Item | Value |
---|---|
geneid | 132949 |
ensemblid | ENSG00000157426.14 |
hgncid | 23993 |
symbol | AASDH |
name | aminoadipate-semialdehyde dehydrogenase |
refseq_nuc | NM_181806.4 |
refseq_prot | NP_861522.2 |
ensembl_nuc | ENST00000205214.11 |
ensembl_prot | ENSP00000205214.6 |
mane_status | MANE Select |
chr | chr4 |
start | 56338290 |
end | 56387491 |
strand | - |
ver | v1.2 |
region | chr4:56338290-56387491 |
region5000 | chr4:56333290-56392491 |
regionname0 | AASDH_chr4_56338290_56387491 |
regionname5000 | AASDH_chr4_56333290_56392491 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1098 | 130 | 26 | 16 | 73 | 8 | 6 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0002 | 0/0 | 1098 | 92 | 16 | 19 | 50 | 2 | 5 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0003 | 0/1 | 1098 | 77 | 25 | 24 | 6 | 6 | 15 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0004 | 0/0 | 1098 | 54 | 2 | 0 | 44 | 0 | 8 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0005 | 0/0 | 1097 | 8 | 8 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1092): Show |
chr4 | 56333290 | 56392491 |
a0006 | 0/0 | 1098 | 4 | 4 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0007 | 0/0 | 1098 | 4 | 3 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0008 | 0/0 | 1098 | 2 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0009 | 0/0 | 1098 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0010 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0011 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0012 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0013 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0014 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0015 | 0/0 | 145 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(140): Show |
chr4 | 56333290 | 56392491 |
a0016 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0017 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
a0018 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | MTLQE others(1093): Show |
chr4 | 56333290 | 56392491 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3294 | 87 | 19 | 12 | 46 | 5 | 4 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0001c0005 | 0/0 | 3294 | 40 | 4 | 4 | 27 | 3 | 2 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0001c0010 | 0/0 | 3294 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0001c0019 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0002c0002 | 0/0 | 3294 | 82 | 16 | 19 | 40 | 2 | 5 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0002c0006 | 0/0 | 3294 | 9 | 0 | 0 | 9 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0002c0024 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0003c0003 | 0/1 | 3294 | 77 | 25 | 24 | 6 | 6 | 15 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0004c0004 | 0/0 | 3294 | 53 | 2 | 0 | 43 | 0 | 8 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0004c0025 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0005c0007 | 0/0 | 3291 | 8 | 8 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3286): Show |
chr4 | 56333290 | 56392491 | ||
a0006c0008 | 0/0 | 3294 | 4 | 4 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0007c0009 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0007c0020 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0008c0012 | 0/0 | 3294 | 2 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0009c0011 | 0/0 | 3294 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0010c0016 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0011c0018 | 0/0 | 3294 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0012c0023 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0013c0021 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0014c0022 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0015c0013 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0016c0015 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0017c0017 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 | ||
a0018c0014 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ATGAC others(3289): Show |
chr4 | 56333290 | 56392491 |
acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3581 | 87 | 19 | 12 | 46 | 5 | 4 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0001c0005t0001 | 0/0 | 3581 | 39 | 4 | 4 | 26 | 3 | 2 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0001c0005t0005 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0001c0010t0001 | 0/0 | 3581 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0001c0019t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0002c0002t0001 | 0/0 | 3581 | 81 | 15 | 19 | 40 | 2 | 5 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0002c0002t0007 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0002c0006t0001 | 0/0 | 3581 | 9 | 0 | 0 | 9 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0002c0024t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0003c0003t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0003c0003t0002 | 0/1 | 3585 | 76 | 24 | 24 | 6 | 6 | 15 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3580): Show |
chr4 | 56333290 | 56392491 |
a0004c0004t0001 | 0/0 | 3581 | 52 | 2 | 0 | 42 | 0 | 8 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0004c0004t0006 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0004c0025t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0005c0007t0003 | 0/0 | 3578 | 8 | 8 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3573): Show |
chr4 | 56333290 | 56392491 |
a0006c0008t0001 | 0/0 | 3581 | 4 | 4 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0007c0009t0004 | 0/0 | 3581 | 3 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0007c0020t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0008c0012t0001 | 0/0 | 3581 | 2 | 0 | 1 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0009c0011t0002 | 0/0 | 3585 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3580): Show |
chr4 | 56333290 | 56392491 |
a0010c0016t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0011c0018t0001 | 0/0 | 3581 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0012c0023t0002 | 0/0 | 3585 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3580): Show |
chr4 | 56333290 | 56392491 |
a0013c0021t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0014c0022t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0015c0013t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0016c0015t0001 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0017c0017t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
a0018c0014t0001 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | ACGTA others(3576): Show |
chr4 | 56333290 | 56392491 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0004 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0005t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0010t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0010t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0001c0019t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0002t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0002c0024t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0003c0003t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0004t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0004c0025t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0005c0007t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0006c0008t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0006c0008t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0006c0008t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0006c0008t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0007c0009t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0007c0009t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0007c0020t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0008c0012t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0008c0012t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0009c0011t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0009c0011t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0010c0016t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0011c0018t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0012c0023t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0013c0021t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0014c0022t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0015c0013t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0016c0015t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0017c0017t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
a0018c0014t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0001 | g0305 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00140 | hp1 | a0003 | c0003 | t0002 | g0270 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00140 | hp2 | a0003 | c0003 | t0002 | g0260 | EUR | GBR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00280 | hp1 | a0003 | c0003 | t0002 | g0025 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00280 | hp2 | a0003 | c0003 | t0002 | g0258 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0304 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00323 | hp2 | a0003 | c0003 | t0002 | g0239 | EUR | FIN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00408 | hp1 | a0004 | c0004 | t0001 | g0172 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00423 | hp1 | a0004 | c0004 | t0001 | g0146 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00423 | hp2 | a0004 | c0004 | t0001 | g0139 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00438 | hp1 | a0004 | c0004 | t0001 | g0140 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00544 | hp1 | a0001 | c0005 | t0001 | g0309 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00609 | hp2 | a0003 | c0003 | t0002 | g0243 | EAS | CHS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00639 | hp1 | a0003 | c0003 | t0002 | g0271 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00735 | hp1 | a0003 | c0003 | t0002 | g0027 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00738 | hp1 | a0003 | c0003 | t0002 | g0247 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00738 | hp2 | a0003 | c0003 | t0002 | g0277 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00741 | hp1 | a0003 | c0003 | t0002 | g0252 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG00741 | hp2 | a0003 | c0003 | t0002 | g0265 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0303 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01070 | hp1 | a0003 | c0003 | t0002 | g0010 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01070 | hp2 | a0001 | c0005 | t0001 | g0284 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01071 | hp2 | a0003 | c0003 | t0002 | g0010 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0291 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01081 | hp2 | a0003 | c0003 | t0002 | g0025 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01109 | hp1 | a0001 | c0005 | t0001 | g0321 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01167 | hp1 | a0003 | c0003 | t0002 | g0264 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01167 | hp2 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0261 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01169 | hp2 | a0003 | c0003 | t0002 | g0328 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01175 | hp2 | a0003 | c0003 | t0002 | g0274 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01243 | hp1 | a0003 | c0003 | t0002 | g0251 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01255 | hp1 | a0003 | c0003 | t0002 | g0327 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01258 | hp1 | a0003 | c0003 | t0002 | g0295 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01261 | hp1 | a0008 | c0012 | t0001 | g0153 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01346 | hp1 | a0003 | c0003 | t0002 | g0027 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01358 | hp1 | a0003 | c0003 | t0002 | g0253 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01433 | hp1 | a0003 | c0003 | t0002 | g0266 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0196 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01516 | hp1 | a0001 | c0005 | t0001 | g0301 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0197 | EUR | IBS | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01884 | hp1 | a0005 | c0007 | t0003 | g0033 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01891 | hp1 | a0004 | c0004 | t0001 | g0021 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01993 | hp2 | a0003 | c0003 | t0002 | g0010 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02015 | hp1 | a0004 | c0004 | t0001 | g0022 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02027 | hp2 | a0001 | c0005 | t0001 | g0051 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02040 | hp1 | a0001 | c0005 | t0001 | g0050 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02055 | hp1 | a0003 | c0003 | t0002 | g0275 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02055 | hp2 | a0003 | c0003 | t0002 | g0262 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02056 | hp1 | a0001 | c0005 | t0001 | g0313 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02056 | hp2 | a0003 | c0003 | t0002 | g0272 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02080 | hp2 | a0004 | c0004 | t0001 | g0136 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02083 | hp1 | a0003 | c0003 | t0002 | g0245 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02129 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02145 | hp1 | a0005 | c0007 | t0003 | g0040 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02145 | hp2 | a0006 | c0008 | t0001 | g0326 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02148 | hp1 | a0003 | c0003 | t0002 | g0294 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CDX | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02257 | hp1 | a0007 | c0009 | t0004 | g0029 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02258 | hp1 | a0003 | c0003 | t0002 | g0045 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02258 | hp2 | a0007 | c0009 | t0004 | g0029 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02293 | hp2 | a0001 | c0005 | t0001 | g0298 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02300 | hp2 | a0003 | c0003 | t0002 | g0297 | AMR | PEL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02451 | hp1 | a0003 | c0003 | t0002 | g0250 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02523 | hp2 | a0004 | c0004 | t0001 | g0145 | EAS | KHV | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02622 | hp1 | a0003 | c0003 | t0002 | g0289 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02622 | hp2 | a0003 | c0003 | t0002 | g0292 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02630 | hp1 | a0005 | c0007 | t0003 | g0038 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02647 | hp1 | a0001 | c0005 | t0001 | g0322 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0220 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0329 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02717 | hp2 | a0003 | c0003 | t0002 | g0263 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02735 | hp2 | a0003 | c0003 | t0002 | g0026 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02809 | hp1 | a0003 | c0003 | t0002 | g0003 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02809 | hp2 | a0001 | c0010 | t0001 | g0281 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02895 | hp1 | a0010 | c0016 | t0001 | g0218 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02895 | hp2 | a0003 | c0003 | t0002 | g0241 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02896 | hp1 | a0003 | c0003 | t0002 | g0049 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02896 | hp2 | a0003 | c0003 | t0002 | g0003 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02897 | hp1 | a0003 | c0003 | t0002 | g0046 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02897 | hp2 | a0003 | c0003 | t0002 | g0240 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02976 | hp1 | a0001 | c0010 | t0001 | g0280 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03041 | hp1 | a0005 | c0007 | t0003 | g0039 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03041 | hp2 | a0006 | c0008 | t0001 | g0059 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03130 | hp1 | a0003 | c0003 | t0002 | g0269 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03130 | hp2 | a0006 | c0008 | t0001 | g0061 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03139 | hp1 | a0005 | c0007 | t0003 | g0037 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03195 | hp1 | a0007 | c0009 | t0004 | g0331 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03195 | hp2 | a0003 | c0003 | t0002 | g0047 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03209 | hp1 | a0003 | c0003 | t0002 | g0052 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03209 | hp2 | a0001 | c0019 | t0001 | g0064 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03225 | hp1 | a0005 | c0007 | t0003 | g0034 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03239 | hp1 | a0003 | c0003 | t0002 | g0278 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03453 | hp1 | a0005 | c0007 | t0003 | g0036 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03453 | hp2 | a0003 | c0003 | t0002 | g0044 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03490 | hp1 | a0003 | c0003 | t0002 | g0279 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0148 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03491 | hp1 | a0003 | c0003 | t0002 | g0249 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03491 | hp2 | a0011 | c0018 | t0001 | g0167 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03492 | hp1 | a0003 | c0003 | t0002 | g0248 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03492 | hp2 | a0004 | c0004 | t0001 | g0138 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03516 | hp1 | a0003 | c0003 | t0002 | g0276 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03516 | hp2 | a0002 | c0002 | t0007 | g0330 | AFR | ESN | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03579 | hp1 | a0003 | c0003 | t0002 | g0048 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03579 | hp2 | a0012 | c0023 | t0002 | g0043 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03654 | hp2 | a0008 | c0012 | t0001 | g0154 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03688 | hp1 | a0001 | c0005 | t0001 | g0308 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03688 | hp2 | a0003 | c0003 | t0002 | g0286 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03704 | hp1 | a0004 | c0004 | t0001 | g0130 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0215 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03710 | hp2 | a0003 | c0003 | t0002 | g0273 | SAS | PJL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03831 | hp2 | a0004 | c0004 | t0001 | g0041 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03834 | hp1 | a0001 | c0005 | t0001 | g0319 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03834 | hp2 | a0003 | c0003 | t0002 | g0238 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03942 | hp1 | a0003 | c0003 | t0002 | g0257 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0132 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04115 | hp1 | a0003 | c0003 | t0002 | g0288 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0296 | SAS | BEB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04199 | hp1 | a0004 | c0004 | t0001 | g0143 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04204 | hp1 | a0004 | c0004 | t0001 | g0133 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04204 | hp2 | a0003 | c0003 | t0002 | g0259 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0268 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0026 | SAS | STU | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18522 | hp1 | a0006 | c0008 | t0001 | g0060 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18522 | hp2 | a0003 | c0003 | t0002 | g0042 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18612 | hp2 | a0004 | c0004 | t0001 | g0137 | EAS | CHB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18906 | hp1 | a0001 | c0005 | t0001 | g0307 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18939 | hp1 | a0004 | c0025 | t0001 | g0126 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18940 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18941 | hp2 | a0004 | c0004 | t0001 | g0129 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18944 | hp2 | a0001 | c0005 | t0001 | g0285 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18946 | hp2 | a0004 | c0004 | t0006 | g0031 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18947 | hp2 | a0001 | c0005 | t0001 | g0028 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18948 | hp1 | a0004 | c0004 | t0001 | g0147 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18954 | hp2 | a0013 | c0021 | t0001 | g0325 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18957 | hp1 | a0001 | c0005 | t0001 | g0302 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18957 | hp2 | a0004 | c0004 | t0001 | g0224 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18959 | hp1 | a0001 | c0005 | t0001 | g0324 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18960 | hp2 | a0004 | c0004 | t0001 | g0149 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18961 | hp1 | a0002 | c0006 | t0001 | g0024 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18961 | hp2 | a0004 | c0004 | t0001 | g0152 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18962 | hp1 | a0001 | c0005 | t0001 | g0316 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18962 | hp2 | a0004 | c0004 | t0001 | g0008 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18963 | hp1 | a0004 | c0004 | t0001 | g0008 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18964 | hp2 | a0009 | c0011 | t0002 | g0206 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18966 | hp1 | a0014 | c0022 | t0001 | g0109 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0246 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0169 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18968 | hp2 | a0002 | c0006 | t0001 | g0024 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18969 | hp1 | a0002 | c0024 | t0001 | g0234 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18969 | hp2 | a0004 | c0004 | t0001 | g0134 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18972 | hp1 | a0004 | c0004 | t0001 | g0144 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18977 | hp1 | a0004 | c0004 | t0001 | g0020 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18979 | hp1 | a0007 | c0020 | t0001 | g0092 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18982 | hp1 | a0004 | c0004 | t0001 | g0173 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18982 | hp2 | a0002 | c0006 | t0001 | g0237 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18984 | hp1 | a0004 | c0004 | t0001 | g0222 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18985 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18985 | hp2 | a0001 | c0005 | t0001 | g0032 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18986 | hp1 | a0004 | c0004 | t0001 | g0135 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18986 | hp2 | a0009 | c0011 | t0002 | g0205 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18989 | hp1 | a0003 | c0003 | t0002 | g0287 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18989 | hp2 | a0001 | c0005 | t0001 | g0317 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18992 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18992 | hp2 | a0015 | c0013 | t0001 | g0067 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18994 | hp2 | a0004 | c0004 | t0001 | g0141 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18997 | hp2 | a0016 | c0015 | t0001 | g0188 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18998 | hp2 | a0001 | c0005 | t0001 | g0311 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18999 | hp2 | a0002 | c0006 | t0001 | g0229 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19001 | hp1 | a0004 | c0004 | t0001 | g0223 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19001 | hp2 | a0001 | c0005 | t0001 | g0320 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19002 | hp2 | a0004 | c0004 | t0001 | g0171 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19003 | hp2 | a0004 | c0004 | t0001 | g0142 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19005 | hp1 | a0004 | c0004 | t0001 | g0156 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19007 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19009 | hp2 | a0001 | c0005 | t0001 | g0323 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19010 | hp1 | a0002 | c0006 | t0001 | g0189 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19011 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19011 | hp2 | a0001 | c0005 | t0001 | g0300 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19030 | hp2 | a0003 | c0003 | t0002 | g0290 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19043 | hp1 | a0005 | c0007 | t0003 | g0035 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19055 | hp1 | a0004 | c0004 | t0001 | g0020 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19057 | hp2 | a0004 | c0004 | t0001 | g0127 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19058 | hp2 | a0001 | c0005 | t0001 | g0242 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0244 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19063 | hp1 | a0004 | c0004 | t0001 | g0225 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19064 | hp1 | a0002 | c0006 | t0001 | g0228 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19064 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19066 | hp1 | a0002 | c0006 | t0001 | g0231 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19066 | hp2 | a0004 | c0004 | t0001 | g0155 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19070 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19075 | hp1 | a0001 | c0005 | t0001 | g0318 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19077 | hp1 | a0001 | c0005 | t0001 | g0299 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19077 | hp2 | a0002 | c0006 | t0001 | g0230 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19079 | hp1 | a0001 | c0005 | t0005 | g0030 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19080 | hp2 | a0004 | c0004 | t0001 | g0221 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19081 | hp1 | a0001 | c0005 | t0001 | g0312 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19081 | hp2 | a0004 | c0004 | t0001 | g0008 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19082 | hp1 | a0001 | c0005 | t0001 | g0310 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19083 | hp2 | a0001 | c0005 | t0001 | g0028 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19084 | hp1 | a0004 | c0004 | t0001 | g0170 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19085 | hp1 | a0001 | c0005 | t0001 | g0314 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19085 | hp2 | a0004 | c0004 | t0001 | g0128 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19086 | hp1 | a0002 | c0006 | t0001 | g0236 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19088 | hp1 | a0001 | c0005 | t0001 | g0306 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19091 | hp2 | a0004 | c0004 | t0001 | g0131 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19240 | hp1 | a0017 | c0017 | t0001 | g0211 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA19240 | hp2 | a0004 | c0004 | t0001 | g0021 | AFR | YRI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20129 | hp1 | a0003 | c0003 | t0002 | g0003 | AFR | ASW | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20129 | hp2 | a0003 | c0003 | t0002 | g0293 | AFR | ASW | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20805 | hp1 | a0003 | c0003 | t0002 | g0267 | EUR | TSI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20905 | hp1 | a0003 | c0003 | t0002 | g0255 | SAS | GIH | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20905 | hp2 | a0004 | c0004 | t0001 | g0151 | SAS | GIH | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | CLM | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03471 | hp1 | a0003 | c0003 | t0002 | g0256 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
HG03471 | hp2 | a0001 | c0005 | t0001 | g0058 | AFR | MSL | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18955 | hp1 | a0004 | c0004 | t0001 | g0150 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | USA | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA20300 | hp2 | a0018 | c0014 | t0001 | g0282 | AFR | USA | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0315 | AFR | LWK | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
homoSapiens | chm13v2 | a0003 | c0003 | t0002 | g0254 | REF | REF | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | AASDH_chr4_56333290_56392491 | AASDH | chr4 | 56333290 | 56392491 |
view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338591 | C | T | 1 | a0017 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3108G>A | p.Met1036Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 3280/3581 | 3108/3297 | 1036/1098 | chr4 | 56338591 | |||
chr4:56338611 | A | C | 5 | a0002a0007a0010others(2): Show | 99 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(96): Show |
missense_variant | MODERATE | c.3088T>G | p.Tyr1030Asp | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 3260/3581 | 3088/3297 | 1030/1098 | chr4 | 56338611 | |||
chr4:56342905 | C | T | 1 | a0010 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.2837G>A | p.Cys946Tyr | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/15 | 3009/3581 | 2837/3297 | 946/1098 | chr4 | 56342905 | |||
chr4:56345186 | T | C | 5 | a0002a0009a0010others(2): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
missense_variant | MODERATE | c.2593A>G | p.Thr865Ala | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/15 | 2765/3581 | 2593/3297 | 865/1098 | chr4 | 56345186 | |||
chr4:56349392 | T | C | 2 | a0006a0018 | 5 | HG02145.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.2359A>G | p.Ile787Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2531/3581 | 2359/3297 | 787/1098 | chr4 | 56349392 | |||
chr4:56349428 | T | C | 1 | a0013 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.2323A>G | p.Ile775Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2495/3581 | 2323/3297 | 775/1098 | chr4 | 56349428 | |||
chr4:56349431 | C | T | 1 | a0016 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.2320G>A | p.Val774Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2492/3581 | 2320/3297 | 774/1098 | chr4 | 56349431 | |||
chr4:56349511 | G | A | 2 | a0003a0012 | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
missense_variant | MODERATE | c.2240C>T | p.Ala747Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2412/3581 | 2240/3297 | 747/1098 | chr4 | 56349511 | |||
chr4:56349637 | G | A | 1 | a0008 | 2 | HG01261.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.2114C>T | p.Ala705Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2286/3581 | 2114/3297 | 705/1098 | chr4 | 56349637 | |||
chr4:56349803 | C | T | 1 | a0011 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1948G>A | p.Asp650Asn | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2120/3581 | 1948/3297 | 650/1098 | chr4 | 56349803 | |||
chr4:56355182 | T | C | 3 | a0004a0008a0014 | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
missense_variant&splice_region_variant | MODERATE | c.1103A>G | p.Lys368Arg | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/15 | 1275/3581 | 1103/3297 | 368/1098 | chr4 | 56355182 | |||
chr4:56371486 | C | T | 1 | a0018 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.826G>A | p.Val276Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/15 | 998/3581 | 826/3297 | 276/1098 | chr4 | 56371486 | |||
chr4:56378269 | GTTC | G | 1 | a0005 | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
conservative_inframe_deletion | MODERATE | c.544_546delGAA | p.Glu182del | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/15 | 718/3581 | 544/3297 | 182/1098 | chr4 | 56378269 | |||
chr4:56378283 | T | C | 1 | a0012 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.533A>G | p.Glu178Gly | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/15 | 705/3581 | 533/3297 | 178/1098 | chr4 | 56378283 | |||
chr4:56378379 | C | T | 1 | a0015 | 1 | NA18992.hp2 | stop_gained | HIGH | c.437G>A | p.Trp146* | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/15 | 609/3581 | 437/3297 | 146/1098 | chr4 | 56378379 | |||
chr4:56382550 | G | C | 2 | a0004a0008 | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
missense_variant | MODERATE | c.278C>G | p.Pro93Arg | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/15 | 450/3581 | 278/3297 | 93/1098 | chr4 | 56382550 | |||
chr4:56384119 | T | C | 2 | a0004a0008 | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
missense_variant | MODERATE | c.181A>G | p.Ile61Val | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/15 | 353/3581 | 181/3297 | 61/1098 | chr4 | 56384119 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338750 | C | T | 1 | a0001c0019 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2949G>A | p.Pro983Pro | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 3121/3581 | 2949/3297 | 983/1098 | chr4 | 56338750 | |||
chr4:56349314 | G | T | 2 | a0002c0006a0002c0024 | 10 | NA18961.hp1 NA18968.hp2 NA18969.hp1 others(7): Show |
synonymous_variant | LOW | c.2437C>A | p.Arg813Arg | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/15 | 2609/3581 | 2437/3297 | 813/1098 | chr4 | 56349314 | |||
chr4:56353426 | G | A | 16 | a0001c0005a0001c0010a0002c0002others(13): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
synonymous_variant | LOW | c.1554C>T | p.Asp518Asp | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/15 | 1726/3581 | 1554/3297 | 518/1098 | chr4 | 56353426 | |||
chr4:56353429 | G | A | 1 | a0005c0007 | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
synonymous_variant | LOW | c.1551C>T | p.Ile517Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/15 | 1723/3581 | 1551/3297 | 517/1098 | chr4 | 56353429 | |||
chr4:56353447 | C | T | 8 | a0002c0002a0002c0006a0002c0024others(5): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
synonymous_variant | LOW | c.1533G>A | p.Pro511Pro | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/15 | 1705/3581 | 1533/3297 | 511/1098 | chr4 | 56353447 | |||
chr4:56371517 | G | A | 2 | a0003c0003a0012c0023 | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
synonymous_variant | LOW | c.795C>T | p.Ser265Ser | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/15 | 967/3581 | 795/3297 | 265/1098 | chr4 | 56371517 | |||
chr4:56371559 | A | G | 1 | a0004c0025 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.753T>C | p.Leu251Leu | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/15 | 925/3581 | 753/3297 | 251/1098 | chr4 | 56371559 | |||
chr4:56382561 | C | T | 1 | a0001c0010 | 2 | HG02809.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.267G>A | p.Glu89Glu | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/15 | 439/3581 | 267/3297 | 89/1098 | chr4 | 56382561 | |||
chr4:56382564 | G | A | 1 | a0002c0024 | 1 | NA18969.hp1 | synonymous_variant | LOW | c.264C>T | p.Ile88Ile | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/15 | 436/3581 | 264/3297 | 88/1098 | chr4 | 56382564 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338310 | C | CTTCT | 3 | a0003c0003t0002a0009c0011t0002a0012c0023t0002 | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*88_*91dupAGAA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 91 | chr4 | 56338310 | ||||||
chr4:56338329 | G | A | 1 | a0005c0007t0003 | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*73C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 73 | chr4 | 56338329 | ||||||
chr4:56338336 | T | C | 1 | a0002c0002t0007 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 15/15 | 66 | chr4 | 56338336 | ||||||
chr4:56387405 | C | T | 1 | a0004c0004t0006 | 1 | NA18946.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/15 | 3106 | chr4 | 56387405 | ||||||
chr4:56387411 | T | C | 1 | a0007c0009t0004 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-92A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/15 | chr4 | 56387411 | |||||||
chr4:56387451 | C | T | 1 | a0001c0005t0005 | 1 | NA19079.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/15 | 3152 | chr4 | 56387451 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:56338794 | A | G | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.2908-3T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56338794 | |||||||
chr4:56338892 | G | A | 2 | a0003c0003t0002g0046a0003c0003t0002g0049 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2908-101C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56338892 | |||||||
chr4:56339033 | G | A | 1 | a0002c0002t0001g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2908-242C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339033 | |||||||
chr4:56339093 | C | G | 2 | a0005c0007t0003g0035a0005c0007t0003g0037 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2908-302G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339093 | |||||||
chr4:56339162 | A | AT | 87 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(84): Show | 98 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(95): Show |
intron_variant | MODIFIER | c.2908-372dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339162 | |||||||
chr4:56339165 | T | A | 2 | a0003c0003t0002g0277a0003c0003t0002g0279 | 2 | HG00738.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2908-374A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339165 | |||||||
chr4:56339191 | T | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.2908-400A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339191 | |||||||
chr4:56339204 | A | C | 26 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(23): Show | 29 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2908-413T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339204 | |||||||
chr4:56339210 | G | C | 3 | a0003c0003t0002g0046a0003c0003t0002g0049a0003c0003t0002g0052 | 3 | HG02896.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2908-419C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339210 | |||||||
chr4:56339292 | C | T | 1 | a0002c0002t0001g0202 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2908-501G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339292 | |||||||
chr4:56339293 | G | A | 2 | a0003c0003t0002g0248a0003c0003t0002g0249 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2908-502C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339293 | |||||||
chr4:56339344 | A | G | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2908-553T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339344 | |||||||
chr4:56339387 | C | T | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.2908-596G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339387 | |||||||
chr4:56339396 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2908-605G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339396 | |||||||
chr4:56339461 | A | G | 1 | a0002c0002t0001g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2908-670T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339461 | |||||||
chr4:56339477 | G | A | 1 | a0004c0004t0001g0136 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2908-686C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339477 | |||||||
chr4:56339622 | A | G | 263 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(260): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2908-831T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339622 | |||||||
chr4:56339668 | T | C | 171 | a0001c0001t0001g0166a0001c0005t0001g0011a0001c0005t0001g0028others(168): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.2908-877A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339668 | |||||||
chr4:56339680 | G | C | 2 | a0002c0002t0001g0191a0002c0002t0001g0198 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2908-889C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339680 | |||||||
chr4:56339703 | A | T | 1 | a0008c0012t0001g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2908-912T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339703 | |||||||
chr4:56339748 | C | CA | 22 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(19): Show | 25 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2908-958dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | |||||||
chr4:56339748 | C | CAA | 71 | a0001c0001t0001g0125a0002c0002t0001g0002a0002c0002t0001g0009others(68): Show | 81 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.2908-959_2908-958d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | |||||||
chr4:56339748 | C | CAAA | 130 | a0001c0001t0001g0166a0001c0005t0001g0242a0001c0005t0001g0299others(127): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2908-960_2908-958d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | |||||||
chr4:56339748 | C | CAAAA | 38 | a0001c0005t0001g0011a0001c0005t0001g0032a0001c0005t0001g0050others(35): Show | 40 | HG00323.hp1 HG00544.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.2908-961_2908-958d others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | |||||||
chr4:56339748 | CA | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0073others(4): Show | 7 | HG00099.hp2 HG01515.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2908-958delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339748 | |||||||
chr4:56339830 | A | AAG | 170 | a0001c0001t0001g0166a0001c0005t0001g0011a0001c0005t0001g0028others(167): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2908-1041_2908-104 others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339830 | |||||||
