Item | Value |
---|---|
geneid | 29997 |
ensemblid | ENSG00000105373.19 |
hgncid | 4333 |
symbol | NOP53 |
name | NOP53 ribosome biogenesis factor |
refseq_nuc | NM_015710.5 |
refseq_prot | NP_056525.2 |
ensembl_nuc | ENST00000246802.10 |
ensembl_prot | ENSP00000246802.4 |
mane_status | MANE Select |
chr | chr19 |
start | 47745546 |
end | 47757058 |
strand | + |
ver | v1.2 |
region | chr19:47745546-47757058 |
region5000 | chr19:47740546-47762058 |
regionname0 | NOP53_chr19_47745546_47757058 |
regionname5000 | NOP53_chr19_47740546_47762058 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 478 | 222 | 45 | 42 | 89 | 13 | 33 | 66 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0002 | 1/1 | 478 | 124 | 14 | 22 | 74 | 3 | 9 | 52 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0003 | 0/0 | 478 | 23 | 18 | 5 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0004 | 0/0 | 478 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0005 | 0/0 | 478 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0006 | 0/0 | 478 | 4 | 0 | 0 | 2 | 0 | 2 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0007 | 0/0 | 478 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0008 | 0/0 | 478 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0009 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0010 | 0/0 | 478 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0011 | 0/0 | 478 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0012 | 0/0 | 478 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0013 | 0/0 | 88 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(83): Show |
chr19 | 47740546 | 47762058 |
a0014 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
a0015 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | MAAGG others(473): Show |
chr19 | 47740546 | 47762058 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1434 | 160 | 5 | 32 | 89 | 5 | 29 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0003 | 0/0 | 1434 | 25 | 24 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0005 | 0/0 | 1434 | 11 | 1 | 5 | 0 | 5 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0006 | 0/0 | 1434 | 10 | 1 | 4 | 0 | 2 | 3 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0008 | 0/0 | 1434 | 8 | 8 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0012 | 0/0 | 1434 | 4 | 4 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0019 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0022 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0023 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0001c0027 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0002c0002 | 1/1 | 1434 | 115 | 9 | 21 | 72 | 2 | 9 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0002c0009 | 0/0 | 1434 | 5 | 5 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0002c0015 | 0/0 | 1434 | 2 | 0 | 1 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0002c0021 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0002c0025 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0003c0004 | 0/0 | 1434 | 23 | 18 | 5 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0004c0007 | 0/0 | 1434 | 9 | 9 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0005c0010 | 0/0 | 1434 | 5 | 5 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0006c0011 | 0/0 | 1434 | 4 | 0 | 0 | 2 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0007c0013 | 0/0 | 1434 | 4 | 4 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0008c0014 | 0/0 | 1434 | 3 | 3 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0009c0018 | 0/0 | 1434 | 2 | 0 | 2 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0010c0017 | 0/0 | 1434 | 2 | 0 | 0 | 0 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0011c0016 | 0/0 | 1434 | 2 | 0 | 0 | 2 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0012c0024 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0013c0028 | 0/0 | 1406 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1401): Show |
chr19 | 47740546 | 47762058 | ||
a0014c0026 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 | ||
a0015c0020 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | ATGGC others(1429): Show |
chr19 | 47740546 | 47762058 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1504 | 160 | 5 | 32 | 89 | 5 | 29 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0003t0001 | 0/0 | 1504 | 25 | 24 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0005t0001 | 0/0 | 1504 | 11 | 1 | 5 | 0 | 5 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0006t0001 | 0/0 | 1504 | 3 | 1 | 1 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0006t0002 | 0/0 | 1505 | 7 | 0 | 3 | 0 | 2 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1500): Show |
chr19 | 47740546 | 47762058 |
a0001c0008t0001 | 0/0 | 1504 | 8 | 8 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0012t0001 | 0/0 | 1504 | 4 | 4 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0019t0002 | 0/0 | 1505 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1500): Show |
chr19 | 47740546 | 47762058 |
a0001c0022t0001 | 0/0 | 1504 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0023t0001 | 0/0 | 1504 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0001c0027t0001 | 0/0 | 1504 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0002c0002t0001 | 1/1 | 1504 | 115 | 9 | 21 | 72 | 2 | 9 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0002c0009t0001 | 0/0 | 1504 | 5 | 5 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0002c0015t0001 | 0/0 | 1504 | 2 | 0 | 1 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0002c0021t0001 | 0/0 | 1504 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0002c0025t0001 | 0/0 | 1504 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0003c0004t0001 | 0/0 | 1504 | 19 | 18 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0003c0004t0003 | 0/0 | 1504 | 4 | 0 | 4 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0004c0007t0001 | 0/0 | 1504 | 9 | 9 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0005c0010t0001 | 0/0 | 1504 | 5 | 5 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0006c0011t0001 | 0/0 | 1504 | 4 | 0 | 0 | 2 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0007c0013t0001 | 0/0 | 1504 | 4 | 4 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0008c0014t0001 | 0/0 | 1504 | 3 | 3 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0009c0018t0001 | 0/0 | 1504 | 2 | 0 | 2 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0010c0017t0001 | 0/0 | 1504 | 2 | 0 | 0 | 0 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0011c0016t0001 | 0/0 | 1504 | 2 | 0 | 0 | 2 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0012c0024t0001 | 0/0 | 1504 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0013c0028t0001 | 0/0 | 1476 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1471): Show |
chr19 | 47740546 | 47762058 |
a0014c0026t0001 | 0/0 | 1504 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
a0015c0020t0001 | 0/0 | 1504 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | CTTCC others(1499): Show |
chr19 | 47740546 | 47762058 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 79 | 3 | 17 | 46 | 3 | 10 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0003 | 0/0 | 21 | 1 | 6 | 13 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0005t0001g0006 | 0/0 | 9 | 1 | 3 | 0 | 5 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0005t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0005t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0006t0001g0007 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0006t0002g0007 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0006t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0006t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0008t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0008t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0008t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0008t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0012t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0012t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0019t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0022t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0023t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0001c0027t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0002 | 1/0 | 49 | 4 | 9 | 34 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0004 | 0/0 | 18 | 0 | 5 | 11 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0005 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0017 | 0/1 | 4 | 0 | 1 | 1 