116 | C | T | 2 | a0013c0022t0003g0019 a0018c0019t0003g0056 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3040-33G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012116 | |||||||
chr17:69012119 | T | C | 2 | a0001c0021t0003g0020 a0014c0015t0003g0052 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3040-36A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012119 | |||||||
chr17:69012241 | C | T | 1 | a0001c0007t0001g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3040-158G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012241 | |||||||
chr17:69012318 | G | A | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.3040-235C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012318 | |||||||
chr17:69012355 | T | C | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3040-272A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012355 | |||||||
chr17:69012412 | T | C | 2 | a0001c0001t0003g0160 a0003c0003t0003g0040 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3040-329A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012412 | |||||||
chr17:69012574 | C | G | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3040-491G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012574 | |||||||
chr17:69012597 | A | T | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3040-514T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012597 | |||||||
chr17:69012665 | A | G | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3040-582T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012665 | |||||||
chr17:69012667 | T | C | 11 | a0001c0001t0001g0239 a0003c0003t0003g0036 a0003c0003t0003g0037 others(8): Show |
11 | HG00639.hp2 HG01361.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3040-584A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012667 | |||||||
chr17:69012772 | T | A | 1 | a0002c0002t0002g0098 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3040-689A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012772 | |||||||
chr17:69012824 | T | C | 167 | a0001c0001t0001g0239 a0001c0001t0003g0160 a0001c0001t0006g0008 others(164): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.3040-741A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012824 | |||||||
chr17:69012911 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | NA19009.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3040-828G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012911 | |||||||
chr17:69012912 | G | A | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3040-829C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012912 | |||||||
chr17:69012916 | A | G | 2 | a0001c0008t0001g0258 a0016c0017t0003g0184 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3040-833T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012916 | |||||||
chr17:69012927 | T | A | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3040-844A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69012927 | |||||||
chr17:69013007 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3040-924T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013007 | |||||||
chr17:69013029 | G | A | 1 | a0002c0002t0002g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3040-946C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013029 | |||||||
chr17:69013180 | T | G | 1 | a0002c0002t0002g0127 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3040-1097A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013180 | |||||||
chr17:69013447 | A | AG | 6 | a0001c0008t0001g0185 a0001c0008t0001g0186 a0001c0008t0001g0187 others(3): Show |
6 | HG02647.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3040-1365dupC | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013447 | |||||||
chr17:69013689 | AGACACTG others(11): Show |
A | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3040-1624_3040-160 others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013689 | |||||||
chr17:69013768 | C | T | 10 | a0001c0001t0001g0183 a0003c0003t0004g0005 a0003c0003t0004g0006 others(7): Show |
12 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.3040-1685G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013768 | |||||||
chr17:69013829 | G | GTACTT | 4 | a0003c0003t0004g0022 a0013c0022t0003g0019 a0018c0019t0003g0056 others(1): Show |
4 | HG02451.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3040-1751_3040-174 others(9): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013829 | |||||||
chr17:69013884 | C | G | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3040-1801G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69013884 | |||||||
chr17:69014323 | A | AAAT | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3039+1927_3039+192 others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014323 | |||||||
chr17:69014384 | T | G | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3039+1869A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014384 | |||||||
chr17:69014400 | T | C | 1 | a0002c0002t0002g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3039+1853A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014400 | |||||||
chr17:69014474 | C | G | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+1779G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014474 | |||||||
chr17:69014716 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0008g0245 a0001c0001t0008g0246 |
3 | HG00323.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3039+1537C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014716 | |||||||
chr17:69014958 | A | G | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3039+1295T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69014958 | |||||||
chr17:69015027 | C | G | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3039+1226G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015027 | |||||||
chr17:69015121 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0163 |
3 | HG03490.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3039+1132C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015121 | |||||||
chr17:69015159 | C | CA | 20 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(17): Show |
24 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.3039+1093dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015159 | |||||||
chr17:69015345 | G | A | 7 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3039+908C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015345 | |||||||
chr17:69015363 | C | T | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3039+890G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015363 | |||||||
chr17:69015383 | C | T | 1 | a0003c0003t0001g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3039+870G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015383 | |||||||
chr17:69015593 | T | C | 1 | a0001c0008t0001g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3039+660A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015593 | |||||||
chr17:69015613 | A | ATAATT | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3039+635_3039+639d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015613 | |||||||
chr17:69015726 | A | T | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3039+527T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015726 | |||||||
chr17:69015863 | T | C | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3039+390A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015863 | |||||||
chr17:69015969 | TTG | T | 121 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(118): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.3039+282_3039+283d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015969 | |||||||
chr17:69015969 | TTGTG | T | 30 | a0001c0021t0003g0020 a0003c0003t0001g0007 a0003c0003t0001g0030 others(27): Show |
34 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.3039+280_3039+283d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015969 | |||||||
chr17:69015969 | TTGTGTG | T | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+278_3039+283d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015969 | |||||||
chr17:69015983 | G | A | 1 | a0003c0003t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3039+270C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69015983 | |||||||
chr17:69016094 | G | A | 19 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(16): Show |
23 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.3039+159C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016094 | |||||||
chr17:69016100 | G | A | 1 | a0015c0024t0002g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3039+153C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016100 | |||||||
chr17:69016102 | G | A | 1 | a0015c0024t0002g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3039+151C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016102 | |||||||
chr17:69016102 | GTA | G | 20 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0001t0001g0235 others(17): Show |
25 | HG01081.hp2 HG01099.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.3039+149_3039+150d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016102 | |||||||
chr17:69016102 | GTATA | G | 26 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0003c0003t0001g0021 others(23): Show |
28 | HG00639.hp2 HG01361.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.3039+147_3039+150d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016102 | |||||||
chr17:69016104 | A | G | 116 | a0001c0001t0003g0160 a0001c0007t0001g0088 a0001c0007t0001g0113 others(113): Show |
123 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.3039+149T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016104 | |||||||
chr17:69016106 | A | G | 14 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0002c0002t0002g0077 others(11): Show |
19 | HG01346.hp1 HG02055.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3039+147T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016106 | |||||||
chr17:69016108 | A | G | 4 | a0007c0010t0002g0118 a0007c0010t0002g0140 a0007c0010t0002g0141 others(1): Show |
4 | HG01496.hp2 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3039+145T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016108 | |||||||
chr17:69016113 | T | C | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3039+140A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016113 | |||||||
chr17:69016119 | T | C | 3 | a0001c0001t0003g0160 a0013c0022t0003g0019 a0018c0019t0003g0056 |
3 | HG02451.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3039+134A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016119 | |||||||
chr17:69016119 | T | TAC | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3039+133_3039+134i others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016119 | |||||||
chr17:69016119 | TATATAC | T | 7 | a0001c0007t0001g0156 a0002c0002t0002g0009 a0002c0002t0002g0076 others(4): Show |
8 | HG00140.hp1 HG00544.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.3039+128_3039+133d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016119 | |||||||
chr17:69016121 | T | C | 17 | a0001c0001t0003g0160 a0003c0003t0003g0036 a0003c0003t0003g0037 others(14): Show |
17 | HG00639.hp2 HG00733.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.3039+132A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016121 | |||||||
chr17:69016121 | TATAC | T | 91 | a0001c0007t0001g0088 a0001c0007t0001g0113 a0001c0007t0001g0115 others(88): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.3039+128_3039+131d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016121 | |||||||
