Item | Value |
---|---|
geneid | 1356 |
ensemblid | ENSG00000047457.14 |
hgncid | 2295 |
symbol | CP |
name | ceruloplasmin |
refseq_nuc | NM_000096.4 |
refseq_prot | NP_000087.2 |
ensembl_nuc | ENST00000264613.11 |
ensembl_prot | ENSP00000264613.6 |
mane_status | MANE Select |
chr | chr3 |
start | 149172497 |
end | 149221829 |
strand | - |
ver | v1.2 |
region | chr3:149172497-149221829 |
region5000 | chr3:149167497-149226829 |
regionname0 | CP_chr3_149172497_149221829 |
regionname5000 | CP_chr3_149167497_149226829 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1065 | 298 | 43 | 53 | 149 | 13 | 39 | 117 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0002 | 1/0 | 1065 | 47 | 32 | 4 | 0 | 5 | 5 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0003 | 0/0 | 1065 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0004 | 0/0 | 1065 | 5 | 0 | 2 | 0 | 0 | 3 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0005 | 0/0 | 1065 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0006 | 0/0 | 1065 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0007 | 0/0 | 1065 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0008 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0009 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0010 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0011 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0012 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0013 | 0/0 | 1065 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0014 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0015 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0016 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
a0017 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | MKILI others(1060): Show |
chr3 | 149167497 | 149226829 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3195 | 276 | 40 | 40 | 144 | 13 | 38 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0003 | 0/0 | 3195 | 8 | 0 | 8 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0005 | 0/0 | 3195 | 6 | 0 | 5 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0010 | 0/0 | 3195 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0014 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0018 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0019 | 0/0 | 3195 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0021 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0025 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0001c0027 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0002c0002 | 1/0 | 3195 | 41 | 28 | 2 | 0 | 5 | 5 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0002c0006 | 0/0 | 3195 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0002c0011 | 0/0 | 3195 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0003c0004 | 0/0 | 3195 | 8 | 6 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0004c0009 | 0/0 | 3195 | 3 | 0 | 2 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0004c0013 | 0/0 | 3195 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0005c0008 | 0/0 | 3195 | 3 | 2 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0006c0007 | 0/0 | 3195 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0007c0012 | 0/0 | 3195 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0008c0024 | 0/0 | 3195 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0009c0029 | 0/0 | 3195 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0010c0015 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0011c0016 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0012c0028 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0013c0017 | 0/0 | 3195 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0014c0023 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0015c0022 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0016c0026 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 | ||
a0017c0020 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ATGAA others(3190): Show |
chr3 | 149167497 | 149226829 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4452 | 218 | 20 | 33 | 119 | 9 | 36 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0001t0002 | 0/0 | 4452 | 34 | 10 | 3 | 19 | 1 | 1 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0001t0003 | 0/0 | 4453 | 10 | 8 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0001c0001t0004 | 0/0 | 4452 | 7 | 0 | 1 | 4 | 1 | 1 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0001t0006 | 0/0 | 4453 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0001c0001t0008 | 0/0 | 4452 | 3 | 0 | 1 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0001t0010 | 0/0 | 4452 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0003t0001 | 0/0 | 4452 | 6 | 0 | 6 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0003t0007 | 0/0 | 4452 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0005t0001 | 0/0 | 4452 | 6 | 0 | 5 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0010t0001 | 0/0 | 4452 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0014t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0018t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0019t0002 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0021t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0025t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0001c0027t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0002c0002t0001 | 1/0 | 4452 | 26 | 16 | 1 | 0 | 4 | 4 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0002c0002t0002 | 0/0 | 4452 | 6 | 6 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0002c0002t0003 | 0/0 | 4453 | 5 | 4 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0002c0002t0005 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0002c0002t0007 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0002c0002t0009 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0002c0002t0011 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0002c0006t0002 | 0/0 | 4452 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0002c0011t0002 | 0/0 | 4452 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0003c0004t0001 | 0/0 | 4452 | 5 | 3 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0003c0004t0002 | 0/0 | 4452 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0004c0009t0001 | 0/0 | 4452 | 3 | 0 | 2 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0004c0013t0002 | 0/0 | 4452 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0005c0008t0001 | 0/0 | 4452 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0005c0008t0006 | 0/0 | 4453 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0006c0007t0005 | 0/0 | 4453 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0007c0012t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0007c0012t0012 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0008c0024t0001 | 0/0 | 4452 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0009c0029t0001 | 0/0 | 4452 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0010c0015t0009 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4448): Show |
chr3 | 149167497 | 149226829 |
a0011c0016t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0012c0028t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0013c0017t0007 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0014c0023t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0015c0022t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0016c0026t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
a0017c0020t0002 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | ACTTC others(4447): Show |
chr3 | 149167497 | 149226829 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0008g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0008g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0007g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0010t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0010t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0014t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0018t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0019t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0021t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0025t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0027t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0304 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0007g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0011g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0011t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0009t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0009t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0009t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0013t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0005c0008t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0005c0008t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0005c0008t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0006c0007t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0006c0007t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0006c0007t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0007c0012t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0007c0012t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0008c0024t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0009c0029t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0010c0015t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0011c0016t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0012c0028t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0013c0017t0007g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0014c0023t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0015c0022t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0016c0026t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0017c0020t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0302 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0258 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00408 | hp2 | a0001 | c0021 | t0001 | g0129 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0098 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00733 | hp2 | a0002 | c0011 | t0002 | g0020 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00735 | hp2 | a0002 | c0011 | t0002 | g0020 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00738 | hp2 | a0001 | c0005 | t0001 | g0047 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0091 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01081 | hp1 | a0008 | c0024 | t0001 | g0252 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01099 | hp2 | a0005 | c0008 | t0001 | g0118 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0048 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01109 | hp1 | a0001 | c0005 | t0001 | g0036 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01109 | hp2 | a0009 | c0029 | t0001 | g0211 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0092 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0311 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0093 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01169 | hp1 | a0003 | c0004 | t0001 | g0310 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01192 | hp1 | a0004 | c0009 | t0001 | g0255 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0283 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01346 | hp2 | a0001 | c0003 | t0007 | g0094 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01358 | hp2 | a0001 | c0003 | t0007 | g0321 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0015 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0306 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0015 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01952 | hp1 | a0001 | c0005 | t0001 | g0045 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01993 | hp2 | a0001 | c0005 | t0001 | g0046 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02055 | hp2 | a0005 | c0008 | t0006 | g0216 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02074 | hp2 | a0001 | c0027 | t0001 | g0210 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0294 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0291 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02273 | hp2 | a0004 | c0009 | t0001 | g0082 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02572 | hp2 | a0007 | c0012 | t0012 | g0218 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02615 | hp1 | a0003 | c0004 | t0001 | g0313 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02615 | hp2 | a0005 | c0008 | t0006 | g0331 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02622 | hp1 | a0010 | c0015 | t0009 | g0328 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02630 | hp1 | a0003 | c0004 | t0002 | g0225 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02647 | hp2 | a0011 | c0016 | t0001 | g0102 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02683 | hp2 | a0002 | c0002 | t0007 | g0303 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02698 | hp2 | a0004 | c0013 | t0002 | g0018 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02717 | hp2 | a0012 | c0028 | t0001 | g0336 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02723 | hp1 | a0001 | c0010 | t0001 | g0222 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02735 | hp1 | a0004 | c0013 | t0002 | g0018 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0232 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0285 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02886 | hp2 | a0001 | c0010 | t0001 | g0221 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0330 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0220 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02922 | hp2 | a0003 | c0004 | t0002 | g0226 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02965 | hp1 | a0002 | c0002 | t0003 | g0280 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0290 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03098 | hp2 | a0002 | c0006 | t0002 | g0270 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03139 | hp1 | a0002 | c0006 | t0002 | g0269 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03195 | hp1 | a0003 | c0004 | t0002 | g0224 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03195 | hp2 | a0006 | c0007 | t0005 | g0299 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0297 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03225 | hp1 | a0002 | c0006 | t0002 | g0272 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0339 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0312 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03486 | hp2 | a0001 | c0014 | t0001 | g0217 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03490 | hp1 | a0001 | c0019 | t0002 | g0181 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03516 | hp1 | a0007 | c0012 | t0001 | g0219 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03516 | hp2 | a0002 | c0006 | t0002 | g0271 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0223 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0308 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03688 | hp1 | a0013 | c0017 | t0007 | g0298 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03710 | hp1 | a0004 | c0009 | t0001 | g0262 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0305 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0021 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18522 | hp2 | a0006 | c0007 | t0005 | g0301 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0281 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18945 | hp1 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18968 | hp2 | a0014 | c0023 | t0001 | g0158 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18972 | hp2 | a0015 | c0022 | t0001 | g0055 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18985 | hp1 | a0001 | c0005 | t0001 | g0044 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0237 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19030 | hp1 | a0016 | c0026 | t0001 | g0167 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0275 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19043 | hp1 | a0002 | c0002 | t0005 | g0279 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0277 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19059 | hp2 | a0001 | c0025 | t0001 | g0070 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19064 | hp2 | a0001 | c0018 | t0001 | g0146 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19077 | hp1 | a0017 | c0020 | t0002 | g0169 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0274 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0268 | AFR | ASW | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20805 | hp2 | a0002 | c0002 | t0011 | g0307 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0284 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0334 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0282 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG06807 | hp1 | a0006 | c0007 | t0005 | g0300 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA21309 | hp1 | a0002 | c0002 | t0009 | g0095 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0273 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0031 | REF | REF | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0304 | REF | REF | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149177860 | C | T | 1 | a0017 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.2998G>A | p.Gly1000Ser | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/19 | 3035/4452 | 2998/3198 | 1000/1065 | chr3 | 149177860 | |||