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0009t0001g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0015t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0015t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0021t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0002c0025t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0003c0004t0003g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0004c0007t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0004c0007t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0004c0007t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0005c0010t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0005c0010t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0006c0011t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0006c0011t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0006c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0006c0011t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0007c0013t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0008c0014t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0009c0018t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0010c0017t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0011c0016t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0012c0024t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0013c0028t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0014c0026t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
a0015c0020t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0006 | t0002 | g0007 | EUR | GBR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0028 | EUR | GBR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00280 | hp1 | a0001 | c0019 | t0002 | g0007 | EUR | FIN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00280 | hp2 | a0001 | c0005 | t0001 | g0006 | EUR | FIN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00323 | hp2 | a0001 | c0005 | t0001 | g0006 | EUR | FIN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00642 | hp1 | a0002 | c0015 | t0001 | g0063 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00738 | hp1 | a0003 | c0004 | t0001 | g0018 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00741 | hp1 | a0001 | c0006 | t0002 | g0007 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01069 | hp1 | a0003 | c0004 | t0003 | g0019 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0087 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01071 | hp2 | a0001 | c0005 | t0001 | g0006 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01192 | hp2 | a0001 | c0005 | t0001 | g0006 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01243 | hp1 | a0001 | c0006 | t0001 | g0007 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01255 | hp1 | a0001 | c0006 | t0002 | g0007 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01255 | hp2 | a0009 | c0018 | t0001 | g0003 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01257 | hp1 | a0012 | c0024 | t0001 | g0001 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0050 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01346 | hp1 | a0001 | c0006 | t0002 | g0007 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01496 | hp1 | a0001 | c0005 | t0001 | g0083 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01496 | hp2 | a0009 | c0018 | t0001 | g0003 | AMR | CLM | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01515 | hp2 | a0001 | c0005 | t0001 | g0006 | EUR | IBS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01517 | hp1 | a0002 | c0021 | t0001 | g0028 | EUR | IBS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01517 | hp2 | a0001 | c0005 | t0001 | g0006 | EUR | IBS | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01884 | hp1 | a0001 | c0008 | t0001 | g0032 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01884 | hp2 | a0001 | c0008 | t0001 | g0031 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01891 | hp1 | a0003 | c0004 | t0001 | g0077 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01891 | hp2 | a0003 | c0004 | t0001 | g0010 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01928 | hp2 | a0003 | c0004 | t0003 | g0019 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01943 | hp2 | a0001 | c0005 | t0001 | g0006 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG01993 | hp2 | a0003 | c0004 | t0003 | g0019 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0010 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02056 | hp2 | a0006 | c0011 | t0001 | g0114 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02145 | hp1 | a0003 | c0004 | t0001 | g0018 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02145 | hp2 | a0007 | c0013 | t0001 | g0020 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | CDX | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02258 | hp1 | a0001 | c0022 | t0001 | g0082 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02258 | hp2 | a0003 | c0004 | t0001 | g0010 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02280 | hp2 | a0003 | c0004 | t0001 | g0067 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02293 | hp1 | a0003 | c0004 | t0003 | g0019 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02572 | hp2 | a0008 | c0014 | t0001 | g0021 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02615 | hp1 | a0004 | c0007 | t0001 | g0024 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02615 | hp2 | a0002 | c0009 | t0001 | g0002 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02622 | hp1 | a0004 | c0007 | t0001 | g0086 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02622 | hp2 | a0001 | c0008 | t0001 | g0030 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0081 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02647 | hp1 | a0002 | c0009 | t0001 | g0002 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02647 | hp2 | a0003 | c0004 | t0001 | g0072 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02683 | hp1 | a0001 | c0006 | t0001 | g0007 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02717 | hp1 | a0002 | c0009 | t0001 | g0002 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02717 | hp2 | a0004 | c0007 | t0001 | g0008 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02723 | hp2 | a0003 | c0004 | t0001 | g0074 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02809 | hp2 | a0004 | c0007 | t0001 | g0008 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02886 | hp2 | a0008 | c0014 | t0001 | g0021 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02895 | hp1 | a0002 | c0009 | t0001 | g0002 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02896 | hp1 | a0003 | c0004 | t0001 | g0010 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02896 | hp2 | a0004 | c0007 | t0001 | g0024 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02897 | hp2 | a0004 | c0007 | t0001 | g0024 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02922 | hp1 | a0001 | c0027 | t0001 | g0033 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02922 | hp2 | a0003 | c0004 | t0001 | g0068 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02965 | hp2 | a0005 | c0010 | t0001 | g0008 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0080 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0018 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02976 | hp2 | a0004 | c0007 | t0001 | g0008 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03041 | hp1 | a0007 | c0013 | t0001 | g0020 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03041 | hp2 | a0001 | c0012 | t0001 | g0112 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03098 | hp1 | a0003 | c0004 | t0001 | g0065 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03098 | hp2 | a0005 | c0010 | t0001 | g0110 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03139 | hp1 | a0003 | c0004 | t0001 | g0075 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03195 | hp1 | a0001 | c0012 | t0001 | g0023 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03195 | hp2 | a0005 | c0010 | t0001 | g0008 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03209 | hp1 | a0008 | c0014 | t0001 | g0021 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03209 | hp2 | a0001 | c0012 | t0001 | g0023 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03225 | hp1 | a0001 | c0008 | t0001 | g0069 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03225 | hp2 | a0001 | c0008 | t0001 | g0031 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0018 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0071 