chr4:56339908 | C | T | 1 | a0004c0004t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2908-1117G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56339908 | |||||||
chr4:56340028 | G | T | 1 | a0002c0002t0001g0113 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2908-1237C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340028 | |||||||
chr4:56340077 | G | GAGAA | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2908-1290_2908-128 others(8): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340077 | |||||||
chr4:56340087 | T | C | 1 | a0002c0002t0001g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2908-1296A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340087 | |||||||
chr4:56340133 | C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG01109.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2908-1342G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340133 | |||||||
chr4:56340147 | C | T | 1 | a0001c0005t0001g0314 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2908-1356G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340147 | |||||||
chr4:56340164 | A | T | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2908-1373T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340164 | |||||||
chr4:56340226 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2908-1435G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340226 | |||||||
chr4:56340319 | G | A | 1 | a0003c0003t0002g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2908-1528C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340319 | |||||||
chr4:56340379 | G | A | 1 | a0001c0005t0001g0309 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2908-1588C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340379 | |||||||
chr4:56340410 | T | C | 1 | a0009c0011t0002g0205 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2908-1619A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340410 | |||||||
chr4:56340430 | C | G | 1 | a0002c0002t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2908-1639G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340430 | |||||||
chr4:56340474 | C | T | 1 | a0004c0004t0001g0144 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2908-1683G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340474 | |||||||
chr4:56340608 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2908-1817G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340608 | |||||||
chr4:56340998 | A | C | 5 | a0003c0003t0002g0010a0003c0003t0002g0258a0003c0003t0002g0260others(2): Show | 7 | HG00140.hp2 HG00280.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2907+1837T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56340998 | |||||||
chr4:56341022 | G | A | 207 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(204): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2907+1813C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341022 | |||||||
chr4:56341178 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1657T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341178 | |||||||
chr4:56341181 | T | C | 2 | a0002c0002t0001g0177a0016c0015t0001g0188 | 2 | NA18997.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2907+1654A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341181 | |||||||
chr4:56341389 | C | CT | 84 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0095others(81): Show | 96 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.2907+1445dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTT | 10 | a0002c0002t0001g0108a0002c0002t0001g0178a0002c0002t0001g0181others(7): Show | 10 | HG01074.hp1 HG01346.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.2907+1444_2907+144 others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTT | 8 | a0002c0002t0001g0180a0005c0007t0003g0033a0005c0007t0003g0034others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.2907+1443_2907+144 others(7): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTTTTTT others(2): Show |
28 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(25): Show | 35 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2907+1437_2907+144 others(13): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTTTTTT others(3): Show |
25 | a0003c0003t0002g0027a0003c0003t0002g0044a0003c0003t0002g0047others(22): Show | 26 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2907+1436_2907+144 others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTTTTTT others(4): Show |
8 | a0003c0003t0002g0045a0003c0003t0002g0046a0003c0003t0002g0049others(5): Show | 8 | HG01175.hp2 HG01258.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1435_2907+144 others(15): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTTTTTT others(5): Show |
3 | a0003c0003t0002g0256a0003c0003t0002g0293a0018c0014t0001g0282 | 3 | HG03471.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2907+1434_2907+144 others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTTTTTT others(6): Show |
2 | a0003c0003t0002g0290a0003c0003t0002g0292 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2907+1433_2907+144 others(17): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTTTTTT others(7): Show |
3 | a0001c0010t0001g0280a0003c0003t0002g0240a0003c0003t0002g0241 | 3 | HG02895.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2907+1432_2907+144 others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | C | CTTTTTTT others(10): Show |
1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2907+1429_2907+144 others(21): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | CT | C | 52 | a0001c0001t0001g0125a0001c0001t0001g0166a0003c0003t0002g0263others(49): Show | 60 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.2907+1445delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341389 | CTTTTTT | C | 35 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(32): Show | 38 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2907+1440_2907+144 others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341389 | |||||||
chr4:56341424 | C | T | 1 | a0004c0004t0001g0152 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2907+1411G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341424 | |||||||
chr4:56341446 | G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1389C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341446 | |||||||
chr4:56341559 | A | AT | 127 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0071others(124): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2907+1275dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341559 | |||||||
chr4:56341559 | AT | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+1275delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341559 | |||||||
chr4:56341591 | C | T | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2907+1244G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341591 | |||||||
chr4:56341676 | C | T | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2907+1159G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341676 | |||||||
chr4:56341840 | G | A | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2907+995C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341840 | |||||||
chr4:56341941 | G | A | 52 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(49): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.2907+894C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56341941 | |||||||
chr4:56342004 | C | T | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2907+831G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342004 | |||||||
chr4:56342038 | T | C | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.2907+797A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342038 | |||||||
chr4:56342043 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+792G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342043 | |||||||
chr4:56342063 | G | C | 3 | a0004c0004t0001g0137a0004c0004t0001g0152a0004c0004t0001g0156 | 3 | NA18612.hp2 NA18961.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2907+772C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342063 | |||||||
chr4:56342110 | C | CA | 56 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0125others(53): Show | 65 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2907+724dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342110 | |||||||
chr4:56342110 | CA | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0099others(12): Show | 16 | HG00408.hp1 HG01346.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.2907+724delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342110 | |||||||
chr4:56342110 | CAAAAAAA others(9): Show |
C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2907+709_2907+724d others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342110 | |||||||
chr4:56342111 | A | C | 1 | a0017c0017t0001g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2907+724T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342111 | |||||||
chr4:56342165 | TAA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2907+668_2907+669d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342165 | |||||||
chr4:56342284 | A | G | 1 | a0003c0003t0002g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2907+551T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342284 | |||||||
chr4:56342393 | A | G | 1 | a0002c0002t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2907+442T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342393 | |||||||
chr4:56342594 | T | C | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.2907+241A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342594 | |||||||
chr4:56342604 | T | C | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2907+231A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342604 | |||||||
chr4:56342651 | C | T | 1 | a0003c0003t0002g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2907+184G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342651 | |||||||
chr4:56342789 | A | T | 149 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(146): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2907+46T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 14/14 | chr4 | 56342789 | |||||||
chr4:56343295 | C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0073others(2): Show | 6 | HG01081.hp1 HG01192.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.2775+267G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343295 | |||||||
chr4:56343340 | AAAC | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.2775+219_2775+221d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343340 | |||||||
chr4:56343359 | A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+203T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343359 | |||||||
chr4:56343363 | T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+199A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343363 | |||||||
chr4:56343365 | C | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+197G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343365 | |||||||
chr4:56343365 | CAT | C | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2775+195_2775+196d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343365 | |||||||
chr4:56343365 | CATAT | C | 226 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(223): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.2775+193_2775+196d others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343365 | |||||||
chr4:56343369 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+193A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343369 | |||||||
chr4:56343480 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2775+82G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 13/14 | chr4 | 56343480 | |||||||
chr4:56343873 | A | C | 2 | a0001c0005t0001g0303a0001c0005t0001g0321 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2653-189T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56343873 | |||||||
chr4:56344034 | G | A | 2 | a0002c0002t0001g0119a0002c0002t0001g0121 | 2 | NA18975.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2653-350C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344034 | |||||||
chr4:56344056 | A | C | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2653-372T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344056 | |||||||
chr4:56344159 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653-475A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344159 | |||||||
chr4:56344164 | A | T | 1 | a0003c0003t0002g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2653-480T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344164 | |||||||
chr4:56344170 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653-486C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344170 | |||||||
chr4:56344257 | C | T | 1 | a0004c0004t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2653-573G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344257 | |||||||
chr4:56344343 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653-659G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344343 | |||||||
chr4:56344344 | A | C | 2 | a0001c0005t0001g0307a0001c0005t0001g0322 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2653-660T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344344 | |||||||
chr4:56344348 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2653-664A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344348 | |||||||
chr4:56344600 | C | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2652+527G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344600 | |||||||
chr4:56344740 | T | C | 1 | a0004c0004t0001g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2652+387A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344740 | |||||||
chr4:56344940 | C | CT | 9 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0283others(6): Show | 10 | HG00438.hp2 HG01261.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2652+186dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344940 | |||||||
chr4:56344940 | CT | C | 115 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0005t0001g0011others(112): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.2652+186delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344940 | |||||||
chr4:56344944 | T | C | 79 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(76): Show | 90 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.2652+183A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344944 | |||||||
chr4:56344945 | T | C | 4 | a0002c0002t0001g0185a0002c0002t0001g0198a0002c0002t0001g0217others(1): Show | 4 | HG01943.hp1 NA18953.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.2652+182A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344945 | |||||||
chr4:56344948 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2652+179A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56344948 | |||||||
chr4:56345090 | C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2652+37G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 12/14 | chr4 | 56345090 | |||||||
chr4:56345366 | A | G | 59 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0023others(56): Show | 67 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.2489-76T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345366 | |||||||
chr4:56345623 | C | T | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2489-333G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345623 | |||||||
chr4:56345676 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2489-386T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345676 | |||||||
chr4:56345705 | A | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0104 | 2 | NA18941.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2489-415T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345705 | |||||||
chr4:56345884 | C | G | 3 | a0003c0003t0002g0263a0003c0003t0002g0275a0003c0003t0002g0289 | 3 | HG02055.hp1 HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2489-594G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345884 | |||||||
chr4:56345935 | G | A | 1 | a0003c0003t0002g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2489-645C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56345935 | |||||||
chr4:56346044 | G | A | 3 | a0001c0005t0001g0285a0001c0005t0001g0299a0001c0005t0001g0300 | 3 | NA18944.hp2 NA19011.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2489-754C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346044 | |||||||
chr4:56346098 | T | C | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2489-808A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346098 | |||||||
chr4:56346148 | T | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0164 | 2 | NA18940.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2489-858A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346148 | |||||||
chr4:56346243 | G | A | 3 | a0004c0004t0001g0130a0004c0004t0001g0138a0004c0004t0001g0148 | 3 | HG03490.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2489-953C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346243 | |||||||
chr4:56346437 | A | G | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2489-1147T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346437 | |||||||
chr4:56346569 | G | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2489-1279C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346569 | |||||||
chr4:56346613 | A | C | 2 | a0003c0003t0002g0269a0003c0003t0002g0276 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2489-1323T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346613 | |||||||
chr4:56346620 | A | G | 2 | a0003c0003t0002g0269a0003c0003t0002g0276 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2489-1330T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346620 | |||||||
chr4:56346849 | C | T | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2489-1559G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346849 | |||||||
chr4:56346879 | C | CAAAAATT others(329): Show |
1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2489-1590_2489-158 others(340): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346879 | |||||||
chr4:56346997 | C | T | 1 | a0002c0002t0001g0009 | 3 | HG01243.hp2 HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2489-1707G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56346997 | |||||||
chr4:56347026 | G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2489-1736C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347026 | |||||||
chr4:56347040 | T | TA | 18 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0010t0001g0280others(15): Show | 18 | HG00423.hp2 HG01175.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2489-1751dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347040 | |||||||
chr4:56347041 | A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100 | 4 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489-1751T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347041 | |||||||
chr4:56347124 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2489-1834A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347124 | |||||||
chr4:56347137 | A | G | 1 | a0002c0002t0001g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2489-1847T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347137 | |||||||
chr4:56347692 | G | A | 202 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(199): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2488+1571C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347692 | |||||||
chr4:56347705 | C | A | 1 | a0018c0014t0001g0282 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2488+1558G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347705 | |||||||
chr4:56347776 | C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2488+1487G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347776 | |||||||
chr4:56347891 | A | C | 1 | a0003c0003t0002g0291 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2488+1372T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347891 | |||||||
chr4:56347903 | A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+1360T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347903 | |||||||
chr4:56347958 | C | G | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2488+1305G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56347958 | |||||||
chr4:56348200 | T | G | 113 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(110): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2488+1063A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348200 | |||||||
chr4:56348241 | C | T | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.2488+1022G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348241 | |||||||
chr4:56348258 | C | CT | 14 | a0002c0002t0001g0226a0002c0002t0001g0235a0003c0003t0001g0220others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2488+1004dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348258 | |||||||
chr4:56348422 | T | G | 1 | a0004c0004t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2488+841A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348422 | |||||||
