Item | Value |
---|---|
geneid | 316 |
ensemblid | ENSG00000138356.14 |
hgncid | 553 |
symbol | AOX1 |
name | aldehyde oxidase 1 |
refseq_nuc | NM_001159.4 |
refseq_prot | NP_001150.3 |
ensembl_nuc | ENST00000374700.7 |
ensembl_prot | ENSP00000363832.2 |
mane_status | MANE Select |
chr | chr2 |
start | 200586014 |
end | 200671495 |
strand | + |
ver | v1.2 |
region | chr2:200586014-200671495 |
region5000 | chr2:200581014-200676495 |
regionname0 | AOX1_chr2_200586014_200671495 |
regionname5000 | AOX1_chr2_200581014_200676495 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1338 | 279 | 52 | 54 | 131 | 8 | 33 | 99 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0002 | 0/1 | 1338 | 38 | 1 | 11 | 18 | 2 | 5 | 13 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0003 | 0/0 | 1338 | 26 | 21 | 0 | 0 | 2 | 3 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0004 | 0/0 | 1338 | 8 | 0 | 4 | 4 | 0 | 0 | 4 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0005 | 0/0 | 1338 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0006 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0007 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0008 | 0/0 | 965 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(960): Show |
chr2 | 200581014 | 200676495 |
a0009 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0010 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0011 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0012 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0013 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0014 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0015 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0016 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0017 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0018 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
a0019 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | MDRAS others(1333): Show |
chr2 | 200581014 | 200676495 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 4014 | 265 | 42 | 53 | 130 | 7 | 32 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0005 | 0/0 | 4014 | 5 | 5 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0008 | 0/0 | 4014 | 3 | 3 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0014 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0019 | 0/0 | 4014 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0020 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0027 | 0/0 | 4014 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0029 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0001c0031 | 0/0 | 4014 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0002c0002 | 0/1 | 4014 | 38 | 1 | 11 | 18 | 2 | 5 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0003c0003 | 0/0 | 4014 | 17 | 13 | 0 | 0 | 2 | 2 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0003c0006 | 0/0 | 4014 | 4 | 4 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0003c0009 | 0/0 | 4014 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0003c0018 | 0/0 | 4014 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0003c0026 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0003c0030 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0004c0004 | 0/0 | 4014 | 8 | 0 | 4 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0005c0007 | 0/0 | 4014 | 4 | 0 | 0 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0006c0010 | 0/0 | 4014 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0007c0028 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0008c0025 | 0/0 | 4014 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0009c0015 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0010c0023 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0011c0017 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0012c0021 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0013c0024 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0014c0012 | 0/0 | 4014 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0015c0022 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0016c0016 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0017c0013 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0018c0011 | 0/0 | 4014 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 | ||
a0019c0032 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ATGGA others(4009): Show |
chr2 | 200581014 | 200676495 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4928 | 140 | 31 | 22 | 67 | 2 | 18 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0001t0002 | 0/0 | 4926 | 119 | 8 | 31 | 61 | 5 | 14 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0001t0005 | 1/0 | 4928 | 4 | 3 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0001t0008 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0001t0010 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0005t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0005t0002 | 0/0 | 4926 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0005t0004 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0005t0006 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0008t0001 | 0/0 | 4928 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0008t0002 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0014t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0019t0002 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0020t0001 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0027t0002 | 0/0 | 4926 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0001c0029t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0001c0031t0001 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0002c0002t0002 | 0/0 | 4926 | 7 | 0 | 0 | 7 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0002c0002t0003 | 0/1 | 4928 | 30 | 0 | 11 | 11 | 2 | 5 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0002c0002t0007 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0003c0003t0001 | 0/0 | 4928 | 10 | 6 | 0 | 0 | 2 | 2 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0003c0003t0004 | 0/0 | 4926 | 6 | 6 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0003c0003t0006 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0003c0006t0001 | 0/0 | 4928 | 4 | 4 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0003c0009t0001 | 0/0 | 4928 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0003c0018t0001 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0003c0026t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0003c0030t0002 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0004c0004t0001 | 0/0 | 4928 | 7 | 0 | 3 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0004c0004t0002 | 0/0 | 4926 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0005c0007t0002 | 0/0 | 4926 | 4 | 0 | 0 | 4 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0006c0010t0007 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0006c0010t0009 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0007c0028t0001 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0008c0025t0003 | 0/0 | 4928 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0009c0015t0002 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0010c0023t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0011c0017t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0012c0021t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0013c0024t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0014c0012t0001 | 0/0 | 4928 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0015c0022t0002 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0016c0016t0002 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0017c0013t0002 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4921): Show |
chr2 | 200581014 | 200676495 |
a0018c0011t0001 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
a0019c0032t0001 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | ACTCG others(4923): Show |
chr2 | 200581014 | 200676495 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0005g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0008g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0001t0010g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0005t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0005t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0005t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0005t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0008t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0008t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0014t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0019t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0020t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0027t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0029t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0001c0031t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0002c0002t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0003t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0006t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0009t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0009t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0018t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0026t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0003c0030t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0004c0004t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0005c0007t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0005c0007t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0005c0007t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0005c0007t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0006c0010t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0006c0010t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0007c0028t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0008c0025t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0009c0015t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0010c0023t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0011c0017t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0012c0021t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0013c0024t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0014c0012t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0015c0022t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0016c0016t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0017c0013t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0018c0011t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
a0019c0032t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0294 | EUR | GBR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00140 | hp2 | a0001 | c0019 | t0002 | g0149 | EUR | GBR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | FIN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00408 | hp1 | a0005 | c0007 | t0002 | g0221 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00408 | hp2 | a0007 | c0028 | t0001 | g0312 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00423 | hp2 | a0001 | c0001 | t0008 | g0343 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00642 | hp1 | a0004 | c0004 | t0001 | g0301 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | CHS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0364 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00738 | hp1 | a0001 | c0027 | t0002 | g0030 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01106 | hp1 | a0002 | c0002 | t0003 | g0047 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0068 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01255 | hp2 | a0008 | c0025 | t0003 | g0285 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01346 | hp1 | a0002 | c0002 | t0003 | g0044 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0066 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01361 | hp1 | a0002 | c0002 | t0003 | g0072 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01515 | hp1 | a0003 | c0003 | t0001 | g0243 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01515 | hp2 | a0002 | c0002 | t0003 | g0046 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0248 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01517 | hp2 | a0002 | c0002 | t0003 | g0045 | EUR | IBS | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01884 | hp2 | a0001 | c0005 | t0002 | g0215 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01934 | hp2 | a0002 | c0002 | t0003 | g0071 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01943 | hp2 | a0002 | c0002 | t0003 | g0200 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01981 | hp1 | a0004 | c0004 | t0002 | g0288 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01993 | hp2 | a0004 | c0004 | t0001 | g0300 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02040 | hp1 | a0002 | c0002 | t0003 | g0049 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02055 | hp2 | a0003 | c0009 | t0001 | g0098 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02071 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02148 | hp2 | a0002 | c0002 | t0003 | g0067 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CDX | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02258 | hp1 | a0003 | c0006 | t0001 | g0095 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02258 | hp2 | a0001 | c0005 | t0004 | g0296 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02273 | hp1 | a0004 | c0004 | t0001 | g0299 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02273 | hp2 | a0002 | c0002 | t0003 | g0065 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0069 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0217 | EAS | KHV | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02602 | hp1 | a0001 | c0031 | t0001 | g0080 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02622 | hp2 | a0009 | c0015 | t0002 | g0075 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02647 | hp1 | a0003 | c0003 | t0004 | g0274 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02698 | hp1 | a0002 | c0002 | t0003 | g0082 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02723 | hp1 | a0003 | c0003 | t0004 | g0212 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02723 | hp2 | a0003 | c0003 | t0004 | g0094 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02809 | hp2 | a0010 | c0023 | t0001 | g0249 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02886 | hp1 | a0003 | c0003 | t0001 | g0091 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0097 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02895 | hp1 | a0003 | c0006 | t0001 | g0093 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02965 | hp1 | a0001 | c0008 | t0002 | g0201 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02970 | hp1 | a0001 | c0008 | t0001 | g0051 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02976 | hp1 | a0011 | c0017 | t0001 | g0064 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02976 | hp2 | a0003 | c0006 | t0001 | g0122 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0096 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03041 | hp2 | a0012 | c0021 | t0001 | g0257 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03130 | hp2 | a0003 | c0003 | t0004 | g0207 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03209 | hp1 | a0003 | c0003 | t0004 | g0074 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03209 | hp2 | a0001 | c0029 | t0001 | g0077 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03225 | hp2 | a0003 | c0026 | t0001 | g0211 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0060 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03453 | hp2 | a0006 | c0010 | t0007 | g0279 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03486 | hp2 | a0002 | c0002 | t0007 | g0250 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03491 | hp1 | a0002 | c0002 | t0003 | g0263 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0272 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03540 | hp1 | a0001 | c0005 | t0006 | g0076 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03540 | hp2 | a0013 | c0024 | t0001 | g0213 | AFR | GWD | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0053 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03669 | hp2 | a0002 | c0002 | t0003 | g0041 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03704 | hp2 | a0003 | c0018 | t0001 | g0220 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0247 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0363 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03927 | hp1 | a0014 | c0012 | t0001 | g0197 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0351 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04204 | hp2 | a0003 | c0003 | t0001 | g0259 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | STU | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18522 | hp2 | a0003 | c0030 | t0002 | g0216 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18747 | hp2 | a0015 | c0022 | t0002 | g0107 | EAS | CHB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18906 | hp1 | a0001 | c0014 | t0001 | g0352 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18906 | hp2 | a0001 | c0005 | t0002 | g0061 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0347 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18950 | hp1 | a0001 | c0001 | t0010 | g0179 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0152 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18960 | hp1 | a0016 | c0016 | t0002 | g0112 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18960 | hp2 | a0004 | c0004 | t0001 | g0303 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18974 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18977 | hp2 | a0004 | c0004 | t0001 | g0326 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18978 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18979 | hp1 | a0005 | c0007 | t0002 | g0240 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18987 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19004 | hp1 | a0001 | c0020 | t0001 | g0228 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19007 | hp1 | a0004 | c0004 | t0001 | g0304 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19007 | hp2 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0210 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19056 | hp1 | a0005 | c0007 | t0002 | g0208 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19060 | hp1 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19062 | hp1 | a0004 | c0004 | t0001 | g0302 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19070 | hp1 | a0017 | c0013 | t0002 | g0140 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19074 | hp2 | a0018 | c0011 | t0001 | g0171 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19082 | hp1 | a0005 | c0007 | t0002 | g0238 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19082 | hp2 | a0002 | c0002 | t0003 | g0151 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19240 | hp1 | a0019 | c0032 | t0001 | g0275 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0287 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0159 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0292 | EUR | TSI | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0366 | AMR | CLM | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02109 | hp1 | a0003 | c0009 | t0001 | g0360 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02109 | hp2 | a0003 | c0003 | t0004 | g0209 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02486 | hp2 | a0001 | c0008 | t0001 | g0361 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03471 | hp1 | a0006 | c0010 | t0009 | g0278 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
HG06807 | hp2 | a0003 | c0006 | t0001 | g0106 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0224 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA20300 | hp2 | a0003 | c0003 | t0006 | g0328 | AFR | USA | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0365 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
NA21309 | hp2 | a0003 | c0003 | t0001 | g0246 | AFR | LWK | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0026 | REF | REF | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0054 | REF | REF | AOX1_chr2_200581014_200676495 | AOX1 | chr2 | 200581014 | 200676495 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200599627 | T | C | 1 | a0018 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.317T>C | p.Ile106Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/35 | 412/4928 | 317/4017 | 106/1338 | chr2 | 200599627 | |||
chr2:200599743 | G | A | 1 | a0014 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.433G>A | p.Gly145Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/35 | 528/4928 | 433/4017 | 145/1338 | chr2 | 200599743 | |||
chr2:200609017 | A | G | 1 | a0019 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.941A>G | p.Gln314Arg | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 11/35 | 1036/4928 | 941/4017 | 314/1338 | chr2 | 200609017 | |||
chr2:200612631 | G | A | 1 | a0017 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.1286G>A | p.Arg429Gln | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/35 | 1381/4928 | 1286/4017 | 429/1338 | chr2 | 200612631 | |||
chr2:200613946 | T | A | 1 | a0009 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1591T>A | p.Ser531Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/35 | 1686/4928 | 1591/4017 | 531/1338 | chr2 | 200613946 | |||
chr2:200620738 | T | A | 1 | a0004 | 8 | HG00642.hp1 HG01981.hp1 HG01993.hp2 others(5): Show |
missense_variant | MODERATE | c.1793T>A | p.Ile598Asn | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/35 | 1888/4928 | 1793/4017 | 598/1338 | chr2 | 200620738 | |||
chr2:200620761 | G | A | 1 | a0016 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.1816G>A | p.Val606Met | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/35 | 1911/4928 | 1816/4017 | 606/1338 | chr2 | 200620761 | |||
chr2:200621220 | G | A | 1 | a0011 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1975G>A | p.Ala659Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/35 | 2070/4928 | 1975/4017 | 659/1338 | chr2 | 200621220 | |||
chr2:200634833 | C | T | 1 | a0005 | 4 | HG00408.hp1 NA18979.hp1 NA19056.hp1 others(1): Show |
missense_variant | MODERATE | c.2264C>T | p.Thr755Ile | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/35 | 2359/4928 | 2264/4017 | 755/1338 | chr2 | 200634833 | |||
chr2:200634886 | G | T | 1 | a0007 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.2317G>T | p.Val773Leu | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/35 | 2412/4928 | 2317/4017 | 773/1338 | chr2 | 200634886 | |||
chr2:200651022 | C | T | 1 | a0008 | 1 | HG01255.hp2 | stop_gained | HIGH | c.2896C>T | p.Gln966* | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/35 | 2991/4928 | 2896/4017 | 966/1338 | chr2 | 200651022 | |||
chr2:200659241 | C | G | 1 | a0013 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.3248C>G | p.Ala1083Gly | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/35 | 3343/4928 | 3248/4017 | 1083/1338 | chr2 | 200659241 | |||
chr2:200659279 | G | A | 1 | a0012 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3286G>A | p.Gly1096Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/35 | 3381/4928 | 3286/4017 | 1096/1338 | chr2 | 200659279 | |||
chr2:200661607 | A | G | 3 | a0003 a0006 a0013 |
29 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(26): Show |
missense_variant | MODERATE | c.3404A>G | p.Asn1135Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/35 | 3499/4928 | 3404/4017 | 1135/1338 | chr2 | 200661607 | |||
chr2:200662889 | G | A | 1 | a0015 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.3463G>A | p.Glu1155Lys | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/35 | 3558/4928 | 3463/4017 | 1155/1338 | chr2 | 200662889 | |||
chr2:200668648 | T | C | 1 | a0010 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.3643T>C | p.Tyr1215His | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/35 | 3738/4928 | 3643/4017 | 1215/1338 | chr2 | 200668648 | |||
chr2:200669666 | A | G | 3 | a0002 a0006 a0008 |
40 | HG00621.hp1 HG00673.hp2 HG01106.hp1 others(37): Show |
missense_variant | MODERATE | c.3890A>G | p.His1297Arg | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/35 | 3985/4928 | 3890/4017 | 1297/1338 | chr2 | 200669666 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200613804 | G | A | 1 | a0001c0014 | 1 | NA18906.hp1 | splice_region_variant&synonymous_variant | LOW | c.1449G>A | p.Arg483Arg | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/35 | 1544/4928 | 1449/4017 | 483/1338 | chr2 | 200613804 | |||
chr2:200616016 | T | C | 1 | a0003c0009 | 2 | HG02055.hp2 HG02109.hp1 |
synonymous_variant | LOW | c.1657T>C | p.Leu553Leu | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/35 | 1752/4928 | 1657/4017 | 553/1338 | chr2 | 200616016 | |||
chr2:200621192 | C | T | 1 | a0001c0031 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1947C>T | p.Asp649Asp | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/35 | 2042/4928 | 1947/4017 | 649/1338 | chr2 | 200621192 | |||
chr2:200627439 | A | G | 4 | a0001c0005 a0001c0029 a0003c0030 others(1): Show |
8 | HG01884.hp2 HG02258.hp2 HG02976.hp1 others(5): Show |
synonymous_variant | LOW | c.2211A>G | p.Gln737Gln | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/35 | 2306/4928 | 2211/4017 | 737/1338 | chr2 | 200627439 | |||
chr2:200636928 | C | G | 1 | a0001c0027 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.2364C>G | p.Thr788Thr | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/35 | 2459/4928 | 2364/4017 | 788/1338 | chr2 | 200636928 | |||
chr2:200636982 | G | A | 1 | a0003c0018 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.2418G>A | p.Ala806Ala | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/35 | 2513/4928 | 2418/4017 | 806/1338 | chr2 | 200636982 | |||
chr2:200641112 | C | T | 5 | a0001c0005 a0001c0008 a0003c0009 others(2): Show |
12 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
synonymous_variant | LOW | c.2583C>T | p.Asn861Asn | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/35 | 2678/4928 | 2583/4017 | 861/1338 | chr2 | 200641112 | |||
chr2:200641115 | T | C | 1 | a0001c0019 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.2586T>C | p.Asp862Asp | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/35 | 2681/4928 | 2586/4017 | 862/1338 | chr2 | 200641115 | |||
chr2:200651090 | G | A | 1 | a0001c0020 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.2964G>A | p.Leu988Leu | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/35 | 3059/4928 | 2964/4017 | 988/1338 | chr2 | 200651090 | |||
chr2:200668740 | C | T | 1 | a0003c0006 | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.3735C>T | p.Pro1245Pro | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/35 | 3830/4928 | 3735/4017 | 1245/1338 | chr2 | 200668740 | |||
chr2:200668797 | A | G | 1 | a0003c0006 | 4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.3792A>G | p.Ser1264Ser | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/35 | 3887/4928 | 3792/4017 | 1264/1338 | chr2 | 200668797 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200586027 | G | A | 1 | a0001c0001t0008 | 1 | HG00423.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-82G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/35 | chr2 | 200586027 | |||||||
chr2:200670851 | T | C | 2 | a0001c0005t0004 a0003c0003t0004 |
7 | HG02109.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*172T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 172 | chr2 | 200670851 | ||||||
chr2:200670923 | C | T | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(42): Show |
365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 244 | chr2 | 200670923 | ||||||
chr2:200671058 | T | G | 4 | a0001c0005t0006 a0002c0002t0003 a0003c0003t0006 others(1): Show |
32 | HG01106.hp1 HG01123.hp2 HG01192.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*379T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 379 | chr2 | 200671058 | ||||||
chr2:200671172 | C | T | 1 | a0001c0001t0010 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*493C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 493 | chr2 | 200671172 | ||||||
chr2:200671207 | G | A | 2 | a0002c0002t0003 a0008c0025t0003 |
30 | HG01106.hp1 HG01123.hp2 HG01192.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 528 | chr2 | 200671207 | ||||||
chr2:200671272 | CAT | C | 17 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(14): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*598_*599delAT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 598 | INFO_REALIGN_3_PRIME | chr2 | 200671272 | |||||
chr2:200671290 | C | A | 2 | a0002c0002t0007 a0006c0010t0007 |
2 | HG03453.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*611C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 611 | chr2 | 200671290 | ||||||
chr2:200671384 | A | C | 1 | a0006c0010t0009 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 35/35 | 705 | chr2 | 200671384 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200586239 | C | G | 3 | a0001c0001t0002g0364 a0001c0001t0002g0365 a0002c0002t0003g0366 |
3 | HG00733.hp1 HG01123.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.45+86C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586239 | |||||||
chr2:200586277 | T | C | 1 | a0001c0001t0002g0005 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.45+124T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586277 | |||||||
chr2:200586283 | C | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(277): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.45+130C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586283 | |||||||
chr2:200586291 | C | G | 1 | a0001c0001t0002g0363 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.45+138C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586291 | |||||||
chr2:200586545 | T | G | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+392T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586545 | |||||||
chr2:200586655 | C | A | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+502C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586655 | |||||||