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03486 | hp2 | a0005 | c0010 | t0001 | g0008 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03516 | hp1 | a0007 | c0013 | t0001 | g0020 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03540 | hp1 | a0001 | c0008 | t0001 | g0070 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0010 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03669 | hp2 | a0001 | c0006 | t0002 | g0085 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03688 | hp1 | a0010 | c0017 | t0001 | g0001 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03831 | hp1 | a0001 | c0006 | t0002 | g0084 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03831 | hp2 | a0001 | c0023 | t0001 | g0014 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03942 | hp1 | a0010 | c0017 | t0001 | g0001 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0041 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0060 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04204 | hp1 | a0006 | c0011 | t0001 | g0115 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | YRI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18906 | hp1 | a0007 | c0013 | t0001 | g0020 | AFR | YRI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | YRI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18965 | hp2 | a0013 | c0028 | t0001 | g0092 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18970 | hp2 | a0002 | c0015 | t0001 | g0059 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18971 | hp1 | a0011 | c0016 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18977 | hp1 | a0014 | c0026 | t0001 | g0105 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18978 | hp2 | a0011 | c0016 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18991 | hp1 | a0015 | c0020 | t0001 | g0005 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19000 | hp2 | a0006 | c0011 | t0001 | g0111 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19030 | hp1 | a0003 | c0004 | t0001 | g0010 | AFR | LWK | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19030 | hp2 | a0001 | c0008 | t0001 | g0032 | AFR | LWK | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | LWK | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | LWK | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19063 | hp2 | a0002 | c0025 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | YRI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA19240 | hp2 | a0001 | c0008 | t0001 | g0030 | AFR | YRI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | ASW | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20129 | hp2 | a0004 | c0007 | t0001 | g0008 | AFR | ASW | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20752 | hp2 | a0001 | c0006 | t0002 | g0007 | EUR | TSI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20805 | hp1 | a0001 | c0005 | t0001 | g0006 | EUR | TSI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0052 | EUR | TSI | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20905 | hp2 | a0006 | c0011 | t0001 | g0113 | SAS | GIH | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02109 | hp2 | a0002 | c0009 | t0001 | g0002 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02486 | hp2 | a0005 | c0010 | t0001 | g0008 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG02559 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | ACB | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03471 | hp1 | a0001 | c0012 | t0001 | g0023 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG03471 | hp2 | a0004 | c0007 | t0001 | g0008 | AFR | MSL | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | USA | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20300 | hp1 | a0003 | c0004 | t0001 | g0010 | AFR | USA | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | USA | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | LWK | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
NA21309 | hp2 | a0001 | c0006 | t0001 | g0007 | AFR | LWK | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0017 | REF | REF | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0002 | REF | REF | NOP53_chr19_47740546_47762058 | NOP53 | chr19 | 47740546 | 47762058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:47745607 | C | A | 1 | a0003 | 23 | HG00738.hp1 HG01069.hp1 HG01891.hp1 others(20): Show |
missense_variant | MODERATE | c.48C>A | p.Ser16Arg | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/13 | 62/1504 | 48/1437 | 16/478 | chr19 | 47745607 | |||
chr19:47745618 | C | T | 2 | a0005 a0009 |
7 | HG01255.hp2 HG01496.hp2 HG02486.hp2 others(4): Show |
missense_variant | MODERATE | c.59C>T | p.Ser20Phe | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/13 | 73/1504 | 59/1437 | 20/478 | chr19 | 47745618 | |||
chr19:47745650 | G | C | 1 | a0006 | 4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
missense_variant | MODERATE | c.91G>C | p.Asp31His | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/13 | 105/1504 | 91/1437 | 31/478 | chr19 | 47745650 | |||
chr19:47746979 | AGAGGCCC others(21): Show |
A | 1 | a0013 | 1 | NA18965.hp2 | frameshift_variant | HIGH | c.238_265delGAGGCCCC others(20): Show |
p.Glu80fs | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/13 | 252/1504 | 238/1437 | 80/478 | chr19 | 47746979 | |||
chr19:47750996 | C | T | 1 | a0014 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.487C>T | p.Arg163Trp | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/13 | 501/1504 | 487/1437 | 163/478 | chr19 | 47750996 | |||
chr19:47752515 | C | T | 1 | a0008 | 3 | HG02572.hp2 HG02886.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.673C>T | p.Pro225Ser | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/13 | 687/1504 | 673/1437 | 225/478 | chr19 | 47752515 | |||
chr19:47754612 | C | T | 1 | a0010 | 2 | HG03688.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.851C>T | p.Thr284Met | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 7/13 | 865/1504 | 851/1437 | 284/478 | chr19 | 47754612 | |||
chr19:47754818 | C | T | 1 | a0008 | 3 | HG02572.hp2 HG02886.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.980C>T | p.Thr327Met | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/13 | 994/1504 | 980/1437 | 327/478 | chr19 | 47754818 | |||
chr19:47754884 | A | G | 1 | a0011 | 2 | NA18971.hp1 NA18978.hp2 |
missense_variant | MODERATE | c.1046A>G | p.His349Arg | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/13 | 1060/1504 | 1046/1437 | 349/478 | chr19 | 47754884 | |||
chr19:47755460 | A | G | 12 | a0001 a0003 a0004 others(9): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
missense_variant | MODERATE | c.1166A>G | p.Gln389Arg | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/13 | 1180/1504 | 1166/1437 | 389/478 | chr19 | 47755460 | |||
chr19:47755496 | A | C | 2 | a0004 a0005 |
14 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
missense_variant | MODERATE | c.1202A>C | p.Asp401Ala | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/13 | 1216/1504 | 1202/1437 | 401/478 | chr19 | 47755496 | |||
chr19:47755516 | C | T | 1 | a0012 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1222C>T | p.Arg408Trp | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/13 | 1236/1504 | 1222/1437 | 408/478 | chr19 | 47755516 | |||
chr19:47755806 | C | T | 1 | a0007 | 4 | HG02145.hp2 HG03041.hp1 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.1280C>T | p.Ser427Leu | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/13 | 1294/1504 | 1280/1437 | 427/478 | chr19 | 47755806 | |||
chr19:47756540 | A | G | 1 | a0015 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.1309A>G | p.Ile437Val | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 11/13 | 1323/1504 | 1309/1437 | 437/478 | chr19 | 47756540 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:47745577 | T | C | 3 | a0001c0006 a0001c0019 a0006c0011 |
15 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(12): Show |
synonymous_variant | LOW | c.18T>C | p.Ser6Ser | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/13 | 32/1504 | 18/1437 | 6/478 | chr19 | 47745577 | |||
chr19:47745667 | G | A | 1 | a0001c0005 | 11 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(8): Show |
synonymous_variant | LOW | c.108G>A | p.Arg36Arg | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/13 | 122/1504 | 108/1437 | 36/478 | chr19 | 47745667 | |||
chr19:47745668 | C | A | 1 | a0001c0005 | 11 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(8): Show |
synonymous_variant | LOW | c.109C>A | p.Arg37Arg | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/13 | 123/1504 | 109/1437 | 37/478 | chr19 | 47745668 | |||