chr3:149179596 | C | T | 1 | a0013 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.2621G>A | p.Cys874Tyr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/19 | 2658/4452 | 2621/3198 | 874/1065 | chr3 | 149179596 | |||
chr3:149182034 | T | C | 1 | a0007 | 2 | HG02572.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2525A>G | p.Glu842Gly | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/19 | 2562/4452 | 2525/3198 | 842/1065 | chr3 | 149182034 | |||
chr3:149183513 | C | T | 1 | a0005 | 3 | HG01099.hp2 HG02055.hp2 HG02615.hp2 |
missense_variant | MODERATE | c.2378G>A | p.Arg793His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/19 | 2415/4452 | 2378/3198 | 793/1065 | chr3 | 149183513 | |||
chr3:149186652 | C | T | 1 | a0011 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1945G>A | p.Ala649Thr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/19 | 1982/4452 | 1945/3198 | 649/1065 | chr3 | 149186652 | |||
chr3:149188142 | G | A | 1 | a0015 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.1774C>T | p.Leu592Phe | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/19 | 1811/4452 | 1774/3198 | 592/1065 | chr3 | 149188142 | |||
chr3:149198428 | G | A | 1 | a0004 | 5 | HG01192.hp1 HG02273.hp2 HG02698.hp2 others(2): Show |
missense_variant | MODERATE | c.1652C>T | p.Thr551Ile | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/19 | 1689/4452 | 1652/3198 | 551/1065 | chr3 | 149198428 | |||
chr3:149198448 | T | A | 15 | a0001 a0003 a0004 others(12): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
missense_variant | MODERATE | c.1632A>T | p.Glu544Asp | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/19 | 1669/4452 | 1632/3198 | 544/1065 | chr3 | 149198448 | |||
chr3:149199720 | T | C | 1 | a0014 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1493A>G | p.Gln498Arg | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/19 | 1530/4452 | 1493/3198 | 498/1065 | chr3 | 149199720 | |||
chr3:149202185 | T | C | 1 | a0008 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1265A>G | p.Lys422Arg | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/19 | 1302/4452 | 1265/3198 | 422/1065 | chr3 | 149202185 | |||
chr3:149206277 | G | A | 1 | a0003 | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
missense_variant | MODERATE | c.1099C>T | p.Arg367Cys | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/19 | 1136/4452 | 1099/3198 | 367/1065 | chr3 | 149206277 | |||
chr3:149209276 | T | A | 1 | a0016 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.716A>T | p.Tyr239Phe | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/19 | 753/4452 | 716/3198 | 239/1065 | chr3 | 149209276 | |||
chr3:149210317 | C | T | 1 | a0010 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.457G>A | p.Glu153Lys | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/19 | 494/4452 | 457/3198 | 153/1065 | chr3 | 149210317 | |||
chr3:149212498 | G | T | 1 | a0006 | 3 | HG03195.hp2 HG06807.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.347C>A | p.Pro116His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 384/4452 | 347/3198 | 116/1065 | chr3 | 149212498 | |||
chr3:149212523 | G | A | 1 | a0012 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.322C>T | p.His108Tyr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 359/4452 | 322/3198 | 108/1065 | chr3 | 149212523 | |||
chr3:149212609 | G | A | 1 | a0009 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.236C>T | p.Thr79Ile | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 273/4452 | 236/3198 | 79/1065 | chr3 | 149212609 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149177861 | G | A | 1 | a0001c0021 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2997C>T | p.His999His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/19 | 3034/4452 | 2997/3198 | 999/1065 | chr3 | 149177861 | |||
chr3:149177867 | A | G | 3 | a0001c0019 a0002c0011 a0004c0013 |
5 | HG00733.hp2 HG00735.hp2 HG02698.hp2 others(2): Show |
synonymous_variant | LOW | c.2991T>C | p.His997His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/19 | 3028/4452 | 2991/3198 | 997/1065 | chr3 | 149177867 | |||
chr3:149178596 | A | G | 1 | a0001c0018 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.2697T>C | p.Val899Val | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/19 | 2734/4452 | 2697/3198 | 899/1065 | chr3 | 149178596 | |||
chr3:149186647 | T | G | 1 | a0001c0003 | 8 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
synonymous_variant | LOW | c.1950A>C | p.Gly650Gly | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/19 | 1987/4452 | 1950/3198 | 650/1065 | chr3 | 149186647 | |||
chr3:149202175 | A | G | 1 | a0001c0010 | 2 | HG02723.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.1275T>C | p.Tyr425Tyr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/19 | 1312/4452 | 1275/3198 | 425/1065 | chr3 | 149202175 | |||
chr3:149206338 | G | A | 1 | a0001c0025 | 1 | NA19059.hp2 | splice_region_variant&synonymous_variant | LOW | c.1038C>T | p.Ala346Ala | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/19 | 1075/4452 | 1038/3198 | 346/1065 | chr3 | 149206338 | |||
chr3:149207406 | A | G | 1 | a0001c0005 | 6 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(3): Show |
synonymous_variant | LOW | c.993T>C | p.Pro331Pro | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/19 | 1030/4452 | 993/3198 | 331/1065 | chr3 | 149207406 | |||
chr3:149209323 | C | G | 1 | a0002c0006 | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.669G>C | p.Val223Val | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/19 | 706/4452 | 669/3198 | 223/1065 | chr3 | 149209323 | |||
chr3:149210306 | T | G | 1 | a0001c0027 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.468A>C | p.Thr156Thr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/19 | 505/4452 | 468/3198 | 156/1065 | chr3 | 149210306 | |||
chr3:149212584 | C | T | 1 | a0001c0014 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.261G>A | p.Pro87Pro | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 298/4452 | 261/3198 | 87/1065 | chr3 | 149212584 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149172557 | G | A | 1 | a0001c0001t0004 | 7 | HG00323.hp1 HG00597.hp1 HG01081.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1157C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 1157 | chr3 | 149172557 | ||||||
chr3:149172802 | G | C | 1 | a0001c0001t0010 | 2 | NA18945.hp1 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*912C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 912 | chr3 | 149172802 | ||||||
chr3:149172835 | T | G | 2 | a0001c0001t0006 a0005c0008t0006 |
4 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*879A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 879 | chr3 | 149172835 | ||||||
chr3:149172885 | A | AT | 8 | a0001c0001t0003 a0001c0001t0006 a0002c0002t0003 others(5): Show |
25 | HG00738.hp1 HG01243.hp1 HG01255.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*828dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 828 | chr3 | 149172885 | ||||||
chr3:149172945 | C | T | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(13): Show |
78 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*769G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 769 | chr3 | 149172945 | ||||||
chr3:149172946 | A | G | 4 | a0002c0002t0005 a0002c0002t0009 a0006c0007t0005 others(1): Show |
6 | HG02622.hp1 HG03195.hp2 HG06807.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*768T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 768 | chr3 | 149172946 | ||||||
chr3:149173205 | T | G | 1 | a0001c0001t0008 | 3 | HG00733.hp1 HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*509A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 509 | chr3 | 149173205 | ||||||
chr3:149173240 | A | G | 2 | a0002c0002t0005 a0006c0007t0005 |
4 | HG03195.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*474T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 474 | chr3 | 149173240 | ||||||
chr3:149173341 | G | C | 1 | a0002c0002t0011 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 373 | chr3 | 149173341 | ||||||
chr3:149173455 | G | A | 1 | a0007c0012t0012 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*259C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 259 | chr3 | 149173455 | ||||||
chr3:149173577 | G | A | 3 | a0001c0003t0007 a0002c0002t0007 a0013c0017t0007 |
4 | HG01346.hp2 HG01358.hp2 HG02683.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*137C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 137 | chr3 | 149173577 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149173734 | T | C | 4 | a0001c0001t0006g0232 a0001c0001t0006g0277 a0005c0008t0006g0216 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3182-4A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149173734 | |||||||
chr3:149173862 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0127 others(7): Show |
12 | HG01109.hp1 HG01192.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.3182-132T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149173862 | |||||||
chr3:149174041 | T | C | 4 | a0001c0003t0007g0094 a0001c0003t0007g0321 a0002c0002t0007g0303 others(1): Show |
4 | HG01346.hp2 HG01358.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.3182-311A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174041 | |||||||
chr3:149174094 | A | G | 4 | a0001c0001t0001g0267 a0002c0002t0001g0003 a0002c0002t0001g0285 others(1): Show |
6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3182-364T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174094 | |||||||
chr3:149174125 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3182-395T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174125 | |||||||
chr3:149174180 | T | G | 340 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.3182-450A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174180 | |||||||
chr3:149174387 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3182-657A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174387 | |||||||
chr3:149174703 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3182-973T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174703 | |||||||
chr3:149175148 | T | A | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3181+1102A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175148 | |||||||
chr3:149175149 | T | A | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3181+1101A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175149 | |||||||
chr3:149175150 | T | G | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3181+1100A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175150 | |||||||
chr3:149175296 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3181+954A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175296 | |||||||
chr3:149175339 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0103 |
3 | NA18965.hp1 NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3181+911C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175339 | |||||||
chr3:149175449 | A | G | 1 | a0002c0002t0001g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3181+801T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175449 | |||||||
chr3:149175664 | A | AGT | 14 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0153 others(11): Show |
16 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.3181+584_3181+585d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(3): Show |
15 | a0001c0001t0003g0176 a0001c0001t0003g0263 a0001c0001t0003g0265 others(12): Show |
15 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3181+576_3181+585d others(12): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(5): Show |
45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(42): Show |
47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.3181+574_3181+585d others(14): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(7): Show |
41 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0064 others(38): Show |
44 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.3181+572_3181+585d others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(9): Show |
7 | a0001c0001t0002g0159 a0001c0001t0002g0168 a0001c0001t0002g0249 others(4): Show |
7 | HG01346.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3181+570_3181+585d others(18): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(11): Show |
9 | a0001c0001t0002g0001 a0001c0001t0002g0243 a0001c0001t0002g0316 others(6): Show |
14 | HG01070.hp2 HG01071.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.3181+568_3181+585d others(20): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(13): Show |
2 | a0001c0001t0003g0244 a0004c0013t0002g0018 |
3 | HG02698.hp2 HG02735.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3181+566_3181+585d others(22): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(15): Show |
3 | a0001c0001t0003g0245 a0001c0001t0006g0277 a0005c0008t0006g0331 |
3 | HG02615.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3181+564_3181+585d others(24): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175664 | A | AGTGTGTG others(17): Show |
4 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0264 others(1): Show |
5 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.3181+562_3181+585d others(26): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | |||||||
chr3:149175667 | G | GTGTGTGT others(7): Show |
1 | a0010c0015t0009g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3181+582_3181+583i others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175667 | |||||||
chr3:149175783 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3181+467T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175783 | |||||||
chr3:149175877 | C | T | 5 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0263 others(2): Show |
5 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.3181+373G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175877 | |||||||
chr3:149176003 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0144 |
2 | NA18949.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.3181+247T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149176003 | |||||||
chr3:149176004 | C | T | 1 | a0008c0024t0001g0252 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3181+246G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149176004 | |||||||
chr3:149176570 | T | G | 3 | a0001c0019t0002g0181 a0002c0011t0002g0020 a0004c0013t0002g0018 |
5 | HG00733.hp2 HG00735.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.3019-158A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176570 | |||||||
chr3:149176577 | A | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG00323.hp2 HG01255.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3019-165T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176577 | |||||||
chr3:149176878 | C | T | 1 | a0001c0005t0001g0046 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3019-466G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176878 | |||||||
chr3:149176898 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3019-486T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176898 | |||||||
chr3:149176901 | A | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0243 a0001c0001t0002g0334 |
8 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3019-489T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176901 | |||||||
chr3:149177243 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3018+597T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177243 | |||||||
chr3:149177264 | C | T | 6 | a0002c0002t0005g0279 a0002c0002t0009g0095 a0006c0007t0005g0299 others(3): Show |
6 | HG02622.hp1 HG03195.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.3018+576G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177264 | |||||||
chr3:149177339 | A | G | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(53): Show |
58 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.3018+501T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177339 | |||||||
chr3:149177744 | G | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0050 others(16): Show |
21 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.3018+96C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177744 | |||||||
chr3:149178044 | A | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0067 a0001c0001t0002g0278 others(2): Show |
7 | HG00408.hp1 HG00673.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.2879-65T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178044 | |||||||
chr3:149178218 | G | A | 7 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0244 others(4): Show |
7 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2878+197C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178218 | |||||||
chr3:149178318 | T | C | 11 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0244 others(8): Show |
11 | HG00738.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2878+97A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178318 | |||||||
chr3:149178359 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2878+56A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178359 | |||||||
chr3:149178403 | A | C | 4 | a0001c0001t0001g0267 a0002c0002t0001g0003 a0002c0002t0001g0285 others(1): Show |