chr2:200586686 | A | G | 1 | a0001c0001t0002g0362 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.45+533A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586686 | |||||||
chr2:200586723 | A | G | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+570A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586723 | |||||||
chr2:200586868 | C | G | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+715C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586868 | |||||||
chr2:200586870 | G | A | 1 | a0003c0009t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.45+717G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586870 | |||||||
chr2:200586903 | C | T | 2 | a0003c0009t0001g0098 a0003c0009t0001g0360 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.45+750C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586903 | |||||||
chr2:200586924 | A | G | 83 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(80): Show |
83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.45+771A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586924 | |||||||
chr2:200586931 | A | G | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+778A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200586931 | |||||||
chr2:200587103 | C | CA | 11 | a0001c0001t0001g0006 a0001c0001t0001g0105 a0001c0001t0001g0280 others(8): Show |
11 | HG02738.hp2 HG04199.hp2 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+960dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200587103 | ||||||
chr2:200587112 | AACC | A | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+961_45+963delCC others(1): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200587112 | ||||||
chr2:200587114 | C | A | 2 | a0001c0001t0002g0289 a0001c0008t0001g0361 |
2 | HG01361.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.45+961C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587114 | |||||||
chr2:200587115 | C | A | 2 | a0001c0008t0001g0361 a0006c0010t0009g0278 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.45+962C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587115 | |||||||
chr2:200587124 | C | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(102): Show |
107 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.45+971C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587124 | |||||||
chr2:200587126 | A | C | 2 | a0001c0008t0002g0201 a0002c0002t0002g0202 |
2 | HG02965.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.45+973A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587126 | |||||||
chr2:200587137 | A | C | 1 | a0018c0011t0001g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.45+984A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587137 | |||||||
chr2:200587753 | A | G | 1 | a0001c0001t0002g0359 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.45+1600A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200587753 | |||||||
chr2:200588025 | G | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
6 | NA18947.hp2 NA18948.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+1872G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588025 | |||||||
chr2:200588111 | G | T | 1 | a0003c0006t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.45+1958G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588111 | |||||||
chr2:200588229 | C | G | 9 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+2076C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588229 | |||||||
chr2:200588273 | A | G | 9 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+2120A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588273 | |||||||
chr2:200588329 | T | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(109): Show |
114 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.45+2176T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588329 | |||||||
chr2:200588334 | T | A | 7 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+2181T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588334 | |||||||
chr2:200588451 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0002g0014 |
3 | HG02132.hp1 NA18961.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.45+2298T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588451 | |||||||
chr2:200588726 | C | CT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
14 | HG01975.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+2594dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+2588_45+2594dup others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.45+2583_45+2584ins others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(4): Show |
1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+2584_45+2594dup others(11): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0282 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+2580_45+2594dup others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0283 a0001c0001t0002g0284 a0003c0030t0002g0216 |
3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.45+2579_45+2594dup others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0218 a0001c0001t0002g0286 a0001c0001t0002g0287 others(3): Show |
6 | HG01070.hp2 HG01255.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+2578_45+2594dup others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(11): Show |
36 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(33): Show |
36 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.45+2577_45+2594dup others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(12): Show |
46 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0239 others(43): Show |
46 | HG00408.hp2 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.45+2576_45+2594dup others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(13): Show |
36 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0258 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.45+2575_45+2594dup others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(14): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0268 a0001c0001t0001g0269 others(11): Show |
15 | HG01243.hp2 HG01261.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+2574_45+2594dup others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0105 a0001c0001t0001g0357 a0001c0001t0002g0276 others(2): Show |
5 | HG01106.hp2 HG01358.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+2594_45+2595ins others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0358 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.45+2594_45+2595ins others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | CT | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG00597.hp1 HG02965.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+2594delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588726 | CTT | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(101): Show |
106 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.45+2593_45+2594del others(2): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200588726 | ||||||
chr2:200588754 | G | A | 1 | a0003c0003t0004g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2601G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588754 | |||||||
chr2:200588905 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0218 a0001c0001t0001g0232 others(12): Show |
16 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+2752C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200588905 | |||||||
chr2:200589028 | G | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0218 others(104): Show |
108 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.45+2875G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589028 | |||||||
chr2:200589225 | C | A | 43 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.45+3072C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589225 | |||||||
chr2:200589346 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+3193A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589346 | |||||||
chr2:200589501 | G | A | 10 | a0001c0001t0002g0092 a0001c0005t0002g0215 a0003c0003t0001g0091 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+3348G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589501 | |||||||
chr2:200589520 | G | A | 10 | a0001c0001t0002g0092 a0001c0005t0002g0215 a0003c0003t0001g0091 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+3367G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589520 | |||||||
chr2:200589566 | C | A | 44 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(41): Show |
44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.45+3413C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589566 | |||||||
chr2:200589612 | TAGC | T | 10 | a0001c0001t0002g0092 a0001c0005t0002g0215 a0003c0003t0001g0091 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+3462_45+3464del others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200589612 | ||||||
chr2:200589620 | TGG | T | 85 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.45+3469_45+3470del others(2): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chr2 | 200589620 | ||||||
chr2:200589726 | G | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0261 a0001c0001t0002g0262 others(2): Show |
5 | HG01934.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3420G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589726 | |||||||
chr2:200589902 | G | A | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-3244G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200589902 | |||||||
chr2:200590035 | C | T | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-3111C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590035 | |||||||
chr2:200590098 | C | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-3048C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590098 | |||||||
chr2:200590417 | A | C | 2 | a0002c0002t0003g0263 a0002c0002t0003g0272 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.46-2729A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590417 | |||||||
chr2:200590446 | T | G | 2 | a0003c0003t0001g0210 a0003c0003t0004g0209 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.46-2700T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590446 | |||||||
chr2:200590522 | C | A | 1 | a0002c0002t0002g0099 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.46-2624C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590522 | |||||||
chr2:200590585 | A | C | 1 | a0001c0001t0002g0104 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.46-2561A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590585 | |||||||
chr2:200590622 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.46-2524G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200590622 | |||||||
chr2:200591000 | C | T | 44 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(41): Show |
44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.46-2146C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591000 | |||||||
chr2:200591051 | A | G | 54 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(51): Show |
54 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-2095A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591051 | |||||||
chr2:200591113 | T | C | 8 | a0001c0001t0001g0203 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-2033T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591113 | |||||||
chr2:200591207 | C | T | 48 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.46-1939C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591207 | |||||||
chr2:200591240 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.46-1906G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591240 | |||||||
chr2:200591325 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.46-1821G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591325 | |||||||
chr2:200591361 | A | T | 48 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.46-1785A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591361 | |||||||
chr2:200591435 | G | A | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.46-1711G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591435 | |||||||
chr2:200591495 | G | A | 1 | a0016c0016t0002g0112 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.46-1651G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591495 | |||||||
chr2:200591508 | T | A | 1 | a0015c0022t0002g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.46-1638T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591508 | |||||||
chr2:200591522 | G | A | 48 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.46-1624G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591522 | |||||||
chr2:200591530 | T | C | 1 | a0001c0001t0002g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.46-1616T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591530 | |||||||
chr2:200591555 | C | T | 1 | a0014c0012t0001g0197 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.46-1591C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591555 | |||||||
chr2:200591622 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0261 a0001c0001t0002g0262 others(2): Show |
5 | HG01934.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-1524G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591622 | |||||||
chr2:200591667 | A | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0218 others(20): Show |
24 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.46-1479A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591667 | |||||||
chr2:200591671 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0002g0108 |
2 | HG00609.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.46-1475G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591671 | |||||||
chr2:200591724 | T | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-1422T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591724 | |||||||
chr2:200591769 | C | G | 43 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.46-1377C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591769 | |||||||
chr2:200591786 | G | A | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-1360G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200591786 | |||||||
chr2:200592549 | G | GC | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-597_46-596insC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592549 | |||||||
chr2:200592747 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0307 others(1): Show |
4 | HG02486.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-399G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592747 | |||||||
chr2:200592801 | C | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0002c0002t0002g0099 |
3 | HG00423.hp1 NA18612.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.46-345C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592801 | |||||||
chr2:200592887 | T | C | 54 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(51): Show |
54 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-259T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200592887 | |||||||
chr2:200593027 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0269 |
2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.46-119A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200593027 | |||||||
chr2:200593048 | G | T | 1 | a0010c0023t0001g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-98G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200593048 | |||||||
chr2:200593104 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.46-42T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 1/34 | chr2 | 200593104 | |||||||
chr2:200593204 | G | A | 1 | a0002c0002t0003g0110 | 1 | NA18968.hp1 | splice_donor_variant&intron_variant | HIGH | c.103+1G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593204 | |||||||
chr2:200593220 | T | C | 1 | a0001c0008t0002g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103+17T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593220 | |||||||
chr2:200593485 | T | TA | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.103+283dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr2 | 200593485 | ||||||
chr2:200593690 | G | A | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0002g0111 others(4): Show |
7 | HG06807.hp1 NA18960.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+487G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593690 | |||||||
chr2:200593737 | A | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.103+534A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200593737 | |||||||
chr2:200594040 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.103+837G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594040 | |||||||
chr2:200594139 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.103+936T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594139 | |||||||
chr2:200594296 | G | A | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.104-976G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594296 | |||||||
chr2:200594305 | G | A | 1 | a0001c0001t0002g0020 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.104-967G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594305 | |||||||
chr2:200594441 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(104): Show |
109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.104-831T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594441 | |||||||
chr2:200594722 | A | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
19 | HG00597.hp1 HG00639.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.104-550A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594722 | |||||||
chr2:200594855 | C | T | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.104-417C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594855 | |||||||
chr2:200594889 | T | A | 3 | a0001c0001t0001g0117 a0001c0001t0005g0002 a0001c0001t0005g0116 |
4 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-383T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594889 | |||||||
chr2:200594988 | C | T | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.104-284C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200594988 | |||||||
chr2:200595048 | T | C | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.104-224T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 2/34 | chr2 | 200595048 | |||||||
chr2:200595381 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(104): Show |
109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.200+13A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595381 | |||||||
chr2:200595539 | A | G | 2 | a0003c0003t0001g0210 a0003c0003t0004g0209 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.200+171A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595539 | |||||||
chr2:200595553 | T | A | 2 | a0003c0003t0001g0097 a0006c0010t0007g0279 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.200+185T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595553 | |||||||
chr2:200595584 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.200+216C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595584 | |||||||
chr2:200595593 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(104): Show |
109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.200+225G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595593 | |||||||
chr2:200595599 | T | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.200+231T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595599 | |||||||
chr2:200595828 | T | C | 1 | a0003c0003t0004g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.200+460T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595828 | |||||||
chr2:200595965 | G | T | 1 | a0001c0001t0001g0329 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.200+597G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200595965 | |||||||
chr2:200596118 | G | C | 303 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(300): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.200+750G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596118 | |||||||
chr2:200596315 | T | C | 1 | a0001c0001t0002g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.200+947T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596315 | |||||||
chr2:200596368 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
23 | HG00597.hp1 HG00639.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.200+1000C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596368 | |||||||
chr2:200596515 | G | A | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201-882G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596515 | |||||||
chr2:200596659 | G | T | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-738G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596659 | |||||||
chr2:200596761 | GTTTA | G | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-625_201-622del others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr2 | 200596761 | ||||||
chr2:200596981 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.201-416C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200596981 | |||||||
chr2:200597002 | A | G | 2 | a0003c0003t0001g0097 a0006c0010t0007g0279 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.201-395A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597002 | |||||||
chr2:200597091 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(104): Show |
109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.201-306G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597091 | |||||||
chr2:200597160 | C | A | 47 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(44): Show |
47 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.201-237C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597160 | |||||||
chr2:200597230 | C | A | 8 | a0001c0001t0001g0203 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-167C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 3/34 | chr2 | 200597230 | |||||||
chr2:200597608 | C | T | 1 | a0003c0003t0001g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.309+103C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597608 | |||||||
chr2:200597634 | C | T | 48 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.309+129C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597634 | |||||||
chr2:200597926 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | NA18944.hp2 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+421T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597926 | |||||||
chr2:200597966 | G | A | 1 | a0003c0006t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.309+461G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597966 | |||||||
chr2:200597984 | A | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(266): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.309+479A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200597984 | |||||||
chr2:200598099 | C | T | 2 | a0001c0001t0001g0229 a0010c0023t0001g0249 |
2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.309+594C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598099 | |||||||
chr2:200598295 | T | G | 44 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(41): Show |
44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.309+790T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598295 | |||||||
chr2:200598399 | T | C | 1 | a0003c0003t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.309+894T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598399 | |||||||
chr2:200598565 | A | G | 1 | a0012c0021t0001g0257 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.310-1055A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598565 | |||||||
chr2:200598652 | GA | G | 133 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(130): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.310-966delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chr2 | 200598652 | ||||||
chr2:200598655 | T | G | 133 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(130): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.310-965T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598655 | |||||||
chr2:200598787 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0218 others(22): Show |
26 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.310-833T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200598787 | |||||||
chr2:200599005 | G | A | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.310-615G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599005 | |||||||
chr2:200599262 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.310-358C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599262 | |||||||
chr2:200599372 | G | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(131): Show |
137 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.310-248G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599372 | |||||||
chr2:200599441 | C | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.310-179C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599441 | |||||||
chr2:200599490 | C | T | 2 | a0001c0005t0002g0215 a0001c0008t0001g0361 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.310-130C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599490 | |||||||
chr2:200599496 | G | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0085 others(1): Show |
4 | HG00597.hp1 HG03927.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-124G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599496 | |||||||
chr2:200599537 | A | G | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.310-83A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599537 | |||||||
chr2:200599572 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(222): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.310-48T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 4/34 | chr2 | 200599572 | |||||||
chr2:200599807 | C | A | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+61C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200599807 | |||||||
chr2:200599842 | C | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0218 others(106): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.436+96C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200599842 | |||||||
chr2:200599931 | C | T | 8 | a0001c0001t0001g0203 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.436+185C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200599931 | |||||||
chr2:200600042 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.436+296T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600042 | |||||||
chr2:200600069 | C | G | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.436+323C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600069 | |||||||
chr2:200600229 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.436+483A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600229 | |||||||
chr2:200600245 | T | C | 1 | a0002c0002t0002g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.436+499T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600245 | |||||||
chr2:200600475 | C | CG | 53 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(50): Show |
53 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.436+737dupG | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200600475 | ||||||
chr2:200600475 | CG | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(198): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.436+737delG | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200600475 | ||||||
chr2:200600478 | G | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.436+732G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600478 | |||||||
chr2:200600503 | T | C | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+757T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600503 | |||||||
chr2:200600568 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0218 others(20): Show |
24 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.436+822C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600568 | |||||||
chr2:200600660 | G | A | 1 | a0003c0003t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.436+914G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600660 | |||||||
chr2:200600789 | T | C | 1 | a0001c0008t0002g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.436+1043T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600789 | |||||||
chr2:200600834 | T | A | 43 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+1088T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600834 | |||||||
chr2:200600949 | G | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(222): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.436+1203G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600949 | |||||||
chr2:200600995 | T | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(222): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.436+1249T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200600995 | |||||||
chr2:200601073 | C | CTTT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0105 a0001c0001t0001g0117 others(129): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.437-1195_437-1193d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | ||||||
chr2:200601073 | C | CTTTT | 25 | a0001c0001t0001g0004 a0001c0001t0001g0187 a0001c0001t0001g0188 others(22): Show |
26 | HG00621.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.437-1196_437-1193d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | ||||||
chr2:200601073 | C | CTTTTT | 11 | a0001c0001t0001g0194 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
11 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-1197_437-1193d others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | ||||||
chr2:200601073 | CT | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0085 others(7): Show |
10 | HG00597.hp1 HG03225.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1193delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | ||||||
chr2:200601073 | CTT | C | 87 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.437-1194_437-1193d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601073 | ||||||
chr2:200601118 | G | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0273 a0003c0003t0004g0274 |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-1166G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601118 | |||||||