chr19:47747018 | C | T | 1 | a0001c0027 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.276C>T | p.Gly92Gly | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/13 | 290/1504 | 276/1437 | 92/478 | chr19 | 47747018 | |||
chr19:47750197 | C | G | 1 | a0001c0008 | 8 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
synonymous_variant | LOW | c.309C>G | p.Thr103Thr | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/13 | 323/1504 | 309/1437 | 103/478 | chr19 | 47750197 | |||
chr19:47751082 | C | T | 2 | a0004c0007 a0005c0010 |
14 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.573C>T | p.Pro191Pro | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/13 | 587/1504 | 573/1437 | 191/478 | chr19 | 47751082 | |||
chr19:47751088 | C | T | 1 | a0002c0025 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.579C>T | p.Tyr193Tyr | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/13 | 593/1504 | 579/1437 | 193/478 | chr19 | 47751088 | |||
chr19:47751542 | T | C | 1 | a0006c0011 | 4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
synonymous_variant | LOW | c.621T>C | p.Val207Val | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/13 | 635/1504 | 621/1437 | 207/478 | chr19 | 47751542 | |||
chr19:47752547 | A | G | 10 | a0001c0001 a0001c0005 a0001c0022 others(7): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
synonymous_variant | LOW | c.705A>G | p.Ala235Ala | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/13 | 719/1504 | 705/1437 | 235/478 | chr19 | 47752547 | |||
chr19:47752553 | C | A | 1 | a0002c0009 | 5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.711C>A | p.Ala237Ala | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/13 | 725/1504 | 711/1437 | 237/478 | chr19 | 47752553 | |||
chr19:47752553 | C | G | 1 | a0002c0021 | 1 | HG01517.hp1 | synonymous_variant | LOW | c.711C>G | p.Ala237Ala | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/13 | 725/1504 | 711/1437 | 237/478 | chr19 | 47752553 | |||
chr19:47752556 | G | A | 1 | a0001c0022 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.714G>A | p.Val238Val | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/13 | 728/1504 | 714/1437 | 238/478 | chr19 | 47752556 | |||
chr19:47754550 | G | A | 1 | a0001c0022 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.789G>A | p.Glu263Glu | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 7/13 | 803/1504 | 789/1437 | 263/478 | chr19 | 47754550 | |||
chr19:47754607 | C | T | 1 | a0001c0019 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.846C>T | p.Pro282Pro | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 7/13 | 860/1504 | 846/1437 | 282/478 | chr19 | 47754607 | |||
chr19:47755515 | G | A | 17 | a0001c0001 a0001c0005 a0001c0006 others(14): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
synonymous_variant | LOW | c.1221G>A | p.Gly407Gly | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/13 | 1235/1504 | 1221/1437 | 407/478 | chr19 | 47755515 | |||
chr19:47755807 | G | T | 1 | a0001c0023 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.1281G>T | p.Ser427Ser | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/13 | 1295/1504 | 1281/1437 | 427/478 | chr19 | 47755807 | |||
chr19:47756530 | C | T | 1 | a0006c0011 | 4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1299C>T | p.Pro433Pro | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 11/13 | 1313/1504 | 1299/1437 | 433/478 | chr19 | 47756530 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:47757020 | C | T | 1 | a0003c0004t0003 | 4 | HG01069.hp1 HG01928.hp2 HG01993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*15C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 13/13 | 15 | chr19 | 47757020 | ||||||
chr19:47757038 | T | TA | 2 | a0001c0006t0002 a0001c0019t0002 |
8 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*39dupA | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 13/13 | 40 | INFO_REALIGN_3_PRIME | chr19 | 47757038 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:47745794 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.224+11C>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47745794 | |||||||
chr19:47745795 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.224+12G>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47745795 | |||||||
chr19:47745824 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.224+41C>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47745824 | |||||||
chr19:47745860 | CGTCGGGG | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.224+101_224+107del others(7): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 47745860 | ||||||
chr19:47745870 | C | A | 8 | a0002c0002t0001g0004 a0002c0002t0001g0013 a0002c0002t0001g0027 others(5): Show |
30 | HG01106.hp1 HG01175.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.224+87C>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47745870 | |||||||
chr19:47745880 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.224+97G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47745880 | |||||||
chr19:47745892 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.224+109G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47745892 | |||||||
chr19:47745895 | G | A | 1 | a0003c0004t0001g0065 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.224+112G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47745895 | |||||||
chr19:47746007 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.224+224G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746007 | |||||||
chr19:47746023 | A | G | 1 | a0002c0015t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.224+240A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746023 | |||||||
chr19:47746031 | T | G | 29 | a0001c0003t0001g0009 a0001c0003t0001g0011 a0001c0003t0001g0022 others(26): Show |
62 | HG00738.hp1 HG01069.hp1 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+248T>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746031 | |||||||
chr19:47746101 | T | C | 1 | a0002c0002t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.224+318T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746101 | |||||||
chr19:47746150 | GTA | G | 4 | a0001c0012t0001g0112 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG03041.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+377_224+378del others(2): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 47746150 | ||||||
chr19:47746155 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG01109.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.224+372T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746155 | |||||||
chr19:47746157 | T | C | 1 | a0001c0005t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.224+374T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746157 | |||||||
chr19:47746158 | ATATGTGT others(7): Show |
A | 1 | a0002c0002t0001g0062 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.224+377_224+390del others(14): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 47746158 | ||||||
chr19:47746191 | T | C | 1 | a0002c0002t0001g0013 | 5 | HG02071.hp1 NA18966.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+408T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746191 | |||||||
chr19:47746194 | A | G | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+411A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746194 | |||||||
chr19:47746249 | T | G | 2 | a0003c0004t0001g0067 a0003c0004t0001g0068 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.224+466T>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746249 | |||||||
chr19:47746261 | G | A | 5 | a0001c0008t0001g0030 a0001c0008t0001g0031 a0001c0008t0001g0032 others(2): Show |
8 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+478G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746261 | |||||||
chr19:47746348 | A | G | 2 | a0001c0008t0001g0032 a0001c0008t0001g0070 |
3 | HG01884.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.224+565A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746348 | |||||||
chr19:47746352 | T | C | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+569T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746352 | |||||||
chr19:47746396 | C | T | 1 | a0001c0022t0001g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.225-571C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746396 | |||||||
chr19:47746451 | C | T | 1 | a0002c0002t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.225-516C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746451 | |||||||