chr17:69016123 | T | C | 32 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0225 others(29): Show |
34 | HG00544.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.3039+130A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | |||||||
chr17:69016123 | T | TAC | 18 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0205 others(15): Show |
18 | HG00408.hp1 HG02040.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.3039+128_3039+129d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | |||||||
chr17:69016123 | TAC | T | 9 | a0001c0001t0001g0172 a0002c0002t0002g0078 a0002c0002t0002g0136 others(6): Show |
9 | HG01517.hp2 HG02074.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.3039+128_3039+129d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | |||||||
chr17:69016123 | TACAC | T | 14 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(11): Show |
15 | HG01167.hp1 HG01175.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.3039+126_3039+129d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016123 | |||||||
chr17:69016125 | C | T | 5 | a0001c0001t0001g0181 a0001c0008t0001g0162 a0001c0029t0001g0195 others(2): Show |
5 | HG00099.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3039+128G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016125 | |||||||
chr17:69016127 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3039+126G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016127 | |||||||
chr17:69016137 | C | T | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3039+116G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016137 | |||||||
chr17:69016148 | T | A | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+105A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016148 | |||||||
chr17:69016173 | TATAAC | T | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.3039+75_3039+79del others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 22/38 | chr17 | 69016173 | |||||||
chr17:69016455 | A | G | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2902-65T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016455 | |||||||
chr17:69016489 | A | G | 1 | a0003c0003t0003g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2902-99T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016489 | |||||||
chr17:69016493 | G | C | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2902-103C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016493 | |||||||
chr17:69016532 | T | C | 1 | a0003c0003t0003g0039 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2902-142A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016532 | |||||||
chr17:69016853 | C | CGT | 11 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0001c0008t0001g0162 others(8): Show |
12 | HG00733.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2902-465_2902-464d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016853 | |||||||
chr17:69016947 | T | G | 1 | a0002c0002t0002g0133 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2902-557A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016947 | |||||||
chr17:69016953 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2902-563G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69016953 | |||||||
chr17:69017032 | C | G | 1 | a0002c0004t0002g0106 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2901+624G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69017032 | |||||||
chr17:69017257 | A | C | 10 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(7): Show |
10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2901+399T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69017257 | |||||||
chr17:69017561 | G | A | 5 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(2): Show |
5 | HG00733.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2901+95C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 21/38 | chr17 | 69017561 | |||||||
chr17:69018065 | G | GTCTA | 7 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2768-280_2768-277d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/38 | chr17 | 69018065 | |||||||
chr17:69018155 | A | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2767+258T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 20/38 | chr17 | 69018155 | |||||||
chr17:69018661 | A | G | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2601-82T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018661 | |||||||
chr17:69018700 | A | G | 2 | a0003c0003t0001g0007 a0003c0003t0001g0030 |
3 | HG03491.hp1 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2601-121T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018700 | |||||||
chr17:69018805 | G | A | 1 | a0004c0005t0003g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2601-226C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018805 | |||||||
chr17:69018823 | G | A | 1 | a0019c0023t0003g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2601-244C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018823 | |||||||
chr17:69018828 | T | C | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2601-249A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69018828 | |||||||
chr17:69019138 | T | C | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2601-559A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019138 | |||||||
chr17:69019387 | C | T | 11 | a0001c0021t0003g0020 a0003c0003t0004g0005 a0003c0003t0004g0006 others(8): Show |
13 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2601-808G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019387 | |||||||
chr17:69019516 | A | G | 2 | a0003c0003t0003g0036 a0003c0003t0003g0037 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2600+872T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019516 | |||||||
chr17:69019787 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0163 |
3 | HG03490.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2600+601G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 19/38 | chr17 | 69019787 | |||||||
chr17:69020676 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2402-90T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69020676 | |||||||
chr17:69020713 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2402-127A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69020713 | |||||||
chr17:69020825 | T | G | 2 | a0008c0013t0003g0057 a0008c0020t0003g0055 |
2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2402-239A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69020825 | |||||||
chr17:69021133 | A | G | 1 | a0003c0003t0004g0005 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2402-547T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021133 | |||||||
chr17:69021176 | G | A | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2401+566C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021176 | |||||||
chr17:69021296 | C | G | 1 | a0002c0002t0002g0089 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2401+446G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021296 | |||||||
chr17:69021313 | A | G | 2 | a0008c0013t0003g0058 a0014c0015t0003g0052 |
2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2401+429T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021313 | |||||||
chr17:69021430 | A | G | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2401+312T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021430 | |||||||
chr17:69021678 | G | GTCCT | 31 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0002c0002t0002g0100 others(28): Show |
35 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.2401+60_2401+63dup others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021678 | |||||||
chr17:69021678 | G | GTCCTTCC others(5): Show |
1 | a0003c0003t0003g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2401+52_2401+63dup others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021678 | |||||||
chr17:69021678 | GTCCT | G | 18 | a0001c0001t0001g0247 a0001c0021t0003g0020 a0004c0005t0003g0001 others(15): Show |
22 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2401+60_2401+63del others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021678 | |||||||
chr17:69021697 | C | CTTCCT | 3 | a0013c0022t0003g0019 a0018c0019t0003g0056 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2401+44_2401+45ins others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 18/38 | chr17 | 69021697 | |||||||
chr17:69021900 | T | A | 1 | a0001c0007t0001g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2282-39A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69021900 | |||||||
chr17:69022074 | C | T | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2282-213G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022074 | |||||||
chr17:69022291 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2282-430T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022291 | |||||||
chr17:69022292 | T | C | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2282-431A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022292 | |||||||
chr17:69022315 | C | G | 3 | a0004c0005t0003g0001 a0004c0005t0003g0264 a0004c0005t0003g0266 |
7 | HG01346.hp1 HG02451.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2282-454G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022315 | |||||||
chr17:69022329 | A | AT | 16 | a0001c0001t0001g0181 a0003c0003t0003g0036 a0003c0003t0003g0037 others(13): Show |
17 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2282-469dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022329 | |||||||
chr17:69022350 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2282-489T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022350 | |||||||
chr17:69022431 | C | T | 25 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0004c0005t0003g0001 others(22): Show |
30 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2282-570G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022431 | |||||||
chr17:69022455 | G | C | 1 | a0002c0002t0002g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2282-594C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022455 | |||||||
chr17:69022494 | T | TTG | 10 | a0001c0001t0001g0227 a0001c0007t0001g0088 a0002c0002t0002g0070 others(7): Show |
10 | HG00733.hp1 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2282-635_2282-634d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022494 | |||||||
chr17:69022494 | TTG | T | 12 | a0001c0001t0001g0249 a0001c0001t0003g0160 a0001c0021t0003g0020 others(9): Show |
12 | HG00639.hp2 HG01891.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2282-635_2282-634d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022494 | |||||||
chr17:69022494 | TTGTGTGT others(21): Show |
T | 1 | a0004c0005t0003g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2282-661_2282-634d others(30): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022494 | |||||||
chr17:69022518 | G | A | 3 | a0001c0001t0006g0008 a0013c0022t0003g0019 a0018c0019t0003g0056 |
3 | HG02055.hp1 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2282-657C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022518 | |||||||
chr17:69022518 | G | GTGTA | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2282-658_2282-657i others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022518 | |||||||
chr17:69022520 | A | ATG | 3 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0019c0023t0003g0018 |