chr2:200601126 | C | A | 1 | a0001c0001t0001g0330 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.437-1158C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601126 | |||||||
chr2:200601373 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(104): Show |
109 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.437-911T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601373 | |||||||
chr2:200601612 | G | A | 303 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(300): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.437-672G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601612 | |||||||
chr2:200601632 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.437-652T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601632 | |||||||
chr2:200601632 | T | TA | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(122): Show |
128 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.437-642dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chr2 | 200601632 | ||||||
chr2:200601643 | T | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.437-641T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601643 | |||||||
chr2:200601698 | T | G | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(276): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.437-586T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601698 | |||||||
chr2:200601831 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.437-453G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601831 | |||||||
chr2:200601857 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.437-427C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601857 | |||||||
chr2:200601898 | A | G | 1 | a0002c0002t0002g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.437-386A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601898 | |||||||
chr2:200601913 | G | A | 2 | a0003c0003t0001g0210 a0003c0003t0004g0209 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.437-371G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200601913 | |||||||
chr2:200602009 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(222): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.437-275T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602009 | |||||||
chr2:200602152 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.437-132T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602152 | |||||||
chr2:200602176 | C | G | 1 | a0002c0002t0002g0347 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.437-108C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602176 | |||||||
chr2:200602200 | G | A | 1 | a0003c0006t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.437-84G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602200 | |||||||
chr2:200602231 | C | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.437-53C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 5/34 | chr2 | 200602231 | |||||||
chr2:200602392 | C | T | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.498+47C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602392 | |||||||
chr2:200602417 | TA | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0002g0014 |
3 | HG02132.hp1 NA18961.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.498+73delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602417 | |||||||
chr2:200602508 | A | G | 87 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.498+163A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602508 | |||||||
chr2:200602601 | T | C | 9 | a0001c0001t0002g0206 a0003c0003t0001g0210 a0003c0003t0004g0207 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.498+256T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602601 | |||||||
chr2:200602783 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.498+438T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602783 | |||||||
chr2:200602840 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0002g0174 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.499-427A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200602840 | |||||||
chr2:200603156 | G | T | 8 | a0001c0001t0002g0070 a0002c0002t0003g0065 a0002c0002t0003g0066 others(5): Show |
8 | HG01192.hp2 HG01358.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-111G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 6/34 | chr2 | 200603156 | |||||||
chr2:200603357 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | splice_donor_variant&intron_variant | HIGH | c.588+1G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603357 | |||||||
chr2:200603371 | A | G | 1 | a0011c0017t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.588+15A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603371 | |||||||
chr2:200603456 | G | A | 1 | a0003c0003t0004g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.588+100G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603456 | |||||||
chr2:200603792 | T | C | 87 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.589-225T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603792 | |||||||
chr2:200603797 | G | T | 43 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.589-220G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603797 | |||||||
chr2:200603798 | G | T | 43 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.589-219G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603798 | |||||||
chr2:200603799 | A | T | 43 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.589-218A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603799 | |||||||
chr2:200603880 | G | A | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589-137G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603880 | |||||||
chr2:200603915 | G | C | 6 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-102G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200603915 | |||||||
chr2:200604009 | C | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(103): Show |
108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
splice_region_variant&intron_variant | LOW | c.589-8C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 7/34 | chr2 | 200604009 | |||||||
chr2:200604187 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.669+90T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604187 | |||||||
chr2:200604207 | C | T | 2 | a0003c0003t0001g0210 a0003c0003t0004g0209 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.669+110C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604207 | |||||||
chr2:200604321 | T | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+224T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604321 | |||||||
chr2:200604366 | T | G | 95 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(92): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.669+269T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604366 | |||||||
chr2:200604415 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18947.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.670-281C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604415 | |||||||
chr2:200604426 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-270A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604426 | |||||||
chr2:200604528 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0273 others(2): Show |
6 | HG02647.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-168T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604528 | |||||||
chr2:200604661 | T | C | 1 | a0003c0006t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.670-35T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 8/34 | chr2 | 200604661 | |||||||
chr2:200604902 | G | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(28): Show |
31 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.814+62G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200604902 | |||||||
chr2:200604958 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.814+118A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200604958 | |||||||
chr2:200604963 | T | G | 1 | a0001c0001t0001g0306 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.814+123T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200604963 | |||||||
chr2:200605031 | C | T | 17 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(14): Show |
17 | HG01192.hp1 HG01261.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.814+191C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605031 | |||||||
chr2:200605068 | C | G | 95 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(92): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.814+228C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605068 | |||||||
chr2:200605122 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
23 | HG00597.hp1 HG00639.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.814+282C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605122 | |||||||
chr2:200605225 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0218 a0001c0001t0001g0232 others(12): Show |
16 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.815-311G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605225 | |||||||
chr2:200605263 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0187 a0001c0001t0002g0204 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-273C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605263 | |||||||
chr2:200605312 | A | G | 1 | a0001c0001t0002g0165 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.815-224A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | chr2 | 200605312 | |||||||
chr2:200605510 | A | AT | 29 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(26): Show |
29 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.815-11dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | ||||||
chr2:200605510 | AT | A | 28 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0042 others(25): Show |
28 | HG01106.hp1 HG01123.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.815-11delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | ||||||
chr2:200605510 | ATT | A | 19 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(16): Show |
19 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.815-12_815-11delTT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | ||||||
chr2:200605510 | ATTT | A | 77 | a0001c0001t0001g0117 a0001c0001t0001g0163 a0001c0001t0001g0281 others(74): Show |
77 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.815-13_815-11delTT others(1): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | ||||||
chr2:200605510 | ATTTT | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0120 others(123): Show |
129 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.815-14_815-11delTT others(2): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chr2 | 200605510 | ||||||
chr2:200605631 | G | A | 8 | a0001c0001t0001g0203 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.907+3G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200605631 | |||||||
chr2:200605693 | C | G | 2 | a0001c0001t0001g0227 a0001c0001t0002g0244 |
2 | NA19005.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.907+65C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200605693 | |||||||
chr2:200605991 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.907+363A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200605991 | |||||||
chr2:200606420 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.907+792C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606420 | |||||||
chr2:200606532 | G | A | 7 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.907+904G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606532 | |||||||
chr2:200606609 | C | T | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.907+981C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606609 | |||||||
chr2:200606821 | C | G | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.907+1193C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606821 | |||||||
chr2:200606825 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.907+1197T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606825 | |||||||
chr2:200606889 | C | T | 3 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0365 |
3 | HG01433.hp2 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.907+1261C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606889 | |||||||
chr2:200606957 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.907+1329A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200606957 | |||||||
chr2:200607152 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(224): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.907+1524A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607152 | |||||||
chr2:200607342 | G | A | 1 | a0012c0021t0001g0257 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.908-1642G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607342 | |||||||
chr2:200607359 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0002g0162 |
3 | HG00642.hp2 HG00733.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.908-1625C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607359 | |||||||
chr2:200607540 | G | A | 4 | a0001c0001t0001g0309 a0001c0001t0002g0310 a0002c0002t0002g0099 others(1): Show |
4 | HG00673.hp1 NA18944.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.908-1444G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607540 | |||||||
chr2:200607568 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.908-1416A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607568 | |||||||
chr2:200607569 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.908-1415G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607569 | |||||||
chr2:200607705 | T | C | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.908-1279T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200607705 | |||||||
chr2:200608023 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.908-961G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608023 | |||||||
chr2:200608039 | A | G | 1 | a0003c0018t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.908-945A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608039 | |||||||
chr2:200608046 | G | T | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.908-938G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608046 | |||||||
chr2:200608316 | G | A | 1 | a0002c0002t0003g0040 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.908-668G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608316 | |||||||
chr2:200608389 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.908-595C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608389 | |||||||
chr2:200608734 | A | AC | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(267): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.908-246dupC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | INFO_REALIGN_3_PRIME | chr2 | 200608734 | ||||||
chr2:200608802 | C | A | 1 | a0001c0001t0002g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.908-182C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608802 | |||||||
chr2:200608876 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.908-108G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608876 | |||||||
chr2:200608951 | G | A | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(267): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.908-33G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 10/34 | chr2 | 200608951 | |||||||
chr2:200609456 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1153+42C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609456 | |||||||
chr2:200609511 | C | T | 20 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(17): Show |
20 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1153+97C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609511 | |||||||
chr2:200609514 | A | G | 95 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(92): Show |
95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1153+100A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609514 | |||||||
chr2:200609601 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1153+187T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609601 | |||||||
chr2:200609713 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(267): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1153+299A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609713 | |||||||
chr2:200609826 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0105 others(267): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1153+412A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609826 | |||||||
chr2:200609916 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1153+502A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609916 | |||||||
chr2:200609924 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1153+510G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200609924 | |||||||
chr2:200610076 | C | CT | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0062 others(246): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1153+675dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | INFO_REALIGN_3_PRIME | chr2 | 200610076 | ||||||
chr2:200610096 | G | T | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1153+682G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610096 | |||||||
chr2:200610202 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1153+788G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610202 | |||||||
chr2:200610434 | A | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(21): Show |
24 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1154-950A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610434 | |||||||
chr2:200610599 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1154-785A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610599 | |||||||
chr2:200610732 | C | G | 1 | a0011c0017t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1154-652C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200610732 | |||||||
chr2:200611000 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1154-384C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611000 | |||||||
chr2:200611045 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1154-339A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611045 | |||||||
chr2:200611101 | T | C | 1 | a0003c0003t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1154-283T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611101 | |||||||
chr2:200611151 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(224): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1154-233A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 12/34 | chr2 | 200611151 | |||||||
chr2:200611552 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1263+59T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611552 | |||||||
chr2:200611553 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1263+60C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611553 | |||||||
chr2:200611580 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1263+87G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611580 | |||||||
chr2:200611676 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1263+183C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611676 | |||||||
chr2:200611701 | T | A | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1263+208T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611701 | |||||||
chr2:200611707 | A | AT | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(143): Show |
148 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1263+229dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr2 | 200611707 | ||||||
chr2:200611707 | AT | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1263+229delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chr2 | 200611707 | ||||||
chr2:200611731 | G | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1263+238G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611731 | |||||||
chr2:200611736 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(130): Show |
136 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1263+243G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611736 | |||||||
chr2:200611807 | C | T | 2 | a0001c0001t0002g0164 a0002c0002t0002g0202 |
2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1263+314C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611807 | |||||||
chr2:200611893 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1263+400C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611893 | |||||||
chr2:200611894 | G | A | 9 | a0001c0001t0002g0206 a0003c0003t0001g0210 a0003c0003t0004g0207 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1263+401G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611894 | |||||||
chr2:200611901 | C | T | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1263+408C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611901 | |||||||
chr2:200611947 | C | T | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1263+454C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200611947 | |||||||
chr2:200612107 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1264-502A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200612107 | |||||||
chr2:200612442 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1264-167G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 13/34 | chr2 | 200612442 | |||||||
chr2:200612858 | C | T | 1 | a0003c0003t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1448+65C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200612858 | |||||||
chr2:200613003 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1448+226_1448+235d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613003 | ||||||
chr2:200613003 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0002g0169 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1448+224_1448+235d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613003 | ||||||
chr2:200613003 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0002g0161 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1448+222_1448+235d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613003 | ||||||
chr2:200613004 | G | C | 4 | a0001c0001t0001g0309 a0001c0001t0002g0310 a0002c0002t0002g0099 others(1): Show |
4 | HG00673.hp1 NA18944.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1448+211G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613004 | |||||||
chr2:200613025 | T | TGAGAGA | 37 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(34): Show |
37 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1448+233_1448+234i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613025 | ||||||
chr2:200613027 | T | A | 39 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(36): Show |
39 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1448+234T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613027 | |||||||
chr2:200613027 | T | TGAGAGA | 3 | a0001c0001t0001g0271 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG01106.hp2 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1448+247_1448+252d others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGAGAGAG others(1): Show |
85 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1448+245_1448+252d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGAGAG others(3): Show |
10 | a0001c0001t0001g0354 a0001c0001t0001g0357 a0001c0001t0002g0092 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGA | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0163 |
3 | HG01346.hp2 HG02015.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1448+235_1448+236i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGAG others(3): Show |
2 | a0001c0001t0001g0126 a0001c0001t0002g0176 |
2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGTG others(3): Show |
12 | a0001c0001t0001g0120 a0001c0001t0001g0127 a0001c0001t0001g0128 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGTG others(5): Show |
2 | a0001c0008t0002g0201 a0006c0010t0007g0279 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1448+235_1448+236i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGTG others(3): Show |
63 | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0134 others(60): Show |
64 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGTG others(5): Show |
12 | a0001c0001t0001g0203 a0001c0001t0001g0252 a0001c0001t0001g0255 others(9): Show |
12 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGTG others(5): Show |
8 | a0001c0001t0001g0117 a0001c0001t0002g0102 a0001c0001t0002g0160 others(5): Show |
9 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGTG others(7): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0218 a0001c0001t0001g0232 others(8): Show |
12 | HG00639.hp2 HG01243.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613027 | T | TGTGTGTG others(7): Show |
13 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0189 others(10): Show |
13 | NA18940.hp2 NA18947.hp1 NA18968.hp2 others(10): Show |
intron_variant | MODIFIER | c.1448+235_1448+236i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chr2 | 200613027 | ||||||
chr2:200613313 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1449-491G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613313 | |||||||
chr2:200613449 | T | G | 1 | a0003c0003t0004g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1449-355T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613449 | |||||||
chr2:200613505 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1449-299A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613505 | |||||||
chr2:200613541 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(224): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1449-263G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613541 | |||||||
chr2:200613559 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1449-245G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613559 | |||||||
chr2:200613563 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1449-241T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613563 | |||||||
chr2:200613768 | C | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1449-36C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613768 | |||||||
chr2:200613784 | C | T | 8 | a0001c0001t0001g0203 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1449-20C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 14/34 | chr2 | 200613784 | |||||||
chr2:200613997 | A | C | 2 | a0001c0001t0001g0003 a0001c0001t0002g0162 |
3 | HG00642.hp2 HG00733.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1611+31A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200613997 | |||||||
chr2:200614043 | T | A | 1 | a0001c0001t0002g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1611+77T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614043 | |||||||
chr2:200614055 | G | C | 1 | a0001c0001t0001g0357 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1611+89G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614055 | |||||||
chr2:200614131 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0173 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1611+165T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614131 | |||||||
chr2:200614173 | G | A | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(248): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1611+207G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614173 | |||||||
chr2:200614188 | C | T | 1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1611+222C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614188 | |||||||
chr2:200614214 | T | G | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(291): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1611+248T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614214 | |||||||
chr2:200614370 | A | G | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(291): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1611+404A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614370 | |||||||
chr2:200614417 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1611+451C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614417 | |||||||
chr2:200614733 | C | G | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(248): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1611+767C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614733 | |||||||
chr2:200614804 | C | T | 1 | a0018c0011t0001g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1611+838C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200614804 | |||||||
chr2:200615014 | AT | A | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(287): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1612-946delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chr2 | 200615014 | ||||||
chr2:200615300 | C | T | 7 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-671C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615300 | |||||||
chr2:200615386 | A | G | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(248): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1612-585A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615386 | |||||||
chr2:200615399 | G | A | 5 | a0001c0001t0002g0206 a0003c0003t0004g0207 a0003c0003t0004g0212 others(2): Show |
5 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1612-572G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615399 | |||||||
chr2:200615426 | A | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(109): Show |
113 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1612-545A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615426 | |||||||
chr2:200615599 | G | A | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1612-372G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615599 | |||||||
chr2:200615741 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1612-230G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615741 | |||||||
chr2:200615955 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1612-16T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 15/34 | chr2 | 200615955 | |||||||
chr2:200616069 | C | T | 13 | a0001c0001t0002g0070 a0002c0002t0003g0007 a0002c0002t0003g0040 others(10): Show |