chr19:47746524 | C | G | 1 | a0001c0001t0001g0045 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.225-443C>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746524 | |||||||
chr19:47746525 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.225-442G>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746525 | |||||||
chr19:47746730 | T | G | 1 | a0002c0002t0001g0047 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.225-237T>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746730 | |||||||
chr19:47746850 | C | A | 1 | a0002c0002t0001g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.225-117C>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746850 | |||||||
chr19:47746946 | T | A | 5 | a0001c0006t0001g0007 a0001c0006t0002g0007 a0001c0006t0002g0084 others(2): Show |
11 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.225-21T>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 1/12 | chr19 | 47746946 | |||||||
chr19:47747063 | G | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(63): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.289+32G>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747063 | |||||||
chr19:47747065 | T | C | 1 | a0001c0005t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.289+34T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747065 | |||||||
chr19:47747157 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(63): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.289+126A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747157 | |||||||
chr19:47747323 | G | A | 3 | a0003c0004t0001g0010 a0003c0004t0001g0071 a0003c0004t0001g0072 |
9 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.289+292G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747323 | |||||||
chr19:47747363 | C | T | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.289+332C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747363 | |||||||
chr19:47747408 | CAGGCAGG others(3): Show |
C | 5 | a0001c0008t0001g0030 a0001c0008t0001g0031 a0001c0008t0001g0032 others(2): Show |
8 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+379_289+388del others(10): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747408 | ||||||
chr19:47747457 | G | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.289+426G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747457 | |||||||
chr19:47747590 | C | T | 3 | a0001c0003t0001g0022 a0001c0003t0001g0081 a0007c0013t0001g0020 |
8 | HG02145.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.289+559C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747590 | |||||||
chr19:47747695 | G | A | 1 | a0002c0002t0001g0049 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.289+664G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747695 | |||||||
chr19:47747723 | C | T | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.289+692C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747723 | |||||||
chr19:47747768 | T | C | 1 | a0001c0003t0001g0011 | 7 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+737T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747768 | |||||||
chr19:47747779 | C | CT | 3 | a0002c0002t0001g0005 a0002c0002t0001g0061 a0015c0020t0001g0005 |
11 | HG01978.hp1 HG01978.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+773dupT | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747779 | ||||||
chr19:47747779 | CT | C | 4 | a0001c0001t0001g0109 a0002c0002t0001g0016 a0002c0002t0001g0028 others(1): Show |
7 | HG00099.hp2 HG01169.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+773delT | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747779 | ||||||
chr19:47747779 | CTT | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0106 others(5): Show |
10 | HG00735.hp2 HG02738.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+772_289+773del others(2): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747779 | ||||||
chr19:47747779 | CTTT | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(62): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.289+771_289+773del others(3): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747779 | ||||||
chr19:47747779 | CTTTT | C | 16 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0088 others(13): Show |
31 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.289+770_289+773del others(4): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747779 | ||||||
chr19:47747779 | CTTTTT | C | 5 | a0001c0012t0001g0023 a0004c0007t0001g0008 a0004c0007t0001g0024 others(2): Show |
16 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.289+769_289+773del others(5): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747779 | ||||||
chr19:47747779 | CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0001g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.289+761_289+773del others(13): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47747779 | ||||||
chr19:47747785 | T | C | 2 | a0001c0003t0001g0011 a0002c0002t0001g0050 |
8 | HG01243.hp2 HG01261.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.289+754T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747785 | |||||||
chr19:47747841 | C | T | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.289+810C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747841 | |||||||
chr19:47747912 | C | T | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.289+881C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747912 | |||||||
chr19:47747941 | C | T | 5 | a0004c0007t0001g0008 a0004c0007t0001g0024 a0004c0007t0001g0086 others(2): Show |
14 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.289+910C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747941 | |||||||
chr19:47747971 | G | A | 1 | a0006c0011t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.289+940G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747971 | |||||||
chr19:47747980 | A | G | 1 | a0001c0003t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.289+949A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47747980 | |||||||
chr19:47748022 | C | T | 1 | a0014c0026t0001g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289+991C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748022 | |||||||
chr19:47748071 | C | T | 1 | a0003c0004t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.289+1040C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748071 | |||||||
chr19:47748127 | G | A | 6 | a0001c0012t0001g0023 a0004c0007t0001g0008 a0004c0007t0001g0024 others(3): Show |
17 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.289+1096G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748127 | |||||||
chr19:47748159 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.289+1128A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748159 | |||||||
chr19:47748202 | G | A | 3 | a0006c0011t0001g0113 a0006c0011t0001g0114 a0006c0011t0001g0115 |
3 | HG02056.hp2 HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.289+1171G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748202 | |||||||
chr19:47748204 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(60): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.289+1173C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748204 | |||||||
chr19:47748211 | C | T | 4 | a0001c0003t0001g0011 a0001c0003t0001g0033 a0001c0003t0001g0073 others(1): Show |
10 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+1180C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748211 | |||||||
chr19:47748217 | G | A | 1 | a0002c0002t0001g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.289+1186G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748217 | |||||||
chr19:47748222 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.289+1191G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748222 | |||||||
chr19:47748286 | C | T | 1 | a0008c0014t0001g0021 | 3 | HG02572.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.289+1255C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748286 | |||||||
chr19:47748344 | G | A | 2 | a0001c0001t0001g0014 a0001c0023t0001g0014 |
5 | HG02735.hp2 HG03239.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+1313G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748344 | |||||||
chr19:47748457 | GCTTTAAT others(24): Show |
G | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.289+1427_289+1457d others(33): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748457 | |||||||
chr19:47748504 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.289+1473A>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748504 | |||||||