chr4:56348506 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+757A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348506 | |||||||
chr4:56348606 | C | T | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2488+657G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348606 | |||||||
chr4:56348691 | T | C | 1 | a0002c0002t0001g0200 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2488+572A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348691 | |||||||
chr4:56348832 | C | T | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2488+431G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348832 | |||||||
chr4:56348933 | G | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+330C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56348933 | |||||||
chr4:56349221 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+42A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 11/14 | chr4 | 56349221 | |||||||
chr4:56350102 | A | G | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1693-44T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350102 | |||||||
chr4:56350174 | G | T | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1693-116C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350174 | |||||||
chr4:56350176 | C | T | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1693-118G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350176 | |||||||
chr4:56350177 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1693-119C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350177 | |||||||
chr4:56350364 | G | T | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0012c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693-306C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350364 | |||||||
chr4:56350373 | G | A | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1693-315C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350373 | |||||||
chr4:56350411 | G | A | 2 | a0004c0004t0001g0140a0004c0004t0001g0221 | 2 | HG00438.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1693-353C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350411 | |||||||
chr4:56350426 | C | T | 3 | a0003c0003t0002g0255a0003c0003t0002g0270a0003c0003t0002g0288 | 3 | HG00140.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1693-368G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350426 | |||||||
chr4:56350456 | A | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1693-398T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350456 | |||||||
chr4:56350622 | T | C | 7 | a0002c0002t0001g0201a0002c0002t0001g0202a0002c0002t0001g0203others(4): Show | 7 | NA18949.hp2 NA18954.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693-564A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350622 | |||||||
chr4:56350690 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1693-632A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350690 | |||||||
chr4:56350731 | T | C | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1692+611A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350731 | |||||||
chr4:56350766 | G | A | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1692+576C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350766 | |||||||
chr4:56350773 | A | G | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1692+569T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350773 | |||||||
chr4:56350775 | G | A | 2 | a0004c0004t0001g0145a0004c0004t0001g0146 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1692+567C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350775 | |||||||
chr4:56350785 | T | A | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1692+557A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350785 | |||||||
chr4:56350884 | T | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.1692+458A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350884 | |||||||
chr4:56350915 | T | C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1692+427A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56350915 | |||||||
chr4:56351057 | G | A | 9 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692+285C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351057 | |||||||
chr4:56351130 | T | C | 1 | a0003c0003t0002g0295 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1692+212A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351130 | |||||||
chr4:56351174 | T | C | 121 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(118): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1692+168A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351174 | |||||||
chr4:56351194 | A | G | 1 | a0004c0004t0001g0134 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1692+148T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 10/14 | chr4 | 56351194 | |||||||
chr4:56351506 | C | T | 1 | a0002c0002t0001g0202 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1577-49G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351506 | |||||||
chr4:56351538 | T | C | 1 | a0013c0021t0001g0325 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1577-81A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351538 | |||||||
chr4:56351629 | C | G | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1577-172G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351629 | |||||||
chr4:56351754 | A | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.1577-297T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351754 | |||||||
chr4:56351917 | C | CA | 9 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 10 | HG01258.hp2 HG01433.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1577-461dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351917 | |||||||
chr4:56351917 | CA | C | 139 | a0001c0001t0001g0073a0001c0005t0001g0011a0001c0005t0001g0028others(136): Show | 154 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.1577-461delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56351917 | |||||||
chr4:56352228 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1577-771G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352228 | |||||||
chr4:56352230 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1577-773G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352230 | |||||||
chr4:56352277 | T | A | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.1577-820A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352277 | |||||||
chr4:56352497 | G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG01109.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1576+907C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352497 | |||||||
chr4:56352538 | C | T | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1576+866G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352538 | |||||||
chr4:56352559 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1576+845T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352559 | |||||||
chr4:56352606 | G | A | 1 | a0001c0005t0005g0030 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1576+798C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352606 | |||||||
chr4:56352843 | G | A | 1 | a0001c0005t0001g0285 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1576+561C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352843 | |||||||
chr4:56352971 | C | T | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1576+433G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56352971 | |||||||
chr4:56353009 | CT | C | 10 | a0001c0001t0001g0065a0001c0005t0001g0318a0005c0007t0003g0033others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1576+394delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353009 | |||||||
chr4:56353019 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1576+385A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353019 | |||||||
chr4:56353094 | C | T | 2 | a0003c0003t0002g0269a0003c0003t0002g0276 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1576+310G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353094 | |||||||
chr4:56353209 | T | C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1576+195A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353209 | |||||||
chr4:56353250 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576+154T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353250 | |||||||
chr4:56353263 | G | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576+141C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353263 | |||||||
chr4:56353328 | A | T | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1576+76T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353328 | |||||||
chr4:56353357 | A | G | 113 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(110): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.1576+47T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353357 | |||||||
chr4:56353396 | T | A | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | splice_region_variant&intron_variant | LOW | c.1576+8A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 9/14 | chr4 | 56353396 | |||||||
chr4:56353892 | C | T | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1383+147G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353892 | |||||||
chr4:56353954 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1383+85A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353954 | |||||||
chr4:56353957 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1383+82T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353957 | |||||||
chr4:56353962 | C | A | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1383+77G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 8/14 | chr4 | 56353962 | |||||||
chr4:56354631 | C | T | 1 | a0002c0002t0001g0227 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1210+74G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 7/14 | chr4 | 56354631 | |||||||
chr4:56354827 | A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104-16T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56354827 | |||||||
chr4:56354828 | C | T | 2 | a0001c0005t0001g0303a0001c0005t0001g0321 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1104-17G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56354828 | |||||||
chr4:56354918 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104-107G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56354918 | |||||||
chr4:56355149 | C | A | 1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1103+33G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 6/14 | chr4 | 56355149 | |||||||
chr4:56355448 | A | G | 4 | a0006c0008t0001g0059a0006c0008t0001g0060a0006c0008t0001g0061others(1): Show | 4 | HG03041.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.862-25T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355448 | |||||||
chr4:56355561 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.862-138A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355561 | |||||||
chr4:56355593 | G | GT | 51 | a0001c0001t0001g0015a0001c0001t0001g0079a0001c0001t0001g0080others(48): Show | 60 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.862-171dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355593 | |||||||
chr4:56355593 | GT | G | 109 | a0001c0001t0001g0089a0001c0005t0001g0011a0001c0005t0001g0028others(106): Show | 120 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.862-171delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355593 | |||||||
chr4:56355593 | GTT | G | 88 | a0001c0010t0001g0280a0001c0010t0001g0281a0002c0002t0001g0017others(85): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.862-172_862-171del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355593 | |||||||
chr4:56355594 | T | TG | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.862-172_862-171ins others(1): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355594 | |||||||
chr4:56355596 | T | G | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.862-173A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355596 | |||||||
chr4:56355641 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.862-218G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355641 | |||||||
chr4:56355749 | G | A | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.862-326C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355749 | |||||||
chr4:56355792 | A | T | 208 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(205): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.862-369T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355792 | |||||||
chr4:56355882 | T | A | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.862-459A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355882 | |||||||
chr4:56355932 | A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-509T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56355932 | |||||||
chr4:56356127 | C | T | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.862-704G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356127 | |||||||
chr4:56356211 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.862-788A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356211 | |||||||
chr4:56356260 | A | G | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.862-837T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356260 | |||||||
chr4:56356332 | A | C | 1 | a0003c0003t0002g0267 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.862-909T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356332 | |||||||
chr4:56356345 | T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-922A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356345 | |||||||
chr4:56356368 | C | A | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-945G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356368 | |||||||
chr4:56356463 | A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-1040T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356463 | |||||||
chr4:56356498 | T | C | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.862-1075A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356498 | |||||||
chr4:56356615 | C | A | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.862-1192G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356615 | |||||||
chr4:56356820 | C | T | 1 | a0003c0003t0002g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.862-1397G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356820 | |||||||
chr4:56356875 | C | T | 1 | a0004c0004t0001g0155 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.862-1452G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356875 | |||||||
chr4:56356901 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.862-1478G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56356901 | |||||||
chr4:56357084 | A | G | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.862-1661T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357084 | |||||||
chr4:56357155 | T | A | 52 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(49): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.862-1732A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357155 | |||||||
chr4:56357186 | T | C | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.862-1763A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357186 | |||||||
chr4:56357516 | C | T | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.862-2093G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357516 | |||||||
chr4:56357519 | C | A | 4 | a0004c0004t0001g0020a0004c0004t0001g0127a0004c0004t0001g0131others(1): Show | 5 | NA18977.hp1 NA18994.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-2096G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357519 | |||||||
chr4:56357520 | C | G | 4 | a0004c0004t0001g0020a0004c0004t0001g0127a0004c0004t0001g0131others(1): Show | 5 | NA18977.hp1 NA18994.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-2097G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357520 | |||||||
chr4:56357639 | T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.862-2216A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357639 | |||||||
chr4:56357704 | A | C | 1 | a0003c0003t0002g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.862-2281T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56357704 | |||||||
chr4:56358173 | T | C | 2 | a0004c0004t0001g0145a0004c0004t0001g0146 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.862-2750A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358173 | |||||||
chr4:56358185 | T | A | 1 | a0001c0010t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.862-2762A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358185 | |||||||
chr4:56358316 | C | A | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.862-2893G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358316 | |||||||
chr4:56358353 | A | G | 121 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(118): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.862-2930T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358353 | |||||||
chr4:56358462 | C | T | 7 | a0001c0005t0001g0285a0001c0005t0001g0299a0001c0005t0001g0300others(4): Show | 7 | HG02056.hp1 NA18944.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.862-3039G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358462 | |||||||
chr4:56358463 | G | A | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.862-3040C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358463 | |||||||
chr4:56358838 | T | A | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0012c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.862-3415A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358838 | |||||||
chr4:56358883 | A | C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.862-3460T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56358883 | |||||||
chr4:56359003 | A | G | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-3580T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359003 | |||||||
chr4:56359007 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-3584G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359007 | |||||||
chr4:56359112 | G | GT | 123 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(120): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.862-3690dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359112 | |||||||
chr4:56359299 | C | T | 1 | a0002c0002t0001g0187 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.862-3876G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359299 | |||||||
chr4:56359317 | C | A | 1 | a0002c0002t0001g0213 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.862-3894G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359317 | |||||||
chr4:56359324 | C | CGCCTCCT | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-3908_862-3902d others(9): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359324 | |||||||
chr4:56359338 | T | C | 1 | a0003c0003t0002g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.862-3915A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359338 | |||||||
chr4:56359345 | C | T | 1 | a0002c0002t0001g0227 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.862-3922G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359345 | |||||||
chr4:56359346 | G | A | 1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.862-3923C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359346 | |||||||
chr4:56359369 | C | G | 1 | a0003c0003t0002g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.862-3946G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359369 | |||||||
chr4:56359507 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4084C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359507 | |||||||
chr4:56359535 | G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4112C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359535 | |||||||
chr4:56359550 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.862-4127C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359550 | |||||||
chr4:56359617 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.862-4194C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359617 | |||||||
chr4:56359622 | A | G | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.862-4199T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359622 | |||||||
chr4:56359645 | A | AC | 8 | a0001c0001t0001g0078a0001c0001t0001g0162a0001c0005t0001g0050others(5): Show | 8 | HG01243.hp1 HG02040.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4223dupG | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359645 | |||||||
chr4:56359662 | G | A | 1 | a0002c0002t0001g0019 | 2 | NA18951.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.862-4239C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359662 | |||||||
chr4:56359701 | G | A | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.862-4278C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359701 | |||||||
chr4:56359748 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4325T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359748 | |||||||
chr4:56359908 | A | G | 1 | a0001c0005t0001g0306 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.862-4485T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56359908 | |||||||