13 | HG01192.hp2 HG01358.hp2 HG01361.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1704+6C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616069 | |||||||
chr2:200616212 | A | T | 1 | a0003c0003t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1704+149A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616212 | |||||||
chr2:200616316 | C | T | 2 | a0001c0001t0002g0164 a0002c0002t0002g0202 |
2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1704+253C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616316 | |||||||
chr2:200616337 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1704+274G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616337 | |||||||
chr2:200616422 | G | A | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1704+359G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616422 | |||||||
chr2:200616660 | C | T | 3 | a0001c0001t0002g0324 a0001c0001t0002g0345 a0001c0001t0002g0346 |
3 | HG02129.hp1 NA18992.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1704+597C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616660 | |||||||
chr2:200616713 | C | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(129): Show |
135 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1704+650C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616713 | |||||||
chr2:200616782 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1704+719G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616782 | |||||||
chr2:200616789 | A | G | 10 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1704+726A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616789 | |||||||
chr2:200616856 | G | A | 2 | a0001c0001t0001g0311 a0001c0001t0001g0331 |
2 | HG00597.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1704+793G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200616856 | |||||||
chr2:200617210 | GC | G | 9 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0233 others(6): Show |
9 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1704+1149delC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617210 | ||||||
chr2:200617258 | C | G | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1704+1195C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617258 | |||||||
chr2:200617325 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0218 others(20): Show |
24 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1704+1262G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617325 | |||||||
chr2:200617479 | T | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0117 others(127): Show |
133 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1704+1416T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617479 | |||||||
chr2:200617481 | C | CA | 64 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0019 others(61): Show |
64 | HG00609.hp1 HG00639.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.1704+1443dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | ||||||
chr2:200617481 | C | CAA | 8 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0002g0025 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1704+1442_1704+144 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | ||||||
chr2:200617481 | CA | C | 82 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0125 others(79): Show |
83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1704+1443delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | ||||||
chr2:200617481 | CAA | C | 10 | a0001c0001t0001g0121 a0001c0001t0002g0123 a0001c0001t0002g0161 others(7): Show |
10 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1704+1442_1704+144 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617481 | ||||||
chr2:200617548 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1704+1485A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617548 | |||||||
chr2:200617666 | C | CCATTA | 111 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1704+1606_1704+161 others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200617666 | ||||||
chr2:200617744 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(58): Show |
62 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.1704+1681A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617744 | |||||||
chr2:200617759 | T | C | 1 | a0001c0001t0001g0008 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1704+1696T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617759 | |||||||
chr2:200617864 | G | A | 1 | a0008c0025t0003g0285 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1704+1801G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617864 | |||||||
chr2:200617965 | G | T | 1 | a0001c0001t0002g0365 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1704+1902G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617965 | |||||||
chr2:200617997 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0187 |
2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1704+1934T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200617997 | |||||||
chr2:200618143 | G | T | 341 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(338): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1704+2080G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618143 | |||||||
chr2:200618231 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1704+2168T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618231 | |||||||
chr2:200618365 | A | G | 112 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1705-2285A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618365 | |||||||
chr2:200618393 | T | C | 43 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(40): Show |
43 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.1705-2257T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618393 | |||||||
chr2:200618497 | T | G | 9 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0029 others(6): Show |
9 | HG00738.hp1 HG01258.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1705-2153T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618497 | |||||||
chr2:200618514 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1705-2136A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618514 | |||||||
chr2:200618533 | G | GT | 7 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1705-2110dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200618533 | ||||||
chr2:200618591 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG00733.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1705-2059C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618591 | |||||||
chr2:200618648 | T | C | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-2002T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618648 | |||||||
chr2:200618660 | T | C | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-1990T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618660 | |||||||
chr2:200618711 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1705-1939T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618711 | |||||||
chr2:200618958 | A | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(353): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1705-1692A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200618958 | |||||||
chr2:200619013 | T | C | 24 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(21): Show |
24 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1705-1637T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619013 | |||||||
chr2:200619048 | T | G | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1705-1602T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619048 | |||||||
chr2:200619106 | T | G | 7 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1705-1544T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619106 | |||||||
chr2:200619108 | TC | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0273 others(2): Show |
6 | HG02647.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1705-1538delC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200619108 | ||||||
chr2:200619151 | C | A | 1 | a0003c0026t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1705-1499C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619151 | |||||||
chr2:200619194 | G | A | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG02056.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1705-1456G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619194 | |||||||
chr2:200619202 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1705-1448G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619202 | |||||||
chr2:200619254 | G | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1705-1396G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619254 | |||||||
chr2:200619307 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1705-1343G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619307 | |||||||
chr2:200619342 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(109): Show |
112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1705-1308C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619342 | |||||||
chr2:200619377 | C | G | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-1273C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619377 | |||||||
chr2:200619461 | G | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1705-1189G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619461 | |||||||
chr2:200619467 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(222): Show |
226 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1705-1183A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619467 | |||||||
chr2:200619663 | C | T | 1 | a0001c0008t0002g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1705-987C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619663 | |||||||
chr2:200619673 | G | T | 2 | a0001c0001t0001g0175 a0001c0001t0002g0174 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1705-977G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619673 | |||||||
chr2:200619759 | T | C | 1 | a0001c0008t0002g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1705-891T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619759 | |||||||
chr2:200619849 | A | G | 10 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1705-801A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619849 | |||||||
chr2:200619990 | T | C | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1705-660T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619990 | |||||||
chr2:200619997 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0165 |
2 | HG01255.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1705-653G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200619997 | |||||||
chr2:200620054 | C | G | 1 | a0003c0030t0002g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1705-596C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620054 | |||||||
chr2:200620198 | A | AG | 42 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(39): Show |
42 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.1705-452_1705-451i others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620198 | |||||||
chr2:200620198 | A | AGT | 3 | a0001c0001t0001g0105 a0001c0001t0002g0230 a0005c0007t0002g0208 |
3 | HG02083.hp2 HG04199.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1705-452_1705-451i others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620198 | |||||||
chr2:200620198 | AC | A | 5 | a0001c0001t0002g0206 a0003c0003t0004g0207 a0003c0003t0004g0212 others(2): Show |
5 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705-451delC | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620198 | |||||||
chr2:200620199 | C | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
64 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.1705-451C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620199 | |||||||
chr2:200620199 | C | T | 45 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(42): Show |
45 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.1705-451C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620199 | |||||||
chr2:200620199 | CT | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(108): Show |
112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1705-432delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200620199 | ||||||
chr2:200620199 | CTT | C | 105 | a0001c0001t0001g0117 a0001c0001t0001g0121 a0001c0001t0001g0124 others(102): Show |
106 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1705-433_1705-432d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chr2 | 200620199 | ||||||
chr2:200620200 | T | G | 5 | a0001c0001t0002g0206 a0003c0003t0004g0207 a0003c0003t0004g0212 others(2): Show |
5 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705-450T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620200 | |||||||
chr2:200620202 | T | G | 3 | a0001c0005t0006g0076 a0001c0029t0001g0077 a0009c0015t0002g0075 |
3 | HG02622.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1705-448T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620202 | |||||||
chr2:200620273 | G | A | 1 | a0003c0006t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1705-377G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620273 | |||||||
chr2:200620383 | T | TG | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1705-267_1705-266i others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620383 | |||||||
chr2:200620384 | T | G | 8 | a0001c0001t0001g0267 a0001c0001t0002g0029 a0001c0001t0002g0136 others(5): Show |
8 | HG01884.hp2 HG01993.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1705-266T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620384 | |||||||
chr2:200620393 | G | A | 111 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1705-257G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620393 | |||||||
chr2:200620397 | C | T | 87 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0280 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1705-253C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620397 | |||||||
chr2:200620411 | G | A | 1 | a0007c0028t0001g0312 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1705-239G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620411 | |||||||
chr2:200620550 | C | T | 1 | a0003c0003t0001g0246 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1705-100C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 16/34 | chr2 | 200620550 | |||||||
chr2:200620849 | A | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(107): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1874+30A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200620849 | |||||||
chr2:200620862 | T | A | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1874+43T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200620862 | |||||||
chr2:200620926 | T | G | 117 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(114): Show |
117 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1874+107T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200620926 | |||||||
chr2:200621024 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1875-96G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200621024 | |||||||
chr2:200621107 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(58): Show |
62 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.1875-13G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 17/34 | chr2 | 200621107 | |||||||
chr2:200621294 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2001+48G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621294 | |||||||
chr2:200621461 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2001+215G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621461 | |||||||
chr2:200621593 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(103): Show |
108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2001+347G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621593 | |||||||
chr2:200621641 | C | CT | 11 | a0001c0001t0001g0265 a0001c0001t0001g0280 a0001c0001t0001g0329 others(8): Show |
11 | HG00642.hp1 HG01981.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001+401dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621641 | ||||||
chr2:200621676 | T | TTCTC | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(200): Show |
204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2001+447_2001+450d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621676 | ||||||
chr2:200621676 | T | TTCTCTC | 46 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0019 others(43): Show |
47 | HG00639.hp2 HG01106.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.2001+445_2001+450d others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621676 | ||||||
chr2:200621676 | T | TTCTCTCT others(1): Show |
104 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(101): Show |
106 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.2001+443_2001+450d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | INFO_REALIGN_3_PRIME | chr2 | 200621676 | ||||||
chr2:200621697 | A | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2001+451A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621697 | |||||||
chr2:200621698 | A | C | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2001+452A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621698 | |||||||
chr2:200621700 | T | C | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2001+454T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621700 | |||||||
chr2:200621998 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(103): Show |
108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2001+752C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200621998 | |||||||
chr2:200622180 | T | C | 2 | a0001c0001t0001g0229 a0010c0023t0001g0249 |
2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2001+934T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622180 | |||||||
chr2:200622232 | G | C | 44 | a0001c0001t0001g0105 a0001c0001t0001g0219 a0001c0001t0001g0222 others(41): Show |
44 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.2001+986G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622232 | |||||||
chr2:200622393 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(229): Show |
233 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2001+1147A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622393 | |||||||
chr2:200622401 | T | G | 1 | a0001c0001t0002g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2001+1155T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622401 | |||||||
chr2:200622595 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2002-1266C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622595 | |||||||
chr2:200622634 | C | G | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2002-1227C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622634 | |||||||
chr2:200622720 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2002-1141A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622720 | |||||||
chr2:200622809 | C | A | 1 | a0003c0026t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2002-1052C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200622809 | |||||||
chr2:200623040 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
71 | HG00597.hp1 HG00639.hp1 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.2002-821C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623040 | |||||||
chr2:200623144 | A | T | 1 | a0001c0001t0002g0012 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2002-717A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623144 | |||||||
chr2:200623267 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(229): Show |
233 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2002-594C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623267 | |||||||
chr2:200623443 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(229): Show |
233 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2002-418T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623443 | |||||||
chr2:200623460 | G | T | 1 | a0001c0001t0002g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2002-401G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623460 | |||||||
chr2:200623500 | C | A | 111 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(108): Show |
111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.2002-361C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623500 | |||||||
chr2:200623643 | G | A | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2002-218G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623643 | |||||||
chr2:200623690 | A | G | 341 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(338): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.2002-171A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623690 | |||||||
chr2:200623712 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2002-149T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623712 | |||||||
chr2:200623794 | G | A | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2002-67G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 18/34 | chr2 | 200623794 | |||||||
chr2:200624035 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(224): Show |
228 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.2124+52A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624035 | |||||||
chr2:200624148 | C | A | 1 | a0001c0001t0002g0298 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2124+165C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624148 | |||||||
chr2:200624278 | C | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(21): Show |
24 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2124+295C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624278 | |||||||
chr2:200624336 | T | G | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2124+353T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624336 | |||||||
chr2:200624427 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(107): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2124+444T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624427 | |||||||
chr2:200624439 | G | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG01192.hp1 HG01261.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.2124+456G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624439 | |||||||
chr2:200624619 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2124+636G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624619 | |||||||
chr2:200624695 | T | G | 1 | a0003c0006t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2124+712T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624695 | |||||||
chr2:200624742 | A | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2124+759A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624742 | |||||||
chr2:200624767 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(222): Show |
226 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.2124+784A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624767 | |||||||
chr2:200624829 | T | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(107): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2124+846T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624829 | |||||||
chr2:200624935 | C | T | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2124+952C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624935 | |||||||
chr2:200624943 | C | T | 1 | a0001c0008t0002g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2124+960C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200624943 | |||||||
chr2:200625091 | A | C | 1 | a0002c0002t0002g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2124+1108A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625091 | |||||||
chr2:200625113 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2124+1130C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625113 | |||||||
chr2:200625299 | C | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2124+1316C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625299 | |||||||
chr2:200625347 | G | A | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2124+1364G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625347 | |||||||
chr2:200625626 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0120 others(103): Show |
108 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2124+1643A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200625626 | |||||||
chr2:200626003 | C | T | 1 | a0002c0002t0003g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2125-1350C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626003 | |||||||
chr2:200626004 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2125-1349G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626004 | |||||||
chr2:200626098 | T | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0181 |
2 | HG00621.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2125-1255T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626098 | |||||||
chr2:200626184 | G | A | 356 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(353): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.2125-1169G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626184 | |||||||
chr2:200626300 | G | A | 1 | a0001c0001t0002g0359 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2125-1053G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626300 | |||||||
chr2:200626536 | T | G | 2 | a0003c0009t0001g0098 a0003c0009t0001g0360 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2125-817T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626536 | |||||||
chr2:200626558 | T | A | 341 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(338): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.2125-795T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626558 | |||||||
chr2:200626707 | C | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2125-646C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626707 | |||||||
chr2:200626727 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(313): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.2125-626A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626727 | |||||||
chr2:200626837 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(89): Show |
93 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.2125-516G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200626837 | |||||||
chr2:200627099 | A | T | 6 | a0001c0001t0001g0358 a0001c0001t0002g0324 a0001c0001t0002g0344 others(3): Show |
6 | HG00423.hp2 HG00544.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2125-254A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200627099 | |||||||
chr2:200627202 | C | T | 1 | a0002c0002t0003g0217 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2125-151C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 19/34 | chr2 | 200627202 | |||||||
chr2:200627562 | G | T | 1 | a0002c0002t0003g0050 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2221+113G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200627562 | |||||||
chr2:200627787 | G | A | 2 | a0001c0001t0002g0157 a0003c0003t0001g0097 |
2 | HG02886.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2221+338G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200627787 | |||||||
chr2:200627801 | A | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01192.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2221+352A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200627801 | |||||||
chr2:200628094 | C | T | 3 | a0001c0001t0002g0206 a0003c0003t0004g0212 a0003c0026t0001g0211 |
3 | HG02723.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2221+645C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628094 | |||||||
chr2:200628100 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2221+651G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628100 | |||||||
chr2:200628178 | TACACACA others(7): Show |
T | 1 | a0008c0025t0003g0285 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2221+741_2221+754d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200628178 | ||||||
chr2:200628312 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2221+863T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628312 | |||||||
chr2:200628401 | G | GA | 247 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.2221+957dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200628401 | ||||||
chr2:200628435 | A | G | 8 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2221+986A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628435 | |||||||
chr2:200628579 | A | T | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2221+1130A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628579 | |||||||
chr2:200628695 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2221+1246G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628695 | |||||||
chr2:200628764 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2221+1315A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628764 | |||||||
chr2:200628788 | G | A | 2 | a0001c0005t0006g0076 a0001c0008t0002g0201 |
2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2221+1339G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200628788 | |||||||
chr2:200628925 | T | TCAAA | 3 | a0001c0001t0001g0225 a0001c0001t0001g0242 a0006c0010t0009g0278 |
3 | HG03471.hp1 NA18965.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2221+1501_2221+150 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200628925 | ||||||
chr2:200629019 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2221+1570A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200629019 | |||||||
chr2:200629183 | A | C | 1 | a0001c0001t0002g0241 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2221+1734A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200629183 | |||||||
chr2:200629256 | C | T | 1 | a0001c0001t0002g0344 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2221+1807C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200629256 | |||||||
chr2:200630113 | C | T | 1 | a0009c0015t0002g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2221+2664C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630113 | |||||||
chr2:200630189 | T | C | 339 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(336): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.2221+2740T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630189 | |||||||