3 | HG02280.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2282-661_2282-660d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022520 | |||||||
chr17:69022520 | A | G | 8 | a0001c0001t0006g0008 a0006c0009t0005g0015 a0006c0009t0005g0288 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2282-659T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022520 | |||||||
chr17:69022520 | ATGTGTGT others(1): Show |
A | 3 | a0008c0013t0003g0057 a0008c0020t0003g0055 a0010c0011t0003g0049 |
3 | HG03041.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2282-667_2282-660d others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022520 | |||||||
chr17:69022528 | G | A | 1 | a0010c0011t0003g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2282-667C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022528 | |||||||
chr17:69022647 | C | T | 8 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(5): Show |
8 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2282-786G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022647 | |||||||
chr17:69022660 | G | A | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2282-799C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022660 | |||||||
chr17:69022721 | C | CCT | 25 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0004c0005t0003g0001 others(22): Show |
30 | HG00733.hp1 HG01109.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2282-862_2282-861d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022721 | |||||||
chr17:69022771 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2282-910C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022771 | |||||||
chr17:69022780 | G | T | 1 | a0003c0003t0001g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2282-919C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022780 | |||||||
chr17:69022997 | T | A | 1 | a0004c0005t0003g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2282-1136A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69022997 | |||||||
chr17:69023006 | T | C | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2282-1145A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023006 | |||||||
chr17:69023564 | C | T | 4 | a0004c0005t0003g0001 a0004c0005t0003g0264 a0004c0005t0003g0266 others(1): Show |
8 | HG01346.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2281+650G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023564 | |||||||
chr17:69023638 | C | T | 2 | a0001c0007t0004g0091 a0002c0002t0002g0092 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2281+576G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023638 | |||||||
chr17:69023788 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0235 |
2 | HG01081.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2281+426T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023788 | |||||||
chr17:69023836 | ATTCTTTC others(24): Show |
A | 4 | a0008c0013t0003g0057 a0008c0020t0003g0055 a0010c0011t0003g0049 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2281+347_2281+377d others(33): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023836 | |||||||
chr17:69023868 | T | C | 4 | a0008c0013t0003g0057 a0008c0020t0003g0055 a0010c0011t0003g0049 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2281+346A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023868 | |||||||
chr17:69023869 | G | C | 4 | a0008c0013t0003g0057 a0008c0020t0003g0055 a0010c0011t0003g0049 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2281+345C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023869 | |||||||
chr17:69023886 | C | T | 1 | a0002c0002t0002g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2281+328G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023886 | |||||||
chr17:69023924 | A | G | 1 | a0001c0007t0001g0220 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2281+290T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023924 | |||||||
chr17:69023997 | AT | A | 20 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(17): Show |
22 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2281+216delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69023997 | |||||||
chr17:69024089 | T | C | 2 | a0002c0002t0002g0117 a0002c0002t0002g0153 |
2 | NA18953.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2281+125A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69024089 | |||||||
chr17:69024187 | C | T | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2281+27G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 17/38 | chr17 | 69024187 | |||||||
chr17:69024385 | A | G | 42 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(39): Show |
48 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2142-32T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024385 | |||||||
chr17:69024635 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2142-282C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024635 | |||||||
chr17:69024639 | T | C | 1 | a0004c0005t0003g0282 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2142-286A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024639 | |||||||
chr17:69024693 | T | G | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2142-340A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024693 | |||||||
chr17:69024697 | G | A | 213 | a0001c0001t0001g0017 a0001c0001t0001g0158 a0001c0001t0001g0159 others(210): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2142-344C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024697 | |||||||
chr17:69024849 | G | C | 3 | a0004c0005t0003g0001 a0004c0005t0003g0264 a0004c0005t0003g0266 |
7 | HG01346.hp1 HG02451.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2142-496C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024849 | |||||||
chr17:69024994 | T | C | 115 | a0001c0007t0001g0088 a0001c0007t0001g0113 a0001c0007t0001g0115 others(112): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2142-641A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69024994 | |||||||
chr17:69025015 | A | G | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2142-662T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025015 | |||||||
chr17:69025071 | T | G | 10 | a0001c0021t0003g0020 a0003c0003t0004g0005 a0003c0003t0004g0006 others(7): Show |
12 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2142-718A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025071 | |||||||
chr17:69025073 | C | T | 1 | a0003c0003t0003g0045 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2142-720G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025073 | |||||||
chr17:69025214 | C | T | 4 | a0001c0001t0001g0017 a0003c0003t0001g0035 a0003c0003t0001g0046 others(1): Show |
4 | HG01099.hp2 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142-861G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025214 | |||||||
chr17:69025228 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2142-875G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025228 | |||||||
chr17:69025232 | A | G | 9 | a0003c0003t0004g0005 a0003c0003t0004g0006 a0003c0003t0004g0022 others(6): Show |
11 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2142-879T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025232 | |||||||
chr17:69025353 | G | A | 2 | a0010c0011t0003g0049 a0010c0011t0003g0050 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2142-1000C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025353 | |||||||
chr17:69025419 | T | G | 1 | a0002c0002t0002g0074 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2141+958A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025419 | |||||||
chr17:69025700 | T | C | 5 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0013c0022t0003g0019 others(2): Show |
6 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2141+677A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025700 | |||||||
chr17:69025773 | G | A | 1 | a0002c0002t0002g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2141+604C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025773 | |||||||
chr17:69025994 | C | A | 124 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0001c0007t0001g0088 others(121): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2141+383G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69025994 | |||||||
chr17:69026134 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2141+243C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 16/38 | chr17 | 69026134 | |||||||
chr17:69026600 | C | T | 1 | a0002c0002t0002g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2051-133G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026600 | |||||||
chr17:69026627 | C | T | 2 | a0001c0001t0003g0160 a0003c0003t0004g0023 |
2 | HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2051-160G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026627 | |||||||
chr17:69026644 | A | G | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2051-177T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026644 | |||||||
chr17:69026669 | G | A | 10 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2051-202C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026669 | |||||||
chr17:69026759 | T | C | 20 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(17): Show |
22 | HG00639.hp2 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2050+217A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 15/38 | chr17 | 69026759 | |||||||
chr17:69027138 | G | A | 1 | a0001c0007t0001g0236 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1912-24C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027138 | |||||||
chr17:69027154 | G | A | 14 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(11): Show |
18 | HG01109.hp2 HG01346.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1912-40C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027154 | |||||||
chr17:69027232 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1911+98T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027232 | |||||||
chr17:69027244 | C | G | 10 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0038 others(7): Show |
10 | HG00639.hp2 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1911+86G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 14/38 | chr17 | 69027244 | |||||||
chr17:69027558 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1791+82T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 13/38 | chr17 | 69027558 | |||||||
chr17:69027614 | A | G | 166 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(163): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1791+26T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 13/38 | chr17 | 69027614 | |||||||
chr17:69028043 | T | G | 10 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1616-228A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028043 | |||||||
chr17:69028126 | A | G | 2 | a0003c0003t0004g0024 a0003c0003t0004g0028 |
2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1616-311T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028126 | |||||||
chr17:69028384 | C | T | 2 | a0002c0002t0002g0100 a0002c0002t0002g0122 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615+151G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028384 | |||||||
chr17:69028413 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1615+122G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028413 | |||||||
chr17:69028444 | T | C | 166 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(163): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1615+91A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 12/38 | chr17 | 69028444 | |||||||