chr19:47748523 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.289+1492C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748523 | |||||||
chr19:47748526 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.289+1495A>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748526 | |||||||
chr19:47748537 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0005t0001g0006 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+1506T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748537 | |||||||
chr19:47748546 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.289+1515A>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748546 | |||||||
chr19:47748616 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290-1562G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748616 | |||||||
chr19:47748619 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290-1559T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748619 | |||||||
chr19:47748628 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290-1550C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748628 | |||||||
chr19:47748629 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290-1549T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748629 | |||||||
chr19:47748633 | C | T | 1 | a0001c0008t0001g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.290-1545C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748633 | |||||||
chr19:47748668 | G | A | 4 | a0001c0008t0001g0030 a0001c0008t0001g0031 a0001c0008t0001g0032 others(1): Show |
7 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-1510G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748668 | |||||||
chr19:47748670 | G | A | 1 | a0002c0002t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.290-1508G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748670 | |||||||
chr19:47748724 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.290-1454G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748724 | |||||||
chr19:47748870 | C | T | 1 | a0002c0002t0001g0029 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.290-1308C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748870 | |||||||
chr19:47748899 | C | T | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.290-1279C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47748899 | |||||||
chr19:47749098 | T | A | 1 | a0002c0002t0001g0054 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.290-1080T>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749098 | |||||||
chr19:47749160 | C | CA | 10 | a0001c0003t0001g0076 a0001c0006t0002g0084 a0001c0022t0001g0082 others(7): Show |
13 | HG00738.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-1004dupA | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47749160 | ||||||
chr19:47749160 | C | CAA | 6 | a0001c0012t0001g0023 a0004c0007t0001g0008 a0004c0007t0001g0024 others(3): Show |
17 | HG02486.hp2 HG02615.hp1 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.290-1005_290-1004d others(4): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47749160 | ||||||
chr19:47749211 | TGAGTTGA others(4): Show |
T | 1 | a0001c0001t0001g0103 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.290-965_290-955del others(11): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47749211 | ||||||
chr19:47749229 | G | T | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-949G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749229 | |||||||
chr19:47749285 | C | T | 1 | a0003c0004t0003g0019 | 4 | HG01069.hp1 HG01928.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-893C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749285 | |||||||
chr19:47749318 | G | A | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.290-860G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749318 | |||||||
chr19:47749353 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.290-825T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749353 | |||||||
chr19:47749378 | A | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0081 |
4 | HG02630.hp2 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-800A>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749378 | |||||||
chr19:47749415 | G | C | 1 | a0001c0008t0001g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290-763G>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749415 | |||||||
chr19:47749530 | T | G | 1 | a0013c0028t0001g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.290-648T>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749530 | |||||||
chr19:47749540 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.290-638T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749540 | |||||||
chr19:47749632 | AAGAC | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.290-543_290-540del others(4): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47749632 | ||||||
chr19:47749688 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.290-490C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749688 | |||||||
chr19:47749726 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.290-452C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749726 | |||||||
chr19:47749745 | T | C | 1 | a0013c0028t0001g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.290-433T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749745 | |||||||
chr19:47749748 | CT | C | 6 | a0001c0006t0001g0007 a0001c0006t0002g0007 a0001c0006t0002g0084 others(3): Show |
12 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.290-420delT | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 47749748 | ||||||
chr19:47749758 | T | G | 5 | a0001c0006t0001g0007 a0001c0006t0002g0007 a0001c0006t0002g0084 others(2): Show |
11 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.290-420T>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749758 | |||||||
chr19:47749776 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.290-402T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749776 | |||||||
chr19:47749790 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.290-388A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749790 | |||||||
chr19:47749888 | C | T | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-290C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749888 | |||||||
chr19:47749999 | G | A | 1 | a0002c0002t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.290-179G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47749999 | |||||||
chr19:47750045 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.290-133G>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47750045 | |||||||
chr19:47750122 | G | A | 1 | a0007c0013t0001g0020 | 4 | HG02145.hp2 HG03041.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-56G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47750122 | |||||||
chr19:47750132 | A | T | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-46A>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47750132 | |||||||
chr19:47750137 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.290-41G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47750137 | |||||||
chr19:47750150 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.290-28C>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 2/12 | chr19 | 47750150 | |||||||
chr19:47750322 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.398+36A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750322 | |||||||
chr19:47750373 | G | A | 1 | a0001c0022t0001g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.398+87G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750373 | |||||||
chr19:47750410 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(46): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.398+124C>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750410 | |||||||
chr19:47750653 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.399-255C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750653 | |||||||
chr19:47750693 | C | T | 1 | a0001c0001t0001g0012 | 7 | HG00408.hp2 HG00423.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.399-215C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750693 | |||||||
chr19:47750758 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.399-150A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750758 | |||||||
chr19:47750834 | G | A | 5 | a0001c0008t0001g0030 a0001c0008t0001g0031 a0001c0008t0001g0032 others(2): Show |
8 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.399-74G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750834 | |||||||