chr2:200630210 | T | TA | 34 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0089 others(31): Show |
34 | HG01109.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.2221+2788dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | T | TAAAAAAA others(8): Show |
1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2221+2774_2221+278 others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | T | TAAAAAAA others(9): Show |
1 | a0003c0003t0004g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2221+2773_2221+278 others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | T | TAAAAAAA others(10): Show |
3 | a0001c0001t0002g0206 a0003c0003t0004g0212 a0003c0026t0001g0211 |
3 | HG02723.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2221+2772_2221+278 others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | T | TAAAAAAA others(11): Show |
1 | a0003c0003t0004g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2221+2771_2221+278 others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | TAA | T | 13 | a0001c0001t0002g0150 a0001c0001t0002g0231 a0001c0001t0002g0237 others(10): Show |
13 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2221+2787_2221+278 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | TAAA | T | 85 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
85 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2221+2786_2221+278 others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | TAAAAAAA others(3): Show |
T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0273 a0001c0001t0001g0290 others(10): Show |
14 | HG00733.hp1 HG01884.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2221+2779_2221+278 others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | TAAAAAAA others(5): Show |
T | 18 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(15): Show |
18 | HG01192.hp1 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.2221+2777_2221+278 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | TAAAAAAA others(6): Show |
T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0117 others(82): Show |
88 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.2221+2776_2221+278 others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630210 | TAAAAAAA others(7): Show |
T | 1 | a0001c0019t0002g0149 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2221+2775_2221+278 others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630210 | ||||||
chr2:200630340 | T | C | 75 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(72): Show |
75 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.2221+2891T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630340 | |||||||
chr2:200630390 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2221+2941A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630390 | |||||||
chr2:200630428 | C | T | 3 | a0001c0005t0002g0061 a0001c0005t0004g0296 a0011c0017t0001g0064 |
3 | HG02258.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2221+2979C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630428 | |||||||
chr2:200630486 | G | A | 1 | a0001c0001t0002g0359 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2221+3037G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630486 | |||||||
chr2:200630526 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2221+3077A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630526 | |||||||
chr2:200630537 | T | A | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2221+3088T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630537 | |||||||
chr2:200630548 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2221+3099G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630548 | |||||||
chr2:200630548 | G | GAGGA | 46 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0042 others(43): Show |
46 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.2221+3148_2221+315 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | G | GAGGAAGG others(1): Show |
52 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(49): Show |
52 | HG00597.hp1 HG00639.hp2 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.2221+3144_2221+315 others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | G | GAGGAAGG others(5): Show |
21 | a0001c0001t0001g0013 a0001c0001t0001g0087 a0001c0001t0001g0090 others(18): Show |
21 | HG00741.hp2 HG01258.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.2221+3140_2221+315 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | G | GAGGAAGG others(9): Show |
4 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0002g0032 others(1): Show |
4 | HG02004.hp2 HG03831.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.2221+3136_2221+315 others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | G | GAGGAAGG others(13): Show |
2 | a0001c0001t0002g0031 a0001c0027t0002g0030 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2221+3132_2221+315 others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGA | G | 5 | a0001c0001t0001g0356 a0001c0001t0002g0260 a0001c0001t0002g0362 others(2): Show |
5 | HG02027.hp1 HG02055.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2221+3148_2221+315 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGAAGG others(1): Show |
G | 3 | a0001c0005t0001g0053 a0001c0029t0001g0077 a0003c0030t0002g0216 |
3 | HG03209.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2221+3144_2221+315 others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGAAGG others(5): Show |
G | 3 | a0001c0005t0002g0061 a0001c0005t0004g0296 a0011c0017t0001g0064 |
3 | HG02258.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2221+3140_2221+315 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGAAGG others(9): Show |
G | 19 | a0001c0001t0001g0167 a0001c0001t0001g0203 a0001c0001t0001g0255 others(16): Show |
19 | HG00621.hp1 HG00642.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2221+3136_2221+315 others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGAAGG others(13): Show |
G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0117 others(88): Show |
94 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2221+3132_2221+315 others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGAAGG others(17): Show |
G | 77 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(74): Show |
77 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.2221+3128_2221+315 others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGAAGG others(21): Show |
G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0273 a0001c0001t0001g0290 others(9): Show |
13 | HG00733.hp1 HG02280.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2221+3124_2221+315 others(32): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630548 | GAGGAAGG others(25): Show |
G | 1 | a0001c0001t0002g0148 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2221+3120_2221+315 others(36): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200630548 | ||||||
chr2:200630627 | G | A | 4 | a0001c0008t0001g0361 a0003c0003t0001g0210 a0003c0003t0004g0209 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2221+3178G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630627 | |||||||
chr2:200630634 | G | A | 1 | a0005c0007t0002g0238 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2221+3185G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630634 | |||||||
chr2:200630648 | G | A | 1 | a0003c0003t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2221+3199G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630648 | |||||||
chr2:200630780 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2221+3331T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630780 | |||||||
chr2:200630951 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2221+3502G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200630951 | |||||||
chr2:200631029 | T | C | 1 | a0001c0001t0002g0102 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2221+3580T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631029 | |||||||
chr2:200631388 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2222-3403A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631388 | |||||||
chr2:200631742 | A | C | 2 | a0001c0001t0005g0002 a0001c0001t0005g0116 |
3 | HG02451.hp2 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2222-3049A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631742 | |||||||
chr2:200631796 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2222-2995C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200631796 | |||||||
chr2:200632046 | T | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.2222-2745T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632046 | |||||||
chr2:200632232 | A | G | 4 | a0001c0008t0001g0361 a0003c0003t0001g0210 a0003c0003t0004g0209 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2222-2559A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632232 | |||||||
chr2:200632298 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0021 others(170): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.2222-2493C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632298 | |||||||
chr2:200632312 | TA | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2222-2478delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632312 | |||||||
chr2:200632496 | A | G | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2222-2295A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632496 | |||||||
chr2:200632591 | G | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0233 |
2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2222-2200G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200632591 | |||||||
chr2:200632633 | T | TA | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0021 others(169): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2222-2148dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200632633 | ||||||
chr2:200632633 | T | TAA | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2222-2149_2222-214 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200632633 | ||||||
chr2:200632879 | CT | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(74): Show |
80 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2222-1902delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200632879 | ||||||
chr2:200633009 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0233 |
2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2222-1782G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633009 | |||||||
chr2:200633047 | C | T | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2222-1744C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633047 | |||||||
chr2:200633081 | G | A | 1 | a0001c0005t0004g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2222-1710G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633081 | |||||||
chr2:200633098 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2222-1693C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633098 | |||||||
chr2:200633099 | G | A | 1 | a0001c0008t0002g0201 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2222-1692G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633099 | |||||||
chr2:200633202 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0002g0028 a0001c0001t0002g0036 |
3 | NA18939.hp2 NA18940.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2222-1589G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633202 | |||||||
chr2:200633314 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2222-1477G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633314 | |||||||
chr2:200633349 | T | C | 8 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0004g0296 others(5): Show |
8 | HG02258.hp2 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2222-1442T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633349 | |||||||
chr2:200633562 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0021 others(169): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2222-1229C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200633562 | |||||||
chr2:200634164 | A | AT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
109 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.2222-602dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | ||||||
chr2:200634164 | A | ATT | 14 | a0001c0001t0001g0134 a0001c0001t0001g0196 a0001c0001t0002g0052 others(11): Show |
14 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2222-603_2222-602d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | ||||||
chr2:200634164 | AT | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0166 a0001c0001t0001g0167 others(26): Show |
29 | HG00408.hp1 HG01192.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.2222-602delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | ||||||
chr2:200634164 | ATTT | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0242 a0001c0001t0001g0320 others(3): Show |
6 | HG02622.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2222-604_2222-602d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | ||||||
chr2:200634164 | ATTTT | A | 78 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(75): Show |
78 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2222-605_2222-602d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | ||||||
chr2:200634164 | ATTTTTTT | A | 7 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0008t0001g0051 others(4): Show |
7 | HG02970.hp1 HG02976.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2222-608_2222-602d others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | ||||||
chr2:200634164 | ATTTTTTT others(1): Show |
A | 14 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0271 others(11): Show |
14 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2222-609_2222-602d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634164 | ||||||
chr2:200634255 | A | AAAC | 9 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0002g0215 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2222-521_2222-519d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chr2 | 200634255 | ||||||
chr2:200634268 | A | C | 3 | a0001c0001t0001g0088 a0001c0001t0002g0028 a0001c0001t0002g0036 |
3 | NA18939.hp2 NA18940.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2222-523A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634268 | |||||||
chr2:200634460 | C | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0233 |
2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2222-331C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634460 | |||||||
chr2:200634497 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0002g0174 a0006c0010t0009g0278 |
3 | HG02280.hp1 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2222-294G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634497 | |||||||
chr2:200634556 | A | C | 1 | a0001c0001t0002g0161 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2222-235A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634556 | |||||||
chr2:200634691 | G | A | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2222-100G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634691 | |||||||
chr2:200634737 | G | T | 1 | a0001c0001t0002g0035 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2222-54G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634737 | |||||||
chr2:200634789 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.2222-2A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 20/34 | chr2 | 200634789 | |||||||
chr2:200635054 | G | T | 1 | a0002c0002t0003g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2346+139G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635054 | |||||||
chr2:200635306 | C | G | 1 | a0001c0001t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2346+391C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635306 | |||||||
chr2:200635351 | G | A | 13 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0271 others(10): Show |
13 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2346+436G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635351 | |||||||
chr2:200635421 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0002g0174 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2346+506T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635421 | |||||||
chr2:200635460 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2346+545T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635460 | |||||||
chr2:200635468 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(20): Show |
24 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2346+553G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635468 | |||||||
chr2:200635477 | GGAAA | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(75): Show |
81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2346+565_2346+568d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200635477 | ||||||
chr2:200635638 | C | T | 1 | a0001c0001t0002g0353 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2346+723C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635638 | |||||||
chr2:200635873 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2346+958G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635873 | |||||||
chr2:200635908 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2346+993C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635908 | |||||||
chr2:200635973 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0020t0001g0228 |
3 | NA18942.hp2 NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2347-938C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200635973 | |||||||
chr2:200636046 | G | C | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2347-865G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636046 | |||||||
chr2:200636065 | G | GA | 86 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.2347-843dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636065 | ||||||
chr2:200636117 | C | CT | 105 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
105 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.2347-765dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | ||||||
chr2:200636117 | C | CTT | 39 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0043 others(36): Show |
39 | HG00597.hp1 HG01123.hp1 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.2347-766_2347-765d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | ||||||
chr2:200636117 | C | CTTT | 6 | a0002c0002t0003g0067 a0002c0002t0003g0072 a0003c0003t0004g0207 others(3): Show |
6 | HG01361.hp1 HG02109.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2347-767_2347-765d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | ||||||
chr2:200636117 | CT | C | 16 | a0001c0001t0001g0281 a0001c0001t0002g0165 a0001c0001t0002g0185 others(13): Show |
16 | HG00642.hp1 HG01070.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.2347-765delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | ||||||
chr2:200636117 | CTT | C | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0356 others(11): Show |
14 | HG00408.hp1 HG01106.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2347-766_2347-765d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | ||||||
chr2:200636117 | CTTT | C | 12 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0271 others(9): Show |
12 | HG00280.hp1 HG01099.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2347-767_2347-765d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chr2 | 200636117 | ||||||
chr2:200636422 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2347-489T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636422 | |||||||
chr2:200636450 | A | G | 1 | a0003c0030t0002g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2347-461A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636450 | |||||||
chr2:200636491 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18947.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2347-420G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636491 | |||||||
chr2:200636648 | AT | A | 3 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0003t0004g0094 |
3 | HG02723.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2347-262delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636648 | |||||||
chr2:200636708 | A | G | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2347-203A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636708 | |||||||
chr2:200636845 | A | G | 35 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0271 others(32): Show |
35 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.2347-66A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 21/34 | chr2 | 200636845 | |||||||
chr2:200637121 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2480+77C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637121 | |||||||
chr2:200637349 | T | A | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2480+305T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637349 | |||||||
chr2:200637490 | T | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(20): Show |
24 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2480+446T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637490 | |||||||
chr2:200637599 | G | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0203 a0001c0001t0001g0255 others(4): Show |
7 | HG01109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2480+555G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637599 | |||||||
chr2:200637672 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2481-543T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637672 | |||||||
chr2:200637789 | A | G | 4 | a0001c0001t0001g0134 a0001c0001t0002g0101 a0001c0001t0002g0102 others(1): Show |
4 | HG00544.hp1 NA18961.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2481-426A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637789 | |||||||
chr2:200637912 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(20): Show |
24 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2481-303C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200637912 | |||||||
chr2:200638081 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0002g0289 |
2 | HG01361.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.2481-134T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200638081 | |||||||
chr2:200638175 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(75): Show |
81 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2481-40G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 22/34 | chr2 | 200638175 | |||||||
chr2:200638348 | A | G | 1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2568+46A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638348 | |||||||
chr2:200638362 | C | T | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2568+60C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638362 | |||||||
chr2:200638453 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(114): Show |
120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2568+151A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638453 | |||||||
chr2:200638460 | A | C | 1 | a0001c0001t0002g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2568+158A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638460 | |||||||
chr2:200638539 | G | A | 1 | a0003c0003t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2568+237G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638539 | |||||||
chr2:200638543 | T | C | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2568+241T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638543 | |||||||
chr2:200638594 | G | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(18): Show |
22 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2568+292G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638594 | |||||||
chr2:200638665 | GTTATGTG others(9): Show |
G | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2568+368_2568+383d others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200638665 | ||||||
chr2:200638695 | G | T | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.2568+393G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638695 | |||||||
chr2:200638849 | A | G | 1 | a0001c0005t0002g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2568+547A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200638849 | |||||||
chr2:200638892 | AGCTCAAT others(5): Show |
A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2568+603_2568+614d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200638892 | ||||||
chr2:200639101 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2568+799G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639101 | |||||||
chr2:200639169 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2568+867C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639169 | |||||||
chr2:200639273 | G | A | 13 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0271 others(10): Show |
13 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2568+971G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639273 | |||||||
chr2:200639681 | G | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(71): Show |
74 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.2568+1379G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639681 | |||||||
chr2:200639755 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2569-1343C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639755 | |||||||
chr2:200639762 | C | T | 1 | a0001c0001t0002g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2569-1336C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639762 | |||||||
chr2:200639773 | G | A | 1 | a0004c0004t0001g0302 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2569-1325G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639773 | |||||||
chr2:200639775 | C | G | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2569-1323C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639775 | |||||||
chr2:200639873 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01192.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2569-1225A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639873 | |||||||
chr2:200639894 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2569-1204G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639894 | |||||||
chr2:200639895 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2569-1203G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639895 | |||||||
chr2:200639896 | G | A | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-1202G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639896 | |||||||
chr2:200639977 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
10 | HG00597.hp1 HG02602.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.2569-1121C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639977 | |||||||
chr2:200639992 | G | A | 3 | a0001c0001t0001g0229 a0003c0003t0001g0097 a0010c0023t0001g0249 |
3 | HG02809.hp2 HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2569-1106G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200639992 | |||||||
chr2:200640005 | C | G | 1 | a0001c0001t0002g0108 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2569-1093C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640005 | |||||||
chr2:200640009 | C | A | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-1089C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640009 | |||||||
chr2:200640036 | C | CA | 75 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(72): Show |
75 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2569-1044dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200640036 | ||||||
chr2:200640036 | CA | C | 32 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0079 others(29): Show |
32 | HG01106.hp1 HG01169.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.2569-1044delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chr2 | 200640036 | ||||||
chr2:200640053 | A | G | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-1045A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640053 | |||||||
chr2:200640125 | A | G | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2569-973A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640125 | |||||||
chr2:200640276 | G | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0198 |
2 | NA18968.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2569-822G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640276 | |||||||
chr2:200640326 | C | T | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2569-772C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640326 | |||||||
chr2:200640425 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2569-673A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640425 | |||||||
chr2:200640546 | C | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2569-552C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640546 | |||||||
chr2:200640549 | C | T | 1 | a0010c0023t0001g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2569-549C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640549 | |||||||
chr2:200640965 | T | C | 2 | a0003c0009t0001g0098 a0003c0009t0001g0360 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2569-133T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200640965 | |||||||
chr2:200641006 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0002g0145 |
2 | HG02165.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2569-92G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 23/34 | chr2 | 200641006 | |||||||
chr2:200641199 | G | A | 1 | a0003c0003t0001g0246 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2655+15G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641199 | |||||||
chr2:200641230 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(127): Show |
133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.2655+46C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641230 | |||||||
chr2:200641245 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2655+61C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641245 | |||||||
chr2:200641249 | G | A | 4 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0004g0296 others(1): Show |
4 | HG02258.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2655+65G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641249 | |||||||