chr17:69028658 | T | A | 166 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(163): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1505-13A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028658 | |||||||
chr17:69028742 | C | T | 1 | a0003c0003t0004g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1505-97G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028742 | |||||||
chr17:69028794 | A | G | 9 | a0003c0003t0004g0005 a0003c0003t0004g0006 a0003c0003t0004g0022 others(6): Show |
11 | HG01884.hp1 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1505-149T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028794 | |||||||
chr17:69028798 | C | T | 1 | a0002c0002t0002g0102 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1505-153G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028798 | |||||||
chr17:69028807 | G | A | 7 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505-162C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028807 | |||||||
chr17:69028814 | T | C | 2 | a0002c0002t0002g0126 a0002c0002t0002g0127 |
2 | NA18946.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1505-169A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69028814 | |||||||
chr17:69029019 | G | GT | 15 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(12): Show |
19 | HG01109.hp2 HG01346.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1504+149dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69029019 | |||||||
chr17:69029089 | T | C | 3 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 |
3 | HG00733.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1504+80A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69029089 | |||||||
chr17:69029100 | C | G | 1 | a0002c0002t0002g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1504+69G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 11/38 | chr17 | 69029100 | |||||||
chr17:69029282 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1446-55T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029282 | |||||||
chr17:69029423 | G | A | 1 | a0006c0009t0005g0290 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1446-196C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029423 | |||||||
chr17:69029423 | G | T | 10 | a0001c0008t0001g0162 a0001c0008t0001g0176 a0001c0008t0001g0185 others(7): Show |
10 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1446-196C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029423 | |||||||
chr17:69029465 | G | A | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1446-238C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029465 | |||||||
chr17:69029549 | G | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1446-322C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029549 | |||||||
chr17:69029563 | A | G | 1 | a0001c0008t0001g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1446-336T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029563 | |||||||
chr17:69029614 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1446-387A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029614 | |||||||
chr17:69029710 | G | A | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1446-483C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029710 | |||||||
chr17:69029714 | A | G | 1 | a0006c0009t0005g0290 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1446-487T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029714 | |||||||
chr17:69029790 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0006g0008 a0001c0001t0006g0054 others(1): Show |
5 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446-563C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029790 | |||||||
chr17:69029900 | G | T | 25 | a0001c0021t0003g0020 a0003c0003t0003g0036 a0003c0003t0003g0037 others(22): Show |
27 | HG00639.hp2 HG00733.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1446-673C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69029900 | |||||||
chr17:69030090 | A | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1446-863T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030090 | |||||||
chr17:69030272 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | NA18939.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1446-1045A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030272 | |||||||
chr17:69030412 | G | T | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1446-1185C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030412 | |||||||
chr17:69030485 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1446-1258C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69030485 | |||||||
chr17:69031061 | A | C | 1 | a0002c0004t0002g0257 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1445+1047T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031061 | |||||||
chr17:69031095 | C | G | 1 | a0003c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1445+1013G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031095 | |||||||
chr17:69031202 | T | G | 2 | a0006c0009t0005g0015 a0006c0009t0005g0289 |
3 | HG01069.hp1 HG01071.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1445+906A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031202 | |||||||
chr17:69031729 | A | G | 133 | a0001c0001t0001g0235 a0001c0007t0001g0088 a0001c0007t0001g0113 others(130): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1445+379T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69031729 | |||||||
chr17:69032071 | G | C | 17 | a0001c0001t0003g0160 a0001c0001t0006g0008 a0001c0001t0006g0054 others(14): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1445+37C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69032071 | |||||||
chr17:69032079 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1445+29A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 10/38 | chr17 | 69032079 | |||||||
chr17:69032280 | T | C | 1 | a0002c0002t0002g0145 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.1277-4A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69032280 | |||||||
chr17:69032511 | A | T | 1 | a0003c0003t0001g0046 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1277-235T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69032511 | |||||||
chr17:69032765 | G | T | 3 | a0001c0001t0001g0017 a0013c0022t0003g0019 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1277-489C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69032765 | |||||||
chr17:69033303 | C | CAA | 16 | a0001c0001t0001g0017 a0006c0009t0005g0015 a0006c0009t0005g0288 others(13): Show |
17 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1276+421_1276+422d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | |||||||
chr17:69033303 | C | CAAA | 7 | a0001c0001t0001g0062 a0001c0001t0001g0208 a0001c0001t0006g0008 others(4): Show |
8 | HG01074.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276+420_1276+422d others(5): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | |||||||
chr17:69033303 | C | CAAAA | 223 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(220): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1276+419_1276+422d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | |||||||
chr17:69033303 | C | CAAAAA | 13 | a0001c0001t0001g0082 a0001c0001t0001g0249 a0001c0001t0001g0259 others(10): Show |
13 | HG01952.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276+418_1276+422d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033303 | |||||||
chr17:69033324 | G | C | 45 | a0001c0001t0001g0082 a0001c0007t0001g0088 a0001c0007t0001g0113 others(42): Show |
46 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.1276+402C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033324 | |||||||
chr17:69033682 | C | G | 7 | a0003c0003t0001g0021 a0003c0003t0001g0032 a0003c0003t0001g0034 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276+44G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 9/38 | chr17 | 69033682 | |||||||
chr17:69034131 | T | A | 3 | a0001c0001t0001g0017 a0013c0022t0003g0019 a0019c0023t0003g0018 |
3 | HG02451.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1129-258A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034131 | |||||||
chr17:69034460 | T | G | 138 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(135): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1129-587A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034460 | |||||||
chr17:69034530 | C | A | 1 | a0001c0001t0001g0173 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1129-657G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034530 | |||||||
chr17:69034604 | T | C | 1 | a0007c0010t0002g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1128+642A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034604 | |||||||
chr17:69034605 | T | C | 1 | a0007c0010t0002g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1128+641A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034605 | |||||||
chr17:69034781 | C | T | 1 | a0008c0013t0003g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1128+465G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034781 | |||||||
chr17:69034936 | G | A | 2 | a0013c0022t0003g0019 a0019c0023t0003g0018 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1128+310C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69034936 | |||||||
chr17:69035228 | T | C | 280 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(277): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1128+18A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 8/38 | chr17 | 69035228 | |||||||
chr17:69035622 | A | G | 2 | a0001c0007t0004g0091 a0002c0002t0002g0092 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.942+38T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 7/38 | chr17 | 69035622 | |||||||
chr17:69035974 | G | A | 2 | a0002c0002t0002g0119 a0002c0002t0002g0134 |
2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.801-173C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69035974 | |||||||
chr17:69036071 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.801-270C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036071 | |||||||
chr17:69036128 | G | T | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.801-327C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036128 | |||||||
chr17:69036147 | T | C | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.801-346A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036147 | |||||||
chr17:69036372 | T | C | 1 | a0013c0022t0003g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.801-571A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036372 | |||||||
chr17:69036493 | C | T | 2 | a0003c0003t0001g0007 a0003c0003t0001g0030 |
3 | HG03491.hp1 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.801-692G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036493 | |||||||
chr17:69036871 | C | CA | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0002c0004t0002g0135 others(13): Show |
18 | HG01071.hp1 HG01099.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.801-1071dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | |||||||
chr17:69036871 | C | CAAAA | 65 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0161 others(62): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.801-1074_801-1071d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | |||||||
chr17:69036871 | C | CAAAAA | 41 | a0001c0001t0001g0166 a0001c0001t0001g0181 a0001c0001t0001g0193 others(38): Show |