chr4:56360234 | G | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-4811C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360234 | |||||||
chr4:56360255 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.862-4832T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360255 | |||||||
chr4:56360284 | T | C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.862-4861A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360284 | |||||||
chr4:56360338 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-4915C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360338 | |||||||
chr4:56360471 | A | G | 1 | a0018c0014t0001g0282 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.862-5048T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360471 | |||||||
chr4:56360689 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.862-5266C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360689 | |||||||
chr4:56360692 | C | T | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.862-5269G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360692 | |||||||
chr4:56360728 | A | G | 10 | a0003c0003t0002g0027a0003c0003t0002g0239a0003c0003t0002g0265others(7): Show | 11 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.862-5305T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360728 | |||||||
chr4:56360753 | C | T | 5 | a0006c0008t0001g0059a0006c0008t0001g0060a0006c0008t0001g0061others(2): Show | 5 | HG02145.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.862-5330G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360753 | |||||||
chr4:56360793 | T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0161 | 2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.862-5370A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360793 | |||||||
chr4:56360857 | C | T | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-5434G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360857 | |||||||
chr4:56360886 | A | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.862-5463T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360886 | |||||||
chr4:56360931 | C | T | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-5508G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56360931 | |||||||
chr4:56361133 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.862-5710G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361133 | |||||||
chr4:56361182 | C | T | 113 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(110): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.862-5759G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361182 | |||||||
chr4:56361183 | G | A | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.862-5760C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361183 | |||||||
chr4:56361209 | C | T | 51 | a0002c0002t0001g0002a0002c0002t0001g0023a0002c0002t0001g0177others(48): Show | 57 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.862-5786G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361209 | |||||||
chr4:56361242 | C | G | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.862-5819G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361242 | |||||||
chr4:56361339 | G | A | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-5916C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361339 | |||||||
chr4:56361504 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-6081G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361504 | |||||||
chr4:56361555 | T | C | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.862-6132A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361555 | |||||||
chr4:56361686 | T | C | 1 | a0001c0005t0001g0305 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.862-6263A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361686 | |||||||
chr4:56361774 | C | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-6351G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361774 | |||||||
chr4:56361812 | G | T | 2 | a0002c0002t0001g0112a0002c0002t0001g0116 | 2 | NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.862-6389C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56361812 | |||||||
chr4:56362019 | G | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-6596C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362019 | |||||||
chr4:56362263 | C | G | 87 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(84): Show | 98 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(95): Show |
intron_variant | MODIFIER | c.862-6840G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362263 | |||||||
chr4:56362334 | G | T | 5 | a0001c0005t0001g0301a0001c0005t0001g0303a0001c0005t0001g0304others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.862-6911C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362334 | |||||||
chr4:56362598 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.862-7175T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362598 | |||||||
chr4:56362748 | C | G | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-7325G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362748 | |||||||
chr4:56362805 | G | A | 52 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(49): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.862-7382C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362805 | |||||||
chr4:56362823 | G | A | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.862-7400C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362823 | |||||||
chr4:56362878 | G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0199 | 3 | NA18973.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.862-7455C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362878 | |||||||
chr4:56362898 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.862-7475G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56362898 | |||||||
chr4:56363009 | C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-7586G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363009 | |||||||
chr4:56363044 | T | C | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.862-7621A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363044 | |||||||
chr4:56363058 | G | A | 1 | a0003c0003t0002g0252 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.862-7635C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363058 | |||||||
chr4:56363109 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.862-7686G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363109 | |||||||
chr4:56363110 | G | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-7687C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363110 | |||||||
chr4:56363151 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-7728G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363151 | |||||||
chr4:56363185 | C | A | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.862-7762G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363185 | |||||||
chr4:56363192 | G | A | 1 | a0003c0003t0002g0297 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.862-7769C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363192 | |||||||
chr4:56363195 | G | A | 1 | a0003c0003t0002g0277 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.862-7772C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363195 | |||||||
chr4:56363195 | G | C | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.862-7772C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363195 | |||||||
chr4:56363242 | G | A | 10 | a0004c0004t0001g0020a0004c0004t0001g0127a0004c0004t0001g0128others(7): Show | 11 | NA18955.hp1 NA18960.hp2 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.862-7819C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363242 | |||||||
chr4:56363242 | G | C | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.862-7819C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363242 | |||||||
chr4:56363293 | G | T | 1 | a0002c0002t0001g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.862-7870C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363293 | |||||||
chr4:56363419 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-7996A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363419 | |||||||
chr4:56363447 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+8004C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363447 | |||||||
chr4:56363490 | A | G | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.861+7961T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363490 | |||||||
chr4:56363499 | G | A | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+7952C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363499 | |||||||
chr4:56363713 | C | T | 1 | a0003c0003t0002g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.861+7738G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363713 | |||||||
chr4:56363791 | G | C | 121 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(118): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.861+7660C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363791 | |||||||
chr4:56363792 | G | A | 1 | a0002c0002t0001g0194 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.861+7659C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363792 | |||||||
chr4:56363853 | T | C | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+7598A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363853 | |||||||
chr4:56363854 | G | A | 16 | a0003c0003t0002g0027a0003c0003t0002g0239a0003c0003t0002g0243others(13): Show | 17 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.861+7597C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363854 | |||||||
chr4:56363925 | A | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+7526T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363925 | |||||||
chr4:56363991 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+7460C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56363991 | |||||||
chr4:56364010 | T | C | 114 | a0001c0001t0001g0090a0001c0005t0001g0011a0001c0005t0001g0028others(111): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.861+7441A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364010 | |||||||
chr4:56364052 | C | T | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.861+7399G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364052 | |||||||
chr4:56364091 | T | C | 1 | a0002c0002t0001g0120 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.861+7360A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364091 | |||||||
chr4:56364242 | T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+7209A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364242 | |||||||
chr4:56364291 | T | A | 1 | a0003c0003t0002g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.861+7160A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364291 | |||||||
chr4:56364307 | A | C | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+7144T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364307 | |||||||
chr4:56364384 | T | C | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+7067A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364384 | |||||||
chr4:56364427 | G | A | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+7024C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364427 | |||||||
chr4:56364521 | C | T | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.861+6930G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364521 | |||||||
chr4:56364709 | T | C | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.861+6742A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364709 | |||||||
chr4:56364718 | T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6733A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364718 | |||||||
chr4:56364765 | T | C | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.861+6686A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364765 | |||||||
chr4:56364850 | T | A | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.861+6601A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364850 | |||||||
chr4:56364883 | G | T | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.861+6568C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364883 | |||||||
chr4:56364920 | T | G | 1 | a0002c0002t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.861+6531A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364920 | |||||||
chr4:56364972 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6479A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56364972 | |||||||
chr4:56365076 | C | T | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.861+6375G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365076 | |||||||
chr4:56365095 | A | T | 1 | a0004c0004t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.861+6356T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365095 | |||||||
chr4:56365117 | AAAGAAGG others(728): Show |
A | 1 | a0006c0008t0001g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.861+5599_861+6333d others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365117 | |||||||
chr4:56365198 | G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6253C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365198 | |||||||
chr4:56365226 | T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+6225A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365226 | |||||||
chr4:56365271 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+6180C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365271 | |||||||
chr4:56365276 | T | C | 6 | a0001c0010t0001g0280a0001c0010t0001g0281a0006c0008t0001g0059others(3): Show | 6 | HG02809.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+6175A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365276 | |||||||
chr4:56365300 | G | C | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+6151C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365300 | |||||||
chr4:56365309 | C | A | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.861+6142G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365309 | |||||||
chr4:56365365 | G | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0071a0001c0001t0001g0074others(10): Show | 16 | HG00597.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.861+6086C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365365 | |||||||
chr4:56365373 | C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0161 | 2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.861+6078G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365373 | |||||||
chr4:56365409 | A | C | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+6042T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365409 | |||||||
chr4:56365458 | A | C | 261 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(258): Show | 292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.861+5993T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365458 | |||||||
chr4:56365576 | C | T | 44 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(41): Show | 47 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.861+5875G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365576 | |||||||
chr4:56365604 | T | C | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.861+5847A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365604 | |||||||
chr4:56365606 | C | A | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.861+5845G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365606 | |||||||
chr4:56365614 | T | A | 1 | a0004c0004t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.861+5837A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365614 | |||||||
chr4:56365650 | C | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+5801G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365650 | |||||||
chr4:56365671 | C | T | 1 | a0012c0023t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.861+5780G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365671 | |||||||
chr4:56365696 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.861+5755T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365696 | |||||||
chr4:56365708 | G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+5743C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365708 | |||||||
chr4:56365732 | A | C | 4 | a0003c0003t0002g0262a0003c0003t0002g0290a0003c0003t0002g0292others(1): Show | 4 | HG02055.hp2 HG02622.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.861+5719T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365732 | |||||||
chr4:56365757 | A | G | 44 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(41): Show | 47 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.861+5694T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365757 | |||||||
chr4:56365825 | C | G | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+5626G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365825 | |||||||
chr4:56365866 | G | A | 1 | a0006c0008t0001g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.861+5585C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365866 | |||||||
chr4:56365940 | T | C | 3 | a0003c0003t0002g0255a0003c0003t0002g0270a0003c0003t0002g0288 | 3 | HG00140.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.861+5511A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365940 | |||||||
chr4:56365950 | C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+5501G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365950 | |||||||
chr4:56365967 | T | C | 1 | a0002c0002t0001g0194 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.861+5484A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56365967 | |||||||
chr4:56366011 | G | A | 38 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(35): Show | 41 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.861+5440C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366011 | |||||||
chr4:56366013 | T | C | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861+5438A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366013 | |||||||
chr4:56366128 | G | A | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.861+5323C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366128 | |||||||
chr4:56366236 | C | T | 4 | a0001c0001t0001g0013a0003c0003t0002g0003a0003c0003t0002g0042others(1): Show | 8 | HG00408.hp2 HG01167.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+5215G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366236 | |||||||
chr4:56366237 | G | C | 53 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(50): Show | 56 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.861+5214C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366237 | |||||||
chr4:56366257 | C | G | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.861+5194G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366257 | |||||||
chr4:56366274 | C | T | 2 | a0002c0002t0001g0178a0002c0002t0001g0179 | 2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.861+5177G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366274 | |||||||
chr4:56366301 | G | A | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.861+5150C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366301 | |||||||
chr4:56366398 | C | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+5053G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366398 | |||||||
chr4:56366541 | C | G | 113 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(110): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.861+4910G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366541 | |||||||
chr4:56366570 | G | A | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+4881C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366570 | |||||||
chr4:56366723 | A | G | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.861+4728T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366723 | |||||||
chr4:56366804 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.861+4647G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366804 | |||||||
chr4:56366808 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+4643G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366808 | |||||||
chr4:56366837 | T | G | 52 | a0003c0003t0002g0010a0003c0003t0002g0025a0003c0003t0002g0026others(49): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.861+4614A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366837 | |||||||
chr4:56366867 | C | T | 1 | a0002c0002t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.861+4584G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56366867 | |||||||
chr4:56367040 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+4411T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367040 | |||||||
chr4:56367118 | T | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.861+4333A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367118 | |||||||
chr4:56367164 | C | T | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.861+4287G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367164 | |||||||
chr4:56367170 | G | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+4281C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367170 | |||||||