chr2:200641333 | G | A | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2655+149G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641333 | |||||||
chr2:200641374 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
13 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2655+190G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641374 | |||||||
chr2:200641535 | G | A | 11 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0002g0215 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2655+351G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641535 | |||||||
chr2:200641619 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2655+435G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641619 | |||||||
chr2:200641694 | AT | A | 16 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0356 others(13): Show |
16 | HG00408.hp1 HG01433.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2655+519delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr2 | 200641694 | ||||||
chr2:200641858 | C | G | 8 | a0001c0001t0001g0117 a0001c0001t0001g0203 a0001c0001t0001g0255 others(5): Show |
8 | HG01109.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2655+674C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641858 | |||||||
chr2:200641904 | A | G | 1 | a0001c0001t0002g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2656-706A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641904 | |||||||
chr2:200641990 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2656-620A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200641990 | |||||||
chr2:200642035 | A | C | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2656-575A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642035 | |||||||
chr2:200642078 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2656-532G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642078 | |||||||
chr2:200642086 | A | G | 1 | a0001c0001t0002g0020 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2656-524A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642086 | |||||||
chr2:200642128 | T | TA | 10 | a0001c0001t0001g0265 a0001c0001t0001g0280 a0001c0001t0001g0329 others(7): Show |
10 | HG00642.hp1 HG01993.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.2656-472dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr2 | 200642128 | ||||||
chr2:200642431 | T | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2656-179T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | chr2 | 200642431 | |||||||
chr2:200642455 | C | CAAA | 81 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(78): Show |
82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2656-151_2656-149d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chr2 | 200642455 | ||||||
chr2:200642837 | G | T | 1 | a0004c0004t0001g0302 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2847+36G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642837 | |||||||
chr2:200642849 | C | T | 5 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0225 others(2): Show |
5 | HG02015.hp2 NA18965.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2847+48C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642849 | |||||||
chr2:200642850 | G | T | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+49G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642850 | |||||||
chr2:200642860 | T | G | 2 | a0003c0009t0001g0098 a0003c0009t0001g0360 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2847+59T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642860 | |||||||
chr2:200642899 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2847+98G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642899 | |||||||
chr2:200642954 | C | G | 1 | a0003c0003t0004g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2847+153C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200642954 | |||||||
chr2:200643186 | CT | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(89): Show |
95 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2847+399delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643186 | ||||||
chr2:200643359 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0365 |
2 | NA18987.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2847+558G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643359 | |||||||
chr2:200643384 | T | C | 4 | a0001c0001t0001g0309 a0001c0001t0002g0310 a0002c0002t0002g0099 others(1): Show |
4 | HG00673.hp1 NA18944.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.2847+583T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643384 | |||||||
chr2:200643386 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(78): Show |
82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2847+585T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643386 | |||||||
chr2:200643386 | T | TAC | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2847+597_2847+598d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643386 | ||||||
chr2:200643386 | T | TACAC | 11 | a0001c0001t0002g0092 a0001c0001t0002g0156 a0001c0001t0002g0157 others(8): Show |
11 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.2847+595_2847+598d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643386 | ||||||
chr2:200643398 | C | CACAT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(77): Show |
83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2847+598_2847+599i others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643398 | ||||||
chr2:200643398 | C | CAT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(10): Show |
14 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2847+611_2847+612d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643398 | ||||||
chr2:200643398 | C | CATAT | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2847+609_2847+612d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200643398 | ||||||
chr2:200643400 | T | C | 34 | a0001c0001t0001g0057 a0001c0001t0001g0223 a0001c0001t0001g0226 others(31): Show |
34 | HG00280.hp1 HG00408.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.2847+599T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643400 | |||||||
chr2:200643412 | T | C | 1 | a0017c0013t0002g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2847+611T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643412 | |||||||
chr2:200643552 | G | T | 69 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(66): Show |
69 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2847+751G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643552 | |||||||
chr2:200643710 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(80): Show |
86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2847+909G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643710 | |||||||
chr2:200643837 | G | A | 8 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2847+1036G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200643837 | |||||||
chr2:200644042 | T | C | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2847+1241T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644042 | |||||||
chr2:200644131 | C | G | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+1330C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644131 | |||||||
chr2:200644335 | C | T | 1 | a0002c0002t0003g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2847+1534C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644335 | |||||||
chr2:200644430 | C | A | 1 | a0001c0001t0002g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2847+1629C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644430 | |||||||
chr2:200644431 | T | A | 1 | a0001c0001t0002g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2847+1630T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644431 | |||||||
chr2:200644435 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2847+1634C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644435 | |||||||
chr2:200644516 | T | C | 1 | a0001c0008t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2847+1715T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644516 | |||||||
chr2:200644544 | G | A | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+1743G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200644544 | |||||||
chr2:200645151 | C | CAATATTA others(5): Show |
212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2847+2354_2847+236 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200645151 | ||||||
chr2:200645151 | C | CAGTATTA others(5): Show |
1 | a0001c0005t0004g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2847+2351_2847+235 others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200645151 | ||||||
chr2:200645265 | G | C | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2847+2464G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645265 | |||||||
chr2:200645566 | G | A | 8 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0002g0215 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2847+2765G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645566 | |||||||
chr2:200645573 | G | A | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2847+2772G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645573 | |||||||
chr2:200645617 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2847+2816A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645617 | |||||||
chr2:200645670 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0336 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2847+2869G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645670 | |||||||
chr2:200645696 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(88): Show |
94 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2847+2895G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645696 | |||||||
chr2:200645744 | C | T | 1 | a0003c0030t0002g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2847+2943C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645744 | |||||||
chr2:200645751 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2847+2950G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645751 | |||||||
chr2:200645860 | T | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(78): Show |
82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2847+3059T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645860 | |||||||
chr2:200645932 | TAGTG | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
13 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2847+3134_2847+313 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200645932 | ||||||
chr2:200645974 | C | T | 8 | a0001c0001t0001g0105 a0001c0001t0001g0229 a0001c0001t0001g0282 others(5): Show |
8 | HG02809.hp2 HG02897.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.2847+3173C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645974 | |||||||
chr2:200645979 | C | T | 1 | a0003c0018t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2847+3178C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200645979 | |||||||
chr2:200646224 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0187 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2847+3423C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646224 | |||||||
chr2:200646512 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(78): Show |
82 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2847+3711G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646512 | |||||||
chr2:200646692 | T | C | 1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2847+3891T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646692 | |||||||
chr2:200646754 | T | C | 1 | a0001c0029t0001g0077 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2847+3953T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200646754 | |||||||
chr2:200647035 | T | C | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2848-3939T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647035 | |||||||
chr2:200647136 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2848-3838A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647136 | |||||||
chr2:200647140 | T | TTTTG | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2848-3830_2848-382 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200647140 | ||||||
chr2:200647429 | C | G | 61 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(58): Show |
61 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.2848-3545C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647429 | |||||||
chr2:200647433 | T | C | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2848-3541T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647433 | |||||||
chr2:200647567 | G | A | 9 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0002g0215 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2848-3407G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647567 | |||||||
chr2:200647693 | A | G | 3 | a0001c0001t0001g0042 a0002c0002t0003g0263 a0002c0002t0003g0272 |
3 | HG02698.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2848-3281A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647693 | |||||||
chr2:200647701 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0002g0101 a0001c0001t0002g0102 others(1): Show |
4 | HG00544.hp1 NA18961.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-3273C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200647701 | |||||||
chr2:200647944 | GT | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2848-3023delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200647944 | ||||||
chr2:200648005 | T | A | 7 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0004g0296 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2848-2969T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648005 | |||||||
chr2:200648165 | T | A | 1 | a0003c0030t0002g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2848-2809T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648165 | |||||||
chr2:200648384 | T | G | 31 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0236 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2848-2590T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648384 | |||||||
chr2:200648450 | G | A | 1 | a0008c0025t0003g0285 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2848-2524G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648450 | |||||||
chr2:200648577 | GGT | G | 4 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0225 others(1): Show |
4 | HG02015.hp2 NA18965.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-2395_2848-239 others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chr2 | 200648577 | ||||||
chr2:200648581 | G | C | 4 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0225 others(1): Show |
4 | HG02015.hp2 NA18965.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-2393G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648581 | |||||||
chr2:200648672 | T | C | 9 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0002g0215 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2848-2302T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648672 | |||||||
chr2:200648709 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2848-2265G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648709 | |||||||
chr2:200648945 | C | G | 8 | a0001c0001t0002g0092 a0003c0003t0001g0091 a0003c0003t0001g0096 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2848-2029C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648945 | |||||||
chr2:200648975 | C | G | 272 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(269): Show |
273 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.2848-1999C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648975 | |||||||
chr2:200648993 | A | C | 153 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(150): Show |
153 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.2848-1981A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200648993 | |||||||
chr2:200649017 | G | T | 1 | a0002c0002t0003g0217 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2848-1957G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649017 | |||||||
chr2:200649048 | C | T | 1 | a0001c0005t0002g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2848-1926C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649048 | |||||||
chr2:200649246 | C | A | 1 | a0001c0001t0001g0355 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2848-1728C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649246 | |||||||
chr2:200649255 | G | A | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(65): Show |
68 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2848-1719G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649255 | |||||||
chr2:200649294 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2848-1680T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649294 | |||||||
chr2:200649346 | G | A | 1 | a0019c0032t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2848-1628G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649346 | |||||||
chr2:200649422 | C | G | 10 | a0001c0001t0001g0317 a0001c0001t0001g0332 a0001c0001t0001g0338 others(7): Show |
10 | NA18939.hp1 NA18950.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.2848-1552C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649422 | |||||||
chr2:200649475 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2848-1499G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649475 | |||||||
chr2:200649538 | G | A | 1 | a0002c0002t0002g0347 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2848-1436G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649538 | |||||||
chr2:200649555 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2848-1419C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649555 | |||||||
chr2:200649570 | A | G | 148 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
148 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.2848-1404A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649570 | |||||||
chr2:200649750 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2848-1224C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649750 | |||||||
chr2:200649787 | G | A | 1 | a0003c0030t0002g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2848-1187G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649787 | |||||||
chr2:200649950 | C | G | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2848-1024C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200649950 | |||||||
chr2:200650169 | G | A | 24 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0271 others(21): Show |
24 | HG00280.hp1 HG00741.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.2848-805G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650169 | |||||||
chr2:200650306 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0002g0145 |
2 | HG02165.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2848-668T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650306 | |||||||
chr2:200650582 | A | G | 16 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0001g0271 others(13): Show |
16 | HG00280.hp1 HG00741.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2848-392A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650582 | |||||||
chr2:200650684 | T | C | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2848-290T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650684 | |||||||
chr2:200650696 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2848-278G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650696 | |||||||
chr2:200650793 | T | C | 16 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0356 others(13): Show |
16 | HG00408.hp1 HG01433.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2848-181T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650793 | |||||||
chr2:200650936 | G | A | 16 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0356 others(13): Show |
16 | HG00408.hp1 HG01433.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2848-38G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650936 | |||||||
chr2:200650940 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2848-34C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 25/34 | chr2 | 200650940 | |||||||
chr2:200651216 | T | C | 284 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(281): Show |
285 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.3075+15T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651216 | |||||||
chr2:200651269 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
13 | HG00733.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3075+68G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651269 | |||||||
chr2:200651304 | G | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(7): Show |
11 | HG01243.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3075+103G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651304 | |||||||
chr2:200651574 | C | T | 1 | a0001c0001t0002g0364 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3075+373C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651574 | |||||||
chr2:200651617 | G | T | 8 | a0001c0005t0001g0053 a0001c0005t0002g0061 a0001c0005t0002g0215 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3075+416G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651617 | |||||||
chr2:200651741 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3075+540G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651741 | |||||||
chr2:200651753 | A | G | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3075+552A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651753 | |||||||
chr2:200651913 | C | A | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3075+712C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651913 | |||||||
chr2:200651917 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3075+716C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651917 | |||||||
chr2:200651929 | T | G | 7 | a0001c0001t0001g0120 a0001c0001t0001g0273 a0001c0001t0001g0319 others(4): Show |
7 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3075+728T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651929 | |||||||
chr2:200651962 | C | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
147 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.3075+761C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200651962 | |||||||
chr2:200652030 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3075+829G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652030 | |||||||
chr2:200652042 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3075+841G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652042 | |||||||
chr2:200652062 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3075+861G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652062 | |||||||
chr2:200652078 | C | T | 227 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
227 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.3075+877C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652078 | |||||||
chr2:200652380 | G | A | 121 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
121 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.3075+1179G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652380 | |||||||
chr2:200652441 | G | C | 9 | a0001c0001t0002g0104 a0002c0002t0003g0041 a0002c0002t0003g0044 others(6): Show |
9 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3075+1240G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652441 | |||||||
chr2:200652671 | G | A | 1 | a0003c0003t0006g0328 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3075+1470G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652671 | |||||||
chr2:200652798 | C | G | 9 | a0001c0001t0002g0104 a0002c0002t0003g0041 a0002c0002t0003g0044 others(6): Show |
9 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3075+1597C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652798 | |||||||
chr2:200652834 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3075+1633A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652834 | |||||||
chr2:200652836 | A | G | 238 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
238 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.3075+1635A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652836 | |||||||
chr2:200652859 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
57 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.3075+1658G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652859 | |||||||
chr2:200652890 | C | T | 1 | a0003c0018t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3075+1689C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652890 | |||||||
chr2:200652943 | C | A | 6 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0006t0001g0093 others(3): Show |
6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3075+1742C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200652943 | |||||||
chr2:200653089 | G | A | 3 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0348 |
3 | NA18955.hp2 NA18981.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3075+1888G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653089 | |||||||
chr2:200653321 | G | A | 13 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0129 others(10): Show |
13 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.3075+2120G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653321 | |||||||
chr2:200653466 | A | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0129 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3075+2265A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653466 | |||||||
chr2:200653485 | C | G | 1 | a0001c0001t0002g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3075+2284C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653485 | |||||||
chr2:200653587 | G | A | 2 | a0001c0005t0006g0076 a0003c0003t0001g0259 |
2 | HG03540.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3075+2386G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653587 | |||||||
chr2:200653645 | G | T | 6 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0006t0001g0093 others(3): Show |
6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3075+2444G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653645 | |||||||
chr2:200653661 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0255 others(11): Show |
15 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3075+2460C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653661 | |||||||
chr2:200653878 | T | G | 3 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0348 |
3 | NA18955.hp2 NA18981.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3075+2677T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200653878 | |||||||
chr2:200654074 | C | T | 1 | a0003c0003t0006g0328 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3076-2768C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654074 | |||||||
chr2:200654179 | G | C | 1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3076-2663G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654179 | |||||||
chr2:200654185 | G | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0325 |
2 | NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3076-2657G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654185 | |||||||
chr2:200654206 | C | CA | 22 | a0001c0001t0001g0196 a0001c0001t0001g0258 a0001c0001t0001g0333 others(19): Show |
22 | HG00423.hp1 HG00741.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3076-2609dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | ||||||
chr2:200654206 | CA | C | 53 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(50): Show |
53 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.3076-2609delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | ||||||
chr2:200654206 | CAAAAA | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0058 others(20): Show |
23 | HG00621.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.3076-2613_3076-260 others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | ||||||
chr2:200654206 | CAAAAAA | C | 128 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
128 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.3076-2614_3076-260 others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | ||||||
chr2:200654206 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0363 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3076-2619_3076-260 others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | ||||||
chr2:200654206 | CAAAAAAA others(7): Show |
C | 10 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0129 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.3076-2622_3076-260 others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200654206 | ||||||
chr2:200654361 | T | C | 6 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0006t0001g0093 others(3): Show |
6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076-2481T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654361 | |||||||
chr2:200654410 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
57 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.3076-2432A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654410 | |||||||
chr2:200654485 | A | G | 1 | a0003c0003t0001g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3076-2357A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654485 | |||||||
chr2:200654559 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3076-2283C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654559 | |||||||
chr2:200654968 | G | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0129 a0001c0001t0001g0229 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3076-1874G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200654968 | |||||||
chr2:200655061 | C | T | 1 | a0001c0014t0001g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3076-1781C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655061 | |||||||
chr2:200655230 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3076-1612C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655230 | |||||||
chr2:200655291 | G | C | 6 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0006t0001g0093 others(3): Show |
6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076-1551G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655291 | |||||||