43 | HG00438.hp2 HG00544.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.801-1075_801-1071d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | |||||||
chr17:69036871 | C | CAAAAAA | 19 | a0001c0001t0001g0163 a0001c0001t0001g0172 a0001c0001t0001g0175 others(16): Show |
19 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.801-1076_801-1071d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | |||||||
chr17:69036871 | CA | C | 75 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(72): Show |
81 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.801-1071delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | |||||||
chr17:69036871 | CAA | C | 8 | a0002c0002t0002g0009 a0002c0002t0002g0060 a0002c0002t0002g0061 others(5): Show |
9 | HG00733.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.801-1072_801-1071d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | |||||||
chr17:69036871 | CAAAAAAA others(3): Show |
C | 1 | a0013c0022t0003g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.801-1080_801-1071d others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036871 | |||||||
chr17:69036925 | TA | T | 13 | a0003c0003t0001g0007 a0003c0003t0001g0030 a0003c0003t0001g0031 others(10): Show |
16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.801-1125delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036925 | |||||||
chr17:69036934 | C | T | 141 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0157 others(138): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.801-1133G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69036934 | |||||||
chr17:69037345 | C | T | 102 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.801-1544G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037345 | |||||||
chr17:69037614 | G | T | 3 | a0002c0002t0002g0102 a0002c0002t0007g0128 a0002c0002t0007g0129 |
3 | HG00639.hp1 HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.801-1813C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037614 | |||||||
chr17:69037696 | G | A | 1 | a0019c0023t0003g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.801-1895C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037696 | |||||||
chr17:69037754 | G | T | 141 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0157 others(138): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.801-1953C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037754 | |||||||
chr17:69037975 | A | G | 272 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(269): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.801-2174T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69037975 | |||||||
chr17:69038305 | G | A | 1 | a0002c0002t0002g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.801-2504C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038305 | |||||||
chr17:69038370 | T | C | 1 | a0002c0002t0002g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.801-2569A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038370 | |||||||
chr17:69038371 | G | A | 105 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0161 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.801-2570C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038371 | |||||||
chr17:69038426 | T | C | 45 | a0001c0001t0001g0082 a0001c0007t0001g0088 a0001c0007t0001g0113 others(42): Show |
46 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.801-2625A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038426 | |||||||
chr17:69038630 | A | G | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.801-2829T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038630 | |||||||
chr17:69038695 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.801-2894A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038695 | |||||||
chr17:69038822 | C | T | 1 | a0001c0007t0001g0206 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.801-3021G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038822 | |||||||
chr17:69038934 | G | T | 136 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(133): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.801-3133C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69038934 | |||||||
chr17:69039137 | T | A | 1 | a0003c0003t0001g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.801-3336A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039137 | |||||||
chr17:69039158 | A | G | 1 | a0003c0003t0003g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.801-3357T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039158 | |||||||
chr17:69039247 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.801-3446G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039247 | |||||||
chr17:69039737 | T | G | 242 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(239): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.800+3752A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039737 | |||||||
chr17:69039750 | C | T | 272 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(269): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.800+3739G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039750 | |||||||
chr17:69039944 | CAT | C | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(1): Show |
4 | HG00733.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+3543_800+3544d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69039944 | |||||||
chr17:69040256 | C | T | 13 | a0003c0003t0001g0007 a0003c0003t0001g0030 a0003c0003t0001g0031 others(10): Show |
16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.800+3233G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040256 | |||||||
chr17:69040385 | T | C | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.800+3104A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040385 | |||||||
chr17:69040445 | A | G | 1 | a0006c0009t0005g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.800+3044T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040445 | |||||||
chr17:69040450 | A | G | 7 | a0003c0003t0001g0021 a0003c0003t0001g0032 a0003c0003t0001g0034 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.800+3039T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040450 | |||||||
chr17:69040514 | T | C | 1 | a0001c0007t0001g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.800+2975A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040514 | |||||||
chr17:69040717 | A | T | 1 | a0002c0028t0002g0079 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.800+2772T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040717 | |||||||
chr17:69040845 | TAC | T | 13 | a0003c0003t0001g0007 a0003c0003t0001g0030 a0003c0003t0001g0031 others(10): Show |
16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.800+2642_800+2643d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040845 | |||||||
chr17:69040862 | A | C | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.800+2627T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040862 | |||||||
chr17:69040894 | C | T | 1 | a0004c0005t0003g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.800+2595G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69040894 | |||||||
chr17:69041184 | G | T | 287 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(284): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.800+2305C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041184 | |||||||
chr17:69041215 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.800+2274T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041215 | |||||||
chr17:69041226 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.800+2263G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041226 | |||||||
chr17:69041339 | T | G | 106 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0161 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.800+2150A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041339 | |||||||
chr17:69041452 | A | C | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.800+2037T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041452 | |||||||
chr17:69041635 | G | C | 31 | a0001c0001t0001g0017 a0004c0005t0003g0001 a0004c0005t0003g0263 others(28): Show |
37 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.800+1854C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041635 | |||||||
chr17:69041711 | TA | T | 286 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(283): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.800+1777delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041711 | |||||||
chr17:69041727 | A | T | 1 | a0001c0001t0009g0194 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.800+1762T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041727 | |||||||
chr17:69041729 | T | TCTATTAT others(5): Show |
1 | a0001c0001t0009g0194 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.800+1759_800+1760i others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | |||||||
chr17:69041729 | T | TTATC | 10 | a0001c0001t0001g0017 a0001c0001t0001g0177 a0001c0001t0001g0202 others(7): Show |
10 | HG00408.hp1 HG00408.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.800+1756_800+1759d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | |||||||
chr17:69041729 | T | TTATCTAT others(1): Show |
79 | a0001c0001t0001g0082 a0001c0001t0001g0196 a0001c0001t0001g0203 others(76): Show |
88 | HG00544.hp2 HG00642.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.800+1752_800+1759d others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | |||||||
chr17:69041729 | T | TTATCTAT others(5): Show |
159 | a0001c0001t0001g0011 a0001c0001t0001g0062 a0001c0001t0001g0157 others(156): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.800+1748_800+1759d others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | |||||||
chr17:69041729 | T | TTATCTAT others(9): Show |
8 | a0001c0001t0001g0167 a0001c0001t0001g0201 a0001c0001t0001g0238 others(5): Show |
9 | HG01517.hp2 HG01975.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.800+1744_800+1759d others(18): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | |||||||
chr17:69041729 | T | TTATCTAT others(13): Show |
2 | a0001c0001t0001g0233 a0002c0028t0002g0079 |
2 | HG02080.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.800+1740_800+1759d others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041729 | |||||||
chr17:69041879 | A | G | 287 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(284): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.800+1610T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041879 | |||||||
chr17:69041982 | T | G | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.800+1507A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041982 | |||||||
chr17:69041993 | C | T | 7 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(4): Show |
7 | HG01175.hp2 HG02572.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.800+1496G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69041993 | |||||||
chr17:69042059 | T | G | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(1): Show |
4 | HG00733.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+1430A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042059 | |||||||
chr17:69042107 | A | G | 9 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(6): Show |
10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.800+1382T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042107 | |||||||
chr17:69042178 | CTA | C | 102 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.800+1309_800+1310d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042178 | |||||||