chr4:56367259 | G | C | 4 | a0002c0002t0001g0002a0002c0002t0001g0196a0002c0002t0001g0197others(1): Show | 8 | HG00735.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+4192C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367259 | |||||||
chr4:56367272 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+4179G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367272 | |||||||
chr4:56367277 | C | A | 2 | a0001c0005t0001g0311a0001c0005t0001g0317 | 2 | NA18989.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.861+4174G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367277 | |||||||
chr4:56367404 | T | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+4047A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367404 | |||||||
chr4:56367436 | C | G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0199 | 3 | NA18973.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.861+4015G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367436 | |||||||
chr4:56367448 | T | C | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+4003A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367448 | |||||||
chr4:56367453 | C | A | 1 | a0002c0002t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.861+3998G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367453 | |||||||
chr4:56367466 | T | C | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.861+3985A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367466 | |||||||
chr4:56367470 | T | C | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.861+3981A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367470 | |||||||
chr4:56367471 | G | T | 113 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(110): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.861+3980C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367471 | |||||||
chr4:56367597 | G | C | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.861+3854C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367597 | |||||||
chr4:56367621 | G | T | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.861+3830C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367621 | |||||||
chr4:56367639 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.861+3812A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367639 | |||||||
chr4:56367651 | G | A | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.861+3800C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367651 | |||||||
chr4:56367692 | C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0161 | 2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.861+3759G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367692 | |||||||
chr4:56367875 | C | A | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+3576G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367875 | |||||||
chr4:56367896 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+3555G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367896 | |||||||
chr4:56367918 | A | G | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+3533T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367918 | |||||||
chr4:56367971 | T | C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.861+3480A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367971 | |||||||
chr4:56367972 | G | A | 1 | a0003c0003t0002g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.861+3479C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56367972 | |||||||
chr4:56368028 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.861+3423T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368028 | |||||||
chr4:56368061 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+3390A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368061 | |||||||
chr4:56368103 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+3348T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368103 | |||||||
chr4:56368105 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+3346T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368105 | |||||||
chr4:56368150 | A | C | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+3301T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368150 | |||||||
chr4:56368175 | T | A | 1 | a0007c0009t0004g0029 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.861+3276A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368175 | |||||||
chr4:56368228 | G | A | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.861+3223C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368228 | |||||||
chr4:56368264 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+3187C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368264 | |||||||
chr4:56368334 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.861+3117T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368334 | |||||||
chr4:56368395 | T | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.861+3056A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368395 | |||||||
chr4:56368432 | C | T | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.861+3019G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368432 | |||||||
chr4:56368463 | G | T | 1 | a0003c0003t0002g0239 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.861+2988C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368463 | |||||||
chr4:56368636 | G | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+2815C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368636 | |||||||
chr4:56368651 | T | C | 2 | a0002c0006t0001g0231a0002c0006t0001g0237 | 2 | NA18982.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.861+2800A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368651 | |||||||
chr4:56368709 | G | C | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.861+2742C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368709 | |||||||
chr4:56368733 | G | C | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.861+2718C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368733 | |||||||
chr4:56368808 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2643C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368808 | |||||||
chr4:56368868 | T | TA | 9 | a0001c0001t0001g0091a0002c0002t0001g0198a0003c0003t0002g0044others(6): Show | 9 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.861+2582dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368868 | |||||||
chr4:56368878 | AAC | A | 8 | a0003c0003t0002g0025a0003c0003t0002g0026a0003c0003t0002g0251others(5): Show | 10 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.861+2571_861+2572d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368878 | |||||||
chr4:56368879 | AC | A | 44 | a0003c0003t0002g0010a0003c0003t0002g0027a0003c0003t0002g0238others(41): Show | 47 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.861+2571delG | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368879 | |||||||
chr4:56368897 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2554A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368897 | |||||||
chr4:56368904 | CA | C | 8 | a0001c0001t0001g0071a0003c0003t0002g0044a0003c0003t0002g0045others(5): Show | 8 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2546delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368904 | |||||||
chr4:56368932 | C | T | 1 | a0001c0010t0001g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.861+2519G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368932 | |||||||
chr4:56368978 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+2473G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56368978 | |||||||
chr4:56369120 | T | C | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.861+2331A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369120 | |||||||
chr4:56369308 | G | C | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.861+2143C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369308 | |||||||
chr4:56369341 | C | G | 1 | a0001c0005t0001g0284 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.861+2110G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369341 | |||||||
chr4:56369585 | C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0159others(1): Show | 6 | NA18971.hp1 NA18975.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+1866G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369585 | |||||||
chr4:56369593 | G | A | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.861+1858C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369593 | |||||||
chr4:56369697 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.861+1754G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369697 | |||||||
chr4:56369746 | C | G | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+1705G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369746 | |||||||
chr4:56369837 | G | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+1614C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369837 | |||||||
chr4:56369875 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.861+1576G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369875 | |||||||
chr4:56369944 | T | TAA | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+1505_861+1506d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369944 | |||||||
chr4:56369944 | TA | T | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.861+1506delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369944 | |||||||
chr4:56369957 | A | C | 67 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(64): Show | 75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.861+1494T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369957 | |||||||
chr4:56369958 | A | C | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.861+1493T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56369958 | |||||||
chr4:56370096 | T | C | 2 | a0002c0002t0001g0215a0002c0002t0001g0216 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.861+1355A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370096 | |||||||
chr4:56370160 | T | A | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.861+1291A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370160 | |||||||
chr4:56370165 | C | T | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.861+1286G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370165 | |||||||
chr4:56370181 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+1270C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370181 | |||||||
chr4:56370280 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+1171G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370280 | |||||||
chr4:56370287 | C | T | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.861+1164G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370287 | |||||||
chr4:56370312 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.861+1139G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370312 | |||||||
chr4:56370388 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.861+1063C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370388 | |||||||
chr4:56370416 | G | GA | 5 | a0001c0005t0001g0032a0004c0004t0001g0134a0004c0004t0001g0143others(2): Show | 5 | HG04199.hp1 NA18969.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.861+1034dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370416 | |||||||
chr4:56370531 | G | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+920C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370531 | |||||||
chr4:56370563 | C | T | 1 | a0003c0003t0002g0272 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.861+888G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370563 | |||||||
chr4:56370567 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+884T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370567 | |||||||
chr4:56370620 | A | G | 1 | a0004c0004t0001g0021 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861+831T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370620 | |||||||
chr4:56370657 | A | G | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.861+794T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370657 | |||||||
chr4:56370775 | A | C | 4 | a0006c0008t0001g0059a0006c0008t0001g0060a0006c0008t0001g0061others(1): Show | 4 | HG03041.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.861+676T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370775 | |||||||
chr4:56370824 | T | C | 1 | a0002c0002t0001g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.861+627A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370824 | |||||||
chr4:56370994 | T | G | 96 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(93): Show | 108 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(105): Show |
intron_variant | MODIFIER | c.861+457A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56370994 | |||||||
chr4:56371324 | G | A | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.861+127C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 5/14 | chr4 | 56371324 | |||||||
chr4:56371773 | A | G | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.669-130T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371773 | |||||||
chr4:56371789 | C | A | 2 | a0002c0002t0001g0009a0002c0002t0001g0209 | 4 | HG01243.hp2 HG02109.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-146G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371789 | |||||||
chr4:56371811 | C | A | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.669-168G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371811 | |||||||
chr4:56371856 | A | T | 1 | a0002c0002t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.669-213T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371856 | |||||||
chr4:56371858 | CAG | C | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-217_669-216del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371858 | |||||||
chr4:56371898 | A | G | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.669-255T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371898 | |||||||
chr4:56371941 | T | TA | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.669-299dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371941 | |||||||
chr4:56371986 | C | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0157 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.669-343G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371986 | |||||||
chr4:56371994 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.669-351G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56371994 | |||||||
chr4:56372019 | C | G | 3 | a0004c0004t0001g0008a0004c0004t0001g0129a0004c0025t0001g0126 | 5 | NA18939.hp1 NA18941.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-376G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372019 | |||||||
chr4:56372059 | T | C | 25 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(22): Show | 28 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.669-416A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372059 | |||||||
chr4:56372070 | C | T | 1 | a0001c0005t0001g0301 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.669-427G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372070 | |||||||
chr4:56372472 | A | T | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0012c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-829T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372472 | |||||||
chr4:56372514 | A | G | 49 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.669-871T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372514 | |||||||
chr4:56372643 | T | C | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.669-1000A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372643 | |||||||
chr4:56372666 | TAA | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-1025_669-1024d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372666 | |||||||
chr4:56372727 | T | A | 1 | a0007c0009t0004g0029 | 2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.669-1084A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372727 | |||||||
chr4:56372752 | TATA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-1112_669-1110d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372752 | |||||||
chr4:56372979 | T | C | 1 | a0003c0003t0002g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.669-1336A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56372979 | |||||||
chr4:56373014 | C | T | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.669-1371G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373014 | |||||||
chr4:56373112 | G | A | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669-1469C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373112 | |||||||
chr4:56373213 | C | CCCAAGTT others(3): Show |
1 | a0004c0004t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.669-1571_669-1570i others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373213 | |||||||
chr4:56373214 | A | G | 1 | a0004c0004t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.669-1571T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373214 | |||||||
chr4:56373355 | C | T | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.669-1712G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373355 | |||||||
chr4:56373433 | G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-1790C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373433 | |||||||
chr4:56373434 | C | T | 1 | a0006c0008t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.669-1791G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373434 | |||||||
chr4:56373459 | G | A | 53 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(50): Show | 56 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.669-1816C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373459 | |||||||
chr4:56373614 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-1971G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373614 | |||||||
chr4:56373825 | GTT | G | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.669-2184_669-2183d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373825 | |||||||
chr4:56373828 | C | G | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.669-2185G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373828 | |||||||
chr4:56373832 | T | A | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.669-2189A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373832 | |||||||
chr4:56373833 | A | AT | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.669-2191_669-2190i others(3): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373833 | |||||||
chr4:56373835 | T | C | 262 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(259): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.669-2192A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56373835 | |||||||
chr4:56374011 | C | G | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.669-2368G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374011 | |||||||
chr4:56374215 | C | CTAAAACT others(371): Show |
1 | a0005c0007t0003g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.669-2573_669-2572i others(380): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374215 | |||||||
chr4:56374367 | C | CA | 102 | a0001c0001t0001g0166a0001c0005t0001g0285a0001c0005t0001g0313others(99): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.669-2725dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | |||||||
chr4:56374367 | C | CAA | 22 | a0003c0003t0001g0220a0003c0003t0002g0044a0003c0003t0002g0045others(19): Show | 22 | HG00423.hp1 HG01255.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.669-2725_669-2724i others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | |||||||
chr4:56374367 | C | CAAAAAAA | 5 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0036others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.669-2725_669-2724i others(9): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | |||||||
chr4:56374367 | CAGAAAAA others(8): Show |
C | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.669-2739_669-2725d others(17): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374367 | |||||||
chr4:56374369 | G | A | 173 | a0001c0001t0001g0166a0001c0005t0001g0011a0001c0005t0001g0028others(170): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.669-2726C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374369 | |||||||
chr4:56374390 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.669-2747T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374390 | |||||||
chr4:56374565 | T | C | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.669-2922A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374565 | |||||||
chr4:56374606 | AT | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-2964delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374606 | |||||||
chr4:56374694 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.669-3051G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374694 | |||||||
chr4:56374786 | G | A | 1 | a0002c0002t0001g0213 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.669-3143C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374786 | |||||||