chr2:200655507 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3076-1335T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655507 | |||||||
chr2:200655548 | C | T | 4 | a0001c0001t0002g0123 a0001c0001t0002g0164 a0001c0001t0002g0244 others(1): Show |
4 | NA18948.hp1 NA18977.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076-1294C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655548 | |||||||
chr2:200655875 | A | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
160 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.3076-967A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200655875 | |||||||
chr2:200656130 | C | T | 9 | a0001c0001t0001g0273 a0001c0001t0002g0206 a0003c0003t0001g0210 others(6): Show |
9 | HG02109.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3076-712C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656130 | |||||||
chr2:200656171 | G | A | 1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3076-671G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656171 | |||||||
chr2:200656199 | T | C | 1 | a0010c0023t0001g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3076-643T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656199 | |||||||
chr2:200656286 | C | T | 6 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0006t0001g0093 others(3): Show |
6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076-556C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656286 | |||||||
chr2:200656293 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3076-549A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656293 | |||||||
chr2:200656313 | T | TA | 162 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
162 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(159): Show |
intron_variant | MODIFIER | c.3076-524dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chr2 | 200656313 | ||||||
chr2:200656401 | G | C | 11 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0002g0150 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.3076-441G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656401 | |||||||
chr2:200656511 | C | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
194 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.3076-331C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656511 | |||||||
chr2:200656660 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
218 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.3076-182T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656660 | |||||||
chr2:200656679 | C | T | 1 | a0002c0002t0003g0151 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3076-163C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656679 | |||||||
chr2:200656732 | G | C | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3076-110G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656732 | |||||||
chr2:200656749 | G | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
103 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.3076-93G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656749 | |||||||
chr2:200656762 | C | T | 12 | a0003c0003t0001g0224 a0003c0003t0001g0243 a0003c0003t0001g0246 others(9): Show |
12 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3076-80C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656762 | |||||||
chr2:200656770 | A | T | 9 | a0001c0001t0002g0104 a0002c0002t0003g0041 a0002c0002t0003g0044 others(6): Show |
9 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3076-72A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656770 | |||||||
chr2:200656786 | C | T | 9 | a0003c0003t0001g0224 a0003c0003t0001g0243 a0003c0003t0001g0246 others(6): Show |
9 | HG01515.hp1 HG01517.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.3076-56C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 26/34 | chr2 | 200656786 | |||||||
chr2:200657008 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0055 others(129): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.3171+71A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657008 | |||||||
chr2:200657062 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3171+125G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657062 | |||||||
chr2:200657141 | T | C | 7 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0129 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3171+204T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657141 | |||||||
chr2:200657161 | C | A | 1 | a0003c0003t0006g0328 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3171+224C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657161 | |||||||
chr2:200657161 | C | CAAAAAAA | 11 | a0001c0001t0001g0134 a0001c0001t0001g0271 a0001c0001t0002g0169 others(8): Show |
11 | HG00544.hp1 HG01496.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657161 | ||||||
chr2:200657161 | C | CAAAAAAA others(2): Show |
68 | a0001c0001t0001g0195 a0001c0001t0001g0356 a0001c0001t0002g0018 others(65): Show |
68 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(11): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657161 | ||||||
chr2:200657161 | C | CAAAAAAA others(4): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0001g0236 others(14): Show |
18 | HG00423.hp2 HG02129.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657161 | ||||||
chr2:200657165 | A | AAAAAAAA others(19): Show |
1 | a0003c0003t0004g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(23): Show |
3 | a0001c0001t0001g0273 a0003c0003t0004g0074 a0003c0003t0004g0094 |
3 | HG02723.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(32): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(27): Show |
2 | a0003c0003t0004g0207 a0003c0003t0006g0328 |
2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(36): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(17): Show |
1 | a0003c0003t0004g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(26): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0339 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(14): Show |
3 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0001g0348 |
3 | NA18955.hp2 NA18963.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(23): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(16): Show |
2 | a0001c0001t0002g0327 a0001c0001t0002g0340 |
2 | NA18939.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0002g0341 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(31): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(26): Show |
1 | a0003c0003t0004g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(35): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(30): Show |
1 | a0001c0001t0002g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(39): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0332 a0004c0004t0001g0302 |
2 | NA19062.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(15): Show |
1 | a0004c0004t0001g0300 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(17): Show |
2 | a0001c0001t0001g0078 a0004c0004t0001g0299 |
2 | HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(26): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(19): Show |
2 | a0004c0004t0001g0304 a0004c0004t0001g0326 |
2 | NA18977.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0225 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(30): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(6): Show |
5 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0002g0337 others(2): Show |
5 | NA18942.hp1 NA18943.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0358 a0001c0001t0002g0115 |
2 | NA19060.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(12): Show |
4 | a0001c0001t0001g0227 a0001c0001t0001g0264 a0001c0001t0001g0320 others(1): Show |
4 | HG02056.hp1 NA18948.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(14): Show |
6 | a0001c0001t0001g0280 a0001c0001t0001g0311 a0001c0001t0001g0322 others(3): Show |
6 | HG03942.hp1 NA18945.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(23): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(16): Show |
7 | a0001c0001t0001g0163 a0001c0001t0001g0239 a0001c0001t0001g0323 others(4): Show |
7 | HG02015.hp1 HG02056.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(18): Show |
10 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(7): Show |
10 | HG00597.hp2 HG00673.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(27): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(20): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0222 a0002c0002t0002g0347 |
3 | HG02015.hp2 NA18944.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(29): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(22): Show |
3 | a0001c0001t0001g0219 a0001c0001t0001g0235 a0001c0001t0001g0354 |
3 | HG02155.hp1 HG04199.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(31): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0002g0119 a0014c0012t0001g0197 |
2 | HG03927.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0316 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(19): Show |
2 | a0004c0004t0001g0301 a0007c0028t0001g0312 |
2 | HG00408.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0321 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(30): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(4): Show |
14 | a0001c0001t0001g0172 a0001c0001t0002g0012 a0001c0001t0002g0027 others(11): Show |
14 | HG01943.hp1 HG01975.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.3171+229_3171+230i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0020 a0001c0001t0002g0108 |
2 | HG00609.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0196 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0306 a0001c0001t0001g0317 a0001c0001t0001g0355 |
3 | NA18950.hp2 NA18978.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3171+229_3171+230i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAATA others(5): Show |
1 | a0003c0006t0001g0093 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAATA others(7): Show |
1 | a0003c0006t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAATA others(9): Show |
1 | a0003c0006t0001g0095 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3171+229_3171+230i others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAAAAATA others(13): Show |
1 | a0001c0001t0001g0089 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3171+229_3171+230i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AAT | 7 | a0001c0001t0001g0191 a0001c0001t0001g0199 a0001c0001t0002g0150 others(4): Show |
7 | HG00738.hp2 HG01255.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3171+253_3171+254d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | AATAT | 4 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0233 others(1): Show |
4 | HG03491.hp2 HG03834.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.3171+251_3171+254d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657165 | ||||||
chr2:200657165 | A | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0214 others(13): Show |
17 | HG01109.hp1 HG01243.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.3171+228A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657165 | |||||||
chr2:200657167 | T | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0166 others(1): Show |
5 | HG00733.hp2 HG01261.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.3171+230T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657167 | |||||||
chr2:200657169 | T | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0242 |
3 | HG00733.hp2 HG02293.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.3171+232T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657169 | |||||||
chr2:200657171 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+234T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657171 | |||||||
chr2:200657173 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+236T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657173 | |||||||
chr2:200657175 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+238T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657175 | |||||||
chr2:200657177 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3171+240T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657177 | |||||||
chr2:200657184 | A | AT | 4 | a0001c0001t0001g0001 a0001c0001t0002g0132 a0001c0001t0002g0363 others(1): Show |
5 | HG03831.hp2 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.3171+248dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657184 | ||||||
chr2:200657184 | A | ATTT | 9 | a0001c0001t0002g0025 a0001c0001t0002g0031 a0001c0001t0002g0032 others(6): Show |
9 | HG00738.hp1 HG01081.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3171+248_3171+249i others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657184 | ||||||
chr2:200657184 | A | T | 3 | a0001c0001t0002g0027 a0001c0001t0002g0029 a0001c0001t0002g0070 |
3 | HG01943.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.3171+247A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657184 | |||||||
chr2:200657186 | A | AT | 13 | a0001c0001t0001g0055 a0001c0001t0001g0356 a0001c0001t0002g0005 others(10): Show |
13 | HG00733.hp1 HG01433.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.3171+250dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657186 | ||||||
chr2:200657186 | A | ATTT | 3 | a0001c0001t0002g0178 a0001c0001t0002g0349 a0001c0001t0002g0362 |
3 | NA18967.hp1 NA18992.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3171+250_3171+251i others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657186 | ||||||
chr2:200657186 | A | ATTTTTTT others(5): Show |
1 | a0003c0003t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3171+250_3171+251i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657186 | ||||||
chr2:200657186 | A | T | 23 | a0001c0001t0001g0001 a0001c0001t0002g0025 a0001c0001t0002g0027 others(20): Show |
24 | HG00738.hp1 HG01081.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.3171+249A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657186 | |||||||
chr2:200657188 | A | AT | 14 | a0001c0001t0001g0281 a0001c0001t0002g0130 a0001c0001t0002g0141 others(11): Show |
14 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.3171+252dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657188 | ||||||
chr2:200657188 | A | ATTT | 19 | a0001c0001t0001g0195 a0001c0001t0002g0018 a0001c0001t0002g0028 others(16): Show |
19 | HG00609.hp1 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.3171+252_3171+253i others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657188 | ||||||
chr2:200657188 | A | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(58): Show |
62 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.3171+251A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657188 | |||||||
chr2:200657189 | TA | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(12): Show |
15 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.3171+253delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657189 | |||||||
chr2:200657190 | A | AT | 13 | a0001c0001t0001g0163 a0001c0001t0001g0219 a0001c0001t0001g0222 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.3171+268dupT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(12): Show |
1 | a0003c0003t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(21): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(44): Show |
1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(53): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(21): Show |
1 | a0003c0003t0001g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(30): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(15): Show |
1 | a0003c0003t0001g0243 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(32): Show |
1 | a0003c0009t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(41): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(19): Show |
1 | a0013c0024t0001g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(15): Show |
2 | a0003c0003t0001g0096 a0003c0006t0001g0122 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(16): Show |
1 | a0003c0018t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(25): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(8): Show |
1 | a0003c0003t0001g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(19): Show |
1 | a0003c0030t0002g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(28): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(7): Show |
1 | a0003c0026t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(14): Show |
1 | a0003c0003t0001g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(23): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(6): Show |
1 | a0003c0003t0001g0246 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(15): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0318 |
4 | HG02615.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0267 a0001c0001t0001g0319 a0001c0014t0001g0352 |
3 | HG02818.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATAT others(10): Show |
1 | a0019c0032t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(19): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATTT others(3): Show |
1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATTT others(8): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0258 a0001c0001t0001g0269 |
3 | HG01109.hp1 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATTT others(9): Show |
2 | a0001c0001t0001g0268 a0001c0001t0001g0333 |
2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATATTT others(11): Show |
2 | a0001c0001t0001g0256 a0012c0021t0001g0257 |
2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3171+254_3171+255i others(20): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATTTTT others(7): Show |
1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3171+254_3171+255i others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0229 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3171+254_3171+255i others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATTT | 39 | a0001c0001t0001g0078 a0001c0001t0001g0121 a0001c0001t0001g0271 others(36): Show |
39 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.3171+266_3171+268d others(5): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATTTT | 10 | a0001c0001t0001g0073 a0001c0001t0001g0320 a0001c0001t0002g0113 others(7): Show |
10 | HG02970.hp2 HG03139.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.3171+265_3171+268d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATTTTT | 14 | a0001c0001t0001g0124 a0001c0001t0001g0196 a0001c0001t0001g0239 others(11): Show |
14 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.3171+264_3171+268d others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0002g0206 a0003c0003t0004g0209 a0003c0006t0001g0093 |
3 | HG02109.hp2 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3171+259_3171+268d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATTTTTTT others(5): Show |
3 | a0003c0003t0004g0094 a0003c0003t0004g0212 a0003c0003t0006g0328 |
3 | HG02723.hp1 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3171+257_3171+268d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATTTTTTT others(7): Show |
1 | a0003c0009t0001g0360 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3171+255_3171+268d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | ATTTTTTT others(8): Show |
1 | a0003c0003t0004g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3171+254_3171+268d others(17): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657190 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(126): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.3171+253A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657190 | |||||||
chr2:200657190 | AT | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
14 | HG00639.hp2 HG01123.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3171+268delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chr2 | 200657190 | ||||||
chr2:200657191 | T | TA | 4 | a0001c0001t0001g0266 a0001c0001t0001g0336 a0001c0001t0001g0342 others(1): Show |
4 | HG01123.hp2 HG01981.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3171+254_3171+255i others(3): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657191 | |||||||
chr2:200657192 | T | A | 28 | a0001c0001t0001g0168 a0001c0001t0001g0191 a0001c0001t0001g0223 others(25): Show |
28 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.3171+255T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657192 | |||||||
chr2:200657193 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3171+256T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657193 | |||||||
chr2:200657194 | T | A | 8 | a0001c0001t0002g0174 a0001c0001t0002g0231 a0001c0001t0002g0251 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.3171+257T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657194 | |||||||
chr2:200657383 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0021 others(183): Show |
188 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3171+446G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657383 | |||||||
chr2:200657411 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0176 |
2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.3171+474C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657411 | |||||||
chr2:200657412 | T | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.3171+475T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657412 | |||||||
chr2:200657493 | G | A | 3 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0103 |
3 | NA18939.hp2 NA18940.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.3171+556G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657493 | |||||||
chr2:200657539 | C | T | 1 | a0003c0003t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3171+602C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657539 | |||||||
chr2:200657654 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3171+717C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657654 | |||||||
chr2:200657669 | A | G | 60 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(57): Show |
60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3171+732A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657669 | |||||||
chr2:200657718 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0020t0001g0228 |
3 | NA18942.hp2 NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.3171+781C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657718 | |||||||
chr2:200657899 | G | T | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3171+962G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657899 | |||||||
chr2:200657992 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3171+1055G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200657992 | |||||||
chr2:200658032 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(232): Show |
237 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.3171+1095C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658032 | |||||||
chr2:200658098 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3172-1067C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658098 | |||||||
chr2:200658166 | T | C | 6 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0006t0001g0093 others(3): Show |
6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172-999T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658166 | |||||||
chr2:200658230 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3172-935C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658230 | |||||||
chr2:200658461 | C | G | 29 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0003t0001g0097 others(26): Show |
29 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.3172-704C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658461 | |||||||
chr2:200658616 | C | T | 1 | a0001c0001t0001g0356 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3172-549C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658616 | |||||||
chr2:200658721 | C | T | 2 | a0003c0009t0001g0098 a0003c0009t0001g0360 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3172-444C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658721 | |||||||
chr2:200658746 | T | A | 2 | a0003c0009t0001g0098 a0003c0009t0001g0360 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.3172-419T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658746 | |||||||
chr2:200658808 | G | A | 1 | a0003c0003t0006g0328 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3172-357G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200658808 | |||||||
chr2:200659013 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(241): Show |
246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.3172-152A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659013 | |||||||
chr2:200659027 | G | A | 2 | a0001c0005t0006g0076 a0002c0002t0007g0250 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3172-138G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659027 | |||||||
chr2:200659033 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3172-132A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659033 | |||||||
chr2:200659090 | T | G | 6 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0006t0001g0093 others(3): Show |
6 | HG02258.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172-75T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 27/34 | chr2 | 200659090 | |||||||
chr2:200659391 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0187 a0001c0008t0001g0361 |
3 | HG02145.hp2 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.3300+98A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659391 | |||||||
chr2:200659471 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3300+178C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659471 | |||||||
chr2:200659474 | C | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0120 others(19): Show |
23 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3300+181C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659474 | |||||||
chr2:200659777 | TTC | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(48): Show |
52 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3301-209_3301-208d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659777 | ||||||
chr2:200659777 | TTCTC | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0117 a0001c0001t0001g0129 others(12): Show |
15 | HG02132.hp2 HG02300.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3301-211_3301-208d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659777 | ||||||
chr2:200659782 | TCTCTCAC others(1): Show |
T | 6 | a0001c0001t0001g0120 a0001c0001t0002g0108 a0001c0001t0002g0364 others(3): Show |
6 | HG00609.hp2 HG00733.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.3301-211_3301-204d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | ||||||
chr2:200659782 | TCTCTCAC others(3): Show |
T | 29 | a0001c0001t0001g0236 a0001c0001t0001g0271 a0001c0001t0001g0356 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.3301-211_3301-202d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | ||||||
chr2:200659782 | TCTCTCAC others(5): Show |
T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(86): Show |
90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3301-211_3301-200d others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | ||||||
chr2:200659782 | TCTCTCAC others(7): Show |
T | 1 | a0001c0001t0002g0308 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3301-211_3301-198d others(16): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659782 | ||||||
chr2:200659784 | T | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0334 a0001c0001t0001g0335 others(6): Show |
9 | HG02056.hp2 HG03942.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.3301-211T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659784 | |||||||
chr2:200659786 | T | A | 54 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(51): Show |
54 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.3301-209T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659786 | |||||||
chr2:200659786 | T | TCA | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(22): Show |
26 | HG00639.hp1 HG00639.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.3301-171_3301-170d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | ||||||
chr2:200659786 | T | TCACA | 11 | a0001c0001t0001g0073 a0001c0001t0001g0121 a0001c0001t0001g0166 others(8): Show |
11 | HG01192.hp1 HG01261.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.3301-173_3301-170d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | ||||||
chr2:200659786 | T | TCACACAC others(3): Show |
1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3301-179_3301-170d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | ||||||
chr2:200659786 | T | TCTCACAC others(5): Show |
1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3301-208_3301-207i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | ||||||
chr2:200659786 | TCA | T | 20 | a0001c0001t0001g0062 a0001c0001t0001g0128 a0001c0001t0001g0198 others(17): Show |
21 | HG01192.hp2 HG01358.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.3301-171_3301-170d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | ||||||
chr2:200659786 | TCACACAC others(13): Show |
T | 3 | a0003c0009t0001g0098 a0003c0009t0001g0360 a0006c0010t0009g0278 |
3 | HG02055.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3301-189_3301-170d others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | ||||||
chr2:200659786 | TCACACAC others(15): Show |
T | 1 | a0003c0026t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3301-191_3301-170d others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659786 | ||||||
chr2:200659790 | A | T | 1 | a0002c0002t0003g0050 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3301-205A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | chr2 | 200659790 | |||||||
chr2:200659791 | C | CACACAT | 7 | a0003c0003t0001g0210 a0003c0003t0001g0243 a0003c0003t0001g0248 others(4): Show |
7 | HG01515.hp1 HG01517.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3301-199_3301-198i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659791 | ||||||
chr2:200659793 | C | CACAT | 8 | a0003c0003t0001g0224 a0003c0003t0001g0246 a0003c0003t0001g0247 others(5): Show |