chr19:47750857 | G | A | 1 | a0001c0022t0001g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.399-51G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 3/12 | chr19 | 47750857 | |||||||
chr19:47751135 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(74): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.598+28T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/12 | chr19 | 47751135 | |||||||
chr19:47751193 | G | A | 1 | a0001c0003t0001g0081 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598+86G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/12 | chr19 | 47751193 | |||||||
chr19:47751225 | A | C | 4 | a0004c0007t0001g0008 a0004c0007t0001g0086 a0005c0010t0001g0008 others(1): Show |
11 | HG02486.hp2 HG02622.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.598+118A>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/12 | chr19 | 47751225 | |||||||
chr19:47751287 | C | T | 4 | a0001c0003t0001g0009 a0001c0003t0001g0076 a0001c0003t0001g0078 others(1): Show |
11 | HG02055.hp2 HG02451.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.598+180C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/12 | chr19 | 47751287 | |||||||
chr19:47751450 | T | C | 5 | a0002c0002t0001g0017 a0002c0002t0001g0028 a0002c0002t0001g0053 others(2): Show |
7 | HG00099.hp2 HG01361.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-70T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/12 | chr19 | 47751450 | |||||||
chr19:47751452 | G | C | 5 | a0001c0008t0001g0030 a0001c0008t0001g0031 a0001c0008t0001g0032 others(2): Show |
8 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-68G>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 4/12 | chr19 | 47751452 | |||||||
chr19:47751635 | A | G | 1 | a0013c0028t0001g0092 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.669+45A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47751635 | |||||||
chr19:47751750 | G | T | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.669+160G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47751750 | |||||||
chr19:47751910 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.669+320T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47751910 | |||||||
chr19:47751947 | CA | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.669+367delA | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 47751947 | ||||||
chr19:47752027 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.669+437G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47752027 | |||||||
chr19:47752107 | C | CA | 7 | a0001c0003t0001g0073 a0001c0006t0001g0007 a0001c0006t0002g0007 others(4): Show |
14 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-394dupA | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 47752107 | ||||||
chr19:47752114 | AAAAAT | A | 5 | a0001c0008t0001g0030 a0001c0008t0001g0031 a0001c0008t0001g0032 others(2): Show |
8 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-386_670-382del others(5): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 47752114 | ||||||
chr19:47752159 | C | T | 1 | a0001c0001t0001g0015 | 5 | HG02698.hp1 HG03017.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-353C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47752159 | |||||||
chr19:47752258 | T | C | 14 | a0001c0003t0001g0009 a0001c0003t0001g0076 a0001c0003t0001g0078 others(11): Show |
33 | HG00738.hp1 HG01069.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.670-254T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47752258 | |||||||
chr19:47752275 | C | T | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-237C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47752275 | |||||||
chr19:47752419 | G | A | 6 | a0001c0012t0001g0023 a0004c0007t0001g0008 a0004c0007t0001g0024 others(3): Show |
17 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.670-93G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47752419 | |||||||
chr19:47752475 | C | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0107 |
3 | HG02738.hp2 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.670-37C>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 5/12 | chr19 | 47752475 | |||||||
chr19:47752731 | G | T | 5 | a0001c0006t0001g0007 a0001c0006t0002g0007 a0001c0006t0002g0084 others(2): Show |
11 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.765+124G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47752731 | |||||||
chr19:47752737 | C | T | 1 | a0001c0003t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.765+130C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47752737 | |||||||
chr19:47752873 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG01106.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.765+266A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47752873 | |||||||
chr19:47752940 | A | G | 5 | a0001c0006t0001g0007 a0001c0006t0002g0007 a0001c0006t0002g0084 others(2): Show |
11 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.765+333A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47752940 | |||||||
chr19:47752990 | G | T | 1 | a0002c0002t0001g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.765+383G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47752990 | |||||||
chr19:47753029 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.765+422G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753029 | |||||||
chr19:47753071 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0005t0001g0006 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.765+464G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753071 | |||||||
chr19:47753121 | G | A | 1 | a0001c0003t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.765+514G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753121 | |||||||
chr19:47753165 | C | T | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+558C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753165 | |||||||
chr19:47753171 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(52): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.765+564C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753171 | |||||||
chr19:47753198 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(47): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.765+591C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753198 | |||||||
chr19:47753322 | G | C | 2 | a0002c0002t0001g0058 a0002c0002t0001g0061 |
2 | HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.765+715G>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753322 | |||||||
chr19:47753528 | AC | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.765+923delC | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 47753528 | ||||||
chr19:47753538 | C | T | 1 | a0002c0002t0001g0043 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.765+931C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753538 | |||||||
chr19:47753676 | C | T | 3 | a0001c0003t0001g0011 a0001c0003t0001g0033 a0001c0027t0001g0033 |
9 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.766-851C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753676 | |||||||
chr19:47753725 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.766-802A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753725 | |||||||
chr19:47753869 | C | T | 3 | a0001c0003t0001g0022 a0001c0003t0001g0081 a0007c0013t0001g0020 |
8 | HG02145.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-658C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47753869 | |||||||
chr19:47754148 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.766-379A>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754148 | |||||||
chr19:47754154 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.766-373G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754154 | |||||||
chr19:47754183 | A | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(46): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.766-344A>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754183 | |||||||
chr19:47754208 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-319C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754208 | |||||||
chr19:47754221 | G | A | 1 | a0002c0002t0001g0029 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766-306G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754221 | |||||||
chr19:47754261 | G | A | 1 | a0001c0003t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.766-266G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754261 | |||||||
chr19:47754264 | A | T | 6 | a0001c0012t0001g0023 a0004c0007t0001g0008 a0004c0007t0001g0024 others(3): Show |