6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2878+12T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178403 | |||||||
chr3:149178643 | A | G | 121 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(118): Show |
133 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.2662-12T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178643 | |||||||
chr3:149178754 | A | G | 6 | a0002c0002t0005g0279 a0002c0002t0009g0095 a0006c0007t0005g0299 others(3): Show |
6 | HG02622.hp1 HG03195.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2662-123T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178754 | |||||||
chr3:149178764 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2662-133A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178764 | |||||||
chr3:149178947 | A | G | 7 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0244 others(4): Show |
7 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2662-316T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178947 | |||||||
chr3:149179033 | A | G | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(53): Show |
58 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2662-402T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179033 | |||||||
chr3:149179047 | T | C | 13 | a0001c0001t0001g0267 a0001c0001t0003g0176 a0001c0001t0003g0325 others(10): Show |
15 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2662-416A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179047 | |||||||
chr3:149179242 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2661+314G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179242 | |||||||
chr3:149179423 | A | C | 5 | a0001c0001t0001g0267 a0002c0002t0001g0003 a0002c0002t0001g0285 others(2): Show |
7 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2661+133T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179423 | |||||||
chr3:149179711 | T | TAC | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(89): Show |
98 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.2555-51_2555-50dup others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179711 | T | TACAC | 45 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0039 others(42): Show |
47 | HG00280.hp2 HG00544.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2555-53_2555-50dup others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179711 | T | TACACAC | 35 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0052 others(32): Show |
36 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.2555-55_2555-50dup others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179711 | T | TACACACA others(1): Show |
12 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0043 others(9): Show |
14 | HG00597.hp2 HG02071.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.2555-57_2555-50dup others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179711 | TAC | T | 26 | a0001c0001t0001g0060 a0001c0001t0001g0161 a0001c0001t0001g0197 others(23): Show |
29 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2555-51_2555-50del others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179711 | TACAC | T | 21 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0108 others(18): Show |
23 | HG00280.hp1 HG01070.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2555-53_2555-50del others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179711 | TACACAC | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0116 others(3): Show |
8 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2555-55_2555-50del others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179711 | TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0242 a0007c0012t0012g0218 |
3 | HG02572.hp2 NA19063.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2555-57_2555-50del others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | |||||||
chr3:149179830 | AGGAATTT others(16): Show |
A | 4 | a0001c0001t0001g0267 a0002c0002t0001g0003 a0002c0002t0001g0285 others(1): Show |
6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2555-191_2555-169d others(25): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179830 | |||||||
chr3:149179941 | C | A | 1 | a0002c0002t0002g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2555-279G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179941 | |||||||
chr3:149180022 | A | G | 4 | a0001c0001t0001g0267 a0002c0002t0001g0003 a0002c0002t0001g0285 others(1): Show |
6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2555-360T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180022 | |||||||
chr3:149180177 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2555-515G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180177 | |||||||
chr3:149180214 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0085 others(9): Show |
14 | HG00609.hp1 HG01258.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.2555-552C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180214 | |||||||
chr3:149180299 | A | G | 7 | a0002c0002t0002g0294 a0002c0002t0005g0279 a0002c0002t0009g0095 others(4): Show |
7 | HG02257.hp1 HG02622.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2555-637T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180299 | |||||||
chr3:149180306 | A | G | 4 | a0001c0001t0001g0104 a0001c0001t0001g0143 a0001c0001t0001g0157 others(1): Show |
4 | HG02040.hp2 NA18966.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2555-644T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180306 | |||||||
chr3:149180315 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2555-653G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180315 | |||||||
chr3:149180318 | G | A | 1 | a0002c0002t0002g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2555-656C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180318 | |||||||
chr3:149180388 | T | C | 3 | a0001c0001t0001g0227 a0001c0001t0001g0234 a0001c0001t0001g0240 |
3 | NA18963.hp1 NA18980.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2555-726A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180388 | |||||||
chr3:149180416 | C | A | 3 | a0001c0003t0007g0094 a0001c0003t0007g0321 a0002c0002t0007g0303 |
3 | HG01346.hp2 HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2555-754G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180416 | |||||||
chr3:149180722 | G | T | 1 | a0002c0002t0001g0292 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2555-1060C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180722 | |||||||
chr3:149180751 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2555-1089C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180751 | |||||||
chr3:149180867 | G | T | 6 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0332 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2554+1138C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180867 | |||||||
chr3:149180872 | T | A | 4 | a0001c0001t0001g0267 a0002c0002t0001g0003 a0002c0002t0001g0285 others(1): Show |
6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2554+1133A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180872 | |||||||
chr3:149181005 | C | CGAT | 78 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(75): Show |
80 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.2554+997_2554+999d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181005 | |||||||
chr3:149181158 | G | A | 1 | a0001c0001t0006g0277 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2554+847C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181158 | |||||||
chr3:149181388 | C | T | 4 | a0001c0003t0007g0094 a0001c0003t0007g0321 a0002c0002t0007g0303 others(1): Show |
4 | HG01346.hp2 HG01358.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2554+617G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181388 | |||||||
chr3:149181452 | A | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(81): Show |
87 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2554+553T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181452 | |||||||
chr3:149181487 | A | T | 1 | a0002c0002t0001g0292 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2554+518T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181487 | |||||||
chr3:149181602 | T | G | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(85): Show |
94 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.2554+403A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181602 | |||||||
chr3:149181647 | C | G | 2 | a0002c0002t0001g0292 a0002c0002t0002g0330 |
2 | HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2554+358G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181647 | |||||||
chr3:149181675 | A | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(81): Show |
89 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2554+330T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181675 | |||||||
chr3:149181675 | A | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0133 others(14): Show |
19 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.2554+330T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181675 | |||||||
chr3:149181721 | G | A | 2 | a0007c0012t0001g0219 a0007c0012t0012g0218 |
2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2554+284C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181721 | |||||||
chr3:149181761 | C | T | 1 | a0001c0018t0001g0146 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2554+244G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181761 | |||||||
chr3:149181783 | T | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0267 a0001c0001t0001g0332 others(17): Show |
23 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.2554+222A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181783 | |||||||
chr3:149181848 | T | G | 1 | a0001c0001t0001g0342 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2554+157A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181848 | |||||||
chr3:149181909 | C | T | 10 | a0001c0001t0001g0024 a0001c0001t0001g0332 a0001c0001t0001g0338 others(7): Show |
11 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2554+96G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181909 | |||||||
chr3:149181988 | C | T | 6 | a0001c0001t0001g0197 a0001c0003t0001g0011 a0001c0003t0001g0090 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.2554+17G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181988 | |||||||
chr3:149182185 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2426-52A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182185 | |||||||
chr3:149182259 | C | T | 43 | a0001c0001t0001g0024 a0001c0001t0001g0267 a0001c0001t0001g0335 others(40): Show |
47 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.2426-126G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182259 | |||||||
chr3:149182371 | G | A | 1 | a0007c0012t0012g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2426-238C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182371 | |||||||
chr3:149182381 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(5): Show |
9 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2426-248A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182381 | |||||||
chr3:149182382 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2426-249C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182382 | |||||||
chr3:149182422 | T | C | 49 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0267 others(46): Show |
54 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.2426-289A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182422 | |||||||
chr3:149182489 | A | G | 5 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0093 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426-356T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182489 | |||||||
chr3:149182610 | T | C | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2426-477A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182610 | |||||||
chr3:149182687 | G | A | 20 | a0001c0001t0001g0267 a0001c0014t0001g0217 a0002c0002t0001g0003 others(17): Show |
22 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.2426-554C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182687 | |||||||
chr3:149182812 | G | A | 41 | a0001c0001t0001g0023 a0001c0001t0001g0267 a0001c0001t0001g0324 others(38): Show |
46 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2425+654C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182812 | |||||||
chr3:149182923 | G | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0338 a0001c0001t0001g0342 others(1): Show |
5 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+543C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182923 | |||||||
chr3:149182925 | C | T | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2425+541G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182925 | |||||||
chr3:149183074 | A | C | 54 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0324 others(51): Show |
60 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.2425+392T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183074 | |||||||
chr3:149183116 | A | G | 40 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(37): Show |
45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2425+350T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183116 | |||||||
chr3:149183129 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(31): Show |
38 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2425+337G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183129 | |||||||
chr3:149183130 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0156 |
2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2425+336C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183130 | |||||||
chr3:149183207 | C | A | 40 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(37): Show |
45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2425+259G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183207 | |||||||
chr3:149183242 | C | T | 2 | a0001c0005t0001g0044 a0001c0025t0001g0070 |
2 | NA18985.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.2425+224G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183242 | |||||||
chr3:149183243 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(2): Show |
6 | HG01884.hp1 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2425+223C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183243 | |||||||
chr3:149183257 | T | C | 2 | a0007c0012t0001g0219 a0007c0012t0012g0218 |
2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2425+209A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183257 | |||||||
chr3:149183291 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2425+175T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183291 | |||||||
chr3:149183403 | C | T | 1 | a0002c0002t0005g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2425+63G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183403 | |||||||
chr3:149183404 | G | A | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2425+62C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183404 | |||||||
chr3:149183617 | A | C | 5 | a0002c0002t0001g0295 a0002c0002t0001g0296 a0002c0002t0001g0297 others(2): Show |
5 | HG02630.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2286-12T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183617 | |||||||
chr3:149183619 | AC | A | 68 | a0001c0001t0001g0023 a0001c0001t0001g0166 a0001c0001t0001g0179 others(65): Show |
73 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.2286-15delG | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183619 | |||||||
chr3:149183620 | C | A | 2 | a0001c0001t0003g0325 a0001c0001t0003g0326 |
2 | HG01884.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2286-15G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183620 | |||||||
chr3:149183753 | C | A | 40 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(37): Show |
45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2286-148G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183753 | |||||||
chr3:149183899 | C | A | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2286-294G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183899 | |||||||
chr3:149184023 | TA | T | 26 | a0001c0001t0001g0166 a0001c0001t0001g0179 a0001c0001t0001g0186 others(23): Show |
26 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2286-419delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184023 | |||||||
chr3:149184026 | TTC | T | 22 | a0001c0001t0001g0166 a0001c0001t0001g0179 a0001c0001t0001g0213 others(19): Show |
22 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2286-423_2286-422d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184026 | |||||||
chr3:149184027 | TC | T | 4 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0231 others(1): Show |
4 | HG01175.hp1 HG01175.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2286-423delG | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184027 | |||||||
chr3:149184028 | C | CT | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.2286-424dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184028 | C | CTT | 95 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(92): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2286-425_2286-424d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184028 | C | CTTT | 35 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0085 others(32): Show |
35 | HG00558.hp2 HG00642.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.2286-426_2286-424d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184028 | C | CTTTT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0103 others(11): Show |