8 | HG02647.hp1 HG03209.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.3301-199_3301-198i others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659793 | ||||||
chr2:200659806 | ACACACAC others(15): Show |
A | 2 | a0003c0003t0001g0091 a0003c0003t0001g0096 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3301-181_3301-160d others(24): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659806 | ||||||
chr2:200659812 | ACACACAC others(9): Show |
A | 4 | a0003c0006t0001g0093 a0003c0006t0001g0095 a0003c0006t0001g0106 others(1): Show |
4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3301-175_3301-160d others(18): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chr2 | 200659812 | ||||||
chr2:200660269 | G | T | 1 | a0001c0001t0002g0362 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3375+200G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660269 | |||||||
chr2:200660380 | G | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.3375+311G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660380 | |||||||
chr2:200660504 | G | T | 2 | a0001c0005t0006g0076 a0002c0002t0007g0250 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3375+435G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660504 | |||||||
chr2:200660523 | A | G | 1 | a0001c0008t0001g0361 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3375+454A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660523 | |||||||
chr2:200660534 | A | G | 9 | a0001c0001t0002g0104 a0002c0002t0003g0041 a0002c0002t0003g0044 others(6): Show |
9 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3375+465A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660534 | |||||||
chr2:200660779 | G | T | 1 | a0001c0001t0002g0070 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3375+710G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660779 | |||||||
chr2:200660832 | G | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(205): Show |
210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.3376-747G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660832 | |||||||
chr2:200660945 | G | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | NA18948.hp2 NA18955.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3376-634G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660945 | |||||||
chr2:200660985 | A | G | 7 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0003t0001g0097 others(4): Show |
7 | HG02258.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3376-594A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200660985 | |||||||
chr2:200661159 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(73): Show |
77 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.3376-420G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661159 | |||||||
chr2:200661186 | A | G | 60 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(57): Show |
60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3376-393A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661186 | |||||||
chr2:200661197 | C | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3376-382C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661197 | |||||||
chr2:200661406 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3376-173A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 29/34 | chr2 | 200661406 | |||||||
chr2:200661645 | C | G | 29 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0003t0001g0097 others(26): Show |
29 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.3428+14C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200661645 | |||||||
chr2:200661829 | T | C | 7 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0105 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3428+198T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200661829 | |||||||
chr2:200662023 | C | T | 33 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0057 others(30): Show |
33 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.3428+392C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662023 | |||||||
chr2:200662041 | A | G | 1 | a0001c0020t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3428+410A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662041 | |||||||
chr2:200662049 | T | C | 1 | a0001c0001t0002g0241 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3428+418T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662049 | |||||||
chr2:200662056 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3428+425A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662056 | |||||||
chr2:200662382 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3429-473C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662382 | |||||||
chr2:200662467 | G | A | 1 | a0008c0025t0003g0285 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3429-388G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662467 | |||||||
chr2:200662487 | A | G | 1 | a0002c0002t0003g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3429-368A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662487 | |||||||
chr2:200662495 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3429-360A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662495 | |||||||
chr2:200662516 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0055 others(145): Show |
150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.3429-339G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662516 | |||||||
chr2:200662615 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0195 others(67): Show |
71 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.3429-240G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662615 | |||||||
chr2:200662740 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3429-115A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662740 | |||||||
chr2:200662806 | C | T | 12 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0029 others(9): Show |
12 | HG00738.hp1 HG01081.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3429-49C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 30/34 | chr2 | 200662806 | |||||||
chr2:200663167 | T | C | 7 | a0003c0003t0001g0091 a0003c0003t0001g0096 a0003c0003t0001g0097 others(4): Show |
7 | HG02258.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+198T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663167 | |||||||
chr2:200663212 | G | T | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3543+243G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663212 | |||||||
chr2:200663254 | A | G | 60 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(57): Show |
60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3543+285A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663254 | |||||||
chr2:200663524 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(143): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.3543+555A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663524 | |||||||
chr2:200663545 | A | AACAC | 55 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(52): Show |
55 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.3543+601_3543+604d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | ||||||
chr2:200663545 | A | AACACACA others(1): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0214 others(11): Show |
15 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3543+597_3543+604d others(10): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | ||||||
chr2:200663545 | A | AACACACA others(3): Show |
1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3543+595_3543+604d others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | ||||||
chr2:200663545 | AAC | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0129 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+603_3543+604d others(4): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | ||||||
chr2:200663545 | AACAC | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0283 others(3): Show |
6 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3543+601_3543+604d others(6): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663545 | ||||||
chr2:200663561 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3543+592C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663561 | |||||||
chr2:200663570 | A | T | 19 | a0001c0001t0001g0236 a0001c0001t0001g0356 a0001c0001t0002g0130 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.3543+601A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663570 | |||||||
chr2:200663572 | A | ACACACAC others(13): Show |
1 | a0003c0026t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3543+604_3543+605i others(22): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | ||||||
chr2:200663572 | A | ACACACT | 3 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0242 |
3 | HG02015.hp2 NA18965.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.3543+604_3543+605i others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | ||||||
chr2:200663572 | A | ACACACTC others(3): Show |
2 | a0001c0001t0002g0133 a0001c0001t0002g0142 |
2 | HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.3543+604_3543+605i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | ||||||
chr2:200663572 | A | ACACACTC others(5): Show |
10 | a0003c0003t0001g0224 a0003c0003t0001g0243 a0003c0003t0001g0248 others(7): Show |
10 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.3543+604_3543+605i others(14): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | ||||||
chr2:200663572 | A | ACACTCTC others(3): Show |
7 | a0003c0003t0001g0210 a0003c0003t0001g0246 a0003c0003t0004g0074 others(4): Show |
7 | HG02647.hp1 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+604_3543+605i others(12): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663572 | ||||||
chr2:200663572 | A | T | 38 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0236 others(35): Show |
38 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.3543+603A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663572 | |||||||
chr2:200663574 | T | A | 4 | a0001c0001t0002g0034 a0001c0001t0002g0180 a0001c0008t0002g0201 others(1): Show |
4 | HG01975.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3543+605T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663574 | |||||||
chr2:200663575 | C | G | 18 | a0003c0003t0001g0210 a0003c0003t0001g0224 a0003c0003t0001g0243 others(15): Show |
18 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.3543+606C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663575 | |||||||
chr2:200663577 | C | G | 3 | a0001c0001t0002g0133 a0001c0001t0002g0142 a0003c0030t0002g0216 |
3 | HG02071.hp2 HG02083.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3543+608C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663577 | |||||||
chr2:200663579 | C | G | 17 | a0001c0001t0001g0236 a0001c0001t0001g0356 a0001c0001t0002g0130 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.3543+610C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663579 | |||||||
chr2:200663581 | C | G | 6 | a0001c0001t0001g0271 a0001c0001t0002g0270 a0001c0001t0002g0276 others(3): Show |
6 | HG00741.hp1 HG01106.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3543+612C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663581 | |||||||
chr2:200663583 | C | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(92): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.3543+614C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663583 | |||||||
chr2:200663585 | C | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0180 a0001c0008t0002g0201 |
3 | HG01975.hp1 HG02965.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.3543+616C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663585 | |||||||
chr2:200663596 | T | C | 21 | a0003c0003t0001g0210 a0003c0003t0001g0224 a0003c0003t0001g0243 others(18): Show |
21 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.3543+627T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663596 | |||||||
chr2:200663596 | T | TCTCCC | 17 | a0001c0001t0001g0236 a0001c0001t0001g0356 a0001c0001t0002g0130 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.3543+628_3543+629i others(7): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | ||||||
chr2:200663596 | T | TCTCTCCC | 6 | a0001c0001t0001g0271 a0001c0001t0002g0270 a0001c0001t0002g0276 others(3): Show |
6 | HG00741.hp1 HG01106.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3543+628_3543+629i others(9): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | ||||||
chr2:200663596 | T | TCTCTCTC others(2): Show |
95 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(92): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.3543+628_3543+629i others(11): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | ||||||
chr2:200663596 | T | TCTCTCTC others(4): Show |
3 | a0001c0001t0002g0034 a0001c0001t0002g0180 a0001c0008t0002g0201 |
3 | HG01975.hp1 HG02965.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.3543+628_3543+629i others(13): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200663596 | ||||||
chr2:200663603 | C | T | 1 | a0010c0023t0001g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3543+634C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663603 | |||||||
chr2:200663604 | T | C | 1 | a0003c0026t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3543+635T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663604 | |||||||
chr2:200663618 | G | A | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3543+649G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663618 | |||||||
chr2:200663704 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(234): Show |
239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3543+735A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663704 | |||||||
chr2:200663777 | GA | G | 7 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0129 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+809delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200663777 | |||||||
chr2:200664022 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(72): Show |
76 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3543+1053G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664022 | |||||||
chr2:200664038 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(227): Show |
232 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3543+1069G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664038 | |||||||
chr2:200664119 | CTGTT | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(227): Show |
232 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3543+1168_3543+117 others(8): Show |
AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | INFO_REALIGN_3_PRIME | chr2 | 200664119 | ||||||
chr2:200664271 | G | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0129 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3543+1302G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664271 | |||||||
chr2:200664364 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(227): Show |
232 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3543+1395A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664364 | |||||||
chr2:200664380 | C | T | 4 | a0003c0006t0001g0093 a0003c0006t0001g0095 a0003c0006t0001g0106 others(1): Show |
4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3543+1411C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664380 | |||||||
chr2:200664485 | T | C | 2 | a0003c0003t0001g0246 a0003c0003t0001g0247 |
2 | HG03831.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3543+1516T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664485 | |||||||
chr2:200664719 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3543+1750A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664719 | |||||||
chr2:200664723 | G | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3543+1754G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664723 | |||||||
chr2:200664727 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3543+1758G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664727 | |||||||
chr2:200664743 | C | G | 1 | a0002c0002t0002g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3543+1774C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664743 | |||||||
chr2:200664755 | C | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(234): Show |
239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3543+1786C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664755 | |||||||
chr2:200664901 | C | T | 1 | a0006c0010t0009g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3544-1786C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664901 | |||||||
chr2:200664998 | T | C | 1 | a0001c0001t0001g0356 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3544-1689T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200664998 | |||||||
chr2:200665017 | G | A | 1 | a0001c0005t0006g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3544-1670G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665017 | |||||||
chr2:200665175 | T | C | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0148 |
3 | NA18961.hp1 NA18980.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3544-1512T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665175 | |||||||
chr2:200665177 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(234): Show |
239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3544-1510C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665177 | |||||||
chr2:200665556 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(181): Show |
185 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3544-1131T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665556 | |||||||
chr2:200665785 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3544-902T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200665785 | |||||||
chr2:200666007 | T | C | 60 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(57): Show |
60 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3544-680T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666007 | |||||||
chr2:200666017 | A | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(234): Show |
239 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.3544-670A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666017 | |||||||
chr2:200666042 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
83 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.3544-645C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666042 | |||||||
chr2:200666113 | C | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0124 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3544-574C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666113 | |||||||
chr2:200666243 | C | T | 1 | a0003c0003t0001g0246 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3544-444C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666243 | |||||||
chr2:200666361 | T | G | 1 | a0002c0002t0007g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3544-326T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666361 | |||||||
chr2:200666471 | A | C | 8 | a0003c0003t0001g0224 a0003c0003t0001g0243 a0003c0003t0001g0246 others(5): Show |
8 | HG01515.hp1 HG01517.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.3544-216A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666471 | |||||||
chr2:200666504 | T | C | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3544-183T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666504 | |||||||
chr2:200666537 | C | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(240): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.3544-150C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 31/34 | chr2 | 200666537 | |||||||
chr2:200666911 | T | C | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3609+159T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200666911 | |||||||
chr2:200666934 | G | A | 1 | a0003c0003t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3609+182G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200666934 | |||||||
chr2:200667042 | A | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(246): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.3609+290A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667042 | |||||||
chr2:200667059 | T | C | 61 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(58): Show |
61 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.3609+307T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667059 | |||||||
chr2:200667077 | C | T | 1 | a0003c0003t0006g0328 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3609+325C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667077 | |||||||
chr2:200667121 | C | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(251): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.3609+369C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667121 | |||||||
chr2:200667172 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG01070.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.3609+420G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667172 | |||||||
chr2:200667369 | C | G | 2 | a0003c0003t0006g0328 a0003c0026t0001g0211 |
2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3609+617C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667369 | |||||||
chr2:200667377 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0055 others(145): Show |
150 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.3609+625G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667377 | |||||||
chr2:200667451 | A | C | 1 | a0001c0001t0002g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3609+699A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667451 | |||||||
chr2:200667480 | A | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(243): Show |
248 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.3609+728A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667480 | |||||||
chr2:200667721 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3610-894A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667721 | |||||||
chr2:200667740 | G | A | 2 | a0006c0010t0007g0279 a0006c0010t0009g0278 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3610-875G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667740 | |||||||
chr2:200667757 | G | C | 3 | a0002c0002t0007g0250 a0003c0003t0001g0097 a0003c0026t0001g0211 |
3 | HG02886.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3610-858G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667757 | |||||||
chr2:200667762 | T | C | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3610-853T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667762 | |||||||
chr2:200667765 | A | C | 1 | a0001c0001t0002g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3610-850A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667765 | |||||||
chr2:200667845 | A | G | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3610-770A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667845 | |||||||
chr2:200667902 | A | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
226 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.3610-713A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667902 | |||||||
chr2:200667959 | T | C | 1 | a0003c0003t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3610-656T>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667959 | |||||||
chr2:200667968 | A | G | 1 | a0001c0005t0002g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3610-647A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667968 | |||||||
chr2:200667975 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0166 a0001c0001t0001g0203 others(28): Show |
32 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.3610-640G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200667975 | |||||||
chr2:200668109 | TA | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0333 a0003c0006t0001g0093 others(3): Show |
6 | HG01243.hp2 HG02258.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3610-505delA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668109 | |||||||
chr2:200668110 | A | T | 8 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0153 others(5): Show |
8 | HG01496.hp1 HG02129.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3610-505A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668110 | |||||||
chr2:200668110 | AT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0129 others(30): Show |
34 | HG01109.hp1 HG01261.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3610-493delT | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chr2 | 200668110 | ||||||
chr2:200668113 | T | A | 1 | a0003c0003t0001g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3610-502T>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668113 | |||||||
chr2:200668125 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
220 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.3610-490G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668125 | |||||||
chr2:200668183 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3610-432G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668183 | |||||||
chr2:200668191 | C | T | 1 | a0006c0010t0007g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3610-424C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668191 | |||||||
chr2:200668209 | G | A | 1 | a0014c0012t0001g0197 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3610-406G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668209 | |||||||
chr2:200668248 | G | A | 1 | a0001c0001t0001g0350 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3610-367G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668248 | |||||||
chr2:200668329 | A | C | 1 | a0001c0001t0001g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3610-286A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668329 | |||||||
chr2:200668393 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3610-222G>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668393 | |||||||
chr2:200668401 | G | T | 1 | a0001c0001t0001g0336 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3610-214G>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668401 | |||||||
chr2:200668440 | C | A | 2 | a0002c0002t0007g0250 a0006c0010t0007g0279 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3610-175C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668440 | |||||||
chr2:200668488 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3610-127A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668488 | |||||||
chr2:200668490 | G | A | 2 | a0001c0001t0002g0364 a0001c0001t0002g0365 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3610-125G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668490 | |||||||
chr2:200668492 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
141 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.3610-123C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 32/34 | chr2 | 200668492 | |||||||
chr2:200669006 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3798+203G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669006 | |||||||
chr2:200669165 | C | T | 4 | a0003c0006t0001g0093 a0003c0006t0001g0095 a0003c0006t0001g0106 others(1): Show |
4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798+362C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669165 | |||||||
chr2:200669182 | G | A | 4 | a0003c0006t0001g0093 a0003c0006t0001g0095 a0003c0006t0001g0106 others(1): Show |
4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798+379G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669182 | |||||||
chr2:200669192 | C | G | 1 | a0001c0001t0002g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3799-383C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669192 | |||||||
chr2:200669260 | C | G | 1 | a0001c0001t0002g0139 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3799-315C>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669260 | |||||||
chr2:200669262 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
192 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.3799-313A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669262 | |||||||
chr2:200669293 | A | G | 1 | a0018c0011t0001g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3799-282A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669293 | |||||||
chr2:200669316 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3799-259A>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669316 | |||||||
chr2:200669413 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(135): Show |
140 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.3799-162C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669413 | |||||||
chr2:200669450 | C | CA | 9 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0229 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3799-112dupA | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chr2 | 200669450 | ||||||
chr2:200669461 | A | C | 10 | a0002c0002t0003g0041 a0002c0002t0003g0044 a0002c0002t0003g0045 others(7): Show |
10 | HG01106.hp1 HG01123.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.3799-114A>C | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669461 | |||||||
chr2:200669464 | T | G | 4 | a0003c0006t0001g0093 a0003c0006t0001g0095 a0003c0006t0001g0106 others(1): Show |
4 | HG02258.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3799-111T>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 33/34 | chr2 | 200669464 | |||||||
chr2:200669860 | C | T | 7 | a0001c0005t0004g0296 a0003c0003t0004g0074 a0003c0003t0004g0094 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3966+118C>T | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200669860 | |||||||
chr2:200670066 | A | G | 1 | a0003c0003t0006g0328 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3966+324A>G | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200670066 | |||||||
chr2:200670352 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(135): Show |
140 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.3967-277G>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200670352 | |||||||
chr2:200670553 | C | A | 1 | a0018c0011t0001g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3967-76C>A | AOX1 | ENSG00000138356.14 | transcript | ENST00000374700.7 | protein_coding | 34/34 | chr2 | 200670553 |