chr17:69042182 | T | C | 9 | a0001c0008t0001g0162 a0001c0008t0001g0176 a0001c0008t0001g0185 others(6): Show |
9 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.800+1307A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042182 | |||||||
chr17:69042186 | A | G | 137 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(134): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.800+1303T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042186 | |||||||
chr17:69042409 | C | T | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.800+1080G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042409 | |||||||
chr17:69042513 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.800+976A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042513 | |||||||
chr17:69042791 | A | G | 1 | a0010c0011t0003g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.800+698T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042791 | |||||||
chr17:69042837 | A | G | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG02071.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.800+652T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042837 | |||||||
chr17:69042930 | T | C | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.800+559A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69042930 | |||||||
chr17:69043008 | C | G | 1 | a0001c0029t0001g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.800+481G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043008 | |||||||
chr17:69043080 | CAGTGACA others(50): Show |
C | 4 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+352_800+408del others(57): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043080 | |||||||
chr17:69043094 | C | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.800+395G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043094 | |||||||
chr17:69043133 | T | C | 1 | a0001c0008t0001g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.800+356A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043133 | |||||||
chr17:69043316 | G | A | 9 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(6): Show |
10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.800+173C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043316 | |||||||
chr17:69043458 | C | T | 7 | a0003c0003t0001g0021 a0003c0003t0001g0032 a0003c0003t0001g0034 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.800+31G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 6/38 | chr17 | 69043458 | |||||||
chr17:69043798 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.574-83G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69043798 | |||||||
chr17:69043923 | G | A | 13 | a0003c0003t0001g0007 a0003c0003t0001g0030 a0003c0003t0001g0031 others(10): Show |
16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-208C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69043923 | |||||||
chr17:69043970 | T | A | 4 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-255A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69043970 | |||||||
chr17:69044203 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.573+294G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044203 | |||||||
chr17:69044240 | T | A | 1 | a0001c0007t0001g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.573+257A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044240 | |||||||
chr17:69044270 | T | C | 11 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(8): Show |
13 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.573+227A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044270 | |||||||
chr17:69044468 | T | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.573+29A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 5/38 | chr17 | 69044468 | |||||||
chr17:69044630 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.470-30C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044630 | |||||||
chr17:69044919 | G | A | 105 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0161 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.469+253C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044919 | |||||||
chr17:69044941 | T | TG | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.469+230_469+231ins others(1): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044941 | |||||||
chr17:69044981 | T | G | 1 | a0001c0001t0001g0253 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.469+191A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69044981 | |||||||
chr17:69045014 | C | G | 1 | a0002c0002t0002g0089 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.469+158G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69045014 | |||||||
chr17:69045079 | T | C | 1 | a0002c0002t0002g0076 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.469+93A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69045079 | |||||||
chr17:69045126 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.469+46A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 4/38 | chr17 | 69045126 | |||||||
chr17:69045430 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.305-94A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69045430 | |||||||
chr17:69045467 | T | C | 88 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0161 others(85): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.305-131A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69045467 | |||||||
chr17:69045867 | C | G | 7 | a0003c0003t0001g0021 a0003c0003t0001g0032 a0003c0003t0001g0034 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.305-531G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69045867 | |||||||
chr17:69046055 | G | C | 1 | a0003c0003t0001g0032 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.305-719C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046055 | |||||||
chr17:69046316 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.305-980A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046316 | |||||||
chr17:69046567 | C | T | 1 | a0001c0001t0009g0194 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.305-1231G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046567 | |||||||
chr17:69046599 | T | C | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.305-1263A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046599 | |||||||
chr17:69046621 | T | G | 103 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(100): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.305-1285A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046621 | |||||||
chr17:69046718 | C | T | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.305-1382G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046718 | |||||||
chr17:69046719 | A | G | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.305-1383T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046719 | |||||||
chr17:69046804 | C | G | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.305-1468G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046804 | |||||||
chr17:69046875 | C | CTA | 4 | a0001c0001t0011g0244 a0002c0004t0002g0178 a0003c0003t0001g0007 others(1): Show |
5 | HG02132.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-1541_305-1540d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | C | CTATA | 5 | a0001c0001t0008g0245 a0001c0001t0008g0246 a0003c0003t0001g0021 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-1543_305-1540d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTA | C | 25 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0165 others(22): Show |
26 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.305-1541_305-1540d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATA | C | 67 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0166 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.305-1543_305-1540d others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATATA | C | 9 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(6): Show |
9 | HG00639.hp2 HG02717.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.305-1545_305-1540d others(8): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATATAT others(1): Show |
C | 12 | a0001c0001t0001g0168 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG02572.hp2 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-1547_305-1540d others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATATAT others(3): Show |
C | 7 | a0001c0001t0001g0157 a0001c0007t0001g0088 a0002c0002t0002g0004 others(4): Show |
9 | HG02155.hp2 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.305-1549_305-1540d others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATATAT others(5): Show |
C | 16 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0003g0160 others(13): Show |
16 | HG00438.hp1 HG00642.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.305-1551_305-1540d others(14): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATATAT others(7): Show |
C | 87 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0113 others(84): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.305-1553_305-1540d others(16): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATATAT others(9): Show |
C | 15 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0005c0006t0001g0014 others(12): Show |
18 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.305-1555_305-1540d others(18): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046875 | CTATATAT others(11): Show |
C | 29 | a0001c0001t0001g0017 a0004c0005t0003g0001 a0004c0005t0003g0263 others(26): Show |
34 | HG01074.hp1 HG01109.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.305-1557_305-1540d others(20): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046875 | |||||||
chr17:69046894 | TATATATA others(29): Show |
T | 1 | a0004c0005t0003g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.305-1594_305-1559d others(38): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046894 | |||||||
chr17:69046901 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.305-1566_305-1565i others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046901 | |||||||
chr17:69046926 | T | A | 1 | a0001c0001t0006g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.305-1590A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046926 | |||||||
chr17:69046930 | G | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.305-1594C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046930 | |||||||
chr17:69046937 | T | TTA | 9 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(6): Show |
10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.305-1603_305-1602d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046937 | |||||||
chr17:69046937 | TTA | T | 103 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(100): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.305-1603_305-1602d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69046937 | |||||||
chr17:69047122 | C | G | 1 | a0003c0003t0004g0005 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.305-1786G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047122 | |||||||
chr17:69047209 | A | G | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.305-1873T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047209 | |||||||
chr17:69047256 | T | C | 1 | a0002c0002t0002g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.305-1920A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047256 | |||||||