16 | HG00609.hp1 HG01258.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2286-427_2286-424d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184028 | C | CTTTTT | 6 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0003t0001g0011 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2286-428_2286-424d others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184028 | CT | C | 7 | a0001c0001t0001g0242 a0001c0001t0002g0318 a0001c0001t0002g0320 others(4): Show |
7 | HG01071.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2286-424delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184028 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0068 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2286-437_2286-424d others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184028 | CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0011g0307 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2286-438_2286-424d others(17): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | |||||||
chr3:149184118 | C | T | 40 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(37): Show |
45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2286-513G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184118 | |||||||
chr3:149184196 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(31): Show |
38 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2286-591T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184196 | |||||||
chr3:149184270 | C | T | 34 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(31): Show |
38 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2286-665G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184270 | |||||||
chr3:149184279 | C | G | 6 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0092 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2286-674G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184279 | |||||||
chr3:149184314 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2286-709G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184314 | |||||||
chr3:149184325 | G | A | 33 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(30): Show |
37 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2286-720C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184325 | |||||||
chr3:149184334 | C | G | 1 | a0002c0002t0003g0282 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2286-729G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184334 | |||||||
chr3:149184513 | C | T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(16): Show |
22 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.2285+726G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184513 | |||||||
chr3:149184536 | A | G | 20 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(17): Show |
23 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.2285+703T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184536 | |||||||
chr3:149184546 | C | T | 20 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(17): Show |
22 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.2285+693G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184546 | |||||||
chr3:149184568 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(10): Show |
15 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.2285+671C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184568 | |||||||
chr3:149184636 | A | G | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2285+603T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184636 | |||||||
chr3:149184654 | C | CTAA | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2285+582_2285+584d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184654 | |||||||
chr3:149184809 | G | T | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2285+430C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184809 | |||||||
chr3:149184895 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2285+344C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184895 | |||||||
chr3:149184927 | T | C | 30 | a0001c0001t0001g0166 a0001c0001t0001g0179 a0001c0001t0001g0186 others(27): Show |
30 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2285+312A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184927 | |||||||
chr3:149185029 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2285+210C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185029 | |||||||
chr3:149185068 | G | A | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2285+171C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185068 | |||||||
chr3:149185097 | G | A | 4 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0092 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.2285+142C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185097 | |||||||
chr3:149185101 | TTTG | T | 39 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(36): Show |
44 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.2285+135_2285+137d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185101 | |||||||
chr3:149185142 | CT | C | 20 | a0001c0001t0001g0230 a0001c0014t0001g0217 a0002c0002t0001g0003 others(17): Show |
22 | HG01243.hp1 HG01261.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2285+96delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185142 | |||||||
chr3:149185163 | T | C | 6 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0092 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2285+76A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185163 | |||||||
chr3:149185579 | C | T | 2 | a0007c0012t0001g0219 a0007c0012t0012g0218 |
2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2078-133G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185579 | |||||||
chr3:149185590 | A | ACATAG | 17 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(14): Show |
19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-145_2078-144i others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185590 | |||||||
chr3:149185591 | T | G | 17 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(14): Show |
19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-145A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185591 | |||||||
chr3:149185593 | C | G | 17 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(14): Show |
19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-147G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185593 | |||||||
chr3:149185618 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0214 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2078-172T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185618 | |||||||
chr3:149185638 | A | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(14): Show |
19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-192T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185638 | |||||||
chr3:149185644 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2078-198G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185644 | |||||||
chr3:149185646 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(14): Show |
19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-200G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185646 | |||||||
chr3:149185709 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(33): Show |
40 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.2078-263C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185709 | |||||||
chr3:149185757 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2078-311G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185757 | |||||||
chr3:149185840 | G | A | 24 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0150 others(21): Show |
32 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.2078-394C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185840 | |||||||
chr3:149185864 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2078-418A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185864 | |||||||
chr3:149185927 | G | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(16): Show |
21 | HG00733.hp2 HG00735.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.2078-481C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185927 | |||||||
chr3:149185934 | G | A | 1 | a0002c0002t0005g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2078-488C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185934 | |||||||
chr3:149186049 | T | C | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2077+471A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186049 | |||||||
chr3:149186128 | A | G | 6 | a0002c0002t0001g0291 a0002c0002t0001g0292 a0002c0002t0002g0294 others(3): Show |
6 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2077+392T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186128 | |||||||
chr3:149186136 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(134): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.2077+384C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186136 | |||||||
chr3:149186371 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2077+149A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186371 | |||||||
chr3:149187220 | T | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(246): Show |
274 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1865-488A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187220 | |||||||
chr3:149187496 | C | T | 20 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0243 others(17): Show |
28 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1864+556G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187496 | |||||||
chr3:149187533 | C | G | 1 | a0012c0028t0001g0336 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1864+519G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187533 | |||||||
chr3:149187723 | G | A | 9 | a0001c0001t0001g0230 a0001c0001t0001g0246 a0001c0001t0001g0247 others(6): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1864+329C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187723 | |||||||
chr3:149187939 | G | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0091 others(4): Show |
8 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1864+113C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187939 | |||||||
chr3:149187990 | A | G | 17 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(14): Show |
19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1864+62T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187990 | |||||||
chr3:149188226 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1714-24A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188226 | |||||||
chr3:149188240 | A | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(34): Show |
41 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1714-38T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188240 | |||||||
chr3:149188379 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1714-177C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188379 | |||||||
chr3:149188490 | C | CA | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(129): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1714-289dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | C | CAA | 44 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(41): Show |
54 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1714-290_1714-289d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | C | CAAA | 17 | a0001c0001t0001g0026 a0001c0001t0001g0162 a0001c0001t0001g0194 others(14): Show |
18 | HG00609.hp1 HG00741.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1714-291_1714-289d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | C | CAAAA | 13 | a0001c0001t0001g0117 a0001c0001t0001g0179 a0001c0001t0001g0186 others(10): Show |
13 | HG00738.hp1 HG01261.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.1714-292_1714-289d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | C | CAAAAA | 13 | a0001c0001t0001g0166 a0001c0001t0001g0192 a0001c0001t0001g0213 others(10): Show |
13 | HG01069.hp1 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1714-293_1714-289d others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | CA | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0079 a0001c0001t0001g0165 others(5): Show |
9 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714-289delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | CAAAAAA | C | 18 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(15): Show |
20 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1714-294_1714-289d others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0001g0205 a0001c0003t0001g0011 a0001c0003t0001g0090 others(4): Show |
8 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714-296_1714-289d others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0204 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1714-298_1714-289d others(12): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | CAAAAAAA others(6): Show |
C | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1714-301_1714-289d others(15): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188490 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0006 | 2 | NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1714-302_1714-289d others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | |||||||
chr3:149188491 | A | C | 2 | a0002c0002t0001g0290 a0007c0012t0012g0218 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1714-289T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188491 | |||||||
chr3:149188492 | A | C | 3 | a0002c0002t0001g0220 a0002c0011t0002g0020 a0007c0012t0001g0219 |
4 | HG00733.hp2 HG00735.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714-290T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188492 | |||||||
chr3:149188493 | A | C | 4 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0002c0002t0001g0289 others(1): Show |
4 | HG01433.hp2 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714-291T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188493 | |||||||
chr3:149188494 | A | C | 3 | a0002c0002t0001g0291 a0002c0002t0002g0294 a0002c0002t0002g0330 |
3 | HG02257.hp1 HG02258.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1714-292T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188494 | |||||||
chr3:149188496 | A | C | 1 | a0002c0006t0002g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1714-294T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188496 | |||||||
chr3:149188497 | A | C | 18 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(15): Show |
20 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1714-295T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188497 | |||||||
chr3:149188539 | T | C | 1 | a0005c0008t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1714-337A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188539 | |||||||
chr3:149188596 | TG | T | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-395delC | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188596 | |||||||
chr3:149188866 | A | G | 2 | a0001c0001t0001g0135 a0001c0018t0001g0146 |
2 | NA19064.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1714-664T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188866 | |||||||
chr3:149188974 | T | C | 1 | a0002c0002t0001g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1714-772A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188974 | |||||||
chr3:149189086 | G | C | 1 | a0002c0002t0001g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1714-884C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189086 | |||||||
chr3:149189127 | T | G | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-925A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189127 | |||||||
chr3:149189171 | A | G | 1 | a0001c0019t0002g0181 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1714-969T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189171 | |||||||
chr3:149189410 | C | T | 1 | a0005c0008t0006g0331 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1714-1208G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189410 | |||||||
chr3:149189441 | CT | C | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-1240delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189441 | |||||||
chr3:149189516 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1714-1314A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189516 | |||||||
chr3:149189553 | C | CA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 others(6): Show |
11 | HG02015.hp1 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714-1352dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189553 | |||||||
chr3:149189553 | CA | C | 44 | a0001c0001t0001g0023 a0001c0001t0001g0207 a0001c0001t0001g0324 others(41): Show |
49 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1714-1352delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189553 | |||||||
chr3:149189643 | C | G | 14 | a0001c0001t0002g0004 a0001c0001t0002g0278 a0001c0001t0002g0314 others(11): Show |
16 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1714-1441G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189643 | |||||||
chr3:149189722 | G | A | 12 | a0002c0002t0001g0220 a0002c0002t0001g0287 a0002c0002t0001g0288 others(9): Show |
13 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1714-1520C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189722 | |||||||
chr3:149189813 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0010g0237 |