chr4:56374989 | G | A | 2 | a0004c0004t0001g0145a0004c0004t0001g0146 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.668+3159C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56374989 | |||||||
chr4:56375105 | G | A | 2 | a0002c0002t0001g0226a0002c0002t0001g0235 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.668+3043C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375105 | |||||||
chr4:56375143 | G | A | 7 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(4): Show | 7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.668+3005C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375143 | |||||||
chr4:56375182 | T | C | 1 | a0001c0005t0001g0314 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.668+2966A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375182 | |||||||
chr4:56375192 | A | T | 88 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(85): Show | 100 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.668+2956T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375192 | |||||||
chr4:56375196 | T | C | 113 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(110): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.668+2952A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375196 | |||||||
chr4:56375373 | T | C | 1 | a0001c0005t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668+2775A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375373 | |||||||
chr4:56375476 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.668+2672T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375476 | |||||||
chr4:56375611 | G | A | 10 | a0002c0002t0001g0226a0002c0002t0001g0235a0005c0007t0003g0033others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.668+2537C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375611 | |||||||
chr4:56375766 | T | C | 1 | a0003c0003t0002g0278 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.668+2382A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375766 | |||||||
chr4:56375832 | T | G | 113 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(110): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.668+2316A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375832 | |||||||
chr4:56375888 | C | T | 2 | a0004c0004t0001g0132a0004c0004t0001g0133 | 2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.668+2260G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56375888 | |||||||
chr4:56376019 | C | CT | 69 | a0001c0001t0001g0069a0001c0005t0001g0316a0001c0005t0001g0317others(66): Show | 80 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.668+2128dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | |||||||
chr4:56376019 | C | CTT | 45 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.668+2127_668+2128d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | |||||||
chr4:56376019 | C | CTTT | 26 | a0001c0005t0001g0285a0001c0005t0001g0299a0001c0005t0001g0300others(23): Show | 29 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.668+2126_668+2128d others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | |||||||
chr4:56376019 | CT | C | 25 | a0001c0001t0001g0066a0001c0001t0001g0093a0001c0001t0001g0096others(22): Show | 25 | HG01109.hp2 HG01515.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.668+2128delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376019 | |||||||
chr4:56376055 | G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.668+2093C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376055 | |||||||
chr4:56376084 | T | C | 2 | a0004c0004t0001g0173a0004c0004t0001g0223 | 2 | NA18982.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.668+2064A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376084 | |||||||
chr4:56376105 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.668+2043G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376105 | |||||||
chr4:56376105 | C | T | 210 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(207): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.668+2043G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376105 | |||||||
chr4:56376216 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1932C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376216 | |||||||
chr4:56376411 | T | C | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.668+1737A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376411 | |||||||
chr4:56376416 | T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1732A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376416 | |||||||
chr4:56376434 | G | A | 1 | a0010c0016t0001g0218 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.668+1714C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376434 | |||||||
chr4:56376464 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.668+1684T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376464 | |||||||
chr4:56376538 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1610A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376538 | |||||||
chr4:56376728 | T | C | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.668+1420A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376728 | |||||||
chr4:56376772 | G | A | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.668+1376C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376772 | |||||||
chr4:56376794 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1354T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376794 | |||||||
chr4:56376805 | C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.668+1343G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376805 | |||||||
chr4:56376924 | G | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.668+1224C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56376924 | |||||||
chr4:56377062 | G | A | 1 | a0009c0011t0002g0206 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.668+1086C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377062 | |||||||
chr4:56377066 | CA | C | 51 | a0001c0001t0001g0125a0001c0001t0001g0166a0004c0004t0001g0005others(48): Show | 59 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.668+1081delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377066 | |||||||
chr4:56377066 | CAA | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1080_668+1081d others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377066 | |||||||
chr4:56377070 | A | AAT | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.668+1077_668+1078i others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377070 | |||||||
chr4:56377074 | A | T | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.668+1074T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377074 | |||||||
chr4:56377077 | A | AAT | 44 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(41): Show | 47 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.668+1070_668+1071i others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377077 | |||||||
chr4:56377077 | A | T | 1 | a0001c0005t0001g0298 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.668+1071T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377077 | |||||||
chr4:56377078 | A | AAAT | 84 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(81): Show | 95 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(92): Show |
intron_variant | MODIFIER | c.668+1069_668+1070i others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377078 | |||||||
chr4:56377078 | A | T | 124 | a0001c0001t0001g0068a0001c0001t0001g0125a0002c0002t0001g0115others(121): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.668+1070T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377078 | |||||||
chr4:56377082 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.668+1066A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377082 | |||||||
chr4:56377086 | T | TA | 201 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(198): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.668+1061dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377086 | |||||||
chr4:56377090 | TA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1057delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377090 | |||||||
chr4:56377096 | A | T | 1 | a0002c0002t0001g0114 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.668+1052T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377096 | |||||||
chr4:56377101 | A | AAAATT | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.668+1042_668+1046d others(7): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377101 | |||||||
chr4:56377101 | A | T | 86 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(83): Show | 97 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.668+1047T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377101 | |||||||
chr4:56377164 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.668+984A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377164 | |||||||
chr4:56377506 | C | T | 48 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(45): Show | 55 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.668+642G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377506 | |||||||
chr4:56377578 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+570A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377578 | |||||||
chr4:56377708 | A | G | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.668+440T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377708 | |||||||
chr4:56377779 | T | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.668+369A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377779 | |||||||
chr4:56377949 | C | T | 7 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(4): Show | 7 | HG01884.hp1 HG02145.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.668+199G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377949 | |||||||
chr4:56377958 | A | G | 1 | a0004c0025t0001g0126 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.668+190T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56377958 | |||||||
chr4:56378052 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+96G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 4/14 | chr4 | 56378052 | |||||||
chr4:56378653 | A | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-189T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378653 | |||||||
chr4:56378653 | A | G | 202 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(199): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.352-189T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378653 | |||||||
chr4:56378758 | CTG | C | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.352-296_352-295del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378758 | |||||||
chr4:56378785 | GT | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-322delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378785 | |||||||
chr4:56378881 | T | A | 3 | a0001c0005t0001g0319a0007c0009t0004g0029a0007c0009t0004g0331 | 4 | HG02257.hp1 HG02258.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-417A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378881 | |||||||
chr4:56378889 | A | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-425T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378889 | |||||||
chr4:56378890 | T | A | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-426A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378890 | |||||||
chr4:56378893 | T | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.352-429A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378893 | |||||||
chr4:56378906 | C | T | 1 | a0004c0004t0001g0150 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.352-442G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378906 | |||||||
chr4:56378923 | A | C | 1 | a0003c0003t0002g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.352-459T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378923 | |||||||
chr4:56378970 | G | A | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.352-506C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56378970 | |||||||
chr4:56379040 | C | T | 1 | a0004c0004t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.352-576G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379040 | |||||||
chr4:56379071 | C | T | 207 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(204): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.352-607G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379071 | |||||||
chr4:56379249 | T | G | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.352-785A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379249 | |||||||
chr4:56379340 | C | G | 6 | a0003c0003t0002g0025a0003c0003t0002g0026a0003c0003t0002g0251others(3): Show | 8 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-876G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379340 | |||||||
chr4:56379525 | T | G | 1 | a0002c0002t0001g0198 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.352-1061A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379525 | |||||||
chr4:56379532 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1068T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379532 | |||||||
chr4:56379725 | C | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.352-1261G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379725 | |||||||
chr4:56379801 | T | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1337A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379801 | |||||||
chr4:56379853 | G | A | 68 | a0003c0003t0002g0003a0003c0003t0002g0010a0003c0003t0002g0025others(65): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.352-1389C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379853 | |||||||
chr4:56379965 | C | G | 2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.352-1501G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56379965 | |||||||
chr4:56380143 | G | T | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.352-1679C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56380143 | |||||||
chr4:56380241 | G | T | 3 | a0003c0003t0002g0238a0003c0003t0002g0250a0003c0003t0002g0295 | 3 | HG01258.hp1 HG02451.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.352-1777C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56380241 | |||||||
chr4:56380510 | G | T | 2 | a0002c0002t0001g0178a0002c0002t0001g0179 | 2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.351+1967C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56380510 | |||||||
chr4:56381039 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.351+1438G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381039 | |||||||
chr4:56381157 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+1320G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381157 | |||||||
chr4:56381160 | A | C | 1 | a0001c0005t0001g0242 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.351+1317T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381160 | |||||||
chr4:56381180 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.351+1297G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381180 | |||||||
chr4:56381423 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351+1054G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381423 | |||||||
chr4:56381452 | C | A | 1 | a0002c0002t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.351+1025G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381452 | |||||||
chr4:56381469 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.351+1008A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381469 | |||||||
chr4:56381509 | C | T | 1 | a0014c0022t0001g0109 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.351+968G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381509 | |||||||
chr4:56381584 | C | CA | 19 | a0001c0001t0001g0283a0001c0005t0001g0284a0002c0002t0001g0123others(16): Show | 19 | HG01070.hp2 HG01175.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.351+892dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381584 | |||||||
chr4:56381584 | C | CAA | 43 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(40): Show | 46 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.351+891_351+892dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381584 | |||||||
chr4:56381646 | T | TTC | 39 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(36): Show | 42 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.351+829_351+830dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381646 | |||||||
chr4:56381649 | T | TCA | 7 | a0001c0001t0001g0057a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01109.hp2 HG03098.hp1 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+826_351+827dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCACACAC others(5): Show |
1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.351+816_351+827dup others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCACACAC others(7): Show |
3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG02965.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.351+814_351+827dup others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCACACAC others(9): Show |
2 | a0001c0001t0001g0015a0001c0010t0001g0281 | 3 | HG02809.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.351+812_351+827dup others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCACACAC others(11): Show |
2 | a0002c0002t0001g0108a0003c0003t0002g0277 | 2 | HG00738.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.351+810_351+827dup others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCACACAC others(13): Show |
3 | a0002c0002t0001g0018a0002c0002t0001g0113a0002c0002t0001g0124 | 4 | NA18952.hp2 NA18973.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+808_351+827dup others(20): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(3): Show |
42 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0023others(39): Show | 50 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(5): Show |
24 | a0001c0001t0001g0125a0002c0002t0001g0201a0002c0002t0001g0202others(21): Show | 26 | HG01192.hp1 HG01891.hp2 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(7): Show |
37 | a0002c0002t0001g0207a0002c0002t0001g0214a0003c0003t0002g0240others(34): Show | 43 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(9): Show |
32 | a0002c0002t0001g0215a0002c0002t0001g0216a0003c0003t0002g0010others(29): Show | 36 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(10): Show |
1 | a0004c0004t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(17): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(11): Show |
31 | a0002c0002t0001g0106a0002c0002t0001g0107a0003c0003t0002g0027others(28): Show | 32 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(18): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(13): Show |
20 | a0002c0002t0001g0017a0002c0002t0001g0105a0002c0002t0001g0110others(17): Show | 24 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(20): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(15): Show |
9 | a0002c0002t0001g0019a0002c0002t0001g0114a0002c0002t0001g0115others(6): Show | 10 | HG01123.hp1 HG01496.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(22): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(17): Show |
3 | a0002c0002t0001g0122a0002c0002t0001g0123a0007c0009t0004g0029 | 4 | HG02257.hp1 HG02258.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(24): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCACAC others(15): Show |
1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+827_351+828ins others(22): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCTCAC others(3): Show |
6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+827_351+828ins others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCTCAC others(5): Show |
1 | a0005c0007t0003g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(12): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCTCAC others(7): Show |
1 | a0004c0004t0001g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(14): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCTCAC others(9): Show |
1 | a0005c0007t0003g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.351+827_351+828ins others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381649 | T | TCTCTCAC others(19): Show |
1 | a0001c0001t0001g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.351+827_351+828ins others(26): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381649 | |||||||
chr4:56381653 | A | T | 1 | a0003c0003t0002g0247 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+824T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381653 | |||||||
chr4:56381696 | A | G | 209 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(206): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.351+781T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381696 | |||||||
chr4:56381742 | A | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0157 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.351+735T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381742 | |||||||
chr4:56381976 | G | GTC | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+499_351+500dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56381976 | |||||||