chr17:69047357 | G | C | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.304+1926C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047357 | |||||||
chr17:69047459 | A | G | 1 | a0008c0020t0003g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.304+1824T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047459 | |||||||
chr17:69047495 | G | C | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.304+1788C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047495 | |||||||
chr17:69047515 | A | G | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.304+1768T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047515 | |||||||
chr17:69047713 | A | G | 3 | a0001c0021t0003g0020 a0013c0022t0003g0019 a0019c0023t0003g0018 |
3 | HG01891.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.304+1570T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047713 | |||||||
chr17:69047770 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.304+1513C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69047770 | |||||||
chr17:69048075 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.304+1208A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048075 | |||||||
chr17:69048215 | T | A | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304+1068A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048215 | |||||||
chr17:69048275 | C | T | 5 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+1008G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048275 | |||||||
chr17:69048420 | T | C | 103 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(100): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.304+863A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048420 | |||||||
chr17:69048426 | T | TA | 136 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(133): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.304+856dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048426 | |||||||
chr17:69048428 | C | T | 1 | a0003c0003t0003g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.304+855G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048428 | |||||||
chr17:69048462 | C | T | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.304+821G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048462 | |||||||
chr17:69048654 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.304+629C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048654 | |||||||
chr17:69048721 | C | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.304+562G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048721 | |||||||
chr17:69048753 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0146 a0002c0002t0002g0147 others(2): Show |
7 | NA18980.hp1 NA18992.hp1 NA19058.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+530A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048753 | |||||||
chr17:69048827 | C | A | 23 | a0001c0001t0001g0062 a0002c0002t0002g0002 a0002c0002t0002g0060 others(20): Show |
25 | HG00099.hp2 HG00140.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.304+456G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048827 | |||||||
chr17:69048830 | C | T | 18 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(15): Show |
20 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.304+453G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 3/38 | chr17 | 69048830 | |||||||
chr17:69049569 | T | A | 4 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-79A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049569 | |||||||
chr17:69049762 | T | G | 259 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.97-272A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049762 | |||||||
chr17:69049776 | T | C | 1 | a0002c0002t0002g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.97-286A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049776 | |||||||
chr17:69049796 | G | A | 1 | a0014c0015t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.97-306C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049796 | |||||||
chr17:69049946 | AC | A | 4 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-457delG | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049946 | |||||||
chr17:69049984 | G | A | 1 | a0012c0016t0002g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.97-494C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69049984 | |||||||
chr17:69050101 | T | C | 2 | a0013c0022t0003g0019 a0019c0023t0003g0018 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.97-611A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050101 | |||||||
chr17:69050221 | G | T | 2 | a0003c0003t0001g0021 a0003c0003t0001g0032 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.97-731C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050221 | |||||||
chr17:69050323 | A | AAC | 7 | a0003c0003t0001g0021 a0003c0003t0001g0032 a0003c0003t0001g0034 others(4): Show |
7 | HG01099.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+706_96+707dupGT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050323 | |||||||
chr17:69050343 | AAC | A | 98 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0007t0001g0113 others(95): Show |
107 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.96+686_96+687delGT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | |||||||
chr17:69050343 | AACAC | A | 14 | a0001c0021t0003g0020 a0002c0002t0002g0149 a0003c0003t0001g0007 others(11): Show |
15 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+684_96+687delGT others(2): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | |||||||
chr17:69050343 | AACACAC | A | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0180 others(5): Show |
9 | HG01175.hp2 HG01978.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+682_96+687delGT others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | |||||||
chr17:69050343 | AACACACA others(1): Show |
A | 103 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(100): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.96+680_96+687delGT others(6): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | |||||||
chr17:69050343 | AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | NA19009.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.96+676_96+687delGT others(10): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | |||||||
chr17:69050343 | AACACACA others(7): Show |
A | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+674_96+687delGT others(12): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050343 | |||||||
chr17:69050525 | A | T | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.96+506T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050525 | |||||||
chr17:69050706 | G | A | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+325C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050706 | |||||||
chr17:69050826 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.96+205G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050826 | |||||||
chr17:69050906 | AT | A | 106 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0161 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.96+124delA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69050906 | |||||||
chr17:69051004 | T | C | 1 | a0002c0002t0002g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.96+27A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 2/38 | chr17 | 69051004 | |||||||
chr17:69051185 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-13-46C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69051185 | |||||||
chr17:69051287 | G | A | 140 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0157 others(137): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-13-148C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69051287 | |||||||
chr17:69051372 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13-233T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69051372 | |||||||
chr17:69052235 | C | T | 1 | a0010c0011t0003g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13-1096G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052235 | |||||||
chr17:69052434 | A | G | 4 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-1295T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052434 | |||||||
chr17:69052668 | G | T | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-13-1529C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052668 | |||||||
chr17:69052844 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0180 a0001c0021t0003g0020 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-1705G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69052844 | |||||||
chr17:69053067 | CTCCTTCA others(10): Show |
C | 13 | a0003c0003t0001g0007 a0003c0003t0001g0030 a0003c0003t0001g0031 others(10): Show |
16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-1945_-13-1929d others(19): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69053067 | |||||||
chr17:69053717 | C | A | 3 | a0004c0005t0003g0001 a0004c0005t0003g0265 a0004c0005t0003g0266 |
7 | HG01346.hp1 HG02451.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-2578G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69053717 | |||||||
chr17:69053780 | CTG | C | 80 | a0001c0001t0001g0082 a0001c0007t0001g0088 a0001c0007t0001g0113 others(77): Show |
86 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-13-2643_-13-2642d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69053780 | |||||||
chr17:69054246 | A | G | 140 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0157 others(137): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-13-3107T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054246 | |||||||
chr17:69054386 | G | A | 4 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-3247C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054386 | |||||||
chr17:69054526 | CA | C | 6 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0002c0004t0002g0179 others(3): Show |
6 | HG01167.hp2 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-3388delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054526 | |||||||
chr17:69054726 | T | C | 1 | a0001c0021t0003g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-13-3587A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054726 | |||||||
chr17:69054810 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | NA18953.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-13-3671C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054810 | |||||||
chr17:69054908 | C | A | 1 | a0005c0006t0001g0287 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13-3769G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054908 | |||||||
chr17:69054920 | A | G | 1 | a0002c0004t0002g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-13-3781T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054920 | |||||||
chr17:69054965 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-13-3826T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69054965 | |||||||
chr17:69055105 | C | T | 1 | a0004c0005t0003g0267 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13-3966G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055105 | |||||||
chr17:69055113 | A | G | 1 | a0010c0011t0003g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13-3974T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055113 | |||||||
chr17:69055196 | A | T | 103 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(100): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-13-4057T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055196 | |||||||