2 | NA18990.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1714-1611T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189813 | |||||||
chr3:149190208 | A | G | 12 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(9): Show |
14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-2006T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190208 | |||||||
chr3:149190331 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0140 |
3 | HG03017.hp1 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1714-2129G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190331 | |||||||
chr3:149190386 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1714-2184C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190386 | |||||||
chr3:149190605 | C | T | 12 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(9): Show |
14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-2403G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190605 | |||||||
chr3:149190656 | T | TA | 20 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0071 others(17): Show |
20 | HG00673.hp1 HG01106.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1714-2455dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190656 | |||||||
chr3:149190656 | TA | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0140 a0001c0001t0001g0246 others(32): Show |
39 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1714-2455delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190656 | |||||||
chr3:149190688 | G | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0156 |
2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1714-2486C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190688 | |||||||
chr3:149190812 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0239 |
2 | NA18949.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1714-2610T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190812 | |||||||
chr3:149190899 | A | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0239 |
2 | NA18949.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1714-2697T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190899 | |||||||
chr3:149190921 | C | T | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1714-2719G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190921 | |||||||
chr3:149191106 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(10): Show |
15 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1714-2904C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191106 | |||||||
chr3:149191167 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0198 |
2 | HG01168.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1714-2965A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191167 | |||||||
chr3:149191243 | AT | A | 43 | a0001c0001t0001g0023 a0001c0001t0001g0175 a0001c0001t0001g0195 others(40): Show |
45 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1714-3042delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | |||||||
chr3:149191243 | ATT | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(109): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1714-3043_1714-304 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | |||||||
chr3:149191243 | ATTT | A | 151 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1714-3044_1714-304 others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | |||||||
chr3:149191243 | ATTTT | A | 16 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0135 others(13): Show |
16 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1714-3045_1714-304 others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | |||||||
chr3:149191511 | A | G | 12 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(9): Show |
14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-3309T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191511 | |||||||
chr3:149191550 | T | TAAGATCA others(300): Show |
9 | a0001c0014t0001g0217 a0002c0002t0001g0293 a0002c0002t0002g0268 others(6): Show |
9 | HG02622.hp2 HG02717.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714-3349_1714-334 others(311): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191550 | |||||||
chr3:149191550 | T | TAAGATCA others(301): Show |
8 | a0002c0002t0001g0003 a0002c0002t0001g0285 a0002c0002t0002g0275 others(5): Show |
10 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-3349_1714-334 others(312): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191550 | |||||||
chr3:149191550 | T | TAAGATCA others(302): Show |
2 | a0002c0002t0003g0281 a0002c0002t0003g0283 |
2 | HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1714-3349_1714-334 others(313): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191550 | |||||||
chr3:149192340 | T | C | 2 | a0001c0001t0003g0244 a0001c0001t0003g0245 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1714-4138A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192340 | |||||||
chr3:149192374 | C | T | 31 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0220 others(28): Show |
34 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1714-4172G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192374 | |||||||
chr3:149192484 | T | C | 1 | a0010c0015t0009g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1714-4282A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192484 | |||||||
chr3:149192493 | C | CA | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(154): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1714-4292dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192493 | |||||||
chr3:149192670 | T | TAC | 19 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0285 others(16): Show |
21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-4470_1714-446 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192670 | |||||||
chr3:149192682 | CAT | C | 12 | a0002c0002t0001g0220 a0002c0002t0001g0287 a0002c0002t0001g0288 others(9): Show |
13 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1714-4482_1714-448 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192682 | |||||||
chr3:149192683 | A | G | 2 | a0001c0001t0001g0075 a0001c0021t0001g0129 |
2 | HG00408.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1714-4481T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192683 | |||||||
chr3:149192684 | T | C | 1 | a0001c0014t0001g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1714-4482A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192684 | |||||||
chr3:149192685 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1714-4483T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192685 | |||||||
chr3:149192734 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(137): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1714-4532T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192734 | |||||||
chr3:149192939 | T | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(9): Show |
14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-4737A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192939 | |||||||
chr3:149192981 | T | TAC | 247 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(244): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1714-4781_1714-478 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192981 | |||||||
chr3:149192981 | T | TACAC | 27 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0041 others(24): Show |
27 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1714-4783_1714-478 others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192981 | |||||||
chr3:149192981 | TAC | T | 34 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(31): Show |
38 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1714-4781_1714-478 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192981 | |||||||
chr3:149193391 | G | T | 31 | a0001c0014t0001g0217 a0002c0002t0001g0003 a0002c0002t0001g0220 others(28): Show |
34 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1713+4976C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193391 | |||||||
chr3:149193466 | G | T | 43 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(40): Show |
48 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1713+4901C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193466 | |||||||
chr3:149193528 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1713+4839C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193528 | |||||||
chr3:149193566 | T | G | 26 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(23): Show |
30 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1713+4801A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193566 | |||||||
chr3:149193612 | T | A | 30 | a0002c0002t0001g0003 a0002c0002t0001g0220 a0002c0002t0001g0285 others(27): Show |
33 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+4755A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193612 | |||||||
chr3:149193638 | A | G | 30 | a0002c0002t0001g0003 a0002c0002t0001g0220 a0002c0002t0001g0285 others(27): Show |
33 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+4729T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193638 | |||||||
chr3:149193641 | T | G | 1 | a0001c0001t0002g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1713+4726A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193641 | |||||||
chr3:149193643 | G | C | 30 | a0002c0002t0001g0003 a0002c0002t0001g0220 a0002c0002t0001g0285 others(27): Show |
33 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+4724C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193643 | |||||||
chr3:149193755 | C | T | 1 | a0001c0001t0006g0232 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1713+4612G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193755 | |||||||
chr3:149194160 | G | C | 3 | a0001c0001t0001g0231 a0001c0001t0001g0251 a0008c0024t0001g0252 |
3 | HG01081.hp1 HG01175.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1713+4207C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194160 | |||||||
chr3:149194197 | C | CT | 20 | a0001c0010t0001g0221 a0001c0010t0001g0222 a0002c0002t0001g0003 others(17): Show |
22 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1713+4169dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194197 | |||||||
chr3:149194245 | A | AT | 9 | a0001c0001t0001g0230 a0001c0001t0001g0246 a0001c0001t0001g0247 others(6): Show |
9 | HG00738.hp1 HG01099.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+4121dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194245 | |||||||
chr3:149194245 | A | T | 1 | a0016c0026t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1713+4122T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194245 | |||||||
chr3:149194245 | AT | A | 51 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(48): Show |
56 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.1713+4121delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194245 | |||||||
chr3:149194282 | A | AG | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1713+4084dupC | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194282 | |||||||
chr3:149194352 | C | T | 28 | a0002c0002t0001g0003 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
30 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+4015G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194352 | |||||||
chr3:149194427 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1713+3940G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194427 | |||||||
chr3:149194581 | G | A | 1 | a0001c0014t0001g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1713+3786C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194581 | |||||||
chr3:149194607 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0066 |
2 | NA18998.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1713+3760C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194607 | |||||||
chr3:149194614 | T | TA | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1713+3752dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194614 | |||||||
chr3:149194878 | A | G | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1713+3489T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194878 | |||||||
chr3:149194980 | T | C | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1713+3387A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194980 | |||||||
chr3:149194995 | T | C | 3 | a0001c0001t0001g0332 a0005c0008t0006g0216 a0005c0008t0006g0331 |
3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1713+3372A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194995 | |||||||
chr3:149195035 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1713+3332C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195035 | |||||||
chr3:149195117 | G | A | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+3250C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195117 | |||||||
chr3:149195137 | A | C | 1 | a0003c0004t0002g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1713+3230T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195137 | |||||||
chr3:149195178 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1713+3189A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195178 | |||||||
chr3:149195209 | G | A | 315 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(312): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.1713+3158C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195209 | |||||||
chr3:149195239 | C | A | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+3128G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195239 | |||||||
chr3:149195268 | A | T | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+3099T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195268 | |||||||
chr3:149195339 | G | T | 51 | a0001c0001t0001g0023 a0001c0001t0001g0324 a0001c0001t0001g0327 others(48): Show |
54 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1713+3028C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195339 | |||||||
chr3:149195535 | A | G | 3 | a0001c0001t0001g0332 a0005c0008t0006g0216 a0005c0008t0006g0331 |
3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1713+2832T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195535 | |||||||
chr3:149195564 | G | A | 1 | a0001c0001t0002g0320 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1713+2803C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195564 | |||||||
chr3:149195639 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0322 a0001c0001t0002g0004 others(12): Show |
19 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1713+2728G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195639 | |||||||
chr3:149195640 | G | A | 4 | a0002c0002t0001g0291 a0002c0002t0001g0292 a0002c0002t0002g0294 others(1): Show |
4 | HG02257.hp1 HG02258.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+2727C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195640 | |||||||
chr3:149195649 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0002g0067 |
2 | HG00408.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1713+2718C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195649 | |||||||
chr3:149195707 | C | T | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+2660G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195707 | |||||||
chr3:149195734 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1713+2633G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195734 | |||||||
chr3:149195797 | T | C | 29 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+2570A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195797 | |||||||
chr3:149195858 | A | G | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+2509T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195858 | |||||||
chr3:149195861 | G | A | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+2506C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195861 | |||||||
chr3:149196129 | T | C | 1 | a0003c0004t0002g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1713+2238A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196129 | |||||||
chr3:149196192 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1713+2175A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196192 | |||||||
chr3:149196224 | C | T | 29 | a0001c0001t0001g0133 a0001c0014t0001g0217 a0002c0002t0001g0285 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+2143G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196224 | |||||||
chr3:149196277 | T | C | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1713+2090A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196277 | |||||||
chr3:149196333 | A | G | 2 | a0007c0012t0001g0219 a0007c0012t0012g0218 |
2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1713+2034T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196333 | |||||||
chr3:149196340 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1713+2027A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196340 | |||||||
chr3:149196467 | C | CA | 9 | a0001c0014t0001g0217 a0003c0004t0001g0223 a0003c0004t0001g0310 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+1899dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196467 | |||||||
chr3:149196530 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1713+1837G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196530 | |||||||
chr3:149196702 | G | A | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1713+1665C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196702 | |||||||