chr4:56382171 | C | T | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+306G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382171 | |||||||
chr4:56382253 | G | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+224C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382253 | |||||||
chr4:56382254 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+223G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382254 | |||||||
chr4:56382411 | G | A | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.351+66C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382411 | |||||||
chr4:56382425 | A | G | 45 | a0002c0002t0001g0002a0002c0002t0001g0023a0002c0002t0001g0177others(42): Show | 51 | HG00735.hp2 HG01074.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.351+52T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 3/14 | chr4 | 56382425 | |||||||
chr4:56382624 | T | C | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.231-27A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382624 | |||||||
chr4:56382690 | T | C | 1 | a0011c0018t0001g0167 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.231-93A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382690 | |||||||
chr4:56382776 | C | T | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.231-179G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382776 | |||||||
chr4:56382792 | G | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.231-195C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382792 | |||||||
chr4:56382836 | G | C | 157 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(154): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.231-239C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382836 | |||||||
chr4:56382836 | G | T | 1 | a0003c0003t0002g0286 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.231-239C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382836 | |||||||
chr4:56382926 | G | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.231-329C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382926 | |||||||
chr4:56382974 | T | C | 1 | a0003c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231-377A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382974 | |||||||
chr4:56382982 | G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-385C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382982 | |||||||
chr4:56382988 | C | T | 3 | a0006c0008t0001g0059a0006c0008t0001g0060a0006c0008t0001g0061 | 3 | HG03041.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.231-391G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56382988 | |||||||
chr4:56383016 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231-419G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383016 | |||||||
chr4:56383109 | T | A | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.231-512A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383109 | |||||||
chr4:56383129 | A | C | 90 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(87): Show | 102 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(99): Show |
intron_variant | MODIFIER | c.231-532T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383129 | |||||||
chr4:56383162 | A | AT | 69 | a0003c0003t0001g0220a0003c0003t0002g0003a0003c0003t0002g0010others(66): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.231-566dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383162 | |||||||
chr4:56383200 | T | C | 1 | a0002c0002t0001g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231-603A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383200 | |||||||
chr4:56383219 | C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-622G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383219 | |||||||
chr4:56383225 | A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-628T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383225 | |||||||
chr4:56383226 | C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-629G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383226 | |||||||
chr4:56383227 | A | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-630T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383227 | |||||||
chr4:56383234 | A | G | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-637T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383234 | |||||||
chr4:56383245 | A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-648T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383245 | |||||||
chr4:56383248 | T | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-651A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383248 | |||||||
chr4:56383254 | A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-657T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383254 | |||||||
chr4:56383256 | A | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-659T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383256 | |||||||
chr4:56383278 | G | A | 4 | a0001c0010t0001g0280a0001c0010t0001g0281a0006c0008t0001g0326others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-681C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383278 | |||||||
chr4:56383322 | C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-725G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383322 | |||||||
chr4:56383323 | A | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-726T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383323 | |||||||
chr4:56383324 | C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231-727G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383324 | |||||||
chr4:56383362 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+708G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383362 | |||||||
chr4:56383364 | G | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+706C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383364 | |||||||
chr4:56383365 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+705G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383365 | |||||||
chr4:56383366 | C | A | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+704G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383366 | |||||||
chr4:56383368 | C | G | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+702G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383368 | |||||||
chr4:56383370 | G | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+700C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383370 | |||||||
chr4:56383372 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+698G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383372 | |||||||
chr4:56383373 | T | G | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+697A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383373 | |||||||
chr4:56383376 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+694G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383376 | |||||||
chr4:56383377 | A | C | 1 | a0002c0002t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+693T>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383377 | |||||||
chr4:56383564 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.230+506G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383564 | |||||||
chr4:56383584 | G | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.230+486C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383584 | |||||||
chr4:56383765 | A | T | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.230+305T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383765 | |||||||
chr4:56383777 | T | C | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.230+293A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383777 | |||||||
chr4:56383845 | T | C | 1 | a0001c0005t0001g0320 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.230+225A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383845 | |||||||
chr4:56383918 | T | TA | 259 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0005t0001g0011others(256): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.230+151_230+152ins others(1): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 2/14 | chr4 | 56383918 | |||||||
chr4:56384657 | TA | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-317delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384657 | |||||||
chr4:56384702 | A | T | 1 | a0004c0004t0001g0223 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-42-361T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384702 | |||||||
chr4:56384702 | AT | A | 42 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(39): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-42-362delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384702 | |||||||
chr4:56384795 | C | T | 4 | a0003c0003t0002g0243a0003c0003t0002g0244a0003c0003t0002g0245others(1): Show | 4 | HG00609.hp2 HG02083.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-454G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56384795 | |||||||
chr4:56385027 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42-686G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385027 | |||||||
chr4:56385331 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-990A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385331 | |||||||
chr4:56385348 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1007A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385348 | |||||||
chr4:56385352 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1011A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385352 | |||||||
chr4:56385353 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1012A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385353 | |||||||
chr4:56385354 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1013G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385354 | |||||||
chr4:56385356 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1015G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385356 | |||||||
chr4:56385357 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1016A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385357 | |||||||
chr4:56385358 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1017A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385358 | |||||||
chr4:56385362 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1021G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385362 | |||||||
chr4:56385363 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1022A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385363 | |||||||
chr4:56385364 | G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1023C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385364 | |||||||
chr4:56385369 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1028A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385369 | |||||||
chr4:56385374 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1033A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385374 | |||||||
chr4:56385376 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1035A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385376 | |||||||
chr4:56385377 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1036A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385377 | |||||||
chr4:56385379 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1038G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385379 | |||||||
chr4:56385382 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1041G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385382 | |||||||
chr4:56385383 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1042A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385383 | |||||||
chr4:56385384 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1043G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385384 | |||||||
chr4:56385387 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1046A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385387 | |||||||
chr4:56385391 | G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1050C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385391 | |||||||
chr4:56385392 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1051G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385392 | |||||||
chr4:56385394 | G | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1053C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385394 | |||||||
chr4:56385395 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1054A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385395 | |||||||
chr4:56385397 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1056A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385397 | |||||||
chr4:56385398 | A | T | 2 | a0007c0009t0004g0029a0007c0009t0004g0331 | 3 | HG02257.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-42-1057T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385398 | |||||||
chr4:56385399 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1058A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385399 | |||||||
chr4:56385400 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1059G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385400 | |||||||
chr4:56385403 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1062A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385403 | |||||||
chr4:56385405 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1064G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385405 | |||||||
chr4:56385408 | T | G | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1067A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385408 | |||||||
chr4:56385414 | C | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1073G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385414 | |||||||
chr4:56385415 | T | A | 1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1074A>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385415 | |||||||
chr4:56385417 | G | GAGAAAGA others(7): Show |
1 | a0003c0003t0002g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-1077_-42-1076i others(16): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385417 | |||||||
chr4:56385496 | A | T | 26 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(23): Show | 29 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-42-1155T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385496 | |||||||
chr4:56385679 | C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0168 | 4 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-1338G>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385679 | |||||||
chr4:56385707 | C | T | 48 | a0004c0004t0001g0005a0004c0004t0001g0008a0004c0004t0001g0020others(45): Show | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.-42-1366G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385707 | |||||||
chr4:56385779 | A | AT | 65 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(62): Show | 71 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-42-1439dupA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385779 | |||||||
chr4:56385929 | CT | C | 8 | a0001c0001t0001g0103a0002c0002t0001g0124a0002c0002t0001g0217others(5): Show | 8 | HG01943.hp1 HG01993.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1432delA | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385929 | |||||||
chr4:56385932 | T | TC | 111 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.-43+1429_-43+1430i others(3): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385932 | |||||||
chr4:56385933 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-43+1429A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385933 | |||||||
chr4:56385948 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1414T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385948 | |||||||
chr4:56385972 | C | T | 1 | a0004c0004t0001g0169 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-43+1390G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385972 | |||||||
chr4:56385978 | T | C | 1 | a0005c0007t0003g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-43+1384A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56385978 | |||||||
chr4:56386143 | T | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1219A>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386143 | |||||||
chr4:56386332 | C | T | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+1030G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386332 | |||||||
chr4:56386469 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43+893G>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386469 | |||||||
chr4:56386522 | G | A | 11 | a0004c0004t0001g0005a0004c0004t0001g0022a0004c0004t0001g0169others(8): Show | 15 | HG00408.hp1 HG02015.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+840C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386522 | |||||||
chr4:56386712 | C | G | 211 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0032others(208): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.-43+650G>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386712 | |||||||
chr4:56386720 | G | C | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+642C>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386720 | |||||||
chr4:56386775 | G | A | 89 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0017others(86): Show | 101 | HG00597.hp2 HG00735.hp2 HG01069.hp1 others(98): Show |
intron_variant | MODIFIER | c.-43+587C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386775 | |||||||
chr4:56386799 | C | CA | 108 | a0001c0001t0001g0125a0001c0001t0001g0157a0001c0001t0001g0158others(105): Show | 124 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-43+562dupT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | C | CAA | 19 | a0002c0002t0001g0226a0002c0002t0001g0227a0002c0002t0001g0232others(16): Show | 20 | HG02080.hp1 HG02559.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.-43+561_-43+562dup others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | C | CAAA | 8 | a0003c0003t0002g0238a0003c0003t0002g0239a0005c0007t0003g0033others(5): Show | 8 | HG00323.hp2 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+560_-43+562dup others(3): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | C | CAAAA | 51 | a0001c0001t0001g0283a0001c0005t0001g0242a0001c0010t0001g0280others(48): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.-43+559_-43+562dup others(4): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | C | CAAAAA | 14 | a0001c0005t0001g0284a0001c0005t0001g0285a0003c0003t0002g0286others(11): Show | 14 | HG01070.hp2 HG01074.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-43+558_-43+562dup others(5): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | C | CAAAAAA | 26 | a0001c0005t0001g0011a0001c0005t0001g0028a0001c0005t0001g0298others(23): Show | 29 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-43+557_-43+562dup others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | C | CAAAAAAA | 7 | a0001c0005t0001g0032a0001c0005t0001g0321a0001c0005t0001g0322others(4): Show | 7 | HG01109.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+556_-43+562dup others(7): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | CA | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+562delT | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | CAA | C | 6 | a0003c0003t0002g0044a0003c0003t0002g0045a0003c0003t0002g0046others(3): Show | 6 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+561_-43+562del others(2): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | CAAAAAA | C | 3 | a0003c0003t0002g0003a0003c0003t0002g0042a0012c0023t0002g0043 | 6 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+557_-43+562del others(6): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386799 | CAAAAAAA others(3): Show |
C | 1 | a0004c0004t0001g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-43+553_-43+562del others(10): Show |
AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386799 | |||||||
chr4:56386823 | G | A | 6 | a0005c0007t0003g0035a0005c0007t0003g0036a0005c0007t0003g0037others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+539C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386823 | |||||||
chr4:56386823 | G | T | 2 | a0005c0007t0003g0033a0005c0007t0003g0034 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-43+539C>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386823 | |||||||
chr4:56386825 | A | G | 8 | a0005c0007t0003g0033a0005c0007t0003g0034a0005c0007t0003g0035others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43+537T>C | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386825 | |||||||
chr4:56386875 | A | T | 1 | a0001c0005t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-43+487T>A | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56386875 | |||||||
chr4:56387045 | G | A | 2 | a0003c0003t0002g0327a0003c0003t0002g0328 | 2 | HG01169.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-43+317C>T | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56387045 | |||||||
chr4:56387202 | T | C | 2 | a0002c0002t0001g0329a0002c0002t0007g0330 | 2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-43+160A>G | AASDH | ENSG00000157426.14 | transcript | ENST00000205214.11 | protein_coding | 1/14 | chr4 | 56387202 |