chr17:69055207 | T | C | 1 | a0002c0002t0002g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13-4068A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055207 | |||||||
chr17:69055448 | G | C | 13 | a0003c0003t0001g0007 a0003c0003t0001g0030 a0003c0003t0001g0031 others(10): Show |
16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-4309C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055448 | |||||||
chr17:69055505 | AAC | A | 3 | a0001c0021t0003g0020 a0013c0022t0003g0019 a0019c0023t0003g0018 |
3 | HG01891.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-13-4368_-13-4367d others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055505 | |||||||
chr17:69055788 | T | A | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-13-4649A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055788 | |||||||
chr17:69055842 | A | T | 1 | a0001c0008t0001g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-13-4703T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055842 | |||||||
chr17:69055885 | A | G | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-13-4746T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055885 | |||||||
chr17:69055910 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-13-4771T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055910 | |||||||
chr17:69055934 | C | G | 4 | a0004c0005t0003g0001 a0004c0005t0003g0264 a0004c0005t0003g0265 others(1): Show |
8 | HG01346.hp1 HG02451.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-4795G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69055934 | |||||||
chr17:69056077 | C | T | 260 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(257): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-14+4789G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056077 | |||||||
chr17:69056081 | C | A | 1 | a0002c0002t0002g0153 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-14+4785G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056081 | |||||||
chr17:69056095 | A | T | 9 | a0006c0009t0005g0015 a0006c0009t0005g0288 a0006c0009t0005g0289 others(6): Show |
10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+4771T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056095 | |||||||
chr17:69056331 | G | T | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG01175.hp2 HG02572.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+4535C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056331 | |||||||
chr17:69056720 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-14+4146T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056720 | |||||||
chr17:69056976 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-14+3890A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056976 | |||||||
chr17:69056986 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+3880G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69056986 | |||||||
chr17:69057141 | G | A | 1 | a0003c0003t0003g0045 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-14+3725C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057141 | |||||||
chr17:69057152 | T | C | 33 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0003c0003t0001g0048 others(30): Show |
39 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+3714A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057152 | |||||||
chr17:69057378 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14+3488G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057378 | |||||||
chr17:69057441 | G | C | 17 | a0001c0001t0001g0017 a0001c0001t0006g0008 a0001c0001t0006g0054 others(14): Show |
19 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14+3425C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057441 | |||||||
chr17:69057507 | CTAGGCTT others(13): Show |
C | 13 | a0003c0003t0001g0007 a0003c0003t0001g0030 a0003c0003t0001g0031 others(10): Show |
16 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14+3339_-14+3358d others(22): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057507 | |||||||
chr17:69057574 | A | C | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+3292T>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057574 | |||||||
chr17:69057824 | T | G | 1 | a0002c0004t0002g0257 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-14+3042A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057824 | |||||||
chr17:69057840 | TTCTTG | T | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+3021_-14+3025d others(7): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057840 | |||||||
chr17:69057997 | G | A | 4 | a0008c0013t0003g0057 a0008c0013t0003g0058 a0008c0020t0003g0055 others(1): Show |
4 | HG00733.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2869C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69057997 | |||||||
chr17:69058007 | G | C | 273 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(270): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-14+2859C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058007 | |||||||
chr17:69058049 | A | T | 1 | a0022c0025t0002g0059 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-14+2817T>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058049 | |||||||
chr17:69058066 | T | C | 1 | a0013c0022t0003g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-14+2800A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058066 | |||||||
chr17:69058148 | G | A | 1 | a0002c0002t0002g0154 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-14+2718C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058148 | |||||||
chr17:69058413 | C | T | 4 | a0001c0021t0003g0020 a0003c0003t0001g0048 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2453G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058413 | |||||||
chr17:69058437 | G | C | 5 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0003c0003t0001g0048 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2429C>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058437 | |||||||
chr17:69058439 | G | T | 1 | a0004c0005t0003g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14+2427C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058439 | |||||||
chr17:69058441 | T | C | 4 | a0001c0021t0003g0020 a0003c0003t0001g0048 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2425A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058441 | |||||||
chr17:69058568 | C | G | 232 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(229): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-14+2298G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058568 | |||||||
chr17:69058568 | C | T | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+2298G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058568 | |||||||
chr17:69058589 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-14+2277G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058589 | |||||||
chr17:69058653 | C | A | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+2213G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058653 | |||||||
chr17:69058794 | C | G | 273 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(270): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-14+2072G>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058794 | |||||||
chr17:69058836 | C | CA | 107 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-14+2029dupT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058836 | |||||||
chr17:69058836 | CA | C | 33 | a0001c0001t0001g0017 a0003c0003t0001g0021 a0003c0003t0001g0048 others(30): Show |
39 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+2029delT | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058836 | |||||||
chr17:69058856 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-14+2010T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69058856 | |||||||
chr17:69059172 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0003g0160 |
3 | HG01884.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-14+1694G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059172 | |||||||
chr17:69059404 | A | G | 260 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(257): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-14+1462T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059404 | |||||||
chr17:69059424 | G | A | 1 | a0003c0003t0001g0046 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14+1442C>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059424 | |||||||
chr17:69059448 | C | T | 2 | a0001c0001t0006g0008 a0001c0001t0006g0054 |
3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14+1418G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059448 | |||||||
chr17:69059573 | C | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+1293G>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059573 | |||||||
chr17:69059624 | T | C | 5 | a0001c0001t0001g0017 a0001c0021t0003g0020 a0003c0003t0001g0048 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+1242A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059624 | |||||||
chr17:69059643 | T | C | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+1223A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059643 | |||||||
chr17:69059669 | A | AT | 166 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(163): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-14+1196dupA | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059669 | |||||||
chr17:69059677 | T | A | 4 | a0001c0021t0003g0020 a0003c0003t0001g0048 a0013c0022t0003g0019 others(1): Show |
4 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1189A>T | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059677 | |||||||
chr17:69059712 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-14+1154C>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059712 | |||||||
chr17:69059760 | A | G | 260 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(257): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-14+1106T>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059760 | |||||||
chr17:69059783 | T | C | 1 | a0003c0003t0001g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-14+1083A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69059783 | |||||||
chr17:69060027 | GTTCT | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0054 a0006c0009t0005g0015 others(13): Show |
18 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+835_-14+838del others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060027 | |||||||
chr17:69060142 | T | G | 103 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0007t0001g0088 others(100): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-14+724A>C | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060142 | |||||||
chr17:69060207 | T | C | 1 | a0002c0004t0002g0262 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-14+659A>G | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060207 | |||||||
chr17:69060521 | AAAAC | A | 108 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-14+341_-14+344del others(4): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060521 | |||||||
chr17:69060599 | ATT | A | 28 | a0004c0005t0003g0001 a0004c0005t0003g0263 a0004c0005t0003g0264 others(25): Show |
34 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+265_-14+266del others(2): Show |
ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060599 | |||||||
chr17:69060765 | C | T | 1 | a0002c0002t0002g0016 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-14+101G>A | ABCA9 | ENSG00000154258.17 | transcript | ENST00000340001.9 | protein_coding | 1/38 | chr17 | 69060765 |