chr3:149196737 | T | TA | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1713+1629dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196737 | |||||||
chr3:149196756 | C | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0332 a0001c0001t0001g0335 others(11): Show |
15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1713+1611G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196756 | |||||||
chr3:149196769 | G | GA | 329 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(326): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.1713+1597dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196769 | |||||||
chr3:149196861 | T | C | 27 | a0001c0001t0001g0166 a0001c0001t0001g0179 a0001c0001t0001g0186 others(24): Show |
27 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1713+1506A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196861 | |||||||
chr3:149196916 | C | T | 3 | a0003c0004t0001g0310 a0003c0004t0001g0311 a0003c0004t0001g0312 |
3 | HG01167.hp2 HG01169.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1713+1451G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196916 | |||||||
chr3:149196966 | C | T | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+1401G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196966 | |||||||
chr3:149197009 | C | T | 22 | a0001c0001t0001g0024 a0001c0001t0001g0335 a0001c0001t0001g0337 others(19): Show |
23 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1713+1358G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197009 | |||||||
chr3:149197025 | G | A | 39 | a0001c0001t0001g0024 a0001c0001t0001g0335 a0001c0001t0001g0337 others(36): Show |
40 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.1713+1342C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197025 | |||||||
chr3:149197034 | G | T | 39 | a0001c0001t0001g0024 a0001c0001t0001g0335 a0001c0001t0001g0337 others(36): Show |
40 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.1713+1333C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197034 | |||||||
chr3:149197133 | G | A | 11 | a0001c0014t0001g0217 a0003c0004t0001g0223 a0003c0004t0001g0310 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1713+1234C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197133 | |||||||
chr3:149197141 | A | C | 28 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0293 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+1226T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197141 | |||||||
chr3:149197154 | C | T | 1 | a0002c0002t0001g0287 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1713+1213G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197154 | |||||||
chr3:149197170 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0157 a0001c0001t0001g0160 |
3 | HG02040.hp2 NA18986.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1713+1197C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197170 | |||||||
chr3:149197181 | G | A | 1 | a0007c0012t0012g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1713+1186C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197181 | |||||||
chr3:149197247 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0131 |
2 | HG00642.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1713+1120A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197247 | |||||||
chr3:149197253 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0131 |
2 | HG00642.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1713+1114G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197253 | |||||||
chr3:149197364 | G | A | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1713+1003C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197364 | |||||||
chr3:149197375 | A | G | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1713+992T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197375 | |||||||
chr3:149197384 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1713+983T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197384 | |||||||
chr3:149197513 | G | GA | 17 | a0001c0001t0001g0024 a0001c0001t0001g0332 a0001c0001t0001g0335 others(14): Show |
18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1713+853dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197513 | |||||||
chr3:149197513 | G | GAA | 29 | a0001c0014t0001g0217 a0002c0002t0001g0285 a0002c0002t0001g0286 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+852_1713+853d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197513 | |||||||
chr3:149197657 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1713+710G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197657 | |||||||
chr3:149197787 | T | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1713+580A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197787 | |||||||
chr3:149197798 | G | A | 12 | a0001c0014t0001g0217 a0002c0002t0009g0095 a0003c0004t0001g0223 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1713+569C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197798 | |||||||
chr3:149197835 | A | C | 11 | a0001c0014t0001g0217 a0003c0004t0001g0223 a0003c0004t0001g0310 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1713+532T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197835 | |||||||
chr3:149197841 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1713+526A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197841 | |||||||
chr3:149197934 | T | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1713+433A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197934 | |||||||
chr3:149197959 | C | T | 11 | a0001c0014t0001g0217 a0003c0004t0001g0223 a0003c0004t0001g0310 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1713+408G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197959 | |||||||
chr3:149198046 | G | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0335 a0001c0001t0001g0337 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+321C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149198046 | |||||||
chr3:149198212 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1713+155C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149198212 | |||||||
chr3:149198939 | A | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502-361T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149198939 | |||||||
chr3:149199209 | C | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+503G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199209 | |||||||
chr3:149199217 | G | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+495C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199217 | |||||||
chr3:149199259 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(32): Show |
41 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1501+453G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199259 | |||||||
chr3:149199330 | C | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+382G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199330 | |||||||
chr3:149199425 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1501+287A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199425 | |||||||
chr3:149199877 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0103 a0001c0001t0001g0114 others(7): Show |
11 | HG00408.hp2 HG01258.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1349-13T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149199877 | |||||||
chr3:149199960 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1349-96G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149199960 | |||||||
chr3:149200057 | G | C | 3 | a0001c0001t0001g0332 a0005c0008t0006g0216 a0005c0008t0006g0331 |
3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1349-193C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200057 | |||||||
chr3:149200215 | G | A | 1 | a0002c0002t0001g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1349-351C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200215 | |||||||
chr3:149200499 | C | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1349-635G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200499 | |||||||
chr3:149200554 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1349-690C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200554 | |||||||
chr3:149200858 | C | A | 1 | a0001c0001t0002g0159 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1349-994G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200858 | |||||||
chr3:149200953 | A | G | 1 | a0007c0012t0001g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1349-1089T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200953 | |||||||
chr3:149201016 | G | A | 2 | a0002c0002t0001g0220 a0002c0002t0001g0290 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1348+1086C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201016 | |||||||
chr3:149201107 | G | GGATT | 20 | a0001c0001t0001g0041 a0001c0001t0001g0051 a0001c0001t0001g0054 others(17): Show |
21 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1348+991_1348+994d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201107 | |||||||
chr3:149201107 | GGATT | G | 6 | a0003c0004t0001g0223 a0003c0004t0001g0312 a0003c0004t0001g0313 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+991_1348+994d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201107 | |||||||
chr3:149201107 | GGATTGAT others(1): Show |
G | 5 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0002c0002t0001g0289 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348+987_1348+994d others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201107 | |||||||
chr3:149201134 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1348+968A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201134 | |||||||
chr3:149201157 | T | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(18): Show |
26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1348+945A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201157 | |||||||
chr3:149201186 | A | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348+916T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201186 | |||||||
chr3:149201217 | G | A | 1 | a0001c0001t0004g0163 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1348+885C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201217 | |||||||
chr3:149201322 | C | T | 1 | a0004c0009t0001g0082 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1348+780G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201322 | |||||||
chr3:149201430 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1348+672C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201430 | |||||||
chr3:149201452 | TCTTTAA | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0337 a0001c0001t0001g0340 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+644_1348+649d others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201452 | |||||||
chr3:149201783 | A | G | 1 | a0013c0017t0007g0298 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1348+319T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201783 | |||||||
chr3:149201827 | C | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348+275G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201827 | |||||||
chr3:149201891 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0161 |
2 | NA18968.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1348+211C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201891 | |||||||
chr3:149202047 | T | C | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348+55A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149202047 | |||||||
chr3:149202093 | A | G | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1348+9T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149202093 | |||||||
chr3:149202256 | A | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-15T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202256 | |||||||
chr3:149202431 | C | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-190G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202431 | |||||||
chr3:149202534 | A | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0266 |
3 | NA18960.hp2 NA18975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1209-293T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202534 | |||||||
chr3:149202562 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1209-321T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202562 | |||||||
chr3:149202605 | C | CT | 25 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0052 others(22): Show |
28 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1209-365dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202605 | |||||||
chr3:149202605 | CT | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
121 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1209-365delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202605 | |||||||
chr3:149202605 | CTT | C | 12 | a0001c0001t0001g0162 a0001c0001t0001g0184 a0001c0001t0001g0206 others(9): Show |
12 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1209-366_1209-365d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202605 | |||||||
chr3:149202701 | G | A | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209-460C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202701 | |||||||
chr3:149202711 | C | T | 5 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0091 others(2): Show |
6 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-470G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202711 | |||||||
chr3:149202753 | G | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-512C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202753 | |||||||
chr3:149202811 | A | G | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-570T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202811 | |||||||
chr3:149202908 | C | CT | 42 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0033 others(39): Show |
48 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1209-668dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202908 | |||||||
chr3:149202908 | CT | C | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-668delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202908 | |||||||
chr3:149202938 | A | G | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-697T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202938 | |||||||
chr3:149202947 | C | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-706G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202947 | |||||||
chr3:149202959 | T | G | 1 | a0002c0002t0001g0285 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1209-718A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202959 | |||||||
chr3:149202998 | T | C | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-757A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202998 | |||||||
chr3:149203064 | G | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-823C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203064 | |||||||
chr3:149203087 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1209-846A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203087 | |||||||
chr3:149203107 | C | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-866G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203107 | |||||||
chr3:149203155 | T | C | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-914A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203155 | |||||||
chr3:149203187 | G | A | 3 | a0001c0014t0001g0217 a0007c0012t0001g0219 a0007c0012t0012g0218 |
3 | HG02572.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1209-946C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203187 | |||||||
chr3:149203196 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1209-955A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203196 | |||||||
chr3:149203202 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18959.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1209-961G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203202 | |||||||
chr3:149203216 | A | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(135): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1209-975T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203216 | |||||||
chr3:149203306 | CA | C | 35 | a0001c0001t0001g0166 a0001c0001t0001g0179 a0001c0001t0001g0192 others(32): Show |
41 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1209-1066delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203306 | |||||||
chr3:149203345 | A | C | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1104T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203345 | |||||||
chr3:149203348 | C | A | 4 | a0004c0009t0001g0082 a0004c0009t0001g0255 a0004c0009t0001g0262 others(1): Show |
5 | HG01192.hp1 HG02273.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-1107G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203348 | |||||||
chr3:149203556 | G | T | 1 | a0002c0002t0001g0287 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1209-1315C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203556 | |||||||
chr3:149203558 | T | C | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1317A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203558 | |||||||
chr3:149203638 | C | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1397G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203638 | |||||||
chr3:149203702 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1209-1461G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203702 | |||||||
chr3:149203839 | C | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1598G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203839 | |||||||