17 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.766-263A>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754264 | |||||||
chr19:47754384 | G | T | 1 | a0001c0003t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.766-143G>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754384 | |||||||
chr19:47754386 | T | C | 1 | a0001c0003t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.766-141T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754386 | |||||||
chr19:47754434 | G | A | 5 | a0001c0008t0001g0030 a0001c0008t0001g0031 a0001c0008t0001g0032 others(2): Show |
8 | HG01884.hp1 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-93G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 6/12 | chr19 | 47754434 | |||||||
chr19:47754656 | C | T | 4 | a0001c0003t0001g0011 a0001c0003t0001g0033 a0001c0003t0001g0073 others(1): Show |
10 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.870+25C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 7/12 | chr19 | 47754656 | |||||||
chr19:47754690 | C | T | 23 | a0001c0003t0001g0009 a0001c0003t0001g0011 a0001c0003t0001g0022 others(20): Show |
53 | HG00738.hp1 HG01069.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.871-19C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 7/12 | chr19 | 47754690 | |||||||
chr19:47754898 | G | A | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | splice_region_variant&intron_variant | LOW | c.1053+7G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47754898 | |||||||
chr19:47754899 | C | T | 1 | a0001c0008t0001g0030 | 2 | HG02622.hp2 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.1053+8C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47754899 | |||||||
chr19:47754911 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1053+20G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47754911 | |||||||
chr19:47754986 | G | A | 1 | a0001c0006t0002g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1053+95G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47754986 | |||||||
chr19:47755050 | C | T | 3 | a0001c0003t0001g0011 a0001c0003t0001g0033 a0001c0027t0001g0033 |
9 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1053+159C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47755050 | |||||||
chr19:47755123 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(57): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1054-225G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47755123 | |||||||
chr19:47755273 | G | A | 1 | a0006c0011t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1054-75G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47755273 | |||||||
chr19:47755294 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1054-54T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47755294 | |||||||
chr19:47755314 | C | T | 1 | a0001c0003t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1054-34C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47755314 | |||||||
chr19:47755321 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1054-27A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 8/12 | chr19 | 47755321 | |||||||
chr19:47755526 | G | A | 1 | a0001c0012t0001g0023 | 3 | HG03195.hp1 HG03209.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.1229+3G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/12 | chr19 | 47755526 | |||||||
chr19:47755555 | C | G | 1 | a0006c0011t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1229+32C>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/12 | chr19 | 47755555 | |||||||
chr19:47755569 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(92): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1229+46G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/12 | chr19 | 47755569 | |||||||
chr19:47755649 | A | G | 1 | a0003c0004t0001g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1230-107A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/12 | chr19 | 47755649 | |||||||
chr19:47755741 | C | T | 1 | a0001c0003t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1230-15C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/12 | chr19 | 47755741 | |||||||
chr19:47755744 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1230-12C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 9/12 | chr19 | 47755744 | |||||||
chr19:47755943 | A | G | 4 | a0006c0011t0001g0111 a0006c0011t0001g0113 a0006c0011t0001g0114 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+121A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47755943 | |||||||
chr19:47755949 | A | G | 1 | a0001c0001t0001g0026 | 3 | NA18964.hp2 NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1296+127A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47755949 | |||||||
chr19:47755963 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0036 others(6): Show |
39 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1296+141C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47755963 | |||||||
chr19:47756015 | C | T | 16 | a0001c0003t0001g0009 a0001c0003t0001g0076 a0001c0003t0001g0078 others(13): Show |
35 | HG00738.hp1 HG01069.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1296+193C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756015 | |||||||
chr19:47756021 | C | T | 4 | a0004c0007t0001g0008 a0004c0007t0001g0086 a0005c0010t0001g0008 others(1): Show |
11 | HG02486.hp2 HG02622.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1296+199C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756021 | |||||||
chr19:47756089 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1296+267T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756089 | |||||||
chr19:47756145 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0039 |
4 | NA18942.hp1 NA18955.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+323C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756145 | |||||||
chr19:47756174 | C | G | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1296+352C>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756174 | |||||||
chr19:47756195 | C | T | 1 | a0001c0012t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1297-333C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756195 | |||||||
chr19:47756221 | T | C | 38 | a0001c0003t0001g0009 a0001c0003t0001g0011 a0001c0003t0001g0022 others(35): Show |
77 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.1297-307T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756221 | |||||||
chr19:47756249 | C | T | 3 | a0001c0003t0001g0022 a0001c0003t0001g0081 a0007c0013t0001g0020 |
8 | HG02145.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1297-279C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756249 | |||||||
chr19:47756377 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1297-151C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756377 | |||||||
chr19:47756410 | C | T | 1 | a0002c0002t0001g0042 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1297-118C>T | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756410 | |||||||
chr19:47756431 | G | A | 1 | a0003c0004t0001g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1297-97G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 10/12 | chr19 | 47756431 | |||||||
chr19:47756822 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1430+78T>C | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 12/12 | chr19 | 47756822 | |||||||
chr19:47756850 | ACC | A | 4 | a0003c0004t0001g0018 a0003c0004t0001g0065 a0003c0004t0001g0074 others(1): Show |
7 | HG00738.hp1 HG02145.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1430+110_1430+111d others(4): Show |
NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 47756850 | ||||||
chr19:47756893 | G | A | 6 | a0001c0012t0001g0023 a0004c0007t0001g0008 a0004c0007t0001g0024 others(3): Show |
17 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1431-106G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 12/12 | chr19 | 47756893 | |||||||
chr19:47756920 | G | A | 6 | a0001c0012t0001g0023 a0004c0007t0001g0008 a0004c0007t0001g0024 others(3): Show |
17 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1431-79G>A | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 12/12 | chr19 | 47756920 | |||||||
chr19:47756921 | A | G | 1 | a0001c0012t0001g0023 | 3 | HG03195.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1431-78A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 12/12 | chr19 | 47756921 | |||||||
chr19:47756977 | A | G | 1 | a0001c0003t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1431-22A>G | NOP53 | ENSG00000105373.19 | transcript | ENST00000246802.10 | protein_coding | 12/12 | chr19 | 47756977 |