chr3:149203982 | G | C | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209-1741C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203982 | |||||||
chr3:149203987 | AGT | A | 3 | a0006c0007t0005g0299 a0006c0007t0005g0300 a0006c0007t0005g0301 |
3 | HG03195.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1209-1748_1209-174 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203987 | |||||||
chr3:149204017 | G | A | 1 | a0002c0002t0009g0095 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209-1776C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204017 | |||||||
chr3:149204021 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1209-1780T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204021 | |||||||
chr3:149204031 | G | C | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1790C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204031 | |||||||
chr3:149204056 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(65): Show |
73 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1209-1815C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204056 | |||||||
chr3:149204061 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1209-1820C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204061 | |||||||
chr3:149204065 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1209-1824C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204065 | |||||||
chr3:149204098 | C | T | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1857G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204098 | |||||||
chr3:149204161 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1209-1920A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204161 | |||||||
chr3:149204259 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0322 a0001c0001t0002g0004 others(12): Show |
19 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1208+1909C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204259 | |||||||
chr3:149204530 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1208+1638G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204530 | |||||||
chr3:149205001 | T | TCAA | 21 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(18): Show |
26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1208+1164_1208+116 others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205001 | |||||||
chr3:149205001 | T | TCAACAA | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208+1161_1208+116 others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205001 | |||||||
chr3:149205090 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1208+1078T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205090 | |||||||
chr3:149205143 | C | A | 328 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.1208+1025G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205143 | |||||||
chr3:149205230 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1208+938T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205230 | |||||||
chr3:149205295 | G | A | 8 | a0003c0004t0001g0223 a0003c0004t0001g0310 a0003c0004t0001g0311 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208+873C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205295 | |||||||
chr3:149205374 | G | C | 4 | a0001c0001t0001g0335 a0001c0001t0001g0337 a0001c0001t0001g0340 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208+794C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205374 | |||||||
chr3:149205380 | G | T | 1 | a0001c0001t0003g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1208+788C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205380 | |||||||
chr3:149205500 | A | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG00438.hp1 HG00558.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1208+668T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205500 | |||||||
chr3:149205612 | A | T | 1 | a0001c0001t0002g0314 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1208+556T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205612 | |||||||
chr3:149205753 | G | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0338 a0001c0001t0001g0342 others(1): Show |
5 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+415C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205753 | |||||||
chr3:149205754 | T | C | 1 | a0002c0002t0003g0282 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1208+414A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205754 | |||||||
chr3:149205869 | G | A | 41 | a0001c0001t0001g0166 a0001c0001t0001g0179 a0001c0001t0001g0192 others(38): Show |
47 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1208+299C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205869 | |||||||
chr3:149206390 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1037-51A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206390 | |||||||
chr3:149206414 | C | T | 4 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | NA18980.hp2 NA18989.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-75G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206414 | |||||||
chr3:149206443 | T | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0332 a0001c0001t0001g0335 others(12): Show |
16 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1037-104A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206443 | |||||||
chr3:149206590 | C | T | 1 | a0016c0026t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1037-251G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206590 | |||||||
chr3:149206818 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1037-479C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206818 | |||||||
chr3:149206852 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1036+511T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206852 | |||||||
chr3:149206979 | G | A | 4 | a0002c0002t0001g0291 a0002c0002t0001g0292 a0002c0002t0002g0294 others(1): Show |
4 | HG02257.hp1 HG02258.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+384C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206979 | |||||||
chr3:149207047 | T | C | 34 | a0002c0002t0001g0285 a0002c0002t0001g0286 a0002c0002t0001g0287 others(31): Show |
35 | HG00733.hp2 HG00735.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1036+316A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149207047 | |||||||
chr3:149207631 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(18): Show |
26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.782-14C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207631 | |||||||
chr3:149207738 | T | C | 329 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(326): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.782-121A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207738 | |||||||
chr3:149207744 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.782-127G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207744 | |||||||
chr3:149207779 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(18): Show |
26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.782-162C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207779 | |||||||
chr3:149207865 | C | A | 3 | a0001c0001t0001g0332 a0005c0008t0006g0216 a0005c0008t0006g0331 |
3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.782-248G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207865 | |||||||
chr3:149207977 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0335 a0001c0001t0001g0337 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.782-360A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207977 | |||||||
chr3:149208022 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.782-405C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208022 | |||||||
chr3:149208276 | C | G | 6 | a0001c0001t0001g0332 a0005c0008t0006g0216 a0005c0008t0006g0331 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-659G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208276 | |||||||
chr3:149208329 | T | A | 28 | a0002c0002t0001g0220 a0002c0002t0001g0285 a0002c0002t0001g0286 others(25): Show |
29 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.782-712A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208329 | |||||||
chr3:149208347 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.782-730G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208347 | |||||||
chr3:149208377 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.782-760G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208377 | |||||||
chr3:149208438 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.781+773G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208438 | |||||||
chr3:149208443 | T | C | 26 | a0002c0002t0001g0285 a0002c0002t0001g0286 a0002c0002t0001g0287 others(23): Show |
27 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.781+768A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208443 | |||||||
chr3:149208483 | T | C | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.781+728A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208483 | |||||||
chr3:149208489 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.781+722T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208489 | |||||||
chr3:149208528 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.781+683C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208528 | |||||||
chr3:149208564 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.781+647T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208564 | |||||||
chr3:149208569 | CAAAT | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0266 |
3 | NA18960.hp2 NA18975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.781+638_781+641del others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208569 | |||||||
chr3:149208817 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.781+394C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208817 | |||||||
chr3:149209716 | C | G | 6 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0091 others(3): Show |
7 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-332G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209716 | |||||||
chr3:149209924 | A | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.607+243T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209924 | |||||||
chr3:149209937 | A | T | 6 | a0001c0001t0001g0332 a0005c0008t0006g0216 a0005c0008t0006g0331 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+230T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209937 | |||||||
chr3:149209992 | T | G | 1 | a0001c0001t0001g0332 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.607+175A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209992 | |||||||
chr3:149210028 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.607+139G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210028 | |||||||
chr3:149210038 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.607+129A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210038 | |||||||
chr3:149210059 | C | T | 2 | a0003c0004t0001g0310 a0003c0004t0001g0311 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.607+108G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210059 | |||||||
chr3:149210062 | T | C | 1 | a0006c0007t0005g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.607+105A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210062 | |||||||
chr3:149210065 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.607+102G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210065 | |||||||
chr3:149210106 | G | A | 2 | a0001c0001t0002g0168 a0017c0020t0002g0169 |
2 | NA18962.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.607+61C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210106 | |||||||
chr3:149210138 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.607+29T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210138 | |||||||
chr3:149210506 | T | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0322 others(24): Show |
33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.395-127A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210506 | |||||||
chr3:149210752 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.395-373A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210752 | |||||||
chr3:149210758 | C | T | 1 | a0001c0001t0006g0232 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.395-379G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210758 | |||||||
chr3:149210869 | G | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.395-490C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210869 | |||||||
chr3:149211136 | A | G | 5 | a0001c0003t0001g0011 a0001c0003t0001g0090 a0001c0003t0001g0091 others(2): Show |
6 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.395-757T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211136 | |||||||
chr3:149211148 | A | C | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.395-769T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211148 | |||||||
chr3:149211353 | G | T | 1 | a0002c0002t0003g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.395-974C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211353 | |||||||
chr3:149211591 | T | C | 2 | a0001c0010t0001g0221 a0001c0010t0001g0222 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.394+860A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211591 | |||||||
chr3:149211618 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.394+833G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211618 | |||||||
chr3:149211725 | A | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0322 a0001c0001t0002g0004 others(12): Show |
19 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+726T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211725 | |||||||
chr3:149211818 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.394+633C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211818 | |||||||
chr3:149212011 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.394+440A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212011 | |||||||
chr3:149212013 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394+438C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212013 | |||||||
chr3:149212024 | T | A | 3 | a0006c0007t0005g0299 a0006c0007t0005g0300 a0006c0007t0005g0301 |
3 | HG03195.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.394+427A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212024 | |||||||
chr3:149212032 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.394+419C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212032 | |||||||
chr3:149212064 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.394+387G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212064 | |||||||
chr3:149212121 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.394+330C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212121 | |||||||
chr3:149212123 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.394+328G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212123 | |||||||
chr3:149212130 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.394+321T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212130 | |||||||
chr3:149212135 | T | C | 22 | a0002c0002t0001g0285 a0002c0002t0001g0286 a0002c0002t0001g0287 others(19): Show |
23 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.394+316A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212135 | |||||||
chr3:149212164 | T | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
108 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.394+287A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212164 | |||||||
chr3:149212290 | G | A | 25 | a0002c0002t0001g0285 a0002c0002t0001g0287 a0002c0002t0001g0288 others(22): Show |
26 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.394+161C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212290 | |||||||
chr3:149212292 | C | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.394+159G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212292 | |||||||
chr3:149212309 | T | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(65): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.394+142A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212309 | |||||||
chr3:149212310 | A | T | 5 | a0002c0002t0001g0290 a0003c0004t0001g0223 a0003c0004t0002g0224 others(2): Show |
5 | HG02630.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+141T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212310 | |||||||
chr3:149212326 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+125T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212326 | |||||||
chr3:149212381 | A | C | 1 | a0001c0001t0001g0006 | 2 | NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.394+70T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212381 | |||||||
chr3:149212431 | G | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(63): Show |
71 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.394+20C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212431 | |||||||
chr3:149212952 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.147-254G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149212952 | |||||||
chr3:149213120 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0338 others(2): Show |
7 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-422T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213120 | |||||||
chr3:149213211 | A | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(63): Show |
71 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.147-513T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213211 | |||||||
chr3:149213212 | T | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(63): Show |
71 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.147-514A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213212 | |||||||
chr3:149213269 | G | T | 1 | a0001c0001t0006g0277 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147-571C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213269 | |||||||
chr3:149213318 | C | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0338 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-620G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213318 | |||||||
chr3:149213354 | T | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
8 | HG00597.hp2 HG01433.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.147-656A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213354 | |||||||
chr3:149213524 | G | T | 1 | a0002c0002t0001g0285 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147-826C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213524 | |||||||
chr3:149213630 | GGGTGT | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0342 a0002c0002t0002g0275 |
3 | HG01243.hp2 NA18990.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147-937_147-933del others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213630 | |||||||
chr3:149213631 | G | GGT | 13 | a0001c0001t0001g0335 a0001c0001t0002g0320 a0001c0001t0006g0277 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-935_147-934dup others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213631 | GGT | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(20): Show |
26 | HG00738.hp1 HG02257.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.147-935_147-934del others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213631 | GGTGT | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.147-937_147-934del others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213631 | GGTGTGT | G | 60 | a0001c0001t0001g0019 a0001c0001t0001g0130 a0001c0001t0001g0142 others(57): Show |
69 | HG00323.hp1 HG00558.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.147-939_147-934del others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213631 | GGTGTGTG others(1): Show |
G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0001g0251 others(2): Show |
5 | HG00642.hp2 HG01175.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-941_147-934del others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213631 | GGTGTGTG others(3): Show |
G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0001g0196 others(2): Show |
5 | HG00099.hp2 HG01070.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-943_147-934del others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213631 | GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0034 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.147-945_147-934del others(12): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213631 | GGTGTGTG others(7): Show |
G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.147-947_147-934del others(14): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | |||||||
chr3:149213737 | G | T | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(65): Show |
73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.147-1039C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213737 | |||||||
chr3:149213739 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147-1041C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213739 | |||||||
chr3:149213977 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0338 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-1279C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213977 | |||||||
chr3:149214003 | T | C | 3 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0265 |
3 | HG00738.hp1 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.147-1305A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214003 | |||||||
chr3:149214022 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.147-1324G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214022 | |||||||
chr3:149214029 | T | A | 1 | a0002c0002t0003g0284 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.147-1331A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214029 | |||||||
chr3:149214053 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.147-1355C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214053 | |||||||
chr3:149214171 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.147-1473C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214171 | |||||||
chr3:149214193 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.147-1495C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214193 | |||||||
chr3:149214242 | T | C | 1 | a0001c0001t0002g0329 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.147-1544A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214242 | |||||||
chr3:149214298 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0003g0176 |
2 | HG01255.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.147-1600C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214298 | |||||||
chr3:149214318 | G | A | 1 | a0004c0009t0001g0262 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.147-1620C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214318 | |||||||
chr3:149214353 | T | C | 3 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0003g0265 |
3 | HG00738.hp1 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.147-1655A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214353 | |||||||
chr3:149214374 | A | G | 1 | a0001c0001t0003g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.147-1676T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214374 | |||||||
chr3:149214382 | C | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(65): Show |
73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.147-1684G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214382 | |||||||
chr3:149214506 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.147-1808G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214506 | |||||||
chr3:149214510 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.147-1812A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214510 | |||||||
chr3:149214712 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0266 |
3 | NA18960.hp2 NA18975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.147-2014C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214712 | |||||||
chr3:149214923 | T | C | 1 | a0002c0002t0002g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-2225A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214923 | |||||||
chr3:149214967 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.147-2269G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214967 | |||||||
chr3:149215299 | T | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.147-2601A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215299 | |||||||
chr3:149215491 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0338 a0001c0001t0001g0340 others(4): Show |
8 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.147-2793A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215491 | |||||||
chr3:149215626 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.147-2928A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215626 | |||||||
chr3:149215765 | A | G | 1 | a0001c0001t0006g0277 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147-3067T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215765 | |||||||
chr3:149215884 | A | G | 1 | a0013c0017t0007g0298 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-3186T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215884 | |||||||
chr3:149216009 | C | T | 4 | a0002c0002t0001g0003 a0002c0002t0001g0295 a0002c0002t0001g0296 others(1): Show |
6 | HG02258.hp1 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-3311G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216009 | |||||||
chr3:149216354 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.147-3656A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216354 | |||||||
chr3:149216423 | G | A | 1 | a0002c0002t0002g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-3725C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216423 | |||||||
chr3:149216443 | C | T | 33 | a0001c0001t0001g0335 a0001c0001t0001g0337 a0002c0002t0001g0285 others(30): Show |
34 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.147-3745G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216443 | |||||||
chr3:149216615 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG03239.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-3917C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216615 | |||||||
chr3:149216811 | A | C | 6 | a0002c0002t0003g0280 a0002c0002t0003g0281 a0002c0002t0003g0282 others(3): Show |
6 | HG01243.hp1 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-4113T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216811 | |||||||
chr3:149216874 | A | C | 15 | a0001c0001t0001g0337 a0002c0002t0001g0285 a0002c0002t0001g0286 others(12): Show |
16 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.147-4176T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216874 | |||||||
chr3:149216900 | C | CT | 16 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(13): Show |
16 | HG00733.hp1 HG01074.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.147-4203dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216900 | |||||||
chr3:149216900 | CT | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0185 a0001c0001t0001g0186 others(8): Show |
11 | HG00323.hp2 HG01069.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-4203delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216900 | |||||||
chr3:149216954 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.147-4256C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216954 | |||||||
chr3:149217177 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.146+4470C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217177 | |||||||
chr3:149217445 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.146+4202A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217445 | |||||||
chr3:149217545 | G | A | 1 | a0005c0008t0006g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.146+4102C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217545 | |||||||
chr3:149217640 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.146+4007A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217640 | |||||||
chr3:149217693 | T | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(61): Show |
69 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.146+3954A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217693 | |||||||
chr3:149217850 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.146+3797A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217850 | |||||||
chr3:149217874 | G | A | 1 | a0001c0010t0001g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.146+3773C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217874 | |||||||
chr3:149217879 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.146+3768C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217879 | |||||||
chr3:149218004 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0338 a0001c0001t0001g0340 others(4): Show |
8 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.146+3643G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218004 | |||||||
chr3:149218072 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.146+3575T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218072 | |||||||
chr3:149218106 | A | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.146+3541T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218106 | |||||||
chr3:149218117 | T | A | 1 | a0001c0001t0001g0343 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.146+3530A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218117 | |||||||
chr3:149218442 | C | G | 8 | a0002c0002t0002g0268 a0002c0002t0002g0273 a0002c0002t0002g0274 others(5): Show |
8 | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.146+3205G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218442 | |||||||
chr3:149218466 | G | A | 26 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0190 others(23): Show |
28 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.146+3181C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218466 | |||||||
chr3:149218530 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(126): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.146+3117A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218530 | |||||||
chr3:149218598 | C | T | 8 | a0002c0002t0002g0268 a0002c0002t0002g0273 a0002c0002t0002g0274 others(5): Show |
8 | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.146+3049G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218598 | |||||||
chr3:149218790 | C | T | 47 | a0001c0001t0001g0019 a0001c0001t0001g0215 a0001c0001t0001g0227 others(44): Show |
54 | HG00323.hp1 HG00738.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.146+2857G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218790 | |||||||
chr3:149218941 | T | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.146+2706A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218941 | |||||||
chr3:149218962 | A | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.146+2685T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218962 | |||||||
chr3:149219353 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.146+2294G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219353 | |||||||
chr3:149219404 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146+2243C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219404 | |||||||
chr3:149219444 | C | T | 4 | a0003c0004t0001g0223 a0003c0004t0002g0224 a0003c0004t0002g0225 others(1): Show |
4 | HG02630.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+2203G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219444 | |||||||
chr3:149219971 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0338 |
3 | HG02559.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146+1676G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219971 | |||||||
chr3:149220103 | G | A | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(59): Show |
65 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.146+1544C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220103 | |||||||
chr3:149220131 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | NA19000.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.146+1516G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220131 | |||||||
chr3:149220325 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.146+1322A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220325 | |||||||
chr3:149220354 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.146+1293G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220354 | |||||||
chr3:149220559 | T | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(57): Show |
63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.146+1088A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220559 | |||||||
chr3:149220593 | T | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(57): Show |
63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.146+1054A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220593 | |||||||
chr3:149220705 | C | T | 6 | a0001c0010t0001g0221 a0001c0010t0001g0222 a0001c0014t0001g0217 others(3): Show |
6 | HG02572.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.146+942G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220705 | |||||||
chr3:149220707 | G | A | 2 | a0001c0001t0001g0337 a0012c0028t0001g0336 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.146+940C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220707 | |||||||
chr3:149220868 | A | G | 1 | a0005c0008t0006g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.146+779T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220868 | |||||||
chr3:149220891 | A | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(57): Show |
63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.146+756T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220891 | |||||||
chr3:149220990 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.146+657T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220990 | |||||||
chr3:149221163 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.146+484T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221163 | |||||||
chr3:149221350 | G | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
6 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.146+297C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221350 | |||||||
chr3:149221390 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0338 a0001c0001t0001g0340 others(4): Show |
8 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.146+257C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221390 | |||||||
chr3:149221551 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.146+96A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221551 | |||||||
chr3:149221606 | C | T | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(57): Show |
63 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.146+41G